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2019 update of the WSES guidelines for management of Clostridioides (Clostridium) difficile infection in surgical patients
World Journal of Emergency Surgery volume 14, Article number: 8 (2019)
In the last three decades, Clostridium difficile infection (CDI) has increased in incidence and severity in many countries worldwide. The increase in CDI incidence has been particularly apparent among surgical patients. Therefore, prevention of CDI and optimization of management in the surgical patient are paramount. An international multidisciplinary panel of experts from the World Society of Emergency Surgery (WSES) updated its guidelines for management of CDI in surgical patients according to the most recent available literature. The update includes recent changes introduced in the management of this infection.
In the last three decades, the dramatic worldwide increase in incidence and severity of Clostridium difficile infection (CDI)  has made CDI a global public health challenge [2,3,4,5,6,7,8,9,10,11,12,13,14]. Surgery is a known risk factor for development of CDI yet surgery is also a treatment option in severe cases of CDI [15,16,17,18]. The World Society of Emergency Surgery (WSES) guidelines for management of CDI in surgical patients were published in 2015 . In 2019, the guidelines have been revised and updated. A multidisciplinary expert panel worldwide prepared the manuscript following an in-depth review of the most recent current literature using MEDLINE, EMBASE, and Cochrane Database and aimed to provide an insight into these complex issues. The expert panel met via email to prepare, discuss, and revise the paper. The manuscript was successively reviewed by all members and ultimately re-formulated as the present manuscript.
These guidelines outline clinical recommendations based on the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) hierarchy criteria from Guyatt et al. [20, 21] (Table 1).
Clostridioides difficile (formerly Clostridium difficile) is an anaerobic, spore-forming, Gram-positive bacillus, which may be part of the normal intestinal microbiota in healthy babies [22,23,24,25]. The organism is spread via the oral-fecal route and in hospitalized patients may be acquired through the ingestion of spores from other patients, healthcare personnel’s hands, or from environmental surfaces [26, 27]. C. difficile is the main pathogen associated with nosocomial infections and is the most common cause of diarrhea in hospitalized patients . CDI can present as a spectrum of symptoms ranging from an asymptomatic carriage to fulminant disease with toxic megacolon. The basis for this range of clinical manifestations is not fully understood but is likely related to host and pathogen interactions.
The rapid evolution of antibiotic resistance in C. difficile and the consequent effects on prevention and treatment of CDIs are a matter of concern for public health. Multi-drug resistant (MDR) C. difficile strains are increasing (about 60% of the epidemic strains circulating in hospital settings show resistance to three or more antibiotics) .
C. difficile spores survive the acidic environment of the stomach and germinate in the intestine , which act as a reservoir for C. difficile and can facilitate spread among patients, as well as contribute to the high recurrence rates observed in CDI. The primary toxins produced by this bacterium are toxins A and B . Toxins A and B act as glucosyltransferases, promoting the activation of Rho GTPases leading to disorganization of the cytoskeleton of the colonocyte, and eventual cell death . Since CDI is a toxin-mediated infection, non-toxigenic C. difficile strains are non-pathogenic. The respective roles and importance of toxins A and B have been debated. Toxin A was thought to be the major virulence factor for many years [33,34,35]. It is now established that both toxins A and B are important for inducing colonocyte death and colitis, and there is increasing evidence pointing toward their role in CDI extra-intestinal effects . In addition to toxins A and B, some strains produce a third toxin known as binary toxin [37,38,39,40,41]. Binary toxin has an ADP-ribosyltransferase function, which also leads to actin depolymerization [42, 43]. However, its pathogenetic role is still debated [44, 45].
Asymptomatic C. difficile colonization occurs when C. difficile is detected in the absence of symptoms of infection. Asymptomatic colonized individuals with no clinical signs of CDI can still act as an infection reservoir and transmit C. difficile to others [46, 47]. Asymptomatic colonization with C. difficile may be a crucial factor in the progression to CDI, as carriers of toxigenic strains may be at a higher risk for the development of an infection compared to non-colonized patients . Other data suggests that carriage of non-toxigenic C. difficile may be protective against toxigenic ribotypes . Estimates of prevalence of asymptomatic C. difficile colonization vary considerably between different patient groups. Among healthy adults with no prior risk factors for CDI, asymptomatic colonization prevalence varied between 0 and 15% [50,51,52,53,54,55,56].
Risk factors for CDI may be divided into three general categories: host factors (immune status, comorbidities), exposure to C. difficile spores (hospitalizations, community sources, long-term care facilities), and factors that disrupt normal colonic microbiome (antibiotics, other medications, surgery) .
Risk factors identified to date include age > 65 years, comorbidity or underlying conditions, inflammatory bowel diseases, immunodeficiency (including human immunodeficiency virus infection), malnutrition, obesity, female sex, and low serum albumin level [3, 58]. Patients with comorbidities may have distinct characteristics of their CDI, for example, in type 2 diabetes mellitus, patients with CDI were younger, and sepsis and proton pump inhibitors (PPIs) were important causes, but fever was not a dominant feature .
The effects of prior appendectomy on the development of C. difficile colitis have been debated . A review by Seretis et al.  of five studies conducted retrospectively and published in 2014 reported that an in situ appendix did not impact on the development of CDI. In the retrospective analysis by Clanton et al.  on 55 patients who underwent colectomy for CDI between 2001 and 2011, a prior appendectomy was noted in 24 of 55 patients (44%, 99% CI 0.280–0.606). In another retrospective study of 507 patients , 13 of 119 patients (10.9%) with a previous appendectomy required colectomy compared to 20 of 388 patients (5.2%) with an intact appendix developing fulminant infection and requiring colectomy and increased disease severity, indicated by increased rates of colectomy, occurred in the group with a history of appendectomy (p = 0.03). A sub-group analysis of a large population-based study published in 2013  showed that appendectomy was not associated with adverse outcomes in CDI. Patients with appendectomy before CDI showed no differences in risk factors, treatment, or outcomes including treatment failure, development of severe or severe-complicated CDI, or recurrence rates as compared with patients without appendectomy. Larger prospective studies are needed to assess the impact of prior appendectomy on the development and severity of CDI.
Exposure to Clostridium difficile spores
Factors that increase risk of exposure to C. difficile spores, such as increased duration of hospital stay, increase the risk of CDI. A length of stay > 2 weeks has been shown to be a risk factor for CDI . Hospitals with well-implemented infection prevention and control measures are at lower risk of nosocomial CDI .
Normal flora disruption
The indigenous gut microbiota is a complex community of microorganisms that populates the gastrointestinal tract in a healthy person. This micro-ecosystem plays a crucial role in protecting the intestines by providing resistance to colonization and infection by pathogenic organisms . Gut microbiota has also immeasurable effects on homeostasis of the host . Under normal conditions, the human gut microbiota may impede pathogen colonization through general mechanisms such as direct inhibition through bacteriocins, nutrient depletion (consuming growth-limiting nutrients), or stimulation of host immune defenses , though the exact mechanism by which the microbiota protects against CDI is unknown . Disruption of the normal balance of colonic microbiota as a consequence of antibiotic use or other stressors is, however, of major importance .
Disruption of the normal gut flora allows C. difficile to proliferate and produce toxins. In 1974, Tedesco et al. published a prospective study of clindamycin-associated colitis, which had become endemic in many hospitals . In 200 consecutive patients, administration of clindamycin resulted in diarrhea in 21% and the incidence of endoscopy-diagnosed pseudomembranous colitis was 10%. The study led to a search for an infectious cause of colitis, and it identified C. difficile as the main causative agent .
The risk of CDI is increased up to sixfold during antibiotic therapy and in the subsequent month afterwards . Although nearly all antibiotics have been associated with CDI, clindamycin, third-generation cephalosporins, penicillins, and fluoroquinolones have traditionally been considered to pose the greatest risk [74,75,76,77,78,79,80]. An association between CDI and antimicrobial treatment > 10 days has also been demonstrated [81, 82]. Antibiotics which have been less commonly associated with CDI include macrolides, sulfonamides, and tetracyclines . Even very limited exposure, such as single-dose surgical antibiotic prophylaxis, can increase patients risk for both C. difficile colonization or infection [84,85,86].
Exposure to gastric acid-suppressive medications, such as histamine-2 blockers and PPIs, may be a potential risk factor for development of CDI. Several studies have suggested the association between use of stomach acid-suppressive medications, primarily PPIs, and CDI [87, 88]. In 2012, a systematic review of incident and recurrent CDI in PPI users was published . Forty-two observational studies (30 case-control, 12 cohort) totaling 313,000 participants were evaluated. Despite the substantial statistical and clinical heterogeneity, the findings indicated a probable association between PPI use and incident and recurrent CDI. This risk was further increased by concomitant use of antibiotics and PPI. Other studies suggested that this association may be the result of confounding with the underlying severity of illness and duration of hospital stay . Another meta-analysis about a plausible link between CDI and PPIs was recently published . Pooled analysis of 50 studies showed a significant association between PPI use and risk of developing CDI (odds ratio [OR] = 1.26, 95% confidence interval (CI), 1.12–1.39) as compared with non-users.
Even when compared to other gastric acid-suppressive medication, a recent meta-analysis showed that the use of PPI increased the risk of hospital-acquired CDI (OR = 1.386, 95% CI 1.152–1.668) when compared to H2-antagonist .
Given that PPIs are overprescribed in surgical settings, consideration should be given to stop PPIs, when they are not necessary, especially in patients at high risk of CDI.
The risk of poor clinical outcomes of CDI in patients with nasogastric tube (NGT) insertion is still controversial. In order to assess the outcomes of CDI in patients with NGT insertion, a systematic review and meta-analysis was recently published .
Eight observational studies were included in the analysis to assess the association between NGT insertion and risk of poor outcome of CDI. The pooled relative risk (RR) of severe or complicated clinical outcomes of CDI in patients with NGT insertion was 1.81 (95% CI 1.17–2.81).
This study demonstrated a statistically significant association between NGT insertion and risk of poor outcomes of CDI. This finding may impact clinical management and primary prevention of CDI. Avoidance of unnecessary NGT uses would improve the clinical outcomes of CDI.
Reports have linked the development of CDI in surgical patients to the widespread use of broad-spectrum antibiotics, and the increasing number of elderly and immunocompromised patients undergoing surgical interventions [17, 94, 95].
Abdelsattar et al.  prospectively identified postoperative patients with laboratory-confirmed CDI following general, vascular, or gynecological surgeries at 52 academic and community hospitals in the state of Michigan, USA between July 2012 and September 2013. The highest rates of CDI occurred after lower-extremity amputation (2.6%), followed by bowel resection or repair (0.9%) and gastric or esophageal surgeries (0.7%). Gynecological and endocrine surgeries had the lowest rates of CDI (0.1% and 0%, respectively). Multivariate analysis identified increasing age, chronic immunosuppression, hypoalbuminemia (≤ 3.5 g/dL), and preoperative sepsis to be associated with postoperative CDI.
Zerey et al.  performed a 5-year retrospective analysis of the Agency for Healthcare Research and Quality’s National Inpatient Sample Database representing a stratified 20% sample of hospitals in the United States, from 1999 to 2003. Emergency surgery was at higher risk of CDI than elective surgery. Colectomy, small-bowel resection, and gastric resection were associated with the highest risk of CDI. Patients undergoing cholecystectomy and appendectomy had the lowest risk.
In 2010, Rodriguez et al.  published a retrospective analysis of all general surgery in patients admitted to a large tertiary referral general surgical unit in the UK, between March 2005 and May 2007. Multivariate analysis identified malignancy, gastrointestinal disease, anemia, respiratory disease, cardiovascular disease, diabetes mellitus, gastrointestinal surgery, and age as independently associated with C. difficile.
To assess risk factors for CDI on a surgical ward, in 2012 Kim et al. conducted a retrospective chart review of all patients admitted between January 2010 and July 2011 . The rate of CDI was 0.4% (19/4720 patients). Multivariate analysis showed that colectomy and hospital stays > 10 days were the main risk factors for CDI in the surgical ward.
Using the Japanese Diagnosis Procedure Combination inpatient database, Yasunaga et al.  analyzed factors associated with CDI incidence and outcomes following digestive tract surgery. Of 143,652 patients undergoing digestive tract surgery, CDI was identified in 409 (0.28%) patients. High mortality, long hospital stay, and high costs were associated with post-surgical CDI.
Colorectal surgery is a documented risk factor for CDI [99, 100]. Damle et al.  published a retrospective analysis of patients who developed CDI following colorectal resection. The authors identified adult patients undergoing colorectal surgery between 2008 and 2012 from the US University Health System Consortium database. A total of 84,648 patients met study inclusion criteria. CDI occurred in 1266 (1.5%) patients. The strongest predictors of CDI were emergency procedure, inflammatory bowel disease, and severity of illness score. CDI was associated with a higher rate of complications, intensive care unit (ICU) admission, longer preoperative inpatient stay, 30-day readmission rate, and death within 30 days compared to non-CDI patients.
Recently, a retrospective colectomy database review of the 2015 American College of Surgeons National Surgical Quality Improvement Project  demonstrated that stoma reversal (OR = 2.701, 95% CI 1.966–3.711; p < 0.001), smoking (OR = 1.520, 95% CI 1.063–2.174; p = 0.022), steroids (OR = 1.677, 95% CI 1.005–2.779; p = 0.048), and disseminated cancer (OR = 2.312, 95% CI 1.437–3.719; p = 0.001) were associated with CDI in the 30-day postoperative period.
In 2008, Lumpkins et al. published a retrospective observational study on the incidence of CDI in the critically injured trauma population . Five hundred eighty-one consecutive critically injured trauma patients were followed prospectively for development of CDI, diagnosed by toxin assay. Among 581 patients, 19 cases of CDI were diagnosed (3.3%). ICU length of stay, duration of mechanical ventilation, and hospital length of stay were associated with CDI. The diagnosis was documented with a median delay of 17 days after admission. Fourteen patients (74%) had received antibiotics for confirmed or suspected infection prior to CDI; 4 patients (21%) received only intraoperative prophylaxis, and 1 patient had no antibiotic exposure.
Obesity and bariatric surgery
Obesity as a risk factor for CDI has been debated. Several reports have recently proposed obesity as a novel risk factor for CDI [104,105,106]. On the other hand, Punni et al. , in a case-control study, showed that obesity is not a risk factor for CDI. Importantly, body mass > 35 index has been shown to be an independent risk factor for CDI .
To investigate the impact of the two most common bariatric surgeries on CDI, Roux-en-Y gastric bypass (RYGB), and vertical sleeve gastrectomy (VSG), a retrospective cohort study was recently published . CDI rates were higher after RYGB than VSG in the first 30 days (OR = 2.10; 95% CI, 1.05–4.20) with a similar but not significant trend within 31–120 days.
Knowledge about the link between obesity, bariatric surgery, and CDI is still evolving. Further studies are needed to reveal the exact mechanisms underlying this association. At this stage, we suggest high suspicion for CDI when managing patients with obesity and undergoing bariatric surgery.
Inflammatory bowel disease
Patients with inflammatory bowel disease (IBD) retain an increased risk of developing CDI, along with worse outcomes, higher rates of colectomy, and higher rates of recurrence [110,111,112,113,114,115].
Patients with IBD also appear to have higher rates of asymptomatic carriage of C. difficile . These patients commonly receive various types of immunosuppressive drugs including steroids which have been found to increase the risk of CDI. In addition, they have a different microbiota compared to healthy subjects [117, 118].
A recent retrospective study evaluated the impact of CDI on in-hospital outcomes among adults with IBD hospitalized in the USA . Using the 2007–2013 Nationwide Inpatient Sample, hospitalizations among US adults with Crohn’s disease (CD), ulcerative colitis (UC), and CDI were identified using ICD-9 coding. Hospital charges, hospital length of stay (LOS), and in-hospital mortality was stratified by CD and UC and compared. Predictors of hospital charges, LOS, and in-hospital mortality were evaluated with multivariate regression models and were adjusted for age, sex, race/ethnicity, year, insurance status, hospital characteristics, and CDI. Among 224,500 IBD hospitalizations (174,629 CD and 49,871 UC), overall prevalence of CDI was 1.22% in CD and 3.41% in UC. On multivariate linear regression, CDI was associated with longer LOS among CD (coefficient: 5.30, 95% CI 4.61–5.99; p < 0.001) and UC (coefficient 4.08, 95% CI 3.54–4.62; p < 0.001). Higher hospital charges associated with CDI were seen among CD (coefficient $35,720, 95% CI $30,041–$41,399; p < 0.001) and UC (coefficient $26,009, 95% CI $20,970–$31,046; p < 0.001). CDI among IBD was associated with almost threefold greater risk of in-hospital mortality.
The clinical presentation of an IBD exacerbation and CDI often is indistinguishable and requires a high index of suspicion for adequate treatment . As the symptoms of CDI and an exacerbation of IBD (diarrhea, abdominal pain, fever, and leukocytosis) overlap, the diagnosis of CDI may be delayed . In addition, in IBD patients with ileostomies, the development of acute enteritis manifested as an increase in ileostomy output, nausea, fever, and leukocytosis may also indicate CDI. The same is true for pouchitis, which presents as an increase in the number of stools per day . In one study, 10.7% of patients with ileal pouch anal anastomosis, presenting with pouchitis, were found to have CDI .
Due to high rates of asymptomatic colonization by C. difficile in patients with IBD, only patients with increased diarrhea or new symptoms potentially due to CDI should be tested for C. difficile toxin. Typical findings of CDI on colonoscopy are often absent in patients with IBD (0–13% of cases)  which may be attributed to a weakened inflammatory response. There is no evidence that one antibiotic regimen is better than another for the treatment of CDI in IBD patients. In a survey of North American gastroenterologists, there was no agreement on combination of antibiotics and immunomodulators in patients with an IBD flare and CDI . The American College of Gastroenterology recommended with low-quality supporting evidence, that ongoing immunosuppression can be maintained in patients with CDI and that escalation of immunosuppression should be avoided .
An expert review to synthesize the existing evidence on the management of CDI in patients with underlying inflammatory bowel disease was published in 2017. The review suggested six simple advices of best practice .
Physicians should remain alert to the possibility of CDI in a patient with an IBD exacerbation to ensure rapid diagnosis and treatment. Early surgical consultation is also key for improving outcomes of patients with severe disease. Colectomy with preservation of the rectum may need to be considered for severely ill IBD patients with CDI.
The rate of CDI is increased in solid organ transplant recipients due to ongoing immunosuppression and antibiotic use .
It has also been reported that cancer patients have a higher risk compared with non-cancer patients  due to chemotherapy causing immunosuppression [129, 130].
Patients with HIV/AIDS are also at high risks of being infected with C. difficile too. The risk is stronger in those with low absolute CD4 T cell counts or those who meet clinical criteria for AIDS .
The increased risk may be partially attributed to frequent hospitalization, exposure to antibiotics, and antibiotic prophylaxis for opportunistic infections, but HIV-related alterations in fecal microbiota, gut mucosal integrity, and humoral and cell-mediated immunity may also likely play a role .
Risk factors for community-acquired C. difficile infection
Although predominantly associated with the inpatient health care population, CDI originating in the community has been increasingly reported. The predominant C. difficile ribotypes isolated in the hospital setting correspond with those isolated in the community, suggesting that transmission between these two settings is occurring .
In 2011, an estimated 159,000 community-associated CDI (CA-CDI) occurred in the USA, representing 35% of the total CDI burden .
Risk factors may include increasing outpatient antibiotic prescriptions, acid-suppression medications, asymptomatic carriers in the community, and food or water contamination . A sub-group analysis of a population-based epidemiological study of CDI in Olmsted County, Minnesota in 1991–2005 , identified 157 CA-CDI cases (75% women), with a median age of 50 years. Among them, 40% required hospitalization, 20% had severe, and 4.4% severe-complicated infection, while 20% had treatment failure and 28% had recurrent CDI.
A case-control study from ten US sites from October 2014 to March 2015 analyzed risk factors for CA-CDI . Case patients were defined as persons aged ≥ 18 years with a positive C. difficile specimen collected as an outpatient or within 3 days of hospitalization who had no admission to a health care facility in the prior 12 weeks and no prior CDI diagnosis. Each case patient was matched to one control (persons without CDI). Participants were interviewed about relevant exposures; multivariate conditional logistic regression was performed. More case patients than controls had prior outpatient health care (82.1% vs. 57.9%; p < 0.0001) and antibiotic (62.2% vs. 10.3%; p < 0.0001) exposures. In multivariate analysis, antibiotic exposure—that is, cephalosporin (adjusted matched odds ratio [AmOR], 19.02; 95% CI 1.13–321.39), clindamycin (AmOR, 35.31; 95% CI 4.01–311.14), fluoroquinolone (AmOR, 30.71; 95% CI 2.77–340.05), and beta-lactam and/or beta-lactamase inhibitor combination (AmOR, 9.87; 95% CI 2.76–340.05)—emergency department visit (AmOR, 17.37; 95% CI 1.99–151.22), white race (AmOR 7.67; 95% CI 2.34–25.20), cardiac disease (AmOR, 4.87; 95% CI 1.20–19.80), chronic kidney disease (AmOR, 12.12; 95% CI 1.24–118.89), and IBD (AmOR, 5.13; 95% CI 1.27–20.79) were associated with CA-CDI.
A systematic review and meta-analysis investigated the association between medications and comorbidities with CA-CDI . Twelve publications (n = 56,776 patients) met inclusion criteria. Antimicrobial (OR = 6.18, 95% CI 3.80–10.04) and corticosteroid (OR = 1.81, 95% CI 1.15–2.84) exposure were associated with increased risk of CA-CDI. Among the comorbidities, IBD (OR = 3.72, 95% CI 1.52–9.12), renal failure (OR = 2.64; 95% CI 1.23–5.68), hematologic malignancy (OR = 1.75; 95% CI 1.02–5.68), and diabetes mellitus (OR = 1.15; 95% CI 1.05–1.27) were associated with CA-CDI. Antimicrobial exposure was associated with a higher risk of CA-CDI in the USA, whereas PPI exposure was associated with a higher risk in Europe. The risk of CA-CDI associated with antimicrobial exposure greatly increased in adults older than 65 years.
Risk factors for recurrent CDI
Recurrent CDI (RCDI) can be defined as reappearance of symptoms within eight weeks following the completion of a course of therapy with complete resolution of symptoms.
The key to preventing recurrent infection is identifying those patients at the greatest risk .
In a meta-analysis, Garey et al.  found that continued use of non-C. difficile antibiotics after diagnosis of CDI (OR = 4.23; 95% CI 2.10–8.55; p < 0.001), concomitant receipt of antacid medications (OR = 2.15; 95% CI 1.13–4.08; p = 0.019), and older age (OR = 1.62; 95% CI 1.11–2.36; p = 0.0012) were associated with increased risk of recurrent CDI. Other factors identified in individual studies include age, hospital exposure, comorbid conditions, severe underlying illness, hypoalbuminemia, impaired humoral immunity, poor quality of life, disease severity, and previous recurrent CDI [141,142,143,144].
In order to evaluate current evidence of risk factors for recurrent CDI, a systematic review and meta-analysis  analyzed 33 studies (18,530 patients). The most frequent independent risk factors for recurrent CDI were age ≥ 65 years (RR = 1.63, 95% CI 1.24–2.14; p = 0.0005), additional antibiotics during follow-up (RR = 1.76; 95% CI 1.52–2.05; p < 0.001), use of PPIs (RR = 1.58; 95% CI 1.13–2.21; p = 0.008), and renal failure (RR = 1.59; 95% CI 1.14–2.23; p = 0.007). The risk was also increased in patients previously on fluoroquinolones (RR = 1.42; 95% CI 1.28–1.57; p < 0.001).
The spectrum of symptomatic CDI ranges from mild diarrhea to severe disease or fulminant colitis and as many as 30% of patients may develop recurrent CDI [146, 147].
Though diarrhea is the hallmark symptom of CDI, it may not be present initially, possibly due to colonic dysmotility either from previous underlying conditions or possibly from the disease process itself .
This is especially important in surgical patients who may have a concomitant ileus. Therefore, in surgical patients, it is important to have a high index of suspicion for the development of CDI.
Diarrhea may be accompanied by mild abdominal pain and cramps and if prolonged may result in altered electrolyte balance and dehydration. When this occurs in patients with severe comorbidity, particularly after surgery, non-severe CDI may increase morbidity significantly .
Severe CDI is associated with increased abdominal cramping and pain as well as systemic features such as fever, leukocytosis, and hypoalbuminemia. The absence of diarrhea may signal a progression to fulminant infection . Though a wide variety of severity predictors for severe CDI has been described [151,152,153,154,155,156], international consensus for the definition of severe CDI is lacking [6, 7].
A systematic review identifying risk factors for adverse outcomes of CDI was published by Abou Chakra et al. in 2012 . Except for leukocytosis, albumin, and age, there was much heterogeneity in the data and most studies were limited by small sample sizes.
To investigate the prognostic value of fever, leukocytosis, and renal failure, in 2012 Bauer et al.  analyzed the database of two randomized controlled trials, which contained information on 1105 patients with CDI. They found that both leucocytosis and renal failure were useful predictors of in severe CDI. Miller et al.  in 2013 subsequently published an analysis of the same two clinical therapeutic trials to validate a categorization system to stratify CDI patients into severe or mild-moderate groups. A combination of five simple and commonly available clinical and laboratory variables (ATLAS) measured at the time of CDI diagnosis were able to accurately predict treatment response to CDI therapy. The ATLAS criteria included age, treatment with systemic antibiotics, leucocyte count, serum albumin, and serum creatinine levels.
Any of the following may be predictors of severe CDI:
WBC > 15 × 109/L
Rise in serum creatinine level (≥ 133 μM/L or ≥ 1.5 times premorbid level)
Temperature > 38.5 °C
Albumin < 2.5 g/dL
It has been recently demonstrated that human serum albumin is capable to bind C. difficile toxin A and B thus impairing their internalization into host cells; this could partially explain the increased CDI severity experienced by hypoalbuminemic patients .
The progression to fulminant C. difficile colitis is relatively infrequent  (1–3% of all CDI) though mortality in this group of patients remains high due to the development of toxic megacolon with colonic perforation, peritonitis, and septic shock and subsequent organ dysfunction. Systemic symptoms may not merely result from toxin-induced inflammatory mediators released locally in the colon but likely to the toxins spread into the bloodstream [36, 159, 160].
Studies have demonstrated a significant rise in the number of cases of fulminant colitis associated with multiple organ failure and increased mortality in recent years associated with the hypervirulent 027 strain of C. difficile [161, 162]. Early diagnosis and treatment is therefore important in reducing the mortality associated with fulminant colitis. Patients who present organ failure including increased serum lactate or vasopressor requirements should be assessed immediately with regard to early operative intervention .
Recurrence of symptoms after initial therapy for C. difficile develops in 10–30% of cases, and presents a clinical challenge [144, 163,164,165,166,167]. For a patient with 1–2 previous episodes, the risk of further recurrences is 40–65%.
Recurrences are associated with an impaired immune response to C. difficile toxins and/or alteration of the colonic microbiota.
RCDI may be either a consequence of germinating resident spores remaining in the colon after antibiotic treatment has stopped, or re-infection from an environmental source.
Even though consensus regarding factors associated with CDI recurrence is not universal, algorithms have been developed to predict CDI recurrence with good sensitivity .
Ultimately, distinction between recurrence and reinfection can only be achieved if the strain of C. difficile is “typed” using molecular epidemiology .
Recurrent episodes are less severe compared to initial episodes: in a Canadian study, the authors reported a decline in the proportion of severe cases according to the number of recurrent episodes (47% for initial episodes, 31% for first recurrences, 25% for second, and 17% for third) .
Additional significant consequences of CDI
Patients who develop CDI have increased hospital length-of-stay, higher medical care costs, more hospital re-admissions, and higher mortality [171,172,173]. These consequences are also found in surgical patients with CDI.
In the Zerey et al. analysis , CDI was an independent predictor of increased length of stay, which increased by 16.0 days (95% CI 15.6–16.4 days; p < 0.0001). Total charges increased by $77,483 (95% CI $75,174, $79,793; p < 0.0001), and there was a 3.4-fold increase in the mortality rate (95% CI 3.02–3.77; p < 0.0001) compared with patients who without C. difficile infection.
In the Abdelsattar et al. study , postoperative CDI was independently associated with increased length of stay (mean, 13.7 days vs. 4.5 days), emergency department presentations (18.9 vs. 9.1%), and readmissions (38.9% vs. 7.2%, all p < 0.001).
Data from Nationwide Inpatient Sample database in 2011 of patients who underwent vascular surgery  showed that in patients who had experienced CDI, the median length of stay was 15 days (IQR 9, 25 days) compared to 8.3 days for matched patients without CDI, in-hospital mortality 9.1% (compared to 5.0%), and $13,471 extra cost per hospitalization. The estimated cost associated with CDI in vascular surgery in the USA was about $98 million in 2011. Similarly, data from the National Inpatient Sample in patients undergoing lumbar surgery found that CDI increased length of stay by 8 days, hospital costs by 2-fold, and increased inpatient mortality by 36-fold .
Higher mortality was also observed for liver transplant recipients (from 2000 to 2010) at a Detroit hospital .
The ACS-NSQIP database from 2005 to 2010 was used by Lee et al. to study emergently performed open colectomies for a primary diagnosis of C. difficile colitis in the USA . The overall mortality was 33% (111/335).
A study was performed to quantify additional hospital stay attributable to CDI in four European countries, by analyzing nationwide hospital-episode data . Patients in England had the longest additional hospital stay attributable to CDI at 16.09 days, followed by Germany at 15.47 days, Spain at 13.56 days, and The Netherlands at 12.58 days. Propensity score matching indicated a higher attributable length of stay of 32.42 days in England, 15.31 days in Spain, and 18.64 days in the Netherlands. Outputs from this study consistently demonstrate that in European countries, in patients whose hospitalization is complicated by CDI, the infection causes a statistically significant increase in hospital length of stay.
Recommendations for the management of CDI
Infection prevention and control
An infection control “bundle” strategy should be used to successfully control CDI outbreaks. The “bundle” approach should include multifaceted interventions including antibiotic stewardship, hand hygiene, isolation measures, and environmental disinfection.
Proper antibiotic stewardship in both selecting an appropriate antibiotic and optimizing its dose and duration to prevent and cure an infection may prevent the emergence of C. difficile (Recommendation 1 B).
As CDI is thought to follow disruption of normal bacterial flora of the colon, a consequence of antibiotic use , it is logical that antibiotic stewardship programs may be useful in preventing CDI . Good antibiotic stewardship involves ensuring appropriate antibiotic choices and optimizing antibiotic doses and duration of treatment to prevent and cure an infection while minimizing toxicity and conditions conducive to the development of CDI.
In order to estimate the effectiveness and safety of interventions to improve antibiotic prescribing practices in hospital inpatients in 2017, a systematic review including 221 studies (58 RCTs, and 163 NRS) was published . The results showed a very low level of evidence regarding the effect of interventions to reduce CDI (median − 48.6%, interquartile range − 80.7% to − 19.2%; seven studies).
Another systematic review and meta-analysis quantified the effect of both persuasive (education and guidance) and restrictive (approval required, removal) antimicrobial stewardship programs for CDI . A significant protective role (overall RR = 0.48, 95% CI 0.38–0.62) was found, with the strongest evidence for restrictive program and those with the longest duration. Cephalosporins and quinolones reduction should be an important target for stewardship programs, with a significant expected impact on the incidence of CDI [181, 182].
C. difficile carriers should be placed in contact (enteric) precautions (Recommendation 1 B). Even if further studies are warranted to establish the benefit of screening and the efficacy of infection control measures for asymptomatic carriers.
Prompt identification of patients with CDI is essential, so that appropriate isolation precautions can be put into effect .
This is particularly important in reducing environmental contamination as spores can survive for months in the environment , despite regular use of environmental cleaning agents.
It is important to place patients suspected of having CDI on contact precautions before diagnostic laboratory test confirmation if there is a lag before test results are available .
Contact (enteric) precautions in patients with CDI should be maintained until the resolution of diarrhea, which is demonstrated by passage of formed stool for at least 48 h. There are no studies demonstrating that further extension of contact precautions results in reductions in CDI incidence.
C. difficile carriers should be placed in a private room  with en-suite hand washing and toilet facilities. If a private room is not available, known CDI patients may be cohorted in the same area  though the theoretical risk of transfection with different strains exists. This is supported by a retrospective cohort of 2859 patients published by Chang et al. . Non-infected patients who were roommates or neighbors of a patient with CDI were at higher risk of nosocomial acquisition of CDI (RR 3.94; 95% CI 1.27–12.24).
Recently, there has been growing interest in asymptomatic carriage/colonization of C. difficile since asymptomatic carriers are considered a reservoir for C. difficile. Colonization by toxigenic C. difficile strain seems to be associated with increased risk of progressing to CDI. Zacharioudakis et al.  showed that carriers of toxigenic strains are at a higher risk for the development of an infection compared to non-colonized patients. On the other hand, patients colonized by non-toxigenic strains may be even protected from developing CDI . Conversion of a non-toxigenic strain to a toxin producer by horizontal gene transfer makes the risk assessment of colonization really challenging . More data are needed to assess the precise role of the microbiota and the conditions allowing progression from asymptomatic colonization to CDI, in particular the recognition of the mechanism which may trigger toxin production. Based on current data, screening for asymptomatic carriers and an eradication of C. difficile is not indicated because C. difficile colonization is not believed to be a direct independent precursor for CDI. C. difficile asymptomatic carriers may also play a role in spore dissemination in the hospital and many cases of CDI are thought to be attributable to cross-contamination from asymptomatic carriers. Curry et al.  examined patients for C. difficile colonization and found that 29% of CDIs were linked to asymptomatic C. difficile carriers. Asymptomatic carriers who are colonized at admission appear to contribute to sustaining C. difficile transmission in the ward by the shedding of spores to the environment. The frequency of environmental contamination depends on the C. difficile status of the patient—34% of rooms of patients with asymptomatic colonization and 49% of rooms of CDI patients were found to be contaminated with C. difficile . Infection control measures for asymptomatic carriers may be effective by limiting contamination of the hospital environment and health care workers’ hands, as well as by preventing direct patient-to-patient transmission. Longtin et al.  reported that screening of C. difficile colonization at hospital admission and contact precautions were associated with a significant decrease in the HA-CDI incidence rate (6.9 per 10,000 patient-days in the pre-intervention period vs. 3.0 per 10,000 patient-days during the intervention period; p < 0.001). This study provides the most convincing evidence to date for the significant effect of isolating asymptomatic carriers.
Hand hygiene with soap and water is the cornerstone of the prevention of C. difficile infection. Hand hygiene, contact precautions, and good cleaning and disinfection of patient care equipment and the environment should be used by all health-care workers in contact with any patient with known or suspected CDI (Recommendation 1 B).
In a health-care setting, transmission of C. difficile spores occurs primarily via the contaminated hands of health-care workers, but contact with a contaminated environment, contaminated utensils or medical devices has also been implicated. Hand hygiene with soap and water and the use of contact precautions along with good cleaning and disinfection of the environment and patient equipment should be used by all health-care workers in contact with any patient with known or suspected CDI. Hand hygiene is a cornerstone of prevention of nosocomial infections, including infection due to C. difficile. Alcohol-based hand sanitizers are highly effective against non-spore-forming organisms, but they do not kill C. difficile spores or remove C. difficile from the hands .
Though disposable glove use during care of a patient with CDI may be effective in preventing the transmission of C. difficile, these must be removed at the point of use and the hands should then be thoroughly decontaminated with soap and water.
For environmental cleaning, disinfection with sodium hypochlorite solutions are usually recommended in patient areas where C. difficile transmission is ongoing .
In 2016, a cross-sectional study was conducted in a tertiary care hospital to analyze the impact of location of sinks on hand washing compliance after caring for patients with CDI. Healthcare workers’ hand washing compliance was low, and a poor access to sinks was associated with decreased hand washing compliance .
Environmental decontamination of clinical areas, ideally using hypochlorite agents or a sporicidal product, is recommended; however, in practice, compliance with cleaning protocols is often suboptimal.
In 2017, a qualitative systematic review including 46 studies investigated the impact of specific interventions on CDI rates in acute-care hospitals. The most effective interventions, resulting in a 45% to 85% reduction in CDI, included daily to twice daily disinfection of high-touch surfaces (including bed rails) and terminal cleaning of patient rooms with chlorine-based products. Chlorhexidine bathing and intensified hand-hygiene practices were not effective for reducing CDI rates .
Newer alternatives for environmental decontamination have been introduced, notably hydrogen peroxide vapor (HPV) and, more recently, UV decontamination .
In a study conducted by McCord et al., breakpoint time series analysis indicated a significant reduction (p < 0.001) in the CDI rate at the time when HPV disinfection was implemented, resulting in a reduction in the CDI rate from 1.0 to 0.4 cases per 1000 patient-days in the 24 months before HPV usage compared with the first 24 months of HPV usage .
Recently, a systematic literature review and meta-analysis on the impact of no-touch disinfection methods to decrease HAIs was performed . Statistically significant reduction in CDI (RR = 0.64; 95% CI 0.49–0.84) was observed using UV light no-touch disinfection technology. Important to point out that the new no-touch methods for room disinfection supplement, but do not replace, daily cleaning .
The European Society of Clinical Microbiology and Infectious Diseases (ESCMID) study group for C. difficile (ESGCD) recently published a set of guidelines regarding measures for prevention of C. difficile infection in acute healthcare settings . According to the committee, it is recommended:
To use personal protective equipment (gloves and gowns/disposable aprons) to decrease transmission of C. difficile or incidence of CDI
To use contact precautions to decrease the transmission of C. difficile and reduce the incidence of CDI
To introduce daily environmental sporicidal disinfection and terminal disinfection of rooms of patients with CDI to decrease the transmission of CDI
To perform surveillance of CDI in combination with timely feedback of infection rates on both the hospital and ward level
To implement restriction protocols of antibiotic agents/classes (effective in reducing CDI rates)
To implement protocols to reduce the duration of antibiotic therapy (effective in reducing CDI rates)
Educate healthcare workers on prevention of CDI to enhance their knowledge and skills on prevention strategies
It is not recommended:
To screen for C. difficile to identify colonized/carrier patients as a way of altering the risk of developing CDI in either colonized subjects or other patients and thus reducing CDI rates
To screen health care workers for C. difficile gut colonization as a routine control measure for CDI
The diagnosis of CDI should be based on clinical signs and symptoms in combination with laboratory tests. Stool testing should only be performed on diarrheal stools from at-risk patients with clinically significant diarrhea (≥ 3 loose stools in 24 h) with no obvious alternative explanation (Recommendation 1 C).
For patients with ileus who may be unable to produce stool specimens, polymerase chain reaction testing of perirectal swabs provides an acceptable alternative to stool specimen analysis (Recommendation 2B).
Typing is useful to differentiate C. difficile strains and to obtain epidemiological information. Different typing methods for C. difficile currently available are: restriction endonuclease analysis (REA), pulsed-field gel electrophoresis (PFGE), multi-locus sequence typing (MLST), repetitive-element PCR typing, toxin-typing, multi-locus variable-number tandem-repeat analysis (MLVA), and PCR-ribotyping . C. difficile strains with increased virulence traits (hypervirulent) have been described in the last 15 years. In particular, PCR-ribotype 027, also known as North American pulsed-field gel electrophoresis type 1 (NAP1) or restriction endonuclease analysis group BI, has been associated with increased disease severity, recurrence, and significant mortality .
The diagnosis of C. difficile infection should be suspected in patients with acute diarrhea (≥ 3 loose stools in 24 h) with no obvious alternative explanation (such as laxative use), particularly in the setting of relevant risk factors (including recent antibiotic use, hospitalization, and advanced age).
Prompt and precise diagnosis is important for the effective management of CDI. An accurate diagnosis of CDI requires both clinical symptoms and a positive laboratory test.
Early identification of CDI allows early treatment and can potentially improve outcomes. Rapid isolation of infected patients is important in controlling the transmission of C. difficile .
The diagnosis of CDI is based on the presence of a clinical picture compatible with CDI and microbiological evidence of free toxin and/or the demonstration of toxigenic C. difficile in a diarrhea stool sample . Clinical features include diarrhea (defined as by passage of three or more unformed stools in 24 h), abdominal pain and cramps, abdominal distension, ileus (signs of severely disturbed bowel function), and toxic megacolon.
Since C. difficile can colonize the intestinal tract of healthy individuals, diagnostic testing for CDI should be performed only on diarrheic stools from symptomatic patients. Testing of formed stool can result in false positive tests, which may result in unnecessary antibiotic therapy.
One limitation of the reliance on stool specimens involves patients with suspected severe CDI complicated by ileus as those patients may be unable to produce specimens for testing. For those patients, testing of perirectal swabs may be an accurate and efficient method to detect toxigenic C. difficile. In 2012, Kundrapu et al.  described the results of a prospective study of 139 patients being tested for C. difficile infection by polymerase chain reaction. The sensitivity, specificity, positive predictive value, and negative predictive value of testing perirectal swabs were 95.7%, 100%, 100%, and 99.1%, respectively. The authors concluded that for selected patients, perirectal swabs provided an acceptable alternative to stool specimen analysis.
Clinical context such as a history of recent antibiotic administration and/or residence in hospital are useful in selecting patients for testing. Other signs such as fever, abdominal pain, leukocytosis, in combination with other laboratory tests (e.g., creatinine and serum lactate) are useful for defining the severity of infection.
Nucleic acid amplification tests (NAAT) for C. difficile toxin genes appear to be sensitive and specific and may be used as a standard diagnostic test for CDI. NAAT as single-step algorithm can increase detection of asymptomatic colonization, therefore it should be performed in patients with high suspicion for CDI or included in two-step algorithm starting with toxin-EIA (Recommendation 1 B).
Glutamate dehydrogenase (GDH) screening tests for C. difficile are sensitive but do not differentiate between toxigenic and non-toxigenic strains. They may be used in association with toxin A/B enzyme immunoassays (EIA) testing. Algorithms including screening with an EIA for GDH followed by a toxin assay may be suggested (Recommendation 1 B).
EIA for toxin A/B is fast and inexpensive and has high specificity but it is not recommended alone due to its relatively low sensitivity (Recommendation 1 B).
C. difficile culture is relatively slow but sensitive. It is rarely performed today as a routine diagnostic test. C. difficile culture is recommended for subsequent epidemiological typing and characterization of strains (Recommendation 1 C).
Repeat testing after a first negative sample during the same diarrheal episode may be useful only in selected cases with ongoing clinical suspicion during an epidemic situation or in cases with high clinical suspicion during endemic situations (Recommendation 1 C).
The best standard laboratory test for diagnosis of CDI has not been clearly established .
Currently, there is no single stool test that can be relied upon as the reference standard for the diagnosis of CDI. Several methods are suggested for the diagnosis of CDI, including toxinogenic culture (TC), cell cytotoxicity neutralization assay (CCNA), enzyme immunoassays (EIA) for toxins A, B, and/or glutamate dehydrogenase (GDH), and nucleic acid amplification tests (NAATs).
In the past, TC was accepted by many microbiologists as the method of choice for diagnosis of CDI. The procedure includes stool culture for C. difficile on a selective differential medium (cycloserine, cefoxitin, fructose agar, or CCFA) and an assay to test the colonies for the ability to produce toxins. Despite TC is considered the gold standard method, there are significant issues with TC including slow turnaround time and its inability to detect the presence of toxins in stool. This may also lead to false positive results as up to 7% of asymptomatic hospitalized patients may be colonized with toxigenic C. difficile .
C. difficile culture is also necessary for subsequent epidemiological typing and characterization of strains.
The EIA for toxin A/B has been adopted by most clinical laboratories because it is fast, convenient, and inexpensive . However, studies have shown that sensitivity can be low. Toxin A + B EIA tests have a described sensitivity of 32–98% and a specificity of 84–100% .
GDH is an enzyme produced by C. difficile in relatively large amounts compared with toxins A and B [209, 210]. A positive GDH assay only documents the presence of C. difficile but it does not discriminate between toxigenic and non-toxigenic strains (about 20% of the C. difficile population). Therefore, a second test for toxin production is necessary for confirmation. GDH screening tests for C. difficile used in association to toxin A + B EIA testing gives an accurate test result quickly [207, 208] even if the sensitivity of such strategy is lower than NAATs.
The use of NAATs for the detection of C. difficile from diarrheal stool specimens was documented in the early 1990s. NAATs possess a series of advantages such as excellent sensitivity and specificity, low complexity, simplified reporting, reduced need for repeat testing, and improved turnaround time [209,210,211,212].
In particular, some NAATs such as multiplex NAATs can simultaneously detect C. difficile strains and toxin encoding genes from stool samples .
There are several commercially available NAATs, including a real-time PCR (RT-PCR) assay and loop-mediated isothermal amplification (LAMP) assay, both of which have an overall high analytical sensitivity (80–100%) and specificity (87–99%).
However, although NAATs have a high sensitivity and specificity, not all laboratories routinely perform this assay . Moreover, some limitations have been associated with NAATs .
Although NAAT methods are considered superior to other methods of diagnosing CDI, this testing strategy is unable to accurately distinguish between C. difficile colonization and active disease, which may result in both over diagnosis and overtreatment of CDI, delaying recognition of other causes of diarrheal illness/outbreaks, and resulting in unnecessary exposure to antibiotics used to treat CDI.
A current topic of debate is whether a stool sample that was positive by a molecular assay needs to be tested with a confirmatory toxin assay  given it can also identify toxigenic C. difficile in asymptomatic patients. This underscores the importance of only testing patients with symptoms. There is no evidence suggesting that surgical patients should be diagnosed any differently than general medical patients . It has already been highlighted that immunocompromised patients including those on glucocorticoids, or chemotherapy and post-transplant patients are at increased risk for CDI.
The issue of if or when to retest for CDI is inherently linked to the accuracy of the employed routine testing method. Methods with suboptimal sensitivity for C. difficile (e.g., stand-alone toxin EIAs) led to frequent retesting in some settings. In the absence of clear changes to the clinical presentation of suspected CDI (i.e., change in character of diarrhea or new supporting clinical evidence), repeating testing should not be performed.
CT imaging is suggested for patients with clinical manifestations of severe-complicated C. difficile colitis; however, its sensitivity is not satisfactory for screening purposes (Recommendation 2 B).
In certain clinical settings, adjunct testing methods such as radiologic diagnostic imaging may be useful for diagnosing CDI. Diagnostic computed tomography (CT) imaging can assist with an early diagnosis and may help determine the severity of the disease in patients with CDI .
CT has been studied as an imaging modality for diagnosing C. difficile colitis [219,220,221,222]. Typical CT findings of CDC include colonic wall thickening, dilation, peri-colonic stranding, “accordion sign” (high-attenuation oral contrast in the colonic lumen alternating with low-attenuation inflamed mucosa), “double-halo sign, target sign” (intravenous contrast displaying varying degrees of attenuation caused by submucosal inflammation and hyperemia), and ascites . However, the most common finding, colonic wall thickening, is non-specific and can be found in other forms of colitis, although it may be more pronounced with CDI.
In the study by Kirkpatrick et al. , CT diagnosis of CDC had a sensitivity of 52%, a specificity of 93%, and positive and negative predictive valued 88%, and 67% respectively. Sensitivity would have been increased to 70% with no change in specificity if colonic wall thickness of greater than 4 mm had been used as a diagnostic criteria, in conjunction with the presence of the following factors, colon wall nodularity, accordion sign, peri-colonic stranding, or otherwise unexplained ascites.
Ultrasound may be useful in critically ill patients suspected to have pseudomembranous colitis who cannot be transported to the CT scan suite (Recommendation 2 C).
Point-of-care ultrasound may be useful in diagnosing and managing critically ill patients who cannot be moved to the radiology department .
Ultrasound findings of pseudomembranous colitis in severe cases include a thickened colonic wall with heterogeneous echogeneity as well as narrowing of the colonic lumen . Pseudomembranes can also be visualized as hyperechoic lines covering the mucosa [226,227,228,229].
In the early stages of pseudomembranous colitis, the texture of the colonic wall is preserved. The hypoechoic edematous mucosa and muscularis propria may be thickened with the echogenic submucosa sandwiched between them. The presence of submucosal gaps may indicate extension of tissue damage into deeper structures. Intraperitoneal free fluid is seen in more than 70% of cases [224,225,226,227].
Flexible sigmoidoscopy may be helpful in the diagnosis of C. difficile colitis when there is a high level of clinical suspicion for C. difficile infection (Recommendation 2 B).
Endoscopy should be used sparingly to confirm the diagnosis of CDI since the diagnosis can be usually made by laboratory tests, clinical findings, and imaging. However, colonoscopy may be hazardous in the setting of fulminant colitis where there may be increased risk of perforation .
A study by Johal et al.  described the use of flexible sigmoidoscopy as a tool for the diagnosis of C. difficile colitis when stool assays were negative suggesting that sigmoidoscopy should be considered in all hospitalized patients with diarrhea in whom the stool tests for C. difficile cytotoxin and enteric pathogens are negative.
Unnecessary antibiotic agent(s) should be discontinued if CDI is suspected (Recommendation 1 B).
Unnecessary PPIs should always be discontinued in patients at high risk for CDI (Recommendation 1 C).
Empirical therapy for CDI should be avoided unless there is a strong suspicion for CDI. If a patient has a strong suspicion for severe CDI, empirical therapy for CDI should be considered while awaiting test results (Recommendation 1 C).
In cases of suspected severe CDI, antibiotic agent(s) should be discontinued, if possible .
A meta-analysis addressing factors associated with prolonged symptoms and severe disease due to C. difficile showed that continued use of antibiotics for infections other than CDI is significantly associated with an increased risk of CDI recurrence .
If continued antibiotic therapy is required for treatment of the primary infection, antimicrobial therapy with agents that are less frequently implicated with antibiotic-associated CDI should be used; these include parenteral aminoglycosides, sulfonamides, macrolides, vancomycin, or tetracycline/tigecycline.
Although there is a clinical association between PPI use and CDI , no RCTs studies have studied the relationship between discontinuing or avoiding PPI use and risk of CDI. Thus, a strong recommendation to discontinue PPIs in patients at high risk for CDI regardless of need for PPI will require further evidences. However, stewardship activities to discontinue unneeded PPIs are strongly warranted.
Antibiotic therapy is the first choice for CDI, and specific antibiotic therapy guideline recommendations should be based on the severity of the disease.
When antibiotic therapy is indicated for symptomatic cases with a positive C. difficile toxin result, options include metronidazole, oral or intraluminal vancomycin, and oral fidaxomicin [233,234,235,236,237,238,239].
Oral metronidazole should be limited to the treatment of an initial episode of mild-moderate CDI (Recommendation 2A). Oral vancomycin is recommended for treatment of patients with mild-moderate disease who do not respond to metronidazole (Recommendation 1 A). Repeated or prolonged courses of metronidazole should be avoided due to risk of cumulative and potentially irreversible neurotoxicity (Recommendation 1 B).
Although metronidazole may be associated with more frequent side effects, and there has been a significant increase in treatment failures (especially in patients infected with the emergent 027/BI/NAP1 strain), oral metronidazole 500 mg three times per day for 10 days has been used for treating mild-to-moderate cases of CDI . Repeated or prolonged courses of metronidazole should be avoided due to risk of cumulative and potentially irreversible neurotoxicity .
In recent IDSA guidelines, metronidazole is suggested only for patients with an initial episode of non-severe CDI in settings where access to vancomycin or fidaxomicin is limited .
In 2015, a systematic review and meta-analysis comparing the efficacy and safety of metronidazole monotherapy with vancomycin monotherapy and combination therapy in CDI patients was published . No statistically significant difference in the rate of clinical cure was found between metronidazole and vancomycin for mild CDI (OR = 0.67, 95% CI 0.45–1.00; p = 0.05) or between either monotherapy and combination therapy for CDI (OR = 1.07, 95% CI 0.58–1.96; p = 0.83); however, the rate of clinical cure was lower for metronidazole than for vancomycin for severe CDI (OR = 0.46, 95% CI 0.26–0.80; p = 0.006). No significant difference in the rate of CDI recurrence was found between metronidazole and vancomycin for mild CDI (OR = 0.99, 95% CI 0.40–2.45; p = 0.98) or severe CDI (OR = 0.98, 95% CI (0.63, 1.53); p = 0.94) or between either monotherapy or combination therapy for CDI (OR = 0.91, 95% CI (0.66, 1.26); p = 0.56). In addition, there was no difference in the rate of adverse events (AEs) between metronidazole and vancomycin (OR = 1.18, 95% CI 0.80–1.74; p = 0.41). In contrast, the rate of adverse effects was significantly lower for either monotherapy than for combination therapy (OR = 0.30, 95% CI 0.17–0.51; p < 0.0001).
However, recent data have suggested an overall superiority of vancomycin to metronidazole for the treatment of patients with CDI and oral vancomycin 125 mg four times per day for 10 days is recommended as first choice antibiotic also for moderate cases.
In 2017, in an update of a previously published Cochrane review, moderate quality evidence suggested that vancomycin is superior to metronidazole in all cases of CDI . The differences in effectiveness between these antibiotics were not too large and the advantage of metronidazole is its far lower cost even if liquid vancomycin is cheaper and reduces the cost.
Both oral vancomycin or fidaxomicin are recommended for treatment of all patients with severe CDI (Recommendation 1 A).
In patients in whom oral antibiotics cannot reach the colon, vancomycin may be administered as retention enema via a large rectal tube or catheter (Recommendation 1 B).
Fidaxomicin may be used to treat CDI, especially in patients at higher risk for recurrence (e.g., elderly patients or those receiving concomitant antibiotics) (Recommendation 1A).
Vancomycin orally 125 mg four times daily for 10 days is considered superior to metronidazole in severe C. difficile disease [245,246,247]. This may reflect the superior pharmacokinetic properties of vancomycin which is concentrated in the gut lumen. Doses of up to 500 mg have been used in some patients with severe or fulminant, as defined as hypotension or shock, ileus or megacolon, CDI , although there is little evidence for this in the literature.
Unlike vancomycin delivered enterally, intravenous vancomycin has no effect on CDI since the antibiotic is not excreted into the colon. Vancomycin enema may be an effective therapy for patients who cannot tolerate the oral preparation or patients with ileus who have delayed passage of oral antibiotics from the stomach to the colon .
Trans-stoma vancomycin may also be effective in surgical patients with Hartmann resection, ileostomy, or colon diversion. A single-hospital, retrospective chart review on 47 consecutive patients with C. difficile colitis treated with intracolonic vancomycin (ICV) was published by Kim et al. in 2013 . Thirty-three of 47 patients (70%) with severe C. difficile colitis responded to adjunct intracolonic vancomycin with complete resolution without surgery. Multivariate analysis suggested that failures to intracolonic vancomycin enemas occurred in patients who were older and frail with albumin < 2.5 g/dl. Early surgery should be considered for those patients. Early surgery should also be offered to those patients who are failing maximal medical therapy including ICV enemas.
Fidaxomicin orally 200 mg twice daily for 10 days may be a valid alternative to vancomycin in patients with CDI [250, 251]. Fidaxomicin was non-inferior to vancomycin for initial cure of CDI in two prospective trials [235, 236]. In a first double-blind, randomized, non-inferiority trial , 629 adults with acute symptoms of C. difficile infection and a positive result on a stool toxin test were enrolled and randomly assigned to receive fidaxomicin (200 mg twice daily) or vancomycin (125 mg four times daily) orally for 10 days. The rates of clinical cure with fidaxomicin were non-inferior to those with vancomycin in both the modified intention-to-treat analysis (88.2% with fidaxomicin and 85.8% with vancomycin) and the per-protocol analysis (92.1% and 89.8%, respectively). Significantly fewer patients in the fidaxomicin group than in the vancomycin group had a recurrence of the infection, in both the modified intention-to-treat analysis and the per-protocol analysis. In a second multicenter, double-blind, randomized, non-inferiority trial , 535 patients, 16 years or older with acute, toxin-positive CDI were randomly allocated (1:1) to receive oral fidaxomicin (200 mg every 12 h) or oral vancomycin (125 mg every 6 h) for 10 days. Non-inferiority was shown for both the modified intention-to-treat analysis (15.4% vs. 25.3%; p = 0.005) and the per-protocol analysis (13.3% vs. 24.0%; p = 0.004). Patients receiving concomitant antibiotics for other infections had a higher cure rate with fidaxomicin (46 [90.2%] of 51) than with vancomycin (33 [73.3%] of 45; p = 0.031).
A randomized, controlled, open-label, superiority study, recruited hospitalized adults aged 60 years and older with confirmed CDI at 86 European hospitals extended-pulsed fidaxomicin demonstrated to be superior to standard-dose vancomycin for sustained cure of CDI . Between Nov 6, 2014, and May 5, 2016, 364 patients were enrolled and randomly assigned to receive extended pulsed fidaxomicin or vancomycin. Then, 362 patients received at least one dose of study medication (181 in each group). Further, 124 (70%) of 177 patients in the modified full analysis set receiving extended-pulsed fidaxomicin achieved sustained clinical cure 30 days after end of treatment, compared with 106 (59%) of 179 patients receiving vancomycin (difference 11% [95% CI, 1.0–20.7]; p = 0.030; OR 1.62 [95% CI, 1.04–2.54]). Incidence of treatment-emergent adverse events did not differ between extended-pulsed fidaxomicin (121 [67%] of 181) and vancomycin (128 [71%] of 181) treatment arms.
Fidaxomicin may be useful for treating patients who are considered at high risk for recurrence (elderly patients with multiple comorbidities who are receiving concomitant antibiotics). However, it is important to note that no data on the efficacy of fidaxomicin in severe life-threatening disease are available.
The use of other antibiotics such as tigecycline [253, 254], fusidic acid, teicoplanin, rifamixin , and nitazoxanide  has been described in the literature, but they are not currently recommended for general use.
Patients with fulminant colitis (FC) who progress to systemic toxicity require surgical intervention.
To determine clinical predictors for the development of fulminant colitis in patients with CDI, a 10-year retrospective review of FC patients who underwent colectomy was performed and compared with randomly selected age- and sex-matched non-fulminant CDI patients at a single institution study by Girotra et al. in 2012 . Predictive clinical and laboratory features included age (> 70 years), prior CDI, profound leukocytosis (> 18,000/mm3), hemodynamic instability, use of anti-peristaltic medications, and a clinical trial of increasing abdominal pain, distension and diarrhea.
Another important clinical feature that should be taken into account in patients who are going to experience fulminant colitis is the occurrence of a change in mental status that could reflect significant toxemia .
Patients with severe CDI who progress to systemic toxicity should undergo early surgical consultation and should be evaluated for potential surgical intervention (Recommendation 1 C).
Patients with severe CDI who progress to systemic toxicity are likely to have serious comorbidities. Delaying surgery in this group leads to increased likelihood of adverse outcomes , although some reports show that a short period of medical optimization can improve outcomes before colectomy .
There are no reliable clinical and/or laboratory findings that can predict those patients who will respond to medical therapy and those who will need surgery .
Data comparing mortality rates between surgical and medical treatment for fulminant C. difficile colitis were published in a systematic review by Stewart et al. . Five hundred ten patients with fulminant colitis were identified in 6 studies. Emergency colectomy for patients with FC provided a survival advantage compared with continuing antibiotics. When all 6 studies numbering 510 patients were analyzed, the pooled adjusted odds ratio of mortality comparing surgery with medical therapy, and weighted by the contribution of each study, was 0.70 (0.49–0.99) leading the authors to conclude that emergency colectomy has a therapeutic role in treating complicated CDI.
Patients presenting with organ failure (acute renal failure, mental status changes, or cardiopulmonary compromise) also need prompt intervention since the timing of surgical intervention is the key for survival of patients with FC [262,263,264,265].
Seder et al.  described 6841 patients with CDI and showed a decreased mortality associated with surgery performed before the need for vasopressor requirement, especially in the patients < 65 years old. Hall et al.  reviewed 3237 consecutive cases of CDI and showed an increased mortality rate when surgical exploration was performed after intubation or the development of respiratory failure and the use of vasopressors.
Recently, a risk scoring system (RSS) for daily clinical practice was designed by van der Wilden et al. . Age greater than 70 years was assigned 2 points, white blood cell counts equal to or greater than > 20,000/μL or equal to or less than 2000/μL was assigned 1 point, cardiorespiratory failure was assigned 7 points, and diffuse abdominal tenderness on physical examination was assigned 6 points. A value of 6 points was determined to be the threshold for reliably dividing low-risk (< 6) from high-risk (≥ 6) patients. Only patients with cardiorespiratory failure or diffuse abdominal tenderness were high risk.
Ferrada et al.  reviewed the existing literature on the treatment of CDI and published practice management guidelines (PMG) for the Eastern Association for the Surgery of Trauma (EAST). The authors strongly recommended that adult patients with CDI undergo early surgery before developing shock and requiring vasopressors. Although optimal timing remains controversial, the authors found that it was between 3 and 5 days after diagnosis in patients who are worsening or not clinically improving .
Many factors have been described as predictors of mortality in patients who undergo emergency surgery.
Sailhamer et al.  reviewed the records of 4796 inpatients diagnosed with C. difficile colitis. In 199 patients (4.1%) with fulminant CDI, the in-hospital mortality rate was 34.7%. Independent predictors of mortality included age 70 years or older, severe leukocytosis or leukopenia (white blood cell count, > or = 35,000/μL or < 4000/μL) or bandemia (neutrophil bands, > or = 10%), and cardiorespiratory failure (intubation or vasopressors). Survival rates were higher in patients who were cared for by surgical vs. nonsurgical departments.
The ACS-NSQIP database from 2005 to 2010 was used by Lee et al. to study emergency open colectomies performed for C. difficile colitis in the USA . The overall mortality was 33% (111/335). Age 80 years or older, preoperative dialysis dependence, chronic obstructive pulmonary disease, and wound class III were associated high patient mortality. Thrombocytopenia (platelet count < 150 × 103/mm3), coagulopathy (international normalized ratio > 2.0), and renal insufficiency (blood urea nitrogen > 40 mg/dL) were also associated with a higher mortality.
A systematic review and meta-analysis of outcomes following emergency surgery for CDI was published by Banghu et al. . Thirty-one studies were included, which presented data for 1433 patients. The authors concluded that the strongest predictors for postoperative death were those relating to preoperative physiological status: preoperative intubation, acute renal failure, multiple organ failure and shock requiring vasopressors.
Early diagnosis and treatment is important to reduce the mortality associated with fulminant colitis.
Resection of the entire colon should be considered to treat patients with fulminant colitis (Recommendation 1 B). However, diverting loop ileostomy with colonic lavage is a useful alternative to resection of the entire colon (Recommendation 1 B).
Patients with fulminant colitis should be treated with high dose vancomycin (500 mg, 6 hourly), oral and/or by enema, in combination with intravenous metronidazole (500 mg, 8 hourly) (Recommendation 1 C).
In the Bhangu et al. meta-analysis , the most commonly performed operation for treatment of fulminant colitis (FC) was total colectomy with end ileostomy (89%, 1247/1401). When total colectomy with end ileostomy was not performed, reoperation to resect further bowel was needed in 15.9% (20/126). In the recent meta-analysis by Ferrada et al. , 17 studies comparing colectomy versus other procedures or no surgery as treatment for CDI were analyzed. The authors recommended that total colectomy (versus partial colectomy or other surgery) is the procedure of choice for patients with C. difficile colitis.
To evaluate the role of emergency colectomy in patients with FC, and to identify subgroups of patients that may benefit from it, Lamontagne et al.  published a retrospective observational cohort study of 165 cases of FC requiring ICU admission or prolongation of ICU stay in 2 tertiary care hospitals in Quebec, Canada. Eighty-seven (53%) patients died within 30 days of ICU admission, of whom almost half (38 of 87, 44%) died within 48 h of ICU admission. The independent predictors of 30-day mortality were leukocytosis ≥ 50 × 109/L, lactate ≥ 5 mmol/L, age ≥ 75 years, immunosuppression, and shock requiring vasopressors. Patients who underwent an emergency colectomy were less likely to die than those treated medically. Colectomy was more beneficial in patients aged 65 years or more, in immunocompetent patients and in patients with a leukocytosis ≥ 20 × 109/L or lactate between 2.2 and 4.9 mmol/L.
Diverting loop ileostomy with antegrade colonic lavage may be a colon-preserving alternative to total colectomy [272, 273]. A prospective, nonrandomized, historical control group study was performed at the University of Pittsburgh Medical Center and the Veterans’ Administration Healthcare System, in Pittsburgh between June 2009 and January 2011 . Forty-two patients with FC were managed by a loop ileostomy, intraoperative colonic lavage with warmed polyethylene glycol 3350/electrolyte solution via the ileostomy, and postoperative antegrade instillation of vancomycin flushes via the ileostomy. There was no significant difference in age, sex, pharmacologic immunosuppression, and Acute Physiology and Chronic Health Evaluation-II scores between the studied cohort and historical controls. The operation was accomplished laparoscopically in 35 patients (83%). This treatment strategy resulted in reduced mortality compared to their historical controls. Preservation of the colon was achieved in 39 of 42 patients (93%). Of note, vancomycin antegrade enemas were continued via the ileostomy every 6 h for 10 days and this likely augmented the effect of the defunctioning surgery.
A retrospective multicenter study conducted under the sponsorship of the Eastern Association for the Surgery of Trauma to compare loop ileostomy versus total colectomy as surgical treatment for CDI was published in 2017 . Data from ten centers of patients who presented with CDI requiring surgery between July 1, 2010 and July 30, 2014 were collected. When comparing colectomy and loop ileostomy, there was no statistical difference between these two operative strategies. Univariate pre-procedure predictors of mortality were age, lactate, timing of operation, vasopressor use, and acute renal failure. There was no statistical difference between the APACHE score of patients undergoing either procedure (TC, 22 vs. LI, 16). Adjusted mortality (controlled for pre-procedure confounders) was significantly lower in the loop ileostomy group (17.2% vs. 39.7%; p = 0.002).
Early detection of shock and aggressive management of underlying organ dysfunction are essential for improved outcomes in patients with fulminant colitis (Recommendation 1 C). Supportive measures, including intravenous fluid resuscitation, albumin supplementation, and electrolyte replacement, should be provided to all patients with severe C. difficile infection (Recommendation 1 C).
Early detection and prompt aggressive treatment of the underlying organ dysfunction is an essential component in the management of CDI in critically ill patients.
Severe CDI may present with a fulminant course and may be associated with great morbidity and high mortality. Physiologic support including invasive monitoring in an intensive care unit and aggressive resuscitation are often necessary in fulminant colitis. Diarrhea results in significant volume depletion and electrolyte abnormalities, and fluid and electrolyte imbalance should be promptly corrected.
Although it has been debated, albumin supplementation in patients with severe hypoalbuminemia (< 2 g/dl) should be considered as a supportive measure and also to exploit its anti-toxin properties .
The expert panel suggests measuring intra-abdominal pressure (IAP) when any known risk factor for intra-abdominal hypertension (IAH)/abdominal compartment syndrome (ACS) is present.
Recurrence is diagnosed when CDI recurs < 8 weeks after the resolution of a previous episode, provided the symptoms from the previous episode resolved after completion of the initial treatment and other causes have been excluded. Symptomatic recurrent C. difficile infection (RCDI) occurs in approximately 20% of patients and is challenging . Therefore, patients with recurrent CDI should therefore be treated by experienced clinicians.
Agents that may be used to treat the first recurrence of CDI include vancomycin (particularly if metronidazole was used for the first episode) or fidaxomicin. (Recommendation 1 B).
Antibiotic treatment options for patients with > 1 recurrence of CDI include oral vancomycin therapy using a tapered and pulsed regimen (Recommendation 1C).
For recurrent cases of CDI, oral vancomycin 125 mg four times per day for 14 days or oral fidaxomicin 200 mg twice a day for 10 days is recommended for first recurrence.
Metronidazole is not recommended as initial treatment of recurrent CDI as sustained response rates are lower than those with vancomycin. Furthermore, metronidazole should not be used for long-term therapy because of the potential for cumulative neurotoxicity.
Vancomycin and fidaxomicin are equally effective in resolving CDI symptoms but fidaxomicin has been shown to be associated with a lower likelihood of CDI recurrence after a first recurrence [237, 238, 276]. However, there are no prospective randomized controlled trials investigating the efficacy of fidaxomicin in patients with multiple recurrences of CDI. Vancomycin is often administered using a prolonged tapered and/or pulsed regimen which may be more effective than a standard 10 to 14 days course, although no RCTs have been reported in second or subsequent CDI recurrences .
Limited direct evidence exists to support the use of probiotics in the management of a first episode of CDI as an adjunctive treatment to antibiotics for immunocompetent patients Recommendation 2 B).
The altered composition of gut microbiota in the setting of C. difficile infection has raised interest in the potential role of probiotics . Their use aims to re-colonize and restore the diversity of flora following the disruption due to antibiotic treatment and C. difficile overgrowth.
There is limited direct evidence to support the use of probiotics in the primary prevention of CDI.
Data for primary prevention of CDI often arises from prevention of antibiotic-associated diarrhea trials with CDI as a secondary outcome and are often underpowered for CDI. Thus, meta-analyses may be useful to evaluate if specific probiotics are efficacious for CDI, as this statistical method utilizes the increase in power resulting from pooling different studies together. However, since the recent finding that the efficacy of probiotics are both strain-specific and disease-specific , for valid conclusions to be reached, the meta-analysis must assess efficacy within subgroups of identical probiotic strains (or mixture of strains) and for the same type of disease. A meta-analysis of 22 randomized controlled trials using sub-group analysis for 5 different types of probiotics for primary prevention of CDI found 4/5 (Saccharomyces boulardii I-745, Lactobacillus casei DN114001, a mixture of Lactobacillus acidophilus and Bifidobacterium bifidum, and another mixture of three Lactobacilli strains [L. acidophilus CL1285, L. casei LBC80R, Lactobacillus rhamnosus CLR2]) were effective and one type (L. rhamnosus GG) was not effective . Other systematic reviews and meta-analyses report a protective effect of probiotics [279,280,281,282,283,284], but reviews exploring the contribution of probiotics in CDI prevention can be limited due to heterogeneity between studies, inadequate study power, or significant levels of missing outcome data. In addition, many reviews still fail to account for strain-specificity and pool different types of probiotics together in their analysis [280, 281, 284]. The short-term use of probiotics appeared to be safe and effective when used along with antibiotics in patients who are not immunocompromised or severely debilitated. Probiotics should not be administered to patients at risk of bacteremia or fungemia.
Prophylactic probiotics may be considered for inpatients receiving antibiotics during high-risk period (such as outbreaks) before the disease develops (Recommendation 2 C). Probiotics should be not used in immunocompromised patients (Recommendation 2 C).
Several types of probiotics have been tested on a facility-level intervention as part of an infection control bundle for CDI. In an effort to reduce hospital-wide CDI rates (especially in hospitals having CDI outbreaks), probiotics were given to newly admitted patients receiving antibiotics and continued during either the duration of the antibiotic or duration of the patient’s stay. Although lacking in the rigorous strength from randomized trials, these hospital studies showed a significant reduction of CDI rates for some types of probiotics (L. casei Shirota, Lactobacillus plantarum 299v, and a mixture of three lactobacilli strains, Bio-K+) . This three lactobacilli strain mixture (L. acidophilus CL1285, L. casei LBC80R, and L. rhamnosus CLR2) has been tested in seven other hospitals and found to be effective in reducing CDI rates . However, other types of probiotics need further research, particularly in those at high risk of CDI. Probiotics are contraindicated for immunocompromised patients due to a rare, but serious risk of bacteremia.
Probiotics for prevention of recurrent CDI may be an effective adjunct to standard antibiotic treatment (vancomycin) in patients with at least one prior episode of CDI (Recommendation 2 B).
There have been many case reports and case series reporting fewer recurrences of CDI when some probiotics were used as an adjunctive treatment with vancomycin or metronidazole. However, there are fewer randomized trials for this adjunctive therapy. Two randomized controlled trials found significantly fewer CDI patients developed recurrences when Saccharomyces boulardii I-745 was combined with standard antibiotic therapy [286, 287]. The first trial demonstrated a lower CDI recurrence rate compared with a placebo control group (26% vs. 45%, respectively)  and the second trial found that the combination of S. boulardii (1 g/day) with high dose vancomycin (2 g/day) was more effective than high dose vancomycin and placebo (17% vs. 50% recurrence rate) . The probiotic was not able to reduce CDI recurrences when combined with a lower dose of vancomycin (500 mg/day) or with metronidazole (1 g/day). Other studies with Lactobacillus strains (L. rhamnosus GG or L. plantarum 299v) were stopped prematurely due to enrollment problems . There have no published trials currently combining probiotics with fidaxomicin.
Fecal microbiota transplantation
Fecal microbiota transplantation (FMT) may be an effective option for patients with multiple recurrences of CDI who have failed appropriate antibiotic treatments (Recommendation 2 C).
FMT has been considered as an alternative therapy to treat RCDI [283,284,285,286,287,288,289,290,291,292,293]. It involves infusing intestinal microorganisms (in a suspension of healthy donor stool) into the intestine of patients to restore the intestinal microbiota.
The rationale of FMT is that disruption of the normal balance of colonic flora allows C. difficile strains to grow and produce CDI. By reintroducing normal flora via donor feces, the imbalance may be corrected, and normal bowel function re-established .
FMT has not been widely adopted as a therapeutic tool probably due to concerns regarding safety and acceptability .
A systematic literature review of FMT treatment for RCDI and pseudomembranous colitis was published in 2011 by Gough et al. . In 317 patients treated across 27 case series and reports, FMT was highly effective, showing disease resolution in 92% of cases. In those studies, 35% of patients received FMT via enema, with a response rate of 95%; 23% patients received FMT via naso-jejunal tube by gastroscope, with a response rate of 76%; and 19% via colonoscopy, with a response rate of 89%. Effectiveness varied by route of instillation, relationship to stool donor, volume of FMT given, and treatment before infusion.
Another systematic review was published by Cammarota et al. . Twenty full-text case series, 15 case reports, and 1 randomized controlled study were included for the final analysis. Almost all patients treated with donors’ fecal infusion had experienced recurrent episodes of CD-associated diarrhea despite standard antibiotic treatment. Of a total of 536 patients treated, 467 (87%) had resolution of diarrhea. Diarrhea resolution rates varied according to the site of infusion: 81% in the stomach, 86% in the duodenum/jejunum, 93% in the cecum/ascending colon, and 84% in the distal colon. No severe adverse events were reported with the procedure.
Recently, a review to evaluate the efficacy of FMT in treating recurrent and refractory CDI was published . Thirty-seven studies were included; 7 randomized controlled trials and 30 case series. FMT was more effective than vancomycin (RR = 0.23, 95% CI 0.07–0.80) in resolving recurrent and refractory CDI. Clinical resolution across all studies was 92% (95% CI 89–94%). A significant difference was observed between lower gastrointestinal (GI) and upper GI delivery of FMT 95% (95% CI 92–97%) vs. 88% (95% CI 82–94%) respectively (p = 0.02). There was no difference between fresh and frozen FMT 92% (95% CI 89–95%) vs. 93% (95% CI 87–97%) respectively (p = 0.84). Administering consecutive courses of FMT following failure of first FMT resulted in an incremental effect. Donor screening was consistent but variability existed in recipient preparation and volume of FMT. Serious adverse events were uncommon.
Although FMT has high success rates with long-term durability , few disadvantages still exist. In particular, the manipulation of feces and the classical enteral administration methods are not only laborious but tend to make the procedure rather unattractive for physicians and patients.
In the context of these disadvantages, few efforts have been made to enhance the feasibility and social acceptance of microbiota transplantation.
FMT may be administered via enemas or as a slurry given via a nasogastric tube.
One systematic review which compared various routes of administration included a total of 182 patients (148 received FMT via colonoscopy and 34 received FMT via nasogastric tube) from 12 published studies . Recurrence of CDI after FMT was similar in both the colonoscopy group (8/148, 5.4%) versus the nasogastric tube group (2/34, 5.9%) (p = 1.000). However, the overall rate of cure after FMT was slightly higher in patients receiving FMT by colonoscopy: 85.3% (29 patients, 29/34) in the nasogastric tube group and 93.2% (138 patients, 138/148) in the colonoscopy group (p = 0.162).
A larger and more recent systematic review of 14 studies including 305 patients and comparing FMT delivery by upper and lower gastrointestinal routes also favored lower gastrointestinal delivery . At 30 and 90 days, the risk of clinical failure was 5.6% and 17.9% in the upper gastrointestinal group compared with 4.9% and 8.5% in the lower GI delivery route group, respectively.
More recently, encapsulated preparations of FMT have been used with success. This strategy has the advantage of being less invasive and simpler, which may also result in improved cost-effectiveness [295,296,297,298].
In 2014, Youngster et al.  reported their experience with frozen FMT capsules in 20 patients who had RCDI. Fourteen patients (70%) had resolution of diarrhea after a single treatment, and 4 patients responded after a second treatment, with a clinical resolution rate of 90%.
Patients who are immunocompromised are at increased risk of CDI. During the last 2 years, the first data on FMT in immunocompromised patients began to appear in the medical literature .
A multicenter retrospective series on the use of FMT in immunocompromised patients with recurrent, refractory, or severe CDI was published in 2014 . Immunosuppression included HIV/AIDS (3), solid organ transplantation (19), oncologic condition (7), immunosuppressive therapy for IBD (36), and other medical conditions/medications (15). This series demonstrated the effective use of FMT for CDI in immunocompromised patients with few serious adverse events.
With the increased awareness of the role of native gut microbiome and its role in the gut brain axis, there have been concerns about the long-term effect of transplanted stool, and how the new gut microbiome can affect brain function and immune responses.
Coadjuvant treatment with monoclonal antibodies (bezlotoxumab) may prevent recurrences of CDI, particularly in patients with CDI due to the 027 epidemic strain, in immunocompromised patients and in patients with severe CDI (Recommendation 1 A).
Since the expression of clostridial toxins (TcdA and TcdB) is mandatory for the development of CDI, the development of monoclonal antibodies aimed at preventing the cytotoxic effect of these toxins is a potential strategy for controlling the disease. In 2016, the FDA approved bezlotoxumab to reduce the recurrence of CDI in adult patients receiving antimicrobial therapy for CDI who are at high risk of CDI recurrence. Bezlotoxumab (MK-6072) is a human monoclonal antibody which reduces recurrent CDI by blocking the binding of C. difficile toxin B to host cells, thus limiting epithelial damage and facilitating recovery of the microbiome . Besides bezlotoxumab, another human monoclonal antibody, actoxumab (MK-3415), was recently designed to neutralize C. difficile toxin.
The data from two double-blind, randomized, placebo-controlled, phase 3 trials, MODIFY I and MODIFY II, involving 2655 adults receiving oral standard-of-care antibiotics for primary or recurrent C. difficile infection showed that bezlotoxumab achieved a significant benefit over placebo in the treatment of recurrent CDI. Participants received an infusion of bezlotoxumab (10 mg/kg of body weight), actoxumab plus bezlotoxumab (10 mg/kg each), or placebo; actoxumab alone (10 mg/kg) was given in MODIFY I but discontinued after a planned interim analysis. The primary end point was recurrent infection (new episode after initial clinical cure) within 12 weeks after infusion in the modified intention-to-treat population .
In both trials, the rate of recurrent C. difficile infection was significantly lower with bezlotoxumab alone than with placebo (MODIFY I: 17% [67 of 386] vs. 28% [109 of 395]; adjusted difference, − 10.1 percentage points; 95% CI, − 15.9 to − 4.3; p < 0.001; MODIFY II: 16% [62 of 395] vs. 26% [97 of 378]; adjusted difference, − 9.9 percentage points; 95% CI, − 15.5 to − 4.3; p < 0.001) .
A post-hoc analysis of pooled monoclonal antibodies for C. difficile therapy (MODIFY) I/II data assessed bezlotoxumab efficacy in participants with risk factors for RCDI including age ≥ 65 years, history of CDI, compromised immunity, severe CDI, and ribotype 027/078/244 . Although the patients with only one of the risk factors may benefit from bezlotoxumab, patients with at least three risk factors appeared to have the greatest risk reduction with bezlotoxumab.
Intravenous immunoglobulin (IVIG) should only be used as adjunct therapy in patients with multiple recurrent or fulminant CDI until results from large, randomized controlled trials are available (Recommendation 2 C).
Novel treatment modalities for management of CDI have been developed. IVIG treatment is based on evidence that the level of immune response to C. difficile colonization is the major determinant of the magnitude and duration of clinical manifestations. Passive immunization with IVIG has been successful in several small series. A review by Abourgergi et al.  of 15 small, mostly retrospective and non-randomized studies, documented success with IVIG in the treatment of protracted, recurrent, or severe CDI. The authors concluded that IVIG should only be used as adjunct therapy until results from large, randomized controlled trials are available. Two small retrospective matched cohort studies were published that compared the clinical efficacy of the addition of IVIG to conventional CDI treatment [306, 307]. Neither of these studies found significant differences between the compared cohorts in the main clinical outcomes, although Shahani et al.  noted that in their IVIG cohort, there were significantly older patients with more severe CDI than in the control group. It is reasonable to utilize IVIG therapy in patients diagnosed with hypogammaglobuminemia based on the confirmation of IgG levels below the normal laboratory range.
Enteral nutrition in CDI
Tube feeding patients should be clinically assessed due to their risk for developing CDI (Recommendation 2 C).
It is widely accepted that enteral nutrition (EN) maintains gut mucosal integrity which leads to decreased intestinal permeability, decreased infections, and an improved immunological status. EN during episodes of diarrhea may be well tolerated and may improve enterocyte healing and maintenance of enzyme activity [308,309,310]. Enteral nutrition, however, has also been associated with increased risk of CDI . Bliss et al. evaluated 76 tube-fed and non-tube-fed hospital patients for the development of CDI . Patients were controlled for age, severity of illness, and duration of hospitalization. Patients who were tube-fed were statistically more likely to develop CDI (20% vs. 8% p = 0.03). One of the reasons may be prolonged use of elemental diets. It is known that critically ill patients tolerate feeding well if the feed is given in elemental form and delivered beyond the stomach into the jejunum because it is totally absorbed within the upper small intestine , depriving the colonic microbiota of their source of nutrition, such as dietary fibers, fructose oligosaccharides, and resistant starch . The resultant suppression of colonic fermentation may therefore lead to the disruption of the normal gut flora and the creation of a “permissive” environment for C. difficile colonization and subsequent infection. In feeding tube patients, the conversion of elemental diet feeding to a diet containing adequate indigestible carbohydrate after the first week of critical illness may, in theory, be beneficial.
Puri et al.  reported that daily concomitant treatment with 4 g cholestyramine in patients receiving long-term intravenous ceftriaxone (2 to 4 g ceftriaxone daily, for an average of > 10 weeks) was associated with CDI in only 3 out of 46 patients (6.5%) compared with 23.1% of those receiving ceftriaxone alone. Cholestyramine (or colestyramine) is a hydrophilic, water insoluble, non-digestible basic anion-exchange resin which can bind luminal TcdA and TcdB.
The use of anti-peristaltic agents for the treatment of CDI should be discouraged. If anti-peristaltic agents are used to control persistent symptoms in patients with CDI, they must always be accompanied by medical therapy (Recommendation 2 C).
A review of the literature regarding anti-motility treatment of CDI found 55 patients with CDI who were exposed to anti-motility agents . Nine patients (16%) died, and 27 patients (49%) had unknown outcomes. Seventeen patients (31%) with CDI developed colonic dilation; 5 of these patients with severe CDI died. However, all patients who experienced complications or died were given anti-motility agents alone initially, without an appropriate antibiotic and 23 patients who received metronidazole or vancomycin co-administered with the anti-motility agent experienced no complications. Further study of the role of anti-motility agents in providing symptomatic relief and reducing environmental contamination with infectious stool may be warranted though, until there is clear evidence of benefit, their use in patients with CDI should be avoided.
In the last three decades, the worldwide increase in CDI incidence has been particularly apparent among surgical patients, becoming a global public health challenge. Therefore, prompt and precise diagnosis is paramount for the effective management of CDI, allowing both the immediate implementation of infection prevention and control strategies, and the optimization of treatment in surgical patients, considering the most recent changes introduced in the management of this infection.
Clostridium difficile infection
Recurrent Clostridium difficile infection
Clements AC, Magalhães RJ, Tatem AJ, Paterson DL, Riley TV. Clostridium difficile PCR ribotype 027: assessing the risks of further worldwide spread. Lancet Infect Dis. 2010;10:395–404.
Lessa FC, Gould CV, McDonald LC. Current status of Clostridium difficile infection epidemiology. Clin Infect Dis. 2012;55:65–70.
Goudarzi M, Seyedjavadi SS, Goudarzi H, Mehdizadeh Aghdam E, Nazeri S. Clostridium difficile infection: epidemiology, pathogenesis, risk factors, and therapeutic options. Scientifica (Cairo). 2014;2014:916826.
To KB, Napolitano LM. Clostridium difficile infection: update on diagnosis, epidemiology, and treatment strategies. Surg Infect. 2014;15:490–502.
Eckmann C, Wasserman M, Latif F, Roberts G, Beriot-Mathiot A. Increased hospital length of stay attributable to Clostridium difficile infection in patients with four co-morbidities: an analysis of hospital episode statistics in four European countries. Eur J Health Econ. 2013;14:835–46.
Surawicz CM, Brandt LJ, Binion DG, Ananthakrishnan AN, Curry SR, Gilligan PH, McFarland LV, Mellow M, Zuckerbraun BS. Guidelines for diagnosis, treatment, and prevention of Clostridium difficile infections. Am J Gastroenterol. 2013;108:478–98.
Debast SB, Bauer MP, Kuijper EJ. European Society of Clinical Microbiology and Infectious Diseases. European Society of Clinical Microbiology and Infectious Diseases: update of the treatment guidance document for Clostridium difficile infection. Clin Microbiol Infect. 2014;20(Suppl 2):1–26.
Lessa FC, Mu Y, Bamberg WM, Beldavs ZG, Dumyati GK, Dunn JR, et al. Burden of Clostridium difficile infection in the United States. N Engl J Med. 2015;372:825–34.
Annual Epidemiological Report for 2016 Clostridium difficile infections. https://ecdc.europa.eu/sites/portal/files/documents/AER_for_2016-C-difficile.pdf. Accessed 11 Jan 2019.
Honda H, Yamazaki A, Sato Y, Dubberke ER. Incidence and mortality associated with Clostridium difficile infection at a Japanese tertiary care Centre. Anaerobe. 2014;25:5–10.
Riley TV, Kimura T. The epidemiology of Clostridium difficile infection in Japan: a systematic review. Infect Dis Ther. 2018;7:39–70.
Kim YS, Han DS, Kim YH, Kim WH, Kim JS, Kim HS, et al. Incidence and clinical features of Clostridium difficile infection in Korea: a nationwide study. Epidemiol Infect. 2013;141:189–94.
Wong-McClure RA, Ramírez-Salas E, Mora-Brenes N, Aguero-Sandí L, Morera-Sigler M, Badilla-Vargas X, et al. Long term effect of infection control practices and associated factors during a major Clostridium difficile outbreak in Costa Rica. J Infect Dev Ctries. 2013;7:914–21.
Legenza L, Barnett S, Rose W, Bianchini M, Safdar N, Coetzee R. Epidemiology and outcomes of Clostridium difficile infection among hospitalised patients: results of a multicentre retrospective study in South Africa. BMJ Glob Health. 2018;3(4):e000889.
Zerey M, Paton BL, Lincourt AE, Gersin KS, Kercher KW, Heniford BT. The burden of Clostridium difficile in surgical patients in the United States. Surg Infect. 2007;8:557–66.
Halabi WJ, Nguyen VQ, Carmichael JC, Pigazzi A, Stamos MJ, Mills S. Clostridium difficile colitis in the United States: a decade of trends, outcomes, risk factors for colectomy, and mortality after colectomy. J Am Coll Surg. 2013;217:802–12.
Herzog T, Deleites C, Belyaev O, Chromik AM, Uhl W. Clostridium difficile in visceral surgery. Chirurg. 2015;86:781–6.
Abdelsattar ZM, Krapohl G, Alrahmani L, Banerjee M, Krell RW, Wong SL, et al. Postoperative burden of hospital-acquired Clostridium difficile infection. Infect Control Hosp Epidemiol. 2015;36:40–6.
Sartelli M, Malangoni MA, Abu-Zidan FM, Griffiths EA, Di Bella S, McFarland LV, et al. WSES guidelines for management of Clostridium difficile infection in surgical patients. World J Emerg Surg. 2015;10:38.
Guyatt G, Gutterman D, Baumann MH, Addrizzo-Harris D, Hylek EM, Phillips B, et al. Grading strength of recommendations and quality of evidence in clinical guidelines: report from an American College of Chest Physicians task force. Chest. 2006;129:174–81.
Brozek JL, Akl EA, Jaeschke R, Lang DM, Bossuyt P, Glasziou P, et al. Grading quality of evidence and strength of recommendations in clinical practice guidelines: part 2 of 3. The GRADE approach to grading quality of evidence about diagnostic tests and strategies. Allergy. 2009;64:1109–16.
Viscidi R, Willey S, Bartlett JG. Isolation rates and toxigenic potential of Clostridium difficile isolates from various patient populations. Gastroenterology. 1981;81:5–9.
Samore MH, DeGirolami PC, Tlucko A, Lichtenberg DA, Melvin ZA, Karchmer AW. Clostridium difficile colonization and diarrhea at a tertiary care hospital. Clin Infect Dis. 1994;18:181–7.
Walker KJ, Gilliland SS, Vance-Bryan K, Moody JA, Larsson AJ, Rotschafer JC, Guay DR. Clostridium difficile colonization in residents of long-term care facilities: prevalence and risk factors. J Am Geriatr Soc. 1993;41:940–6.
Linsenmeyer K, O'Brien W, Brecher SM, Strymish J, Rochman A, Itani K, Gupta K. Clostridium difficile screening for colonization during an outbreak setting. Clin Infect Dis. 2018;67:1912–4.
Cheng AC, Ferguson JK, Richards MJ, Robson JM, Gilbert GL, McGregor A, et al. Australasian Society for Infectious Diseases guidelines for the diagnosis and treatment of Clostridium difficile infection. Med J Aust. 2011;194:353–8.
McFarland LV, Mulligan ME, Kwok RY, Stamm WE. Nosocomial acquisition of Clostridium difficile infection. NEJM. 1989;320:204–10.
Magill SS, Edwards JR, Bamberg W, Beldavs ZG, Dumyati G, Kainer MA, et al. Emerging infections program healthcare-associated infections and antimicrobial use prevalence survey team. Multistate point-prevalence survey of health care-associated infections. N Engl J Med. 2014;370:1198–208.
Spigaglia P, Mastrantonio P, Barbanti F. Antibiotic resistances of Clostridium difficile. Adv Exp Med Biol. 2018;1050:137–59.
Shaughnessy MK, Micielli RL, DePestel DD, Arndt J, Strachan CL, Welch KB, Chenoweth CE. Evaluation of hospital room assignment and acquisition of Clostridium difficile infection. Infect Control Hosp Epidemiol. 2011;32:201–6.
Pruitt RN, Lacy DB. Toward a structural understanding of Clostridium difficile toxins a and B. Front Cell Infect Microbiol. 2012;2:28.
Jank T, Giesemann T, Aktories K. Rho-glucosylating Clostridium difficile toxins A and B: new insights into structure and function. Glycobiology. 2007;17:15R–22R.
Kuehne SA, Cartman ST, Heap JT, Kelly ML, Cockayne A, Minton NP. The role of toxin A and toxin B in Clostridium difficile infection. Nature. 2010;467:711–3.
Carter GP, Rood JI, Lyras D. The role of toxin A and toxin B in the virulence of Clostridium difficile. Trends Microbiol. 2012;20:21–9.
Kuehne SA, Collery MM, Kelly ML, Cartman ST, Cockayne A, Minton NP. Importance of toxin A, toxin B, and CDT in virulence of an epidemic Clostridium difficile strain. J Infect Dis. 2014;209:83–6.
Di Bella S, Ascenzi P, Siarakas S, Petrosillo N, di Masi A. Clostridium difficile toxins A and B: insights into pathogenic properties and Extraintestinal effects. Toxins (Basel). 2016;8(5):134.
Warny M, Pepin J, Fang A, Killgore G, Thompson A, Brazier J, et al. Toxin production by an emerging strain of Clostridium difficile associated with outbreaks of severe disease in North America and Europe. Lancet. 2005;366:1079–84.
Eckert C, Coignard B, Hebert M, Tarnaud C, Tessier C, Lemire A, et al. Clinical and microbiological features of Clostridium difficile infections in France: the ICD-RAISIN 2009 national survey. Med Mal Infect. 2013;43:67–74.
Barbut F, Mastrantonio P, Delmée M, Brazier J, Kuijper E. Poxton I; European study group on Clostridium difficile (ESGCD). Prospective study of Clostridium difficile infections in Europe with phenotypic and genotypic characterisation of the isolates. Clin Microbiol Infect. 2007;13:1048–57.
Bauer MP, Notermans DW, van Benthem BH, Brazier JS, Wilcox MH, Rupnik M, et al. Clostridium difficile infection in Europe: a hospital-based survey. Lancet. 2011;377:63–73.
De Rosa FG, Cavallerio P, Corcione S, Parlato C, Fossati L, Serra R, et al. Molecular characterization of toxigenic Clostridium difficile in a northern Italian hospital. Curr Microbiol. 2015;70:154–5.
Geric B, Johnson S, Gerding DN, Grabnar M, Rupnik M. Frequency of binary toxin genes among Clostridium difficile strains that do not produce large clostridial toxins. J Clin Microbiol. 2003;41:5227–32.
Barth H. Uptake of binary actin ADP-ribosylating toxins. Rev Physiol Biochem Pharmacol. 2004;152:165–82.
Bacci S, Mølbak K, Kjeldsen MK, Olsen KE. Binary toxin and death after clostridium difficile infection. Emerg Infect Dis. 2011;17:976–82.
Sundriyal A, Roberts AK, Ling R, McGlashan J, Shone CC, Acharya KR. Expression, purification and cell cytotoxicity of actin-modifying binary toxin from Clostridium difficile. Protein Expr Purif. 2010;74:42–8.
Furuya-Kanamori L, Marquess J, Yakob L, Riley TV, Paterson DL, Foster NF, et al. Asymptomatic Clostridium difficile colonization: epidemiology and clinical implications. BMC Infect Dis. 2015;15:516.
Crobach MJT, Vernon JJ, Loo VG, Kong LY, Péchiné S, Wilcox MH, Kuijper EJ. Understanding Clostridium difficile colonization. Clin Microbiol Rev. 2018;31(2):e00021.
Zacharioudakis IM, Zervou FN, Pliakos EE, Ziakas PD, Mylonakis E. Colonization with toxinogenic C. difficile upon hospital admission, and risk of infection: a systematic review and meta-analysis. Am J Gastroenterol. 2015;110:381–90.
Riley TV, Collins DA, Karunakaran R, Kahar MA, Adnan A, Hassan SA, et al. High prevalence of toxigenic and nontoxigenic Clostridium difficile strains in Malaysia. J Clin Microbiol. 2018;56(6):e00170.
McNamara SE, Abdujamilova N, Somsel P, Gordoncillo MJ, DeDecker JM, Bartlett PC. Carriage of Clostridium difficile and other enteric pathogens among a 4-H avocational cohort. Zoonoses Public Health. 2011;58:192–9.
Arvand M, Moser V, Schwehn C, Bettge-Weller G, Hensgens MP, Kuijper EJ. High prevalence of Clostridium difficile colonization among nursing home residents in Hesse Germany. PLoS One. 2012;7:e30183.
Aronsson B, Mollby R, Nord CE. Antimicrobial agents and Clostridium difficile in acute enteric disease: epidemiological data from Sweden, 1980-1982. J Infect Dis. 1985;151:476–81.
Kato H, Kita H, Karasawa T, Maegawa T, Koino Y, Takakuwa H, et al. Colonisation and transmission of Clostridium difficile in healthy individuals examined by PCR ribotyping and pulsed-field gel electrophoresis. J Med Microbiol. 2001;50:720–7.
Galdys AL, Nelson JS, Shutt KA, Schlackman JL, Pakstis DL, Pasculle AW, et al. Prevalence and duration of asymptomatic Clostridium difficile carriage among healthy subjects in Pittsburgh Pennsylvania. J Clin Microbiol. 2014;52:2406–9.
Stojanović P, Stojanović N, Kocic B, Stanković-Dordević D, Babić T, Stojanović K. Asymptomatic carriers of Clostridium difficile in serbian population. Cent Eur J Med. 2012;7:769–74.
Loo VG, Bourgault AM, Poirier L, Lamothe F, Michaud S, Turgeon N, et al. Host and pathogen factors for Clostridium difficile infection and colonization. N Engl J Med. 2011;365:1693–703.
McFarland LV. Renewed interest in a difficult disease: Clostridium difficile infections—epidemiology and current treatment strategies. Curr Opin Gastroenterol. 2009;25:24–35.
Vecchio AL, Zacur GM. Clostridium difficile infection: an update on epidemiology, risk factors, and therapeutic options. Curr Opin Gastroenterol. 2012;28:1–9.
Hassan SA, Rahman RA, Huda N, Wan Bebakar WM, Lee YY. Hospital-acquired Clostridium difficile infection among patients with type 2 diabetes mellitus in acute medical wards. J R Coll Physicians Edinb. 2013;43:103–7.
Sanders NL, Bollinger RR, Lee R, Thomas S, Parker W. Appendectomy and Clostridium difficile colitis: relationships revealed by clinical observations and immunology. World J Gastroenterol. 2013;19:5607–14.
Seretis C, Seretis F, Goonetilleke K. Appendicectomy and clostridium difficile infection: is there a link? J Clin Med Res. 2014;6:239–41.
Clanton J, Subichin M, Drolshagen K, Daley T, Firstenberg MS. Fulminant Clostridium difficile infection: an association with prior appendectomy? World J Gastrointest Surg. 2013;27:233–8.
Yong FA, Alvarado AM, Wang H, Tsai J, Estes NC. Appendectomy: a risk factor for colectomy in patients with Clostridium difficile. Am J Surg. 2015;209:532–5.
Khanna S, Baddour LM, Dibaise JK, Pardi DS. Appendectomy is not associated with adverse outcomes in clostridium difficile infection: a population-based study. Am J Gastroenterol. 2013;108:626–7.
Huang H, Wu S, Chen R, Xu S, Fang H, Weintraub A, Nord CE. Risk factors of Clostridium difficile infections among patients in a university hospital in Shanghai, China. Anaerobe. 2014;30:65–9.
Walker AS, Eyre DW, Wyllie DH, Dingle KE, Harding RM, O'Connor L, et al. Characterisation of Clostridium difficile hospital ward-based transmission using extensive epidemiological data and molecular typing. PLoS Med. 2012;9:e1001172.
Theriot CM, Young VB. Microbial and metabolic interactions between the gastrointestinal tract and Clostridium difficile infection. Gut Microbes. 2014;5:86–95.
Kamada N, Seo SU, Chen GY, Nunez G. Role of the gut microbiota in immunity and inflammatory disease. Nat Rev Immunol. 2013;13:321–35.
Pérez-Cobas AE, Artacho A, Ott SJ, Moya A, Gosalbes MJ, Latorre A. Structural and functional changes in the gut microbiota associated to Clostridium difficile infection. Front Microbiol. 2014;5:335.
Kamada N, Chen GY, Inohara N, Núñez G. Control of pathogens and pathobionts by the gut microbiota. Nat Immunol. 2013;14:685–90.
Tedesco FJ, Barton RW, Alpers DH. Clindamycin-associated colitis: a prospective study. Ann Intern Med. 1974;81:429–33.
Bartlett JG, Onderdonk AB, Cisneros RL, Kasper DL. Clindamycin-associated colitis due to a toxin-producing species of Clostridium in hamsters. In: Bartlett JG, Onderdonk AB, Cisneros RL, Kasper DL, editors. J Infect Dis. 2004;190:202–9. Commentary
Hensgens MP, Goorhuis A, Dekkers OM, Kuijper EJ. Time interval of increased risk for Clostridium difficile infection after exposure to antibiotics. J Antimicrob Chemother. 2012;67:742–8.
Kazakova SV, Ware K, Baughman B, Bilukha O, Paradis A, Sears S, et al. A hospital outbreak of diarrhea due to an emerging epidemic strain of Clostridium difficile. Arch Intern Med. 2006;166:2518–24.
Muto CA, Pokrywka M, Shutt K, Mendelshon AB, Nouri K, Posey K, et al. A large outbreak of Clostridium difficile–associated disease with an unexpected proportion of deaths and colectomies at a teaching hospital following increased fluoroquinolone use. Infect Control Hosp Epidemiol. 2005;26:273–80.
Loo VG, Poirier L, Miller MA, Oughton M, Libman MB, Michaud S, et al. A predominately clonal multi-institutional outbreak of Clostridium difficile-associated diarrhea with high morbidity and mortality. N Engl J Med. 2005;353:2442–9.
Pépin J, Saheb N, Coulombe MA, Alary ME, Corriveau MP, Authier S, et al. Emergence of fluoroquinolones as the predominant risk factor for Clostridium difficile-associated diarrhea: a cohort study during an epidemic in Quebec. Clin Infect Dis. 2005;41:1254–60.
Dubberke ER, Reske KA, Yan Y, Olsen MA, McDonald LC, Fraser VJ. Clostridium difficile-associated disease in a setting of endemicity: identification of novel risk factors. Clin Infect Dis. 2007;45:1543–9.
Owens RC, Donskey CJ, Gaynes RP, Loo VG, Muto CA. Antimicrobial-associated risk factors for Clostridium difficile infection. Clin Infect Dis. 2008;46:19–31.
McCusker ME, Harris AD, Perencevich E, Roghmann M. Fluoroquinolone use and Clostridium difficile-associated diarrhea. Emerg Infect Dis. 2003;9:730–3.
Gerding DN, Olson MM, Peterson LR, Teasley LR, Gebhard RL, Schwartz ML, Lee JT Jr. Clostridium difficile-associated diarrhea and colitis in adults. Arch Intern Med. 1986;146:95–100.
Brown E, Talbot GH, Axelrod P, Provencher M, Hoegg C. Risk factors for Clostridium difficile toxin-associated diarrhea. Infect Control Hosp Epidemiol. 1990;11:283–90.
Oldfield EC IV, Oldfield EC III, Johnson DA. Clinical update for the diagnosis and treatment of Clostridium difficile infection. World J Gastrointest Pharmacol Ther. 2014;5:1–26.
Privitera G, Scarpellini P, Ortisi G, Nicastro G, Nicolin R, De Lalla F. Prospective study of Clostridium difficile intestinal colonization and disease following single-dose antibiotic prophylaxis in surgery. Antimicrob Agents Chemother. 1991;35:208–10.
Yee J, Dixon CM, McLean AP, Meakins JL. Clostridium difficile disease in a department of surgery. The significance of prophylactic antibiotics. Arch Surg. 1991;126:241–6.
Al-Obaydi W, Smith CD, Foguet P. Changing prophylactic antibiotic protocol for reducing Clostridium difficile-associated diarrhoeal infections. J Orthop Surg (Hong Kong). 2010;18:320–3.
Cunningham R, Dale B, Undy B, Gaunt N. Proton pump inhibitors as a risk factor for Clostridium difficile diarrhoea. J Hosp Infect. 2003;54:243–5.
Dial S, Alrasadi K, Manoukian C, Huang A, Menzies D. Risk of Clostridium difficile diarrhea among hospital inpatients prescribed proton pump inhibitors: cohort and case-control studies. CMAJ. 2004;171:33–8.
Kwok CS, Arthur AK, Anibueze CI, Singh S, Cavallazzi R, Loke YK. Risk of Clostridium difficile infection with acid suppressing drugs and antibiotics: meta-analysis. Am J Gastroenterol. 2012;107:1011–9.
Shah S, Lewis A, Leopold D, Dunstan F, Woodhouse K. Gastric acid suppression does not promote clostridial diarrhoea in the elderly. QJM. 2000;93:175–81.
Cao F, Chen CX, Wang M, Liao HR, Wang MX, Hua SZ, et al. Updated meta-analysis of controlled observational studies: proton-pump inhibitors and risk of Clostridium difficile infection. J Hosp Infect. 2018;98:4–13.
Azab M, Doo L, Doo DH, Elmofti Y, Ahmed M, Cadavona JJ, et al. Comparison of the hospital-acquired Clostridium difficile infection risk of using proton pump inhibitors versus histamine-2 receptor antagonists for prophylaxis and treatment of stress ulcers: a systematic review and meta-analysis. Gut Liver. 2017;11:781–8.
Wijarnpreecha K, Sornprom S, Thongprayoon C, Phatharacharukul P, Cheungpasitporn W. Nasogastric tube and outcomes of Clostridium difficile infection: a systematic review and meta-analysis. J Evid Based Med. 2018;11:40–5.
Kent KC, Rubin MS, Wroblewski L, Hanff PA, Silen W. The impact of Clostridium difficile on a surgical service: a prospective study of 374 patients. Ann Surg. 1998;227:296–301.
McDonald LC, Killgore GE, Thompson A, Owens RC Jr, Kazakova SV, Sambol SP, et al. An epidemic, toxin gene-variant strain of Clostridium difficile. N Engl J Med. 2005;353:2433–41.
Rodrigues MA, Brady RR, Rodrigues J, Graham C, Gibb AP. Clostridium difficile infection in general surgery patients; identification of high-risk populations. Int J Surg. 2010;8:368–72.
Kim MJ, Kim BS, Kwon JW, Ahn SE, Lee SS, Park HC, Lee BH. Risk factors for the development of Clostridium difficile colitis in a surgical ward. J Korean Surg Soc. 2012;83:14–20.
Yasunaga H, Horiguchi H, Hashimoto H, Matsuda S, Fushimi K. The burden of Clostridium difficile-associated disease following digestive tract surgery in Japan. J Hosp Infect. 2012;82:175–80.
Wren SM, Ahmed N, Jamal A, Safadi BY. Preoperative oral antibiotics in colorectal surgery increase the rate of Clostridium difficile colitis. Arch Surg. 2005;140:752–6.
Yeom CH, Cho MM, Baek SK, Bae OS. Risk factors for the development of Clostridium difficile-associated colitis after colorectal Cancer surgery. J Korean Soc Coloproctol. 2010;26:329–33.
Damle RN, Cherng NB, Flahive JM, Davids JS, Maykel JA, Sturrock PR, et al. Clostridium difficile infection after colorectal surgery: a rare but costly complication. J Gastrointest Surg. 2014;18:1804–11.
Skancke M, Vaziri K, Umapathi B, Amdur R, Radomski M, Obias V. Elective stoma reversal has a higher incidence of postoperative Clostridium difficile infection compared with elective colectomy: an analysis using the American College of Surgeons National Surgical Quality Improvement Program and targeted colectomy databases. Dis Colon Rectum. 2018;61:593–8.
Lumpkins K, Bochicchio GV, Joshi M, Gens R, Bochicchio K, Conway A, et al. Clostridium difficile infection in critically injured trauma patients. Surg Infect. 2008;9:497–501.
Bishara J, Farah R, Mograbi J, Khalaila W, Abu-Elheja O, Mahamid M, Nseir W. Obesity as a risk factor for Clostridium difficile infection. Clin Infect Dis. 2013;57:489–93.
Leung J, Burke B, Ford D, Garvin G, Korn C, Sulis C, Bhadelia N. Possible association between obesity and Clostridium difficile infection. Emerg Infect Dis. 2013;19:1791–8.
Nathanson BH, Higgins TL. McGee WT the dangers of extreme body mass index values in patients with Clostridium difficile. Infection. 2017;45:787–93.
Punni E, Pula JL, Asslo F, Baddoura W, DeBari VA. Is obesity a risk factor for Clostridium difficile infection? Obes Res Clin Pract. 2015;9:50–4.
Mulki R, Baumann AJ, Alnabelsi T, Sandhu N, Alhamshari Y, Wheeler DS. Body mass index greater than 35 is associated with severe Clostridium difficile infection. Aliment Pharmacol Ther. 2017;45:75–81.
Hussan H, Ugbarugba E, Bailey MT, Porter K, Needleman B, Noria S, et al. The impact of bariatric surgery on short term risk of Clostridium difficile admissions. Obes Surg. 2018;28:2006–13.
Stallmach A, Anttila VJ, Hell M, Gwynn S, Merino-Amador P, Petrosillo N, et al. Inflammatory bowel disease and Clostridium difficile infection: contrasting views of international clinical professionals. Z Gastroenterol. 2018;56:731.
Navaneethan U, Mukewar S, Venkatesh PG, Lopez R, Shen B, Nitzan O, et al. Clostridium difficile infection is associated with worse long term outcome in patients with ulcerative colitis. J Crohns Colitis. 2012;6:330–6.
Jodorkovsky D, Young Y, Abreu MT. Clinical outcomes of patients with ulcerative colitis and co-existing Clostridium difficile infection. Dig Dis Sci. 2010;55:415–20.
Issa M, Vijayapal A, Graham MB, Beaulieu DB, Otterson MF, Lundeen S, et al. Impact of Clostridium difficile on inflammatory bowel disease. Clin Gastroenterol Hepatol. 2007;5:345–51.
Ananthakrishnan AN, McGinley EL, Binion DG. Excess hospitalisation burden associated with Clostridium difficile in patients with inflammatory bowel disease. Gut. 2008;57:205–10.
Chen Y, Furuya-Kanamori L, Doi SA, Ananthakrishnan AN, Kirk M. Clostridium difficile infection and risk of colectomy in patients with inflammatory bowel disease: a bias-adjusted meta-analysis. Inflamm Bowel Dis. 2017;23:200–7.
Clayton EM, Rea MC, Shanahan F, Quigley EM, Kiely B, Hill C, Ross RP. The vexed relationship between Clostridium difficile and inflammatory bowel disease: an assessment of carriage in an outpatient setting among patients in remission. Am J Gastroenterol. 2009;104:1162–9.
Schneeweiss S, Korzenik J, Solomon DH, Canning C, Lee J, Bressler B. Infliximab and other immunomodulating drugs in patients with inflammatory bowel disease and the risk of serious bacterial infections. Aliment Pharmacol Ther. 2009;30:253–64.
Kariv R, Navaneethan U, Venkatesh PG, Lopez R, Shen B. Impact of Clostridium difficile infection in patients with ulcerative colitis. J Crohns Colitis. 2011;5:34–40.
Rezapour M, Galoosian A, Liu B, Bhuket T, Wong RJ. Clostridium difficile co-infection in inflammatory bowel disease is associated with significantly increased in-hospital mortality. Eur J Gastroenterol Hepatol. 2018;30:1041–6.
Absah I, Faubion WA. Concomitant therapy with methotrexate and anti-TNF-α in pediatric patients with refractory crohn’s colitis: a case series. Inflamm Bowel Dis. 2012;18:1488–92.
Rodemann JF, Dubberke ER, Reske KA, da Seo H, Stone CD. Incidence of Clostridium difficile infection in inflammatory bowel disease. Clin Gastroenterol Hepatol. 2007;5:339–44.
Li Y, Qian J, Queener E, Shen B. Risk factors and outcome of PCR-detected Clostridium difficile infection in ileal pouch patients. Inflamm Bowel Dis. 2013;19:397–403.
Tsironi E, Irving PM, Feakins RM, Rampton DS. “Diversion” colitis caused by Clostridium difficile infection: report of a case. Dis Colon Rectum. 2006;49:1074–7.
Ben-Horin S, Margalit M, Bossuyt P, Maul J, Shapira Y, Bojic D, et al. Prevalence and clinical impact of endoscopic pseudomembranes in patients with inflammatory bowel disease and Clostridium difficile infection. J Crohns Colitis. 2010;4:194–8.
Yanai H, Nguyen GC, Yun L, Lebwohl O, Navaneethan U, Stone CD, et al. Practice of gastroenterologists in treating flaring inflammatory bowel disease patients with clostridium difficile: antibiotics alone or combined antibiotics/immunomodulators? Inflamm Bowel Dis. 2011;17:1540–6.
Khanna S, Shin A, Kelly CP. Management of Clostridium difficile infection in inflammatory bowel disease: expert review from the clinical practice updates committee of the AGA Institute. Clin Gastroenterol Hepatol. 2017;15:166–74.
Honda H, Dubberke ER. Clostridium difficile infection in solid organ transplant recipients. Curr Opin Infect Dis. 2014;27:336–41.
Albright JB, Bonatti H, Mendez J, Kramer D, Stauffer J, Hinder R, et al. Early and late onset Clostridium difficile-associated colitis following liver transplantation. Transpl Int. 2007;20:856–66.
Chopra T, Alangaden GJ, Chandrasekar P. Clostridium difficile infection in cancer patients and hematopoietic stem cell transplant recipients. Expert Rev Anti-Infect Ther. 2010;8:1113–9.
Rodríguez Garzotto A, Mérida García A, Muñoz Unceta N, Galera Lopez MM, Orellana-Miguel MA, Díaz-García CV, et al. Risk factors associated with Clostridium difficile infection in adult oncology patients. Support Care Cancer. 2015;23:1569–77.
Haines CF, Moore RD, Bartlett JG, Sears CL, Cosgrove SE, Carroll K, Gebo KA. Clostridium difficile in a HIV-infected cohort: incidence, risk factors, and clinical outcomes. AIDS. 2013;27:2799–807.
Collini PJ, Kuijper E, Dockrell DH. Clostridium difficile infection in patients with HIV/AIDS. Curr HIV/AIDS Rep. 2013;10:273–82.
Furuya-Kanamori L, Riley TV, Paterson DL, Foster NF, Huber CA, Hong S, et al. Comparison of Clostridium difficile ribotypes circulating in Australian hospitals and communities. J Clin Microbiol. 2016;55:216–25.
Lessa FC, Winston LG, McDonald LC. Emerging infections program C. difficile surveillance team. Burden of Clostridium difficile infection in the United States. N Engl J Med. 2015;372:825–34.
Namiki H, Kobayashi T. Long-term, low-dose of clarithromycin as a cause of community-acquired Clostridium difficile infection in a 5-year-old boy. Oxf Med Case Reports. 2018;2018:omx106.
Khanna S, Pardi DS, Aronson SL, Kammer PP, Baddour LM. Outcomes in community-acquired Clostridium difficile infection. Aliment Pharmacol Ther. 2012;35:613–8.
Gupta A, Khanna S. Community-acquired Clostridium difficile infection: an increasing public health threat. Infect Drug Resist. 2014;7:63–72.
Furuya-Kanamori L, Stone JC, Clark J, McKenzie SJ, Yakob L, Paterson DL, et al. Comorbidities, exposure to medications, and the risk of community-acquired Clostridium difficile infection: a systematic review and meta-analysis. Infect Control Hosp Epidemiol. 2015;36:132–41.
Zainul NH, Ma ZF, Besari A, Siti Asma H, Rahman RA, Collins DA, et al. Prevalence of Clostridium difficile infection and colonization in a tertiary hospital and elderly community of north-eastern peninsular Malaysia. Epidemiol Infect. 2017;145:3012–9.
Garey KW, Sethi S, Yadav Y, DuPont HL. Meta-analysis to assess risk factors for recurrent Clostridium difficile infection. J Hosp Infect. 2008;70:298–304.
Eyre DW, Walker AS, Wyllie D, Dingle KE, Griffiths D, Finney J, et al. Predictors of first recurrence of Clostridium difficile infection: implications for initial management. Clin Infect Dis. 2012;55:77–87.
Zilberberg MD, Reske K, Olsen M, Yan Y, Dubberke ER. Risk factors for recurrent Clostridium difficile infection (CDI) hospitalization among hospitalized patients with an initial CDI episode: a retrospective cohort study. BMC Infect Dis. 2014;14:306.
Rotramel A, Poritz LS, Messaris E, Berg A, Stewart DB. PPI therapy and albumin are better predictors of recurrent Clostridium difficile colitis than choice of antibiotics. J Gastrointest Surg. 2012;16:2267–73.
Petrosillo N. Tackling the recurrence of Clostridium difficile infection. Med Mal Infect. 2018;48:18–22.
Deshpande A, Pasupuleti V, Thota P, Pant C, Rolston DD, Hernandez AV, et al. Risk factors for recurrent Clostridium difficile infection: a systematic review and meta-analysis. Infect Control Hosp Epidemiol. 2015;36:452–60.
Cornely OA, Miller MA, Louie TJ, Crook DW, Gorbach SL. Treatment of first recurrence of Clostridium difficile infection: fidaxomicin versus vancomycin. Clin Infect Dis. 2012;55:154–61.
McFarland LV, Clarridge JE, Beneda HW, Raugi GJ. Fluoroquinolone use and risk factors for Clostridium difficile-associated disease within a veterans administration health care system. Clin Infect Dis. 2007;45:1141–51.
Jaber MR, Olafsson S, Fung WL, Reeves ME. Clinical review of the management of fulminant clostridium difficile infection. Am J Gastroenterol. 2008;103:3195–203.
Kazanowski M, Smolarek S, Kinnarney F, Grzebieniak Z. Clostridium difficile: epidemiology, diagnostic and therapeutic possibilities—a systematic review. Tech Coloproctol. 2014;18:223–32.
Welfare MR, Lalayiannis LC, Martin KE, Corbett S, Marshall B, Sarma JB. Co-morbidities as predictors of mortality in Clostridium difficile infection and derivation of the ARC predictive score. J Hosp Infect. 2011;79:359–63.
Hu MY, Katchar K, Kyne MS, Tummala S, Dreisbach V, et al. Prospective derivation and validation of a clinical prediction rule for recurrent Clostridium difficile infection. Gastroenterology. 2009;136:1206–14.
Voelker R. Increased Clostridium difficile virulence demands new treatment approach. JAMA. 2010;26:2017–9.
Bauer MP, Hensgens MPM, Miller MA, Gerding DN, Wilcox MH, Dale AP, et al. Renal failure and leukocytosis are predictors of a complicated course of Clostridium difficile infection if measured on day of diagnosis. Clin Infect Dis. 2012;55:149–53.
Abou Chakra CN, Pepin J, Valiquette L. Prediction tools for unfavourable outcomes in Clostridium difficile infection: a systematic review. PLoS One. 2012;7:e30258.
Miller MA, Louie T, Mullane K, Weiss K, Lentnek A, Golan Y, et al. Derivation and validation of a simple clinical bedside score (ATLAS) for Clostridium difficile infection which predicts response to therapy. BMC Infect Dis. 2013;13:148.
Cohen SH, Gerding DN, Johnson S, Kelly CP, Loo VG, McDonald LC, et al. Clinical practice guidelines for Clostridium difficile infection in adults: 2010 update by the society for healthcare epidemiology of America (SHEA) and the infectious diseases society of America (IDSA). Infect Control Hosp Epidemiol. 2010;31:431–55.
Di Masi A, Leboffe L, Polticelli F, Tonon F, Zennaro C, Caterino M, et al. Human serum albumin is an essential component of the host defense mechanism against Clostridium difficile intoxication. J Infect Dis. 2018;22:1424–35.
Flegel W, Muller F, Daubener W, Fisher HG, Hadding U, Northoff H. Cytokine response by human monocytes to Clostridium difficile toxin a and toxin B. Infect Immun. 1991;59:3659–66.
Castagliuolo I, Keates AC, Wang CC, Pasha A, Valenick L, Kelly CP, et al. Clostridium difficile toxin a stimulates macrophage- inflammatory protein-2 production in rat intestinal epithelial cells. J Immunol. 1998;160:6039–45.
Dallal RM, Harbrecht BG, Boujoukas AJ, Sirio CA, Farkas LM, Lee KK, Simmons RL. Fulminant Clostridium difficile: an underappreciated and increasing cause of death and complications. Ann Surg. 2002;235:363–72.
Adams SD, Mercer DW. Fulminant Clostridium difficile colitis. Curr Opin Crit Care. 2007;13:450–5.
Malnick SD, Zimhony O. Treatment of Clostridium difficile-associated diarrhea. Ann Pharmacother. 2002;36:1767–75.
McFarland LV, Elmer GW, Surawicz CM. Breaking the cycle: treatment strategies for 163 cases of recurrent Clostridium difficile disease. Am J Gastroenterol. 2002;97:1769–75.
Kelly JP. Can we identify patients at high risk of recurrent Clostridium difficile infection? Clin Microbiol Infect. 2012;18(Suppl 6):21–7.
Fekety R, McFarland LV, Surawicz CM, Greenberg RN, Elmer GW, Mulligan ME. Recurrent Clostridium difficile diarrhea: characteristics of and the risk factors for patients enrolled in a prospective, randomized, double-blinded trial. Clin Infect Dis. 1997;24:324–33.
Johnson S. Recurrent Clostridium difficile infection: a review of risk factors, treatments, and outcomes. J Inf Secur. 2009;58:403–10.
Samie AA, Traub M, Bachmann K, Kopischke K, Theilmann L. Risk factors for recurrence of Clostridium difficile-associated diarrhea. Hepatogastroenterology. 2013;60:1351–4.
LaBarbera FD, Nikiforov I, Parvathenani A, Pramil V, Gorrepati S. A prediction model for Clostridium difficile recurrence. J Community Hosp Intern Med Perspect. 2015;5:26033.
Hookman P, Barkin JS. Clostridium difficile associated infection, diarrhea and colitis. World J Gastroenterol. 2009;15:1554–80.
Sheitoyan-Pesant C, Abou Chakra CN, Pépin J, Marcil-Héguy A, Nault V, Valiquette L. Clinical and healthcare burden of multiple recurrences of Clostridium difficile infection. Clin Infect Dis. 2016;62:574–80.
Tabak YP, Zilberberg MD, Johannes RS, Sun X, McDonald LC. Attributable burden of hospital-onset Clostridium difficile infection: a propensity score matching study. Infect Control Hosp Epidemiol. 2013;34:588–96.
Campbell R, Dean B, Nathanson B, Haidar T, Strauss M, Thomas S. Length of stay and hospital costs among high-risk patients with hospital-origin Clostridium difficile-associated diarrhea. J Med Econ. 2013;16:440–8.
Magalini S, Pepe G, Panunzi S, Spada PL, De Gaetano A, Gui D. An economic evaluation of Clostridium difficile infection management in an Italian hospital environment. Eur Rev Med Pharmacol Sci. 2012;16:2136–41.
Egorova NN, Siracuse JJ, McKinsey JF, Nowygrod R. Trend, risk factors and costs of Clostridium difficile infections in vascular surgery. Ann Vasc Surg. 2015;S0890-5096:00015–1.
Skovrlj B, Guzman JZ, Silvestre J, Al Maaieh M, Qureshi SA. Clostridium difficile colitis in patients undergoing lumbar spine surgery. Spine. 2014;39:1167–73.
Mittal C, Hassan S, Arshad S, Jeepalyam S, Bruni S, Miceli M, et al. Clostridium difficile infection in liver transplant recipients: a retrospective study of rates, risk factors and outcomes. Am J Transplant. 2014;14:1901–7.
Lee DY, Chung EL, Guend H, Whelan RL, Wedderburn RV, Rose KM. Predictors of mortality after emergency colectomy for Clostridium difficile colitis: an analysis of ACS-NSQIP. Ann Surg. 2014;259:148–56.
Piacenti FJ, Leuthner KD. Antimicrobial stewardship and Clostridium difficile-associated diarrhea. J Pharm Pract. 2013;26:506–13.
Feazel LM, Malhotra A, Perencevich EN, Kaboli P, Diekema DJ, Schweizer ML. Effect of antibiotic stewardship programmes on Clostridium difficile incidence: a systematic review and meta-analysis. J Antimicrob Chemother. 2014;69:1748–54.
Davey P, Marwick CA, Scott CL, Charani E, McNeil K, Brown E, et al. Interventions to improve antibiotic prescribing practices forhospital inpatients. Cochrane Database Syst Rev. 2017;2:CD003543.
Dingle KE, Didelot X, Quan TP, Eyre DW, Stoesser N, Golubchik T, et al. Modernising medical microbiology informatics group. Effects of control interventions on Clostridium difficile infection in England: an observational study. Lancet Infect Dis. 2017;17:411–21.
Marufu O, Desai N, Aldred D, Brown T, Eltringham I. Analysis of interventions to reduce the incidence of Clostridium difficile infection at a London teaching hospital trust, 2003-2011. J Hosp Infect. 2014;89:38–45.
Barker AK, Ngam C, Musuuza JS, Vaughn VM, Safdar N. Reducing Clostridium difficile in the inpatient setting: a systematic review of the adherence to and effectiveness of C. difficile prevention bundles. Infect Control Hosp Epidemiol. 2017;38:639–50.
Owens RC. Clostridium difficile-associated disease: an emerging threat to patient safety: insights from the Society of Infectious Diseases Pharmacists. Pharmacotherapy. 2006;26:299–311.
Longtin Y, Paquet-Bolduc B, Gilca R, Garenc C, Fortin E, Longtin J, et al. Effect of detecting and isolating Clostridium difficile carriers at hospital admission on the incidence of C. difficile infections: a quasi-experimental controlled study. JAMA Intern Med. 2016;176:796–804.
Garner JS. Guideline for isolation precautions in hospitals. The hospital infection control practices advisory committee. Infect Control Hosp Epidemiol. 1996;17:53–80.
Vonberg RP, Kuijper EJ, Wilcox MH, Barbut F, Tull P, Gastmeier P, et al. Infection control measures to limit the spread of Clostridium difficile. Clin Microbiol Infect. 2008;14:2–20.
Chang VT, Nelson K. The role of physical proximity in nosocomial diarrhea. Clin Infect Dis. 2000;31:717–22.
Gerding DN, Meyer T, Lee C, Cohen SH, Murthy UK, Poirier A, et al. Administration of spores of nontoxigenic Clostridium difficile strain M3 for prevention of recurrent C. difficile infection: a randomized clinical trial. JAMA. 2015;313:1719–27.
Brouwer MS, Roberts AP, Hussain H, Williams RJ, Allan E, Mullany P. Horizontal gene transfer converts non-toxigenic Clostridium difficile strains into toxin producers. Nat Commun. 2013;4:2601.
Curry SR, Muto CA, Schlackman JL, Pasculle AW, Shutt KA, Marsh JW, Harrison LH. Use of multilocus variable number of tandem repeats analysis genotyping to determine the role of asymptomatic carriers in Clostridium difficile transmission. Clin Infect Dis. 2013;57:1094–102.
Biswas JS, Patel A, Otter JA, van Kleef E, Goldenberg SD. Contamination of the hospital environment from potential Clostridium difficile excretors without active infection. Infect Control Hosp Epidemiol. 2015;36:975–7.
Oughton MT, Loo VG, Dendukuri N, Fenn S, Libman MD. Hand hygiene with soap and ater is superior to alcohol rub and antiseptic wipes for removal of Clostridium difficile. Infect Control Hosp Epidemiol. 2009;30:939–44.
Willt M, Odenhott I, Walder M. Activity of three disinfectants and acidified nitrate against Clostridium difficile spores. Infect Control Hosp Epidemiol. 2003;24:765–8.
Deyneko A, Cordeiro F, Berlin L, Ben-David D, Perna S, Longtin Y. Impact of sink location on hand hygiene compliance after care of patients with Clostridium difficile infection: a cross-sectional study. BMC Infect Dis. 2016;16:203.
Louh IK, Greendyke WG, Hermann EA, Davidson KW, Falzon L, Vawdrey DK, et al. Clostridium difficile infection in acute care hospitals: systematic review and best practices for prevention. Infect Control Hosp Epidemiol. 2017;38:476–82.
Barbut F. How to eradicate Clostridium difficile from the environment. J Hosp Infect. 2015;89:287–95.
McCord J, Prewitt M, Dyakova E, Mookerjee S, Otter JA. Reduction in Clostridium difficile infection associated with the introduction of hydrogen peroxide vapour automated room disinfection. J Hosp Infect. 2016;94:185–7.
Marra AR, Schweizer ML, Edmond MB. No-touch disinfection methods to decrease multidrug-resistant organism infections: a systematic review and meta-analysis. Infect Control Hosp Epidemiol. 2018;39:20–31.
Tschudin-Sutter S, Kuijper EJ, Durovic A, Vehreschild MJGT, Barbut F, Eckert C, et al. Guidance document for prevention of Clostridium difficile infection in acute healthcare settings. Clin Microbiol Infect. 2018;24:1051.
Huber CA, Foster NF, Riley TV, Paterson DL. Challenges for standardization of Clostridium difficile typing methods. J Clin Microbiol. 2013;51:2810–4.
McDonald EG, Lee TC. Clostridium difficile infection. N Engl J Med. 2015;373:286–8.
Barbut F, Surgers L, Eckert C, Visseaux B, Cuingnet M, Mesquita C, et al. Does a rapid diagnosis of Clostridium difficile infection impact on quality of patient management? Clin Microbiol Infect. 2014;20:136–44.
Kundrapu S, Sunkesula VC, Jury LA, Sethi AK, Donskey CJ. Utility of perirectal swab specimens for diagnosis of Clostridium difficile infection. Clin Infect Dis. 2012;55:1527–30.
Carroll KC. Tests for the diagnosis of Clostridium difficile infection: the next generation. Anaerobe. 2011;17:170–4.
Kyne L, Warny M, Qamar A, Kelly CP. Asymptomatic carriage of Clostridium difficile and serum levels of IgG antibody against toxin A. N Engl J Med. 2000;342:390–7.
Planche T, Aghaizu A, Holliman R, Riley P, Poloniecki J, Breathnach A, Krishna S. Diagnosis of Clostridium difficile infection by toxin detection kits: a systematic review. Lancet Infect Dis. 2008;8:777–84.
Brecher SM, Novak-Weekley SM, Nagy E. Laboratory diagnosis of Clostridium difficile infections: there is light at the end of the colon. Clin Infect Dis. 2013;57:1175–81.
Chen S, Gu H, Sun C, Wang H, Wang J. Rapid detection of Clostridium difficile toxins and laboratory diagnosis of Clostridium difficile infections. Infection. 2017;45:255–62.
Gerding DN, Johnson S, Rupnik M, Aktories K. Clostridium difficile binary toxin CDT: mechanism, epidemiology, and potential clinical importance. Gut Microbes. 2014;5:15–27.
Gilligan PH. Optimizing the laboratory diagnosis of Clostridium difficile infection. Clin Lab Med. 2015;35:299–312.
Smits WK, Lyras D, Lacy DB, Wilcox MH, Kuijper EJ. Clostridium difficile infection. Nat Rev Dis Primers. 2016;2:16020.
Lyerly DM, Barroso LA, Wilkins TD. Identification of the latex test-reactive protein of Clostridium difficile as glutamate dehydrogenase. J Clin Microbiol. 1991;29:2639–42.
Polage CR, et al. Outcomes in patients tested for Clostridium difficile toxins. Diagn Microbiol Infect Dis. 2012;74:369–73.
Schmidt ML, Gilligan PH. Clostridium difficile testing algorithms: what is practical and feasible? Anaerobe. 2009;15:270–3.
Planche TD, Davies KA, Coen PG, Finney JM, Monahan IM, Morris KA, et al. Differences in outcome according to Clostridium difficile testing method: a prospective multicentre diagnostic validation study of C. difficile infection. Lancet Infect Dis. 2013;13:936–45.
Martínez-Meléndez A, Camacho-Ortiz A, Morfin-Otero R, Maldonado-Garza HJ, Villarreal-Treviño L, Garza-González E. Current knowledge on the laboratory diagnosis of Clostridium difficile infection. World J Gastroenterol. 2017;23:1552–67.
Napolitano LM, Edmiston CE Jr. Clostridium difficile disease: diagnosis, pathogenesis, and treatment update. Surgery. 2017;162:325–48.
Ros PR, Buetow PC, Pantograg-Brown L, Forsmark CE, Sobin LH. Pseudomembranous colitis. Radiology. 1996;198:1–9.
Merine DS, Fishman EK, Jones B. Pseudomembranous colitis: CT evaluation. J Comput Assist Tomogr. 1987;2:1017–20.
Fishman EK, Kavuru M, Jones B, Kuhlman JE, Merine DS, Lillimoe KD, Siegelman SS. Pseudomembranous colitis: CT evaluation of 26 cases. Radiology. 1991;180:57–60.
Boland GW, Lee MJ, Cats AM, Gaa JA, Saini S, Mueller PR. Antibiotic-induced diarrhea: specificity of abdominal CT for the diagnosis of Clostridium difficile disease. Radiology. 1994;191:103–6.
Wang MF, Ding Z, Zhao J, Jiang CQ, Liu ZS, Qian Q. Current role of surgery for the treatment of fulminant Clostridium difficile colitis. Chin Med J. 2013;126:949–56.
Kirkpatrick ID, Greenberg HM. Evaluating the CT diagnosis of Clostridium difficile colitis: should CT guide therapy? Am J Roentgenol. 2001;176:635–9.
Abu-Zidan FM. Point-of-care ultrasound in critically ill patients: where do we stand? J Emerg Trauma Shock. 2012;5:70–1.
O'Malley ME, Wilson SR. US of gastrointestinal tract abnormalities with CT correlation. Radiographics. 2003;23:59–72.
Downey DB, Wilson SR. Pseudomembranous colitis: sonographic features. Radiology. 1991;180:61–4.
Ramachandran I, Sinha R, Rodgers P. Pseudomembranous colitis revisited: spectrum of imaging findings. Clin Radiol. 2006;61:535–44.
Razzaq R, Sukumar SA. Ultrasound diagnosis of clinically undetected Clostridium difficile toxin colitis. Clin Radiol. 2006;61:446–52.
Johal SS, Hammond J, Solomon K, James PD, Mahida YR. Clostridium difficile associated diarrhoea in hospitalised patients: onset in the community and hospital and role of flexible sigmoidoscopy. Gut. 2004;53:673–7.
Kyne L, Merry C, O’Connell B, Kelly A, Keane C, O’Neill D. Factors associated with prolonged symptoms and severe disease due to Clostridium difficile. Age Ageing. 1999;28:107–13.
Bagdasarian N, Rao K, Malani PN. Diagnosis and treatment of Clostridium difficile in adults: a systematic review. JAMA. 2015;313:398–408.
Bartlett JG. The case for vancomycin as the preferred drug for treatment of Clostridium difficile infection. Clin Infect Dis. 2008;46:1489–92.
Teasley DG, Gerding DN, Olson MM, Peterson LR, Gebhard RL, Schwartz MJ, Lee JT Jr. Prospective randomised trial of metronidazole vs vancomycin for Clostridium difficile-associated diarrhea and colitis. Lancet. 1983;2:1043–6.
Fekety R, Silva J, Buggy B, Deery HG. Treatment of antibiotic-associated colitis with vancomycin. J Antimicrob Chemother. 1984;14:97–102.
Bartlett JG, Tedesco FJ, Shull S, Lowe B, Chang T. Symptomatic relapse after oral vancomycin therapy of antibiotic-associated pseudomembranous colitis. Gastroenterology. 1980;78:431–4.
Louie TJ, Miller MA, Mullane KM, Weiss K, Lentnek A, Golan Y, et al. Fidaxomicin versus vancomycin for Clostridium difficile infection. N Engl J Med. 2011;364:422–31.
Cornely OA, Crook DW, Esposito R, Poirier A, Somero MS, Weiss K, et al. Fidaxomicin versus vancomycin for infection with Clostridium difficile in Europe, Canada, and the USA: a double-blind, non-inferiority, randomised controlled trial. Lancet Infect Dis. 2012;12:281–9.
Gerber M, Ackermann G. OPT-80. A macrocyclic antimicrobial agent for the treatment of clostridium difficile infections: a review. Expert Opin Investig Drugs. 2008;17:547–53.
Nelson RL. Antibiotic treatment for Clostridium difficile-associated diarrhea in adults. Cochrane Database Syst Rev. 2011;11:CD004610.
Goolsby TA, Jakeman B, Gaynes RP. Clinical relevance of metronidazole and peripheral neuropathy: a systematic review of the literature. Int J Antimicrob Agents. 2018;51:319–25.
McDonald LC, Gerding DN, Johnson S, Bakken JS, Carroll KC, Coffin SE, et al. Clinical practice guidelines for Clostridium difficile infection in adults and children: 2017 update by the Infectious Diseases Society of America (IDSA) and Society for Healthcare Epidemiology of America (SHEA). Clin Infect Dis. 2018;66:e1–e48.
Li R, Lu L, Lin Y, Wang M, Liu X. Efficacy and safety of metronidazole monotherapy versus vancomycin monotherapy or combination therapy in patients with Clostridium difficile infection: a systematic review and meta-analysis. PLoS One. 2015;10:e0137252.
Nelson RL, Suda KJ, Evans CT. Antibiotic treatment for Clostridium difficile-associated diarrhoea in adults. Cochrane Database Syst Rev. 2017;3:CD004610.
Zar FA, Bakkanagari SR, Moorthi KM, Davis MB. A comparison of vancomycin and metronidazole for the treatment of Clostridium difficile-associated diarrhea, stratified by disease severity. Clin Infect Dis. 2007;45:302–7.
Al-Nassir WN, Sethi AK, Nerandzic MM, Bobulsky GS, Jump RL, Donskey CJ. Comparison of clinical and microbiological response to treatment of Clostridium difficile -associated disease with metronidazole and vancomycin. Clin Infect Dis. 2008;47:56–62.
Johnson S, Louie TJ, Gerding DN, Cornely OA, Chasan-Taber S, Fitts D, et al. Vancomycin, metronidazole, or tolevamer for Clostridium difficile infection: results from two multinational, randomized, controlled trials. Clin Infect Dis. 2014;59:345–54.
Kim PK, Zhao P, Teperman S. Evolving treatment strategies for severe Clostridium difficile colitis: defining the therapeutic window. In: Sartelli M, Bassetti M, Martin-Loeches I, editors. Abdominal Sepsis. A multidisciplinary approach. Hot topics in acute care surgery and trauma. Cham: Springer; 2018. p. 225–39.
Kim PK, Huh HC, Cohen HW, Feinberg EJ, Ahmad S, Coyle C, et al. Intracolonic vancomycin for severe Clostridium difficile colitis. Surg Infect. 2013;14:532–9.
Eiland EH 3rd, Sawyer AJ, Massie NL. Fidaxomicin use and clinical outcomes for Clostridium difficile-associated diarrhea. Infect Dis Clin Pract (Baltim Md). 2015;23:32–5.
Vargo CA, Bauer KA, Mangino JE, Johnston JE, Goff DA. An antimicrobial stewardship program's real-world experience with fidaxomicin for treatment of Clostridium difficile infection: a case series. Pharmacotherapy. 2014;34:901–9.
Guery B, Menichetti F, Anttila VJ, Adomakoh N, Aguado JM, Bisnauthsing K, et al. Extended-pulsed fidaxomicin versus vancomycin for Clostridium difficile infection in patients 60 years and older (EXTEND): a randomised, controlled, open-label, phase 3b/4 trial. Lancet Infect Dis. 2018;18:296–307.
Herpers BL, Vlaminckx B, Burkhardt O, Blom H, Biemond-Moeniralam HS, Hornef M, et al. Intravenous tigecycline as adjunctive or alternative therapy for severe refractory Clostridium difficile infection. Clin Infect Dis. 2009;48:1732–5.
El-Herte RI, Baban TA, Kanj SS. Recurrent refractory Clostridium difficile colitis treated successfully with rifaximin and tigecycline: a case report and review of the literature. Scand J Infect Dis. 2012;44:228–30.
Musher DM, Logan N, Mehendiratta V, Melgarejo NA, Garud S, Hamill RJ. Clostridium difficile colitis that fails conventional metronidazole therapy: response to nitazoxanide. J Antimicrob Chemother. 2007;59:705–10.
Girotra M, Kumar V, Khan JM, Damisse P, Abraham RR, Aggarwal V, Dutta SK. Clinical predictors of fulminant colitis in patients with Clostridium difficile infection. Saudi J Gastroenterol. 2012;18:133–9.
Kaiser AM, Hogen R, Bordeianou L, Alavi K, Wise PE, Sudan R, CME Committee of the SSAT. Clostridium difficile infection from a surgical perspective. J Gastrointest Surg. 2015;19:1363–77.
Khanna S, Pardi DS. Clostridium difficile infection: new insights into management. Mayo Clin Proc. 2012;87:1106–17.
Clanton J, Fawley R, Haller N, Daley T, Porter J, Paranjape C, Bonilla H. Patience is a virtue: an argument for delayed surgical intervention in fulminant Clostridium difficile colitis. Am Surg. 2014;80:614–9.
Carchman EH, Peitzman AB, Simmons RL, Zuckerbraun BS. The role of acute care surgery in the treatment of severe, complicated Clostridium difficile-associated disease. J Trauma Acute Care Surg. 2012;73:789–800.
Stewart DB, Hollenbeak CS, Wilson MZ. Is colectomy for fulminant Clostridium difficile colitis life saving? A systematic review. Color Dis. 2013;15:798–804.
Ali SO, Welch JP, Dring RJ. Early surgical intervention for fulminant pseudomembranous colitis. Am Surg. 2008;74:20–6.
Chan S, Kelly M, Helme S, Gossage J, Modarai B, Forshaw M. Outcomes following colectomy for Clostridium difficile colitis. Int J Surg. 2009;7:78–81.
Hall JF, Berger D. Outcome of colectomy for Clostridium difficile colitis: a plea for early surgical management. Am J Surg. 2008;196:384–8.
Osman KA, Ahmed MH, Hamad MA, Mathur D. Emergency colectomy for fulminant Clostridium difficile colitis: striking the right balance. Scand J Gastroenterol. 2011;46:1222–7.
Seder CW, Villalba MR Jr, Robbins J, Ivascu FA, Carpenter CF, Dietrich M, Villalba MR Sr. Early colectomy may be associated with improved survival in fulminant Clostridium difficile colitis: an 8-year experience. Am J Surg. 2009;197:302–7.
Van der Wilden GM, Chang Y, Cropano C, Subramanian M, Schipper IB, Yeh DD, et al. Fulminant Clostridium difficile colitis: prospective development of a risk scoring system. J Trauma Acute Care Surg. 2014;76:424–30.
Ferrada P, Velopulos CG, Sultan S, Haut ER, Johnson E, Praba-Egge A, et al. Timing and type of surgical treatment of Clostridium difficile-associated disease: a practice management guideline from the Eastern Association for the Surgery of trauma. J Trauma Acute Care Surg. 2014;76:1484–93.
Sailhamer EA, Carson K, Chang Y, Zacharias N, Spaniolas K, Tabbara M, et al. Fulminant Clostridium difficile colitis: patterns of care and predictors of mortality. Arch Surg. 2009;144:433–9.
Bhangu A, Nepogodiev D, Gupta A, Torrance A, Singh P; West midlands research collaborative. Systematic review and meta-analysis of outcomes following emergency surgery for Clostridium difficile colitis. Br J Surg 2012;99:1501–1513.
Lamontagne F, Labbé AC, Haeck O, Lesur O, Lalancette M, Patino C, et al. Impact of emergency colectomy on survival of patients with fulminant Clostridium difficile colitis during an epidemic caused by a hypervirulent strain. Ann Surg. 2007;245:267–72.
Neal MD, Alverdy JC, Hall DE, Simmons RL, Zuckerbraun BS. Diverting loop ileostomy and colonic lavage: an alternative to total abdominal colectomy for the treatment of severe, complicated Clostridium difficile associated disease. Ann Surg. 2011;254:423–37.
Olivas AD, Umanskiy K, Zuckerbraun B, Alverdy JC. Avoiding colectomy during surgical management of fulminant Clostridium difficile colitis. Surg Infect. 2010;11:299–305.
Ferrada P, Callcut R, Zielinski MD, Bruns B, Yeh DD, Zakrison TL, et al. Loop ileostomy versus total colectomy as surgical treatment for Clostridium difficile-associated disease: an eastern association for the surgery of trauma multicenter trial. J Trauma Acute Care Surg. 2017;83:36–40.
Xu JY, Chen QH, Xie JF, Pan C, Liu SQ, Huang LW, et al. Comparison of the effects of albumin and crystalloid on mortality in adult patients with severe sepsis and septic shock: a meta-analysis of randomized clinical trials. Crit Care. 2014;18:702.
O'Horo JC, Jindai K, Kunzer B, Safdar N. Treatment of recurrent Clostridium difficile infection: a systematic review. Infection. 2014;42:43–59.
McFarland LV, Evans CT, Goldstein EJC. Strain-specificity and disease-specificity of probiotic efficacy: a systematic review and meta-analysis. Front Med (Lausanne). 2018;5:124.
McFarland LV. Primary prevention of Clostridium difficile infections—how difficult can it be? Expert Rev Gastroenterol Hepatol. 2017;11:507–21.
Avadhani A, Miley H. Probiotics for prevention of antibiotic-associated diarrhea and Clostridium difficile-associated disease in hospitalized adults—a meta-analysis. J Am Acad Nurse Pract. 2011;23:269–74.
Goldenberg JZ, Ma SS, Saxton JD, Martzen MR, Vandvik PO, Thorlund K, et al. Probiotics for the prevention of Clostridium difficile-associated diarrhea in adults and children. Cochrane Database Syst Rev. 2013;5:CD006095.
Johnston BC, Ma SS, Goldenberg JZ, Thorlund K, Vandvik PO, Loeb M, et al. Probiotics for the prevention of Clostridium difficile-associated diarrhea: a systematic review and meta-analysis. Ann Intern Med. 2012;157:878–88.
McFarland LV. Meta-analysis of probiotics for the prevention of antibiotic associated diarrhea and the treatment of Clostridium difficile disease. Am J Gastroenterol. 2006;101:812–22.
Johnson S, Maziade PJ, McFarland LV, Trick W, Donskey C, Currie B, et al. Is primary prevention of Clostridium difficile infection possible with specific probiotics? Int J Infect Dis. 2012;16:e786–92.
Goldenberg JZ, Yap C, Lytvyn L, Lo CK, Beardsley J, Mertz D, Johnston BC. Probiotics for the prevention of Clostridium difficile-associated diarrhea in adults and children. Cochrane Database Syst Rev. 2017;12:CD006095.
McFarland LV, Ship N, Auclair J, Milletteu M. Primary prevention of Clostridium difficile infections with a specific probiotic combining Lactobacillus acidophilus, L. casei and L. rhamnosus strains: assessing the evidence. J Hosp Infect. 2018;99:443–52.
McFarland LV, Surawicz CM, Greenberg RN, Fekety R, Elmer GW, Moyer KA, et al. A randomized placebo-controlled trial of Saccharomyces boulardii in combination with standard antibiotics for Clostridium difficile disease. JAMA. 1994;271:1913–8.
Surawicz CM, McFarland LV, Greenberg RN, Rubin M, Fekety R, Mulligan ME, et al. The search for a better treatment for recurrent Clostridium difficile disease: use of high-dose vancomycin combined with Saccharomyces boulardii. Clin Infect Dis. 2000;31:1012–7.
Bakken JS, Borody T, Brandt LJ, Brill JV, Demarco DC, Franzos MA, et al. Treating Clostridium difficile infection with fecal microbiota transplantation. Clin Gastroenterol Hepatol. 2011;9:1044–9.
Gough E, Shaikh H, Manges AR. Systematic review of intestinal microbiota transplantation (fecal bacteriotherapy) for recurrent Clostridium difficile infection. Clin Infect Dis. 2011;53:994–1002.
Cammarota G, Ianiro G, Gasbarrini A. Fecal microbiota transplantation for the treatment of Clostridium difficile infection: a systematic review. J Clin Gastroenterol. 2014;48:693–702.
Quraishi MN, Widlak M, Bhala N, Moore D, Price M, Sharma N, Iqbal TH. Systematic review with meta-analysis: the efficacy of faecal microbiota transplantation for the treatment of recurrent and refractory Clostridium difficile infection. Aliment Pharmacol Ther. 2017;46:479–93.
Orenstein R, Dubberke E, Hardi R, Ray A, Mullane K, Pardi DS, et al. Safety and durability of RBX2660 (microbiota suspension) for recurrent Clostridium difficile infection: results of the PUNCH CD study. Clin Infect Dis. 2016;62:596–602.
Postigo R, Kim JH. Colonoscopic versus nasogastric fecal transplantation for the treatment of Clostridium difficile infection: a review and pooled analysis. Infection. 2012;40:643–8.
Furuya-Kanamori L, Doi SA, Paterson DL, Helms SK, Yakob L, McKenzie SJ, et al. Upper versus lower gastrointestinal delivery for transplantation of fecal microbiota in recurrent or refractory Clostridium difficile infection: a collaborative analysis of individual patient data from 14 studies. J Clin Gastroenterol. 2017;51:145–50.
Hirsch BE, Saraiya N, Poeth K, Schwartz RM, Epstein ME, Honig G. Effectiveness of fecal-derived microbiota transfer using orally administered capsules for recurrent Clostridium difficile infection. BMC Infect Dis. 2015;15:191.
Youngster I, Russell GH, Pindar C, Ziv-Baran T, Sauk J, Hohmann EL. Oral, capsulized, frozen fecal microbiota transplantation for relapsing Clostridium difficile infection. JAMA. 2014;312:1772–8.
Kassam Z, Lee CH, Yuan Y, Hunt RH. Fecal microbiota transplantation for Clostridium difficile infection: systematic review and meta-analysis. Am J Gastroenterol. 2013;108:500–8.
Van Nood E, Vrieze A, Nieuwdorp M, Fuentes S, Zoetendal EG, de Vos WM, et al. Duodenal infusion of donor feces for recurrent Clostridium difficile. N Engl J Med. 2013;368:407–15.
Di Bella S, Gouliouris T, Petrosillo N. Fecal microbiota transplantation (FMT) for Clostridium difficile infection: focus on immunocompromised patients. J Infect Chemother. 2015;21:230–7.
Kelly CR, Ihunnah C, Fischer M, Khoruts A, Surawicz C, Afzali A, et al. Fecal microbiota transplant for treatment of Clostridium difficile infection in immunocompromised patients. Am J Gastroenterol. 2014;109:1065–71.
Bartlett JG. Bezlotoxumab—a new agent for Clostridium difficile infection. N Engl J Med. 2017;376:381–2.
Wilcox MH, Gerding DN, Poxton IR, Kelly C, Nathan R, Birch T, et al. Bezlotoxumab for prevention of recurrent Clostridium difficile infection. N Engl J Med. 2017;376:305–17.
Lübbert C, Nitschmann S. Bezlotoxumab for the secondary prevention of Clostridium difficile infection: MODIFY I and MODIFY II studies. Internist (Berl). 2017;58:639–42.
Gerding DN, Kelly CP, Rahav G, Lee C, Dubberke ER, Kumar PN, et al. Bezlotoxumab for prevention of recurrent Clostridium difficile infection in patients at increased risk for recurrence. Clin Infect Dis. 2018;67:649–56.
Abourgergi MS, Kwon JH. Intravenous immunoglobulin for the treatment of Clostridium difficile infection: a review. Dig Dis Sci. 2011;56:19–26.
Shahani L, Koirala J. Use of intravenous immunoglobulin in severe Clostridium difficile-associated diarrhea. Hosp Pract. 2015;43:154–7.
Juang P, Skledar SJ, Zgheib NK, Paterson DL, Vergis EN, Shannon WD, et al. Clinical outcomes of intravenous immune globulin in severe clostridium difficile-associated diarrhea. Am J Infect Control. 2007;35:131–7.
Sullivan PB. Nutritional management of acute diarrhea. Nutrition. 1998;14:758–62.
Choi EY, Park DA, Park J. Calorie intake of enteral nutrition and clinical outcomes in acutely critically ill patients: a meta-analysis of randomized controlled trials. JPEN J Parenter Enteral Nutr. 2015;39:291–300.
Gerding DN. Acquisition of Clostridium difficile and Clostridium difficile-associated diarrhea in hospitalized patients receiving tube feeding. Ann Intern Med. 1998;129:1012–9.
Bliss DZ, Johnson S, Savik K, et al. Acquisition of C. difficile and C. diff-associated diarrhea in hospitalized patients receiving tube feeding. Ann Intern Med. 1998;129:1012–9.
O'Keefe SJ. A guide to enteral access procedures and enteral nutrition. Nat Rev Gastroenterol Hepatol. 2009;6:207–15.
O'Keefe SJ. Tube feeding, the microbiota, and Clostridium difficile infection. World J Gastroenterol. 2010;16:139–42.
Puri BK, Hakkarainen-Smith J, Monro JA. The potential use of cholestyramine to reduce the risk of developing Clostridium difficile-associated diarrhoea in patients receiving long-term intravenous ceftriaxone. Med Hypotheses. 2015;84:78–80.
Koo HL, Koo DC, Musher DM, DuPont HL. Antimotility agents for the treatment of Clostridium difficile diarrhea and colitis. Clin Infect Dis. 2009;48:598–605.
Availability of data and materials
The authors are responsible for the data described in the manuscript and assure full availability of the study material upon request to the corresponding author.