Review of 58 patients with necrotizing fasciitis in the Netherlands
© The Author(s). 2016
Received: 13 April 2016
Accepted: 23 May 2016
Published: 27 May 2016
Necrotizing fasciitis is a rare, life threatening soft tissue infection, primarily involving the fascia and subcutaneous tissue. In a large cohort of patients presenting with Necrotizing fasciitis in the Netherlands we analysed all available data to determine the causative pathogens and describe clinical management and outcome.
We conducted a retrospective, multicentre cohort study of patients with a necrotizing fasciitis between January 2003 and December 2013 in an university medical hospital and three teaching hospitals in the Netherlands. We only included patients who stayed at the Intensive Care Unit for at least one day.
Fifty-eight patients were included. The mortality rate among those patients was 29.3 %. The central part of the body was affected in 28 patients (48.3 %) and in 21 patients (36.2 %) one of the extremities. Most common comorbidity was cardio vascular diseases in 39.7 %. Thirty-nine patients (67.2 %) were operated within 24 h after presentation. We found a type 1 necrotizing fasciitis in 35 patients (60.3 %) and a type 2 in 23 patients (39.7 %).
Our study, which is the largest study in Europe, reaffirmed that Necrotizing fasciitis is a life threatening disease with a high mortality. Early diagnosis and adequate treatment are necessary to improve the clinical outcome. Clinical awareness off necrotizing fasciitis remains pivotal.
Necrotizing fasciitis (NF) is a part of the Necrotizing Soft Tissue Infections. It’s a rare, life threatening soft tissue infection, primarily involving the fascia and subcutaneous tissue. Although the symptoms were already described in the fifth century BC by Hippocrates [1, 2], even in modern medicine it still has a high mortality rate ranging from 6 to 76 % [1, 3–6]. The term necrotizing fasciitis was introduced by Wilson in 1952 [1, 7].
The rapidly progressive infection can affect any part of the body. The portal of entry usually is a minor injury of the affected site or a surgical wound. However, no definitive cause can be found in 20–50 % [8–10].
Medical conditions associated with necrotizing fasciitis are diabetes mellitus (31–44 %), obesity (28 %), smoking (27 %), alcoholabusus (17 %), cirrhosis (8–15 %), malignancy (3 %), corticosteroid therapy (3 %) and chronic renal failure (3 %) [11, 12].
The incidence of NF is low with 0.4 cases per 100.000 in the United Kingdom .
Clinical symptoms consist of local symptoms like erythema, swelling, changes in skin colouring, intense pain, bullae and sometimes subcutaneous emphysema and general symptoms such as fever, nausea, vomiting and malaise [2, 8, 11].
Necrotizing fasciitis can be classified in four clinical forms, depending on the causative organisms . In Type 1 at least one anaerobic species is isolated with one or more facultative anaerobic streptococci (other than group A) and members of the Enterobacteriaceae (e.g., E.coli, Enterobacter, Klebsiella, Proteus) . Type 2 is generally monomicrobial and caused by hemolytic streptococcus group A, sometimes with co-infection of Staphylococcus aureus. Most articles show type 1 is more common, with a relative incidence up to 75 % [8, 9]. Some studies also describe type 3, caused by the marine Vibrio spp. The portal of entry for this type 3 NF is a puncture wound caused by fish or marine insects and is rarely observed in Europe . Type 4 describes fungal cases of candida NF, which are very rare [2, 15].
The Laboratory Risk Indicator for Necrotizing Fasciitis (LRINEC score)
C-reactive protein (mg/l)
Leucocyte count (109/l)
Appropriate treatment of a patient with NF can only be achieved through close cooperation between the surgeon, intensivist and microbiologist.
The aim of our study was to analyse all available data of a large cohort of patients presenting with NF in four teaching hospitals in the Netherlands. Also, we determined the causative pathogens in our population, described clinical management and clinical outcome in this Dutch cohort and compared that with previous other studies.
The study was designed as a retrospective cohort study.
All consecutive adult patients who were diagnosed with NF were eligible for inclusion at the Radboud University Medical Center Nijmegen (Radboudumc) (a 900 beds university hospital), the Gelderse Vallei Hospital Ede (GVH) (a 500 beds hospital), Rijnstate Hospital Arnhem (RH) (a 950 beds hospital) and Slingeland Hospital Doetinchem (SH) (a 340 beds hospital) between January 2003 and December 2013. These hospitals are located in the Central-Eastern part of the Netherlands, belonging to one surgical training region.
For inclusion, patients had to stay at the intensive care unit for at least one day. Patients were found by hospital data system, diagnostic codes and microbiological results.
Diagnosis of necrotizing fasciitis was proven by histopathologic examination of tissue samples or surgical findings when no tissue sample was analyzed. This means the presence of an affected fascia, which was documented in the procedure note as a necrotizing fasciitis, was diagnostic. Vital parameters (e.g., temperature, blood pressure, heart rate), clinical symptoms of the affected body part and laboratory results at presentation, as well as all demographic data were collected from the patient charts. Results of blood and wound cultures, the number of surgical interventions, operative findings, length of stay at the intensive care unit (ICU), total duration of hospitalization and the mortality rate were documented. For all patients the LRINEC score was calculated from the laboratory findings.
We considered Type 2 FN as caused by a monoculture of hemolytic streptococcus group A (Streptococcus pyogenes), or in rare cases caused by Staphylococcus aureus or hemolytic streptococcus group C or G.
And in contrast Type 1 FN was seen as caused by different combinations of anaerobic bacteria, aerobic gram negative rods from the Enterobacteriaceae group and streptococci other than Streptococcus pyogenes.
A total of 58 patients were included (19 Radboudumc; 15 GVH, 16 RH, 8 SH). Thirty-four patients were male (58.6 %) and 24 were female (41.4 %). The median age was 62 years (range 21–81 years).
Localisation of the fasciitis was in the central part of the body in 28 patients (48.3 %) and in one of the extremities in 21 patients (36.2 %). In 8 patients (13.8 %) there was a combination of central part of the body with one of the extremities. In one patient the head was the affected.
The most common comorbidity was cardiovascular diseases (39.7 %). Other co-morbidities included were obesity (25.9 %), diabetes mellitus (24.1 %) and malignancy (19.0 %). Thirteen patients (22.4 %) had no comorbidities.
Operations prior to necrotizing fasciitis
Inguinal hernia repair
Forty-six patients had a LRINEC score ≥ 6 (79.3 %), 33 patients had a score ≥ 8 (56.9 %) and 8 patients had a score ≥ 10 (13.8 %). The mean LRINEC score was 7.4.
Cultures in necrotizing fasciitis type I, n = 35 patients
Present in mixed culture
Haemolytic streptococci, not group A
Anaerobe gram negative rods, mainly B.fragilis
Anaerobic mixed culture
9 (13 %)
61 (87 %)
70 (100 %)
9 (26 %)
26 (74 %)
35 (100 %)
Treatment and follow up
All patients underwent one or more operations. Thirty-nine patients (67.2 %) were operated within 24 h and 16 patients (27.6 %) underwent their first operation after 24 h. In 3 patients the exact time of operation was not clear.
Forty-nine patients (84.5 %) underwent radical necrotectomy. In 6 cases (10.3 %) an amputation was necessary. In 3 patients the NF was so extensive, that because of poor prognosis, radical necrotectomy was not conducted.
The mean number of debridement procedures of the patients who survived was 2.8 (range 1–8). In 26 patients (44.8 %) we used vacuum assisted closure therapy, which in 12 patients was followed by definitive reconstruction by split skin grafts (Fig. 1b-d). Other patients received split skin grafts without VAC® (Vacuüm Assisted Closure) therapy, primary wound closure or reconstruction by the plastic surgeon.
The mortality was 17 out of 58 patients (29.3 %). The median age of the patients who died was 64 years (range 38–72 years). The median age of the survivors was 59 years (range 21–81 years). Nine patients died within 2 days because of multi organ failure or cessation of treatment due to poor prognosis. Two patients died in the first week after admission. Six patients died several weeks or months (range 15–73 days) after admission because of a new septic period, cardiac failure or general weakness.
From 38 patients histological examinations were taken. In two cases an autopsy was performed. All patients showed typical signs of NF.
The mean duration of hospitalization of the patients who survived was 46 days (range 11–166). The mean stay on the intensive care unit was 11 days (range 1–42).
Necrotizing fasciitis is a part of the Necrotizing Soft Tissue Infections (NSTI) and is a rare life threatening disease that still has a high mortality and morbidity. We included 58 patients with necrotizing fasciitis in four different hospitals. To our knowledge, this study is the first Dutch study and involves one of the largest European cohorts. Previous large studies have been conducted in Asia and Australia [5–7, 19, 20]. Because we exclusively wanted to include patients with the fulminant form of necrotizing fasciitis, patients with NF admitted for at least one day in the intensive care unit, were included. Patients with a subacute fasciitis  or a doubtful diagnosis were excluded from our study.
Many patients presented with classical symptoms like erythema, swelling and tachycardia, had abnormal blood results and had a clear minimal trauma or a surgical wound as the portal of entry. Despite the classical presentation, up to 30 % was not operated on within 24 h after admission. This is consistent with the literature, which shows even higher numbers of delay of surgical treatment up to 40 % [7, 20]. Also, Goh et all describes 71.4 % misdiagnosis of NF as cellulitis or abscess in their systematic review . This illustrates the diagnostic dilemma that is present in a large number of patients.
The LRINEC score can be a useful tool to help diagnose NF . In the initial study, a score of 6 or above was shown to have a positive predictive value of 92 % and a negative predictive value of 96 % . However, no prognostic studies for validating this score, and the cut-off value of ≥6, are available . Twenty-one percent of our patients had a LRINEC score below 6. However, this was a selected group in which the diagnostic process had already been completed. The LRINEC score was used retrospectively and therefore did not aid in the diagnosis. If we want to use the LRINEC score in this way, an adequate validation is necessary.
The most common risk factor for NF in the literature is diabetes mellitus [5, 7, 11, 12, 23, 24], however, there are major differences between studies (Bucca at all 21 %, Wong at all 70.8 %) [6, 25]. In our study only 24.1 % of the patients had diabetes. The most common comorbidity we found was cardiovascular diseases in almost 40 % of the patients. Over 50 % of them had a serious cardiac event like infarction or arrhythmia. The other patients only had hypertension. The number of patients with no comorbidities (22.4 %) is comparable to other studies [5, 19].
Many of the larger studies on NF are published in South East Asia or Australia. These countries live in close relation to marine life. In addition to type 1 and type 2 NF, type 3 was described regularly. We had no patients in our study with NF type 3. Huang described 11.9 % wound cultures with Vibrio spp, it was the most common pathogen leading to bacteraemia (29.5 %) in their population . This difference in pathogens may also have influenced the course of the disease and outcome of patients with NF. In our study we found 60.3 % of patients with type 1 NF and 39.7 % with type 2 NF. This is similar to other studies [3, 8, 9]. Studies with higher numbers of type 2 NF describe up to 63.3 % type 2. These studies used other criteria to distinguish between type 1 and 2, classifying all monomicrobial infections as type 2 [7, 24, 26].
The treatment of patients with NF is challenging and consists of adequate surgical debridement, supportive care by the intensivist and starting broad spectrum antimicrobials [25, 27]. The choice of antibiotics depends on the suspected causative microorganism(s), part of the body that is affected and clinical picture. Antibiotic therapy can be narrowed down as culture results are known. The most important factor is early surgical aggressive debridement, which is associated with a lower mortality when performed within 24 h [17, 18].
Mortality in our study population was 29 %, which is slightly higher than in other reports of patients with NF [5, 7, 10, 19, 20, 24, 25, 28]. This can be explained by the different inclusion criteria and possible different microorganism(s). Due to the inclusion criteria of at least 1 day ICU-stay we possibly included a more seriously ill population compared to other reports.
Recent years have shown an increase in the use of the vacuum assisted therapy . We used the VAC® therapy in nearly half of our patients with good results.
Our study was limited by the retrospective character. Another limitation is, because of the rarity of NF, patients of four different hospitals are included. Different routines in the hospitals, although they belong to the same training regions, and the relative long period of inclusion can explain some missing data.
We present the first Dutch and the largest European study of patients with necrotizing fasciitis. Our study reaffirmed that NF is a life threatening disease with a high mortality. Early diagnosis and adequate treatment are necessary to improve the clinical outcome. Clinical awareness of necrotizing fasciitis remains pivotal.
Our recommendations for further research are a prospective study to validate the LRINEC score and to explore the correlation between the score and clinical outcome.
GVH, Gelderse Vallei Hospital Ede; ICU, Intensive Care Unit; LRINEC, Laboratory Risk Indicator for Necrotizing Fasciitis; NF, Necrotizing Fasciitis (NF); NSTI, Necrotizing Soft Tissue Infections; Radboudumc, Radboud University Medical Center Nijmegen; RH, Rijnstate Hospital Arnhem; SH, Slingeland Hospital Doetinchem; VAC®, Vacuüm Assisted Closure.
No fundings to declare.
Availability of data and materials
Data sharing on request.
SvS, performed the study, collected all data with help of the local surgeons, analysed the data and wrote the manuscript. JdV, microbiological support and supervision, critically revising the manuscript. JB, design of the manuscript, interpretation of data. RM, collected data GVH, critically revising the manuscript. EH, collected data RH, critically revising the manuscript. SL, collected data SH, critically revising the manuscript. ET, conceived the study, collected data RUMC, revising the manuscript critically, supervisor. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
All local ethical committees approved this study.
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- Wong CH, Wang YS. The diagnosis of necrotizing fasciitis. Curr Opin Infect Dis. 2005;18:101–6.View ArticlePubMedGoogle Scholar
- Morgan MS. Diagnosis and management of necrotizing fasciitis: a multiparametric approach. J Hosp Infect. 2010;75:249–57.View ArticlePubMedGoogle Scholar
- McHenry CR, Piotrowski JJ, Petrinic D, Malangoni MA. Determinants of mortality for necrotising soft tissue infections. Ann Surg. 1995;221:558–65.View ArticlePubMedPubMed CentralGoogle Scholar
- Tilkorn DJ, Citak M, Fehmer T, Ring A, Hauser J, Al Benna S, et al. Characteristics and differences in necrotizing fasciitis and gas forming myonecrosis: a series of 36 patients. Scand J Surg. 2012;101(1):51–5.View ArticlePubMedGoogle Scholar
- Su Y-C, Chen H-W, Hong Y-C, Chen C-Y, Hsiao C-T, Chen I-C. Laboratory risk indicator for necrotizing fasciitis score and the outcomes. ANZ J Surg. 2008;78:968–72.View ArticlePubMedGoogle Scholar
- Wong CH, Khin LW, Heng KS, Tan KC, Low CO. The LRINEC (Laboratory Risk Indicator for Necrotizing Fasciits) score: a tool for distinguishing necrotizing fasciitis from other soft tissue infections. Crit Care Med. 2004;32(7):1535–41.View ArticlePubMedGoogle Scholar
- Huang K-F, Hung M-H, Lin Y-S, Lu C-L, Lui C, Chen C-C, Lee Y-H. Independent predictors of mortalitity for necrotizing fasciitis: a retrospective analysis in a single institution. J Trauma. 2011;71:467–73.View ArticlePubMedGoogle Scholar
- Sarani B, Strong M, Pascual J, Schwab CW. Necrotizing fasciitis: current concepts and review of the literature. J Am Coll Surg. 2009;208:279–88.View ArticlePubMedGoogle Scholar
- Wong CH, Chang HC, Pasupathy S, Khin LW, Tan JL, Low CO. Necrotizing fasciitis: clinical presentation, microbiology, and determinants of mortality. J Bone Joint Surg Am. 2003;85-A(8):1454–60.PubMedGoogle Scholar
- Vayvada H, Demirdover C, Menderes A, Karaca C. Necrotising fasciitis in the central part of the body: diagnosis, management and review of the literature. Int Wound J. 2013;10(4):466–72.View ArticlePubMedGoogle Scholar
- Angoules AG, Kontakis G, Drakoulakis E, Vrentzos G, Granick MS, Giannoudis PV. Necrotising fasciitis of upper and lower limb: a systematic review. Injury. 2007;38(5):S19–26.PubMedGoogle Scholar
- Goh T, Goh LG, Ang CH, Wong CH. Early diagnosis of necrotizing fasciitis. Br J Surg. 2014;101(1):119–25.View ArticleGoogle Scholar
- Ellis Simonsen SM, van Orman ER, Hatch BE, Jones SS, Gren LH, Hegmann KT, et al. Cellulitis incidence in a defined population. Epidemiol Infect. 2006;134:293–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Mandell GL, Bennett JE, Dolin R. Principles and practice of infectious diseases. 7th ed. Philadelphia: Churchill Livingstone; 2010. p. 1307–8. Part II.Google Scholar
- Davoudian P, Flint NJ. Necrotizing fasciitis. Contin Educ Anaesth Crit Care Pain. 2012;12(5):245–50.View ArticleGoogle Scholar
- Stevens DL, Baddour LM, Sexton DJ, Edwards MS, Baron EL. Necrotizing soft tissue infections. Available online at: http://www.uptodate.com. Accessed 11 Dec 2014.
- Cheung JP, Fung B, Tang WM, Ip WY. A review of necrotising fasciitis in the extremities. Hong Kong Med J. 2009;15(1):44–52.Google Scholar
- Bilton BD, Zibari GB, McMillan RW, Aultman DF, Dunn G, McDonald JC. Aggressive surgical management of necrotizing fasciitis serves to decrease mortality: a retrospective study. Am Surg. 1998;64:397–400.PubMedGoogle Scholar
- Das DK, Baker MG, Venugopal K. Risk factors, microbiological findings and outcomes of necrotizing fasciitis in New Zealand: a retrospective chart review. BMC Infect Dis. 2012;12:348.View ArticlePubMedPubMed CentralGoogle Scholar
- Nisbet M, Ansell G, Lang S, Taylor S, Dzendrowskyj P, Holland D. Necrotizing fasciitis: review of 82 cases in South Auckland. Intern Med J. 2011;41(7):543–8.View ArticlePubMedGoogle Scholar
- Wong CH, Wang SW. What is a subacute necrotizing fasciitis?: A proposed clinical diagnostic criteria. J Infect. 2006;52(6):415–9.View ArticlePubMedGoogle Scholar
- Holland MJ. Application of the Laboratory Risk Indicator in Necrotizing Fasciitis (LRINEC) score to patients in a tropical tertiary referral centre. Anaesth Intensive Care. 2009;37:588–92.PubMedGoogle Scholar
- Elliott DC, Kufera JA, Meyers RA. Necrotizing soft tissue infections. Risk factors for mortality and strategies for management. Ann Surg. 1996;244:672–83.View ArticleGoogle Scholar
- Kalaivani V, Hiremath BV, Indumathi V. Necrotising soft tissue infection-risk factors for mortality. J Clin Diagn Res. 2013;7(8):1662–5.Google Scholar
- Bucca K, Spencer R, Orford N, Cattigan C, Athan E, McDonald A. Early diagnosis and treatment of necrotizing fasciitis can improve survival: an observational intensive care unit cohort study. ANZ J Surg. 2013;83(5):365–70.View ArticlePubMedGoogle Scholar
- Ryssel H, Germann G, Kloeters O, Radu CA, Reichenberger M. Necrotizing fasciitis of the extremities: 34 cases at a single centre over the past 5 years. Arch Orthop Trauma Surg. 2010;130:1515–22.View ArticlePubMedGoogle Scholar
- Ustin JS, Malangoni MA. Necrotizing soft-tissue infections. Crit Care Med. 2011;39:2156–62.View ArticlePubMedGoogle Scholar
- Arifi HM, Duci SB, Zatriqi VK, Ahmeti HR, Ismajli VH, Gashi MM, et al. A retrospective study of 22 patients with necrotising fasciitis treated at the University Clinical Center of Kosovo (2005–2010). Int Wound J. 2013;10(4):461–5.View ArticlePubMedGoogle Scholar
- Misiakos EP, Bagias G, Patapis P, Sotiropoulos D, Kanavidis P, Machairas A. Current concepts in the management of necrotizing fasciitis. Front Surg. 2014;1:36.View ArticlePubMedPubMed CentralGoogle Scholar