Proposal for a recovery prediction method for patients affected by acute mediastinitis

  • Sławomir Jabłoński1Email author and

    Affiliated with

    • Marcin Kozakiewicz2

      Affiliated with

      World Journal of Emergency Surgery20127:11

      DOI: 10.1186/1749-7922-7-11

      Received: 6 January 2012

      Accepted: 10 May 2012

      Published: 10 May 2012

      Abstract

      Background

      An attempt to find a prediction method of death risk in patients affected by acute mediastinitis. There is not such a tool described in available literature for that serious disease.

      Methods

      The study comprised 44 consecutive cases of acute mediastinitis. General anamnesis and biochemical data were included. Factor analysis was used to extract the risk characteristic for the patients. The most valuable results were obtained for 8 parameters which were selected for further statistical analysis (all collected during few hours after admission). Three factors reached Eigenvalue >1. Clinical explanations of these combined statistical factors are: Factor1 - proteinic status (serum total protein, albumin, and hemoglobin level), Factor2 - inflammatory status (white blood cells, CRP, procalcitonin), and Factor3 - general risk (age, number of coexisting diseases). Threshold values of prediction factors were estimated by means of statistical analysis (factor analysis, Statgraphics Centurion XVI).

      Results

      The final prediction result for the patients is constructed as simultaneous evaluation of all factor scores. High probability of death should be predicted if factor 1 value decreases with simultaneous increase of factors 2 and 3. The diagnostic power of the proposed method was revealed to be high [sensitivity =90%, specificity =64%], for Factor1 [SNC = 87%, SPC = 79%]; for Factor2 [SNC = 87%, SPC = 50%] and for Factor3 [SNC = 73%, SPC = 71%].

      Conclusion

      The proposed prediction method seems a useful emergency signal during acute mediastinitis control in affected patients.

      Introduction

      Severe sepsis is still a major cause of postoperative morbidity and mortality after surgery in patients with acute mediastinitis (AM). The disease is characterized by rapid and severe course and poor prognosis despite undertaken on time aggressive surgical management and supportive treatment in the intensive care conditions. The cause of the failure of the treatment is complex. Local anatomical conditions favor the infection spread in mediastinal anatomical loose tissues and the systemic reaction to infection [1]. An association is emphasized between the increase in mortality and the delay in surgical intervention [14]. The etiology of AM does not remain insignificant. The best chance of survival have the patients previously healthy without earlier mediastinal pathologies in whom infection develops as a result of injury or as a complication related to endoscopic diagnostic procedures [57]. If the disease develops in a patient with previous history of diseases, especially of carcinoma or as the result of complications related to thoracosurgical or cardiosurgical procedures, the death risk increases [810]. It should be expected that a number of factors can affect the final prognosis e.g. age, etiology, delay in diagnosis, the type of surgical procedure, the kind and number of coexisting diseases, the type of a pathogen, postoperative complications and others.

      The management in this severe disease could facilitate categorizing patients into appropriate risk groups in order to undertake the most optimal treatment strategy for the developing severe sepsis. Working out a simple prognostic scale on the basis of the data obtained from the medical history, clinical examination, diagnostic imaging and preliminary biochemical investigations can be one of the useful solutions. Similar prognostic scales are applied in other diseases such as e.g. acute pancreatitis: the Acute Physiology and Chronic Health Evaluation (APACHE II) scale, Ranson criteria, the Atlanta Classification of Severe Acute Pancreatitis [1113]. Scales trying to determine the prognosis for severely sick patients have also been created e.g.: Nutritional Risk Index (NRI) [14, 15] and Prognostic Inflammatory and Nutritional Index(PINI) [16].

      To date no method has been available for the evaluation of the probability of recovery if a patient is affected by acute mediastinitis.

      Therefore, we attempt to find a clinically useful preoperative method of predicting the prognosis for patients with AM on the basis of clinical examination and simple laboratory investigations.

      Material and methods

      In the years 1998–2010, at the Department of Thoracic Surgery, General and Oncological Surgery of the Medical University of Lodz, there were treated 44 consecutive patients with AM. The study group comprised the patients fulfilling modified criteria of mediastinitis diagnosis worked out by Esterra et al. [17], which in the original version were related to descending necrotizing mediastinitis: (1) clinical manifestation of severe infection; (2) demonstration of AM etiological factors; (3) characteristic radiological picture of mediastanitis; (4) isolation of the pathogen in microbiological cultures from the mediastinal area; (5) intraoperative or postmortem documentation of mediastinitis. Exponents of sepsis in the form of: fever, tachycardia, hyperventilation and leucocytosis were observed in all patients.

      The study was given an approval by the institutional Ethical Review Committee (ERC).

      The age of the patients was from 19 to 83 years, mean age 52.5 years (median 54.5). There were 31 men, mean age 50,9 years (median 55) and 13 women, mean age 56.4 years (median 58). Majority of them were referred to our department after earlier treatment in other centers which had an impact on the delay in diagnosis and on appropriate surgical treatment.

      The time of hospitalization was on the average about 3 weeks (23.84 ± 11.96 days, median 21.5). All patients were operated, 14 patients died. The total death rate was 31.82% (38.7% in male and 15.4% in female group).

      The etiology of AM was extremely differentiated (Table 1). Iatrogenic complications were the most frequent cause of mediastinal infection. They were found in 19 patients (43.2%) and associated with esophageal and tracheal surgeries or with injuries to these organs during endoscopy or intubation. Non-iatrogenic esophageal and tracheal injuries were the cause of AM in 11 patients (25%). This group also included perforations caused by a foreign body. Descending AM was detected in 9 patients (20.4%). In 5 patients (11.4%) AM resulted from a spontaneous perforation of advanced esophageal cancer or lung cancer with infiltration to the esophagus (neoplastic etiology).
      Table 1

      Aetiology and surgical procedures in patients with acute mediastinitis

      AETIOLOGY

       

      Number

      Procedure

      Death

      Iatrogenic (19)

       

      Oesophageal endoscopy

      4

      PR-3E SPH-1

      1

       

      Oesophagotomy

      4

      EX-2 PR-2

      2

       

      Nissen operation

      2

      ESPH-1PR-1

      1

       

      Post-intubation tracheal rupture

      2

      PR-2

      0

       

      Complications of thyroid surgery

      2

      CRD + MDV-1 CRD + MDT-1

      0

       

      Oesophageal rupture during intubation

      1

      PR-1

      0

       

      Sternotomy complications in cardiac surgery

      1

      RVM-1

      1

       

      Colonic perforation to retroperitoneal space

      1

      MDV-1

      0

       

      Complications of neurosurgical procedures

      1

      CRD + MDV-1

      0

       

      Complications of funnel chest surgery

      1

      RVM-1

      0

      Traumatic (11)

       

      Oesophageal perforation

      3

      PR-3

      0

       

      Tracheal rupture

      2

      PR-2

      0

       

      Oesophageal rupture (foreign body)

      3

      PR-3

      0

       

      Boerhaave syndrome

      1

      PR-1

      1

       

      Burn of oesophagus with perforation

      1

      ESPH-1

      0

       

      Foreign body in mediastinum (traffic accident)

      1

      MDS-1

      0

      Descending (9)

       

      Dental abscess

      4

      DCUM- 2 CRD + MDT-2

      1

       

      Retropharyngeal abscess

      3

      DCUM- 2 CRD + MDV- 1

      1

       

      Peritonsillar abscess

      2

      CRD + MDT- 1 DCUM- 1

      1

      Neoplastic (4)

       

      Esophageal spontaneous perforation after prosthesis/ stent implantation

      2

      EX + PN-1 EX-1

      2

       

      Spontaneous oesophageal perforation in advanced cancer

      3

      PR-1 EX-1 TD-1

      3

      Legends of surgical procedures:

      - EX: exclusion

      - PR: primary repair

      - ESPH: oesophagectomy

      - MDT: mediastinal drainage by thoracotomy

      - MDV: mediastinal drainage by videothoracoscopy

      - MDS: mediastinal drainage by sternotomy

      - TD: T-tube drainage

      - CRD: cervical drainage

      - PN: pneumonectomy

      - DCUM: drainage of cervix and upper mediastinum

      - RVM: revirage and mediastinal drainage

      All patients underwent surgery. The time from the establishment of the diagnosis of AM to the introduction of surgical treatment ranged from 2 h to 11 days, mean 1.62 days (±1.86), median (1.0). Surgical strategy was determined individually dependently on the etiology, delay from the diagnosis establishment, local conditions and the patient’s general condition. The surgery, first of all, aimed at controlling the infection source and at limiting local inflammation by means of a wide cervical and/or mediastinal drainage through various surgical approaches. A detailed list of the performed surgical procedures and mortality rate of AM patients is presented in Table 1.

      The following clinical risk features were evaluated: age, gender, etiology of coexisting diseases, delay in surgical treatment, isolated pathogens, type of surgical procedure, the number and type of postoperative complications. Then, the association between mortality rate and selected biochemical risk factors was investigated analyzing the following parameters: hemoglobin level, hematocrit, red blood cell count, leucocytosis, platelet count, serum sodium and potassium level, values of the inflammation markers: C-reactive protein (CRP) and procalcitonin (PCT) in preoperative period and on day 3 postoperatively. General and biochemical data were included (Table 2). The factors for which in statistical analysis no association was found with the prognosis were excluded from further studies.
      Table 2

      Data included into this paper from treated patients affected with acute mediastinitis

       

      Age

      Coex_diseas

      HGB

      WBC_pre

      CRP_pre

      PCT_pre

      Proteins

      Albumins

      Average

      52,5455

      1,97727

      11,5677

      15,2432

      202,891

      2,93409

      57,3864

      31,6773

      Standard deviation

      13,7595

      1,42223

      2,14823

      5,14417

      50,1198

      3,92167

      7,35118

      3,90652

      Legend: Coex_diseas – coexisting diseases; HGB – level of hemoglobin in venous blood (g/dl) WBC_pre – white blood cell count in venous blood collected before surgical treatment immediately after department admission [x106/μl]; CRP_pre – C-reactive protein collected before surgical treatment immediately after department admission (mg/l); PCT_pre – procalcitonin in serum collected before surgical treatment immediately after department admission (ng/ml); Proteins – level of total serum proteins (g/l); Albumins – albumin level in serum (g/l).

      Statistical analysis

      Statistical method of the factor analysis was used to extract the risk aspects for the patients (Statgraphics Centurion XVI, StatPoint Technologies, Inc. Warrenton, USA). Then, the clinical value of the extracted factors was evaluated by ANOVA, where the treatment outcome was investigated. Variances were checked by Levene’s test. As p value for this statistics was less than 0.05, Kruskal-Wallis Test was applied to check the significance.

      Finally, the number of significant preoperative factors for the prognosis was reduced to 8 parameters which were grouped into 3 prognostic factors named respectively: proteinic status, inflammatory status and general status arranged dependently on their statistical power. All utilized parameters can be collected in a simple way during examination of the patient directly after admission to the ward and after laboratory investigations (within 2–3 hours).

      The first factor explained as “proteinic status” informs about the initial state of protein metabolism. This parameter is composed of results of laboratory tests of blood: serum protein, albumin and hemoglobin (HGB) level.

      The second factor “inflammatory status” allows to estimate the patient’s septic state on the basis of three laboratory parameters determined prior to the treatment: white blood cell count (WBC_pre), CRP value (CRP_pre), PCT value (PCT_pre).

      The third factor of the prediction schema “general risk” focuses on the evaluation of the patient’s clinical state and includes only two important parameters: age (Age) and the number of coexisting diseases (Coex_disease).

      Coefficients of sensitivity (SNC) and specificity (SPC) were calculated for the extracted factors to check the prediction power of the suggested method. The proposed method is designed for the prediction of recovery. Thus, the result of the test is positive (P) if the test predicts the recovery, and negative (N) if the test does not predict the recovery but i.e. “death”. Respectively, the result of the test is true (T) if the test predicts recovery when the observed result is “recovery”, and the result of the test is false (F) if the test does not predict the recovery. Therefore: TP-patient recovered and predicted as “recovery”, TN-patient died and predicted as “death”, FP-patient died but predicted as “recovery”, and FN - patient recovered but predicted as “death”. Basing on the above definitions, the suggested sensitivity and specificity coefficients equations are:

      Sensitivity coefficient: http://static-content.springer.com/image/art%3A10.1186%2F1749-7922-7-11/MediaObjects/13017_2012_257_IEq1_HTML.gif

      Specificity coefficient: http://static-content.springer.com/image/art%3A10.1186%2F1749-7922-7-11/MediaObjects/13017_2012_257_IEq2_HTML.gif

      Results

      Three factors have been extracted as statistically requested (Eigenvalue > 1), they are presented in Table 3. Together they account for over 69% of the variability in the original data. The initial communality estimates have been set to assume that all of the variability in the data is due to common factors (principal components method). Next, factor loading matrix was calculated. In order to simplify the clinical explanation of the factors, the rotation of the matrix was performed. Table 4 shows the parameters for equations, which estimate the common factors after rotation has been performed. Basing on those scores in the next statistical step, the factor (rotated) equations were constructed:
      http://static-content.springer.com/image/art%3A10.1186%2F1749-7922-7-11/MediaObjects/13017_2012_257_Equ1_HTML.gif
      http://static-content.springer.com/image/art%3A10.1186%2F1749-7922-7-11/MediaObjects/13017_2012_257_Equ2_HTML.gif
      http://static-content.springer.com/image/art%3A10.1186%2F1749-7922-7-11/MediaObjects/13017_2012_257_Equ3_HTML.gif
      where the values of the variables (x) in the equations are standardized by subtracting their means (μ) and dividing by their standard deviations (σ). It also shows the estimated communalities, which can be interpreted as estimating the proportion of the variability in each variable attributable to the extracted factors.
      Table 3

      Factor Analysis – presentation of the factors

      Factor

      Number

      Eigenvalue

      Percent of

      Variance

      Cumulative

      Percentage

      Initial

      Communality

      1

      3,31109

      41,389

      41,389

      1,0

      2

      1,16325

      14,541

      55,929

      1,0

      3

      1,04991

      13,124

      69,053

      1,0

      4

      0,754858

      9,436

      78,489

      1,0

      5

      0,682004

      8,525

      87,014

      1,0

      6

      0,540662

      6,758

      93,772

      1,0

      7

      0,358296

      4,479

      98,251

      1,0

      8

      0,139929

      1,749

      100,000

      1,0

      Note: for 3 factors the Eigenvalue is >1.

      Table 4

      Factor loading matrix after varimax rotation

      Parameter

      Factor score coefficients

      Estimated

      Communality

      Specific

      Variance

       

      Factor1

      Factor2

      Factor3

        

      HGB

      0,712131

      0,152337

      −0,243032

      0,589401

      0,410599

      Proteins

      0,854481

      −0,0461529

      −0,0418942

      0,734023

      0,265977

      Coex_diseas

      −0,131796

      −0,0604516

      0,863627

      0,766875

      0,233125

      WBC_pre

      0,00534419

      0,914729

      0,108861

      0,848609

      0,151391

      Age

      −0,141942

      0,263779

      0,685527

      0,559674

      0,440326

      Albumins

      0,908303

      −0,0949298

      −0,167625

      0,862124

      0,137876

      CRP_pre

      −0,651832

      0,514794

      0,0364827

      0,691229

      0,308771

      PCT_pre

      −0,560482

      0,371643

      0,141625

      0,472317

      0,527683

      Visual presentation of extracted factors is shown in Figure 1. Final factor scores calculated for all factors included into this study, together with easy explanation of their meanings are presented in Table 5.
      http://static-content.springer.com/image/art%3A10.1186%2F1749-7922-7-11/MediaObjects/13017_2012_257_Fig1_HTML.jpg
      Figure 1

      Plot of final factor loading after matrix rotation.

      Table 5

      Factor scores

      Case

      Observed outcome

      Factor1

      Factor2

      Factor3

      Classification result

        

      Proteinic status

      Inflammatory status

      General risk

       
        

      Recovery Prediction

      for > −1.4*

      Recovery Prediction for <1.0*

      Recovery Prediction for <0.4*

       

      1

      Death

      −8,61293

      1,97822

      2,03692

      TN

      2

      Recovery

      −1,89787

      1,01016

      0,60735

      FN

      3

      Death

      −5,67083

      1,17312

      3,18046

      TN

      4

      Recovery

      2,96689

      0,0611059

      −1,30167

      TP

      5

      Death

      −4,61678

      0,759947

      1,84367

      TN

      6

      Death

      −3,58174

      3,35379

      2,15131

      TN

      7

      Recovery

      1,24868

      −0,0408765

      0,219901

      TP

      8

      Recovery

      −2,55507

      0,0101163

      −0,12325

      FN

      9

      Recovery

      0,858724

      0,588775

      0,151806

      TP

      10

      Recovery

      −1,95238

      0,0573994

      0,216068

      FN

      11

      Recovery

      3,64292

      −0,704072

      −0,684944

      TP

      12

      Recovery

      2,6163

      −1,34394

      −2,25436

      TP

      13

      Death

      −4,19034

      4,84986

      0,915751

      TN

      14

      Recovery

      1,82354

      0,0636333

      −1,26561

      TP

      15

      Recovery

      3,03511

      1,12721

      −0,649727

      TP

      16

      Recovery

      3,37817

      −1,38079

      −2,2192

      TP

      17

      Recovery

      0,580244

      −0,316079

      −1,61708

      TP

      18

      Death

      −1,56375

      −2,27389

      −0,389642

      TN

      19

      Death

      −1,78795

      −0,0187813

      −0,789484

      TN

      20

      Recovery

      0,57392

      1,00331

      −0,714067

      TP

      21

      Recovery

      2,86891

      −0,0531427

      −1,05936

      TP

      22

      Recovery

      0,343636

      0,293051

      0,970888

      TP

      23

      Recovery

      1,14208

      −0,965971

      −1,6126

      TP

      24

      Recovery

      5,51418

      −1,06023

      −3,28449

      TP

      25

      Death

      −3,25473

      1,29683

      1,1493

      TN

      26

      Death

      −2,12645

      2,29104

      0,529981

      TN

      27

      Recovery

      2,29387

      0,0084471

      1,6481

      TP

      28

      Death

      0,907509

      −0,6706

      3,7267

      FP

      29

      Recovery

      1,29283

      −1,69442

      0,299441

      TP

      30

      Recovery

      3,45795

      −1,35408

      −2,1628

      TP

      31

      Death

      2,96653

      −1,47445

      −0,86775

      FP

      32

      Recovery

      0,0323576

      −1,55881

      0,509574

      TP

      33

      Recovery

      1,0745

      0,26778

      0,334441

      TP

      34

      Death

      −2,52481

      2,36734

      1,19426

      TN

      35

      Recovery

      1,32141

      1,05543

      0,824733

      TP

      36

      Recovery

      1,29592

      −1,62119

      −2,8627

      TP

      37

      Death

      −5,05654

      0,832591

      1,11692

      TN

      38

      Recovery

      2,11607

      −0,960466

      −0,634111

      TP

      39

      Recovery

      −1,4526

      0,511999

      1,41191

      FN

      40

      Recovery

      −0,871523

      −1,93215

      −0,779669

      TP

      41

      Death

      3,87668

      −2,0661

      −0,280317

      FP

      42

      Recovery

      −1,30349

      −0,759654

      0,880723

      TP

      43

      Recovery

      1,76721

      −1,49925

      −1,44593

      TP

      44

      Recovery

      0,0236466

      −1,21219

      1,07856

      TP

      This table shows the factor scores (prognostic) for each patient from our data file (observation). * − level of dichotomic division of subpopulation: recovery and death, see cross of the lines in density traces (Figure 2). Bold-lack of agreement between prediction and observation. Classification result: TP-true positive, TN-true negative, FP-false positive, FN-false negative.

      There are three separate groups: HGB + Proteins + Albumim, WBC_pre + CRP_pre + PCT_pre, and Age + Coex_diseas.

      According to the above, clinical meaning of the factors was established. Factor1 (F1) is “proteinic status” of the patient, Factor2 (F2) – “inflammatory status”, and Factor3 (F3) – “general risk” understood as the composite of age and number of coexisting diseases. The statistics of these factors in the presented clinical series is shown in Table 6.
      Table 6

      Final statistics of factor scores

      Parameter

      Factor1

      Factor2

      Factor3

       

      Proteinic status

      Inflammatory status

      General risk

      Count

      44

      44

      44

      Average

      9,55 × 10-8

      5,11 × 10-7

      1,36 × 10-7

      Median

      0,72

      −0,005

      0,18

      Standard deviation

      2,98

      1,50

      1,52

      Minimum

      −8,61

      −2,27

      −3,28

      Maximum

      5,51

      4,85

      3,73

      Range

      14,13

      7,12

      7,01

      Standardized skewness

      −1,88

      2,64

      0,26

      Standardized kurtosis

      0,45

      1,94

      −0,01

      Finally, clinical verification was done by checking the extracted factors value in our series of patients concerning the outcome of the treatment as recovery or death (Table 7). ANOVA results are presented in Figure 2 for F1 (F = 21.78, p < 0.0001; Levene`s test = 4.0978, p < 0.05; Kruskal-Wallis test = 11.9168, p < 0.001), for F2 (F = 8.45, p < 0.01; Levene`s test = 8.9967, p < 0.01; Kruskal-Wallis test = 4.9168, p < 0.05), and for F3 (F = 14.18, p < 0.001; Levene`s test = 0.0001, p = 0.9929).
      Table 7

      Final statistics of subgroups (factor scores)

       

      Factor1

      Factor2

      Factor3

       

      Proteinic status

      Inflammatory status

      General risk

       

      death

      recovery

      death

      recovery

      death

      recovery

      Count

      14

      30

      14

      30

      14

      30

      Average

      −2,52

      1,17

      0,89

      −0,41

      1,11

      −0,52

      Median

      −2,89

      1,27

      1,00

      −0,18

      1,13

      −0,64

      Standard deviation

      3,36

      1,89

      2,06

      0,93

      1,41

      1,30

      Minimum

      −8,61

      −2,56

      −2,27

      −1,93

      −0,87

      −3,28

      Maximum

      3,88

      5,51

      4,85

      1,13

      3,73

      1,65

      Range

      12,49

      8,07

      7,12

      3,06

      4,59

      4,93

      Stnd. skewness

      0,64

      −0,19

      0,16

      0,18

      0,41

      −0,70

      Stnd. kurtosis

      0,20

      −0,18

      −0,28

      −1,38

      −0,43

      −0,79

      http://static-content.springer.com/image/art%3A10.1186%2F1749-7922-7-11/MediaObjects/13017_2012_257_Fig2_HTML.jpg
      Figure 2

      Comparison of Proteinic status (Factor 1), Inflammatory status (Factor 2), and General risk (factor 3) in subpopulation of recovery and lethal outcome of acute mediastinitis. The difference is statistically significant.

      The final number of extracted factors was three. Furthermore, the coefficients of sensitivity and specificity were calculated for each factor (for F1: SNC = 87%, SPC = 79%; for F2: SNC = 87%, SPC = 50%; for F3: SNC = 73%, SPC = 71%), and next the prevalence test classification (TP, TN, FP, FN) was performed to establish the whole prognostic power of the method: SNC = 90%, SPC = 64%.

      The schema of the proposed prediction method application is presented in Figure 3.
      http://static-content.springer.com/image/art%3A10.1186%2F1749-7922-7-11/MediaObjects/13017_2012_257_Fig3_HTML.jpg
      Figure 3

      Schema of the application of the recovery prediction method.

      The probability of recovery increases when F1 is higher. In other words, when “proteinic status” is worse the risk of death is higher. As far as the “inflammatory status” (F2) is concerned, in our series, lower scores are observed in recovery outcome cases. The same trend is noticed in the analysis of “general risk” (i.e. F3). When plot (Figure 2) of “proteinic status” is analyzed, the value dividing recovery outcome from death is approximately −1,4 (F1). It should be understood as high probability of the patient’s recovery if the score is higher than −1.4. In case of “inflammatory status” the caesura is located around +1.0 (F2). The prediction of survival is for patients with the score lower than +1.0. Respectively, “general risk” (F3) score lower than +0.4 is a prediction of recovery outcome (as presented in tab.5). The predictable result based on F1 is most of all in compliance with the observed result of the treatment (only 7 variances/44 results). The variances result from the application of 3 factors. It should be known that if 8 parameters are subject of analysis, the whole explanation of variability is possible with 8 factors. The same is visible in density traces (Figure 2) where full strict dichotomic separation of recovery from death outcome subpopulations is impossible. That kind of mutually penetrating subpopulations is often observed in biological sciences.

      Discussion

      Early recognition of septic complications, information about sepsis severity and thus, the ability to predict the prognosis can have a significant impact on the treatment strategy in AM. Access to such data can be of importance in establishing the urgency and type of surgical intervention, monitoring in postoperative period, necessity for repair, the kind of antibiotic-therapy and supportive treatment. In medicine, numerous prognostic scales have been created allowing to assess the prognosis in selected pathological states. However, in available literature we have not found a scale related to acute mediastinitis. Most probably it results from rare prevalence of this disease and difficulty in gathering appropriately rich material within one medical centre. The proposed prognostic method, based on the evaluation of 8 simple and easy to obtain parameters compiled in the form of 3 factors, allows dichotomic categorization of patients into 2 groups as regards the predicted prognosis: survival or death. When the calculated values of individual factors are combined, it is easy to distinguish within first few hours of hospitalization the patients whose prognosis is worse than that of the others. Obviously, the selection of proper parameters for the estimation of the predicted prognosis in the course of AM can be the subject of discussion.

      In practice the first information about the patient’s general condition is obtained during taking the history data. At this stage we can obtain the data regarding patient’s age and coexisting diseases which in the proposed prognostic scale are important for calculating factor 3 values. In critically ill patients with sepsis, older age and coexisting diseases are associated with poor prognosis [1820]. There are several prognostic scales considering the effectof coexisting diseases on the prognosis. The best known are: Charlson Comorbidity Index (CCI), Davies (Stokes) score and Index of Coexisting Diseases (ICED). They are widely applied in the patients dialyzed due to renal failure [2124]. Charlson scale, which estimates similar parameters as our scale but it is based on different methodology, is used most frequently. It takes into account 19 coexisting diseases which are assigned with a score. CCI includes age as one of the evaluated elements and the age scores are counted according to the following scheme: 1 score for each decade over 40 years of age. The total score enables to predict the prognosis [25]. It was demonstrated in C-Y Wang’s study that higher value of CCI (>2) in patients treated surgically due to stage I of lung cancer was associated with higher mortality rate than in the group of patients with lower number of comorbidities; CCI < 2 [26]. The proposed by us prognostic scale is different because the data on the general state (F3) are only one of three estimated elements. If after substituting the data concerning age and coexisting diseases for the given formula for “F3” we obtain the value < +0.4, there increases the chance for the patient’s survival. F3 is important for the whole scale but according to our calculations it has a lower diagnostic value compared to the remaining two factors (SNC = 73%, SPC = 71%). Anticipating the questions why there were not taken into account such obvious clinical risk factors as: etiology, delay in diagnosis or the type of pathogen, we want to explain that the introduction of these data, to our surprise, led in consequence to the weakening of the algorithm diagnostic value. It seems that additional parameters can act the opposite way in the whole pool. Presumably, the factor analysis eliminated less reliable variables leaving those which presented the highest predictive power in the proposed algorithm. For instance, the delay in diagnosis and the time of the introduction of the surgical treatment are not unequivocal parameters. It is worth emphasizing that majority of the patients were hospitalized earlier on other wards, where initially no proper diagnosis was established. Furthermore, they were then subjected to surgical procedures the effect of which could sometimes deteriorate their condition and sometimes improve it partially. Similar remarks concern the bacterial flora which changed in the course of the treatment and finally its distribution was the effect of coincidence, antibiotic therapy and/or infection. It was impossible to classify such internally unstable parameters by the method of factor analysis and attempts of their inclusion into the algorithm had a negative effect on the accuracy of the prediction.

      Laboratory investigations are important elements of the proposed algorithm. The determination of other risk factors, found in already mentioned 2 factors: “proteinic status” and “inflammatory status” using 6 simple biochemical tests, supplements our prognostic method. F1 determines the initial state of the patient’s protein metabolism on the basisof 3 parameters: total protein, albumin and HGB level. Malnutrition and hypoproteinemia are distinctly associated with increased death rate due to infection and neoplastic disease [27, 28]. An objective estimation of malnutrition and protein metabolism is usually difficult, it is based on clinical observation, determination of BMI and biochemical investigations [29]. Among biochemical markers albumin level is most frequently used in malnutrition assessment. Hypoalbuminemia is associated with malnutrition and the decrease of protein level because liver reduces albumin production in favor of more important plasma proteins [16]. In 1988 Busby et al., first described the Nutritional Risk Index (NRI) to score the severity of postoperative complications [14, 15]. It combines two nutritional indicators (albumin and weight loss), which are strictly correlated with higher morbidity and mortality risk in the population of elderly patients [30]. The need of determining ideal body weight, which is difficult in elderly or critically ill patients, is one of the limitations of this scale. Thus, it became necessary to find a formula enabling to calculate ideal body weight, which led to creation of a new, more objective tool – the Geriatric Nutritional Risk Index (GNRI) [31]. Basing on the performed analysis we have demonstrated that there is also a need for inclusion of the hemoglobin level into the prognostic scale. It was included into the markers estimating “proteinic status”. The presence of anemia is a known factor affecting poor prognosis, particularly in combination with other diseases [32, 33]. The studies of Welch et al. demonstrated that general death risk increases with the decrease of HGB concentration and even benign forms of anemia can be associated with the increase of the death risk [34]. The advantage of the suggested prognostic method is the determination of protein metabolism in simpler way than in NRI or GNRI basing only on biochemical tests which is of importance in patients in critical condition. The obtained high diagnostic value for “proteinic status”, corresponding with the final prognosis (SNC = 87%, SPC = 79%) should be . If the value of F1 calculated on the basis of the formula is lower than −1.4, it means a high death risk for the patient.

      We are convinced that in the case of infectious diseases limitation to the assessment of protein metabolism, age and co-existing diseases is not sufficient for the prediction of the prognosis. It seems natural to extend the prognostic scale including biochemical markers of inflammation. White blood cell count (WBC) is the oldest widely used marker. It should be reminded that WBC value is one of the criteria of SIRS and sepsis diagnosis [35]. Fever in combination with elevated WBC count is a quick and cheap way of infection diagnosis but its low diagnostic value is its basic limitation [36]. This parameter in combination with other inflammatory markers still has a wide clinical application both in the diagnosis and monitoring of the results of the treatment. CRP remains one of the most important classic markers for inflammation. It is included into sensitive but little specific acute phase proteins, the level of which increases in inflammation and malignancy [37, 38]. It has been confirmed that initial CRP values were directly associated with total mortality rate in neoplastic disease [39]. However, Matson et al. paid attention to the fact that “normal” plasma CRP level in critically ill patients is rarely the same as in healthy population [40]. The post-mortem studies demonstrated that in patients with cachexia related to malignant carcinoma, in the case of extensive tumor necrosis, significant deviations were observed in the behavior of acute phase proteins [41]. That is why in these cases the determination of CRP alone can appear to be insufficient in the monitoring of inflammation. PCT is a biochemical marker extremely useful in the diagnosis and differentiation of severe infections and septic complications [4244]. The increase of PCT concentration induced by bacterial toxins (with preserved insensitivity to other pro-inflammatory stimuli) and close relation between serum PCT concentration and infection severity are the most important properties of this marker [45, 46]. Taking into account the above mentioned properties we have included serum PCT concentration into F2 evaluation. We think that simultaneous determination of three biochemical markers will enable more precise and more objective assessment of “inflammatory status” eliminating errors resulting from heterogeneity of the investigated group and known deviations in the behavior of the selected markers in some critical morbid states.

      Among the prognostic scales using inflammatory state markers we have not found any similar to ours. Our scale is unique due to the combination of biochemical data of inflammation with simultaneous assessment of the patient’s general condition and protein metabolism. Ingenbleek and Carpentier Prognostic Inflammatory and Nutritional Index (PINI) deserves attention [16]. The scale is based on the evaluation of 4 parameters: 2 markers of malnutrition: albumin and prealbumin, and 2 markers of inflammatory state: CRP and α1acid glycoprotein (AAG). This scoring system may predict morbidity or mortality in hospitalized patients [24]. The normal PINI level in healthy population is <1. The value of PINI (>1) is associated with poor prognosis [16, 47]. PINI has been found to be a reliable indicator of both nutritional status and prognosis in trauma, burns and infection [48, 49] and lately in cancer [50]. PINI is slightly similar to the scale proposed by us, as it considers 2 of 3 analyzed groups of risk factors. In our investigations we did not determine AAG, which is not a marker commonly used in clinical practice in our country, and prealbumin due to its susceptibility to nutrition inhibition, which always occurs in the course of the treatment of AM patients. Other authors also confirmed that nutritional state can affect inflammatory response in patients with advanced carcinoma and the results of PINI prognostic scale [51, 52]. Wunder et al. presented an interesting attempt of working out an independent indicator of early prediction of death in sepsis [53]. The authors, analyzing 33 patients with sepsis of different etiology, noticed that the deviations of the values of PCT and Acute Physiology and Chronic Health Evaluation (APACHE II) were correlated with poor prognosis. Novotny et al. carried out similar studies on a larger group of 160 patients with sepsis resulting from peritonitis or mediastinitis after an anastomotic leak and perforation of a hollow organ [54]. It should be noted that the clinical material presented in this study was to a great extent similar to our material. The authors, owing to combination of both indicators and calculations with the use of binary logistic regression analysis, were able to identify the groups of high and low death risk. In a multivariate analysis, both PCT and APACHE III score were identified as independent, early predictive indicators of sepsis lethality. While 71% of the high-risk patients died of sepsis, 77% of patients assigned to the low-risk group survived the septic complication (sensitivity 71%, specificity 77%) [54]. To compare, the diagnostic value for “inflammatory status” in the suggested method obtained higher sensitivity (87%) but lower specificity (50%). Poor prognosis should be suspected in patients whose value of F2 calculated from the formula is <1.0.

      High death rate in the course of AM points to the need of further studies. Rare prevalence of the disease and high differentiation of the material within one medical centre are the limitations. Thus, introduction of multicentre register of the patients should be taken into consideration. A detailed analysis of the investigated cases in a large representative group of patients can have an influence on the determination of risk factors and on the improvement of the prognosis in patients treated surgically due to AM.

      Conclusion

      We do hope that the proposed prognostic method has a chance to be introduced into the clinical practice which can contribute to the modification of the treatment of patients with AM. It is based on mathematical assessment of own material and devoid of subjective interpretation. Its most important advantages are: inclusion into the assessment of 2 simple clinical data and 6 biochemical tests which can be obtained within first 2–3 hours after the patient’s admission to hospital (duration of laboratory investigations), low costs and simple interpretation of the results. We think that the construction of the method, based on the evaluation of 3 groups of risk factors determining inflammatory, proteinic and general status, will be less sensitive to difficult to foresee deviations of the values of biochemical markers associated with the impact of factors such as: malnutrition, bacteriological etiology, comorbidities, surgical complications and others. To simplify the calculations, the scale can be prepared in a form of automatic electronic “calculator” which provides a ready result after entering appropriate data. The result proving poor prognosis should induce to more aggressive surgical treatment and to modification of antibiotic-therapy and supportive treatment.

      Consent

      Written informed consent was obtained from the patient for publication of this report and any accompanying images.

      Abbreviations

      AM: 

      acute mediastinitis

      APACHE: 

      Acute Physiology and Chronic Health Evaluation

      NRI: 

      Nutritional Risk Index

      PINI: 

      Prognostic Inflammatory and Nutritional Index

      CRP: 

      C-reactive protein

      PCT: 

      Procalcitonin

      HGB: 

      Hemoglobin

      WBC: 

      White blood cell

      pre: 

      Preoperative

      Coex_disease: 

      coexisting diseases

      SNC: 

      Sensitivity

      SPC: 

      Specificity

      P: 

      Positive

      N: 

      Negative

      T: 

      True

      F: 

      False

      TP: 

      True positive

      TN: 

      True negative

      FP: 

      False positive

      FN: 

      False negative

      F1: 

      Factor1

      F2: 

      Factor2

      F3: 

      Factor3

      CCI: 

      Charlson Comorbidity Index

      ICED: 

      Index of Coexisting Diseases

      BMI: 

      Body mass index

      GNRI: 

      Geriatric Nutritional Risk Index

      SIRS: 

      Systemic Inflammatory Response Syndrome

      PINI: 

      Prognostic Inflammatory and Nutritional Index

      AAG: 

      α1acid glycoprotein.

      Declarations

      Acknowledgement

      The authors wish to thank professor Marian Brocki and professor Jacek Rysz for making the hospitalized patients’ data available, for their professional advice in preparing this article and for providing necessary support.

      Authors’ Affiliations

      (1)
      Department of Thoracic Surgery, General and Oncological Surgery, Medical University of Lodz
      (2)
      Department of Maxillofacial Surgery, Medical University of Lodz

      References

      1. Marty-Ané CH, Berthet JP, Alric P, et al.: Management of descending necrotizing mediastinitis: an aggressive treatment for an aggressive disease. Ann Thorac Surg 1999, 68:212–217.PubMedView Article
      2. Muir AD, White J, McGuigan JA, McManus KG, Grahamoraz AN: Treatment and outcomes of oesophageal perforation in a tertiary referral centre. Eur J Cardiothorac Surg 2003, 23:799–804.PubMedView Article
      3. Reeder LB, DeFilippi VJ, Ferguson MK: Current results of therapy for esophageal perforation. Am J Surg 1995, 169:615–617.PubMedView Article
      4. Freeman RK, Vallières E, Verrier ED, Karmy-Jones R, Wood DE: Descending necrotizing mediastinitis: an analysis of the effects of serial surgical debridement on patient mortality. J Thorac Cardiovasc Surg 2000, 119:260–267.PubMedView Article
      5. Bufkin BL, Miller JI, Mansour KA: Esophageal perforation: emphasis on management. Ann Thorac Surg 1996, 61:1447–1452.PubMedView Article
      6. Dubost C, Kaswin D, Duranteau A, Jehanno C, Kaswin R: Esophageal perforation during attempted endotracheal intubation. J Thorac Cardiovasc Surg 1979, 78:44–51.PubMed
      7. Akman C, Kantarci F, Cetinkaya S: Imaging in mediastinitis: a systematic review based on aetiology. Clin Radiol 2004, 59:573–585.PubMedView Article
      8. El Oakley RM, Wright JE: Postoperative mediastinitis: classification and management. Ann Thorac Surg 1996, 61:1030–1036.PubMedView Article
      9. Schroeyers P, Wellens F, Degrieck I, De Geest R, Van Praet F, Vermeulen Y, Vanermen H: Aggressive primary treatment for poststernotomy acute mediastinitis: our experience with omental- and muscle flaps surgery. Eur J Cardiothorac Surg 2001, 20:743–746.PubMedView Article
      10. Jones WG, Ginsberg RJ: Esophageal perforation: a continuing challenge. Ann Thorac Surg 1992, 53:534–543.PubMedView Article
      11. Leung TK, Lee CM, Lin SY, Chen HC, Wang HJ, Shen LK, et al.: Balthazar computed tomography severity index is superior to Ranson criteria and APACHE II scoring system in predicting acute pancreatitis outcome. World J Gastroenterol 2005, 11:6049–6052.PubMed
      12. Blamey SL, Imrie CW, O’Neill J, Gilmour WH, Carter DC: Prognostic factors in acute pancreatitis. Gut 1984, 25:1340–1346.PubMedView Article
      13. Bradley EL: A clinically based classification system for acute pancreatitis. Summary of the International Symposium on Acute Pancreatitis, Atlanta, Ga., September 11 through 13, 1992. Arch Surg 1993, 128:586–590.PubMedView Article
      14. Buzby GP, Knox LS, Crosby LO, et al.: Study protocol: a randomized clinical trialof total parenteral nutrition in malnourished surgical patients. Am J Clin Nutr 1988, 47:366–381.PubMed
      15. Buzby GP, Williford WO, Peterson OL, et al.: A randomized clinical trial of total parenteral nutrition in malnourished surgical patients: the rationale and impact of previous clinical trials and pilot study on protocol design. Am J Clin Nutr 1988, 47:357–365.PubMed
      16. Ingenbleek Y, Carpentier YA: A prognostic inflammatory and nutritional index scoring critically ill patients. Int J Vitam Nutr Res 1985, 55:91–101.PubMed
      17. Estrera AS, Lanay MJ, Grisham JM, et al.: Descending necrotizing mediastinitis. Surg Gynecol Obstet 1983, 157:545–552.PubMed
      18. Martin GS, Mannino DM, Moss M: The effect of age on the development and outcome of adult sepsis. Crit Care Med 2006, 34:15–21.PubMedView Article
      19. Yang Y, Yang KS, Hsann YM, Lim V, Ong BC: The effect of comorbidity and age on hospital mortality and length of stay in patients with sepsis. J Crit Care 2010, 25:398–405.PubMedView Article
      20. Azoulay E, Adrie C, De Lassence A, et al.: Determinants of postintensive care unit mortality: a prospective multicenter study. Crit Care Med 2003, 31:428–432.PubMedView Article
      21. Fried L, Bernardini J, Piraino B: Charlson Comorbidity Index as a predictor of outcomes in incident peritoneal dialysis patients. Am J Kidney Dis 2001, 37:337–342.PubMedView Article
      22. Beddhu S, Bruns FJ, Saul M, Seddon P, Zeidel ML: A simple comorbidity scale predicts clinical outcomes and costs in dialysis patients. Am J Med 2000, 108:609–613.PubMedView Article
      23. Athienites NV, Miskulin DC, Fernandez G, Bunnapradist S, Simon G, Landa M, et al.: Comorbidity assessment in hemodialysis and peritoneal dialysis using the Index of Coexistent Disease. Semin Dial 2000, 13:320–326.PubMedView Article
      24. Davies SJ, Russell L, Bryan J, Phillips L, Russell GI: Comorbidity, urea kinetics and appetite in continuous ambulatory peritoneal dialysis patients: their interrelationship and prediction of survival. Am J Kidney Dis 1995, 26:353–361.PubMedView Article
      25. Charlson ME, Pompei P, Ales KL, MacKenzie CR: A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis 1987, 5:373–383.View Article
      26. Wang C-Y, Lin Y-S, Tzao C, Lee H-C, Huang M-H, Hsu W-H, Hsu H-S: Comparison of Charlson comorbidity index and Kaplan—Feinstein index in patients with stage I lung cancer after surgical resection. Eur J Cardiothorac Surg 2007, 32:877–881.PubMedView Article
      27. Marti J, Armadans L, Vaque J, Segura F, Schwartz S: Protein-calorie malnutrition and lymphocytopenia as predictors of hospital infection in the elderly. Med Clin (Barc) 2001, 116:446–450.
      28. Chen MK, Souba WW, Copeland EM: Nutritional support of the surgical oncology patient. Hematol Oncol Clin North Am 1991, 5:125–145.PubMed
      29. Reynolds TM, Stokes A, Russell L: Assessment of a prognostic biochemical indicator of nutrition and inflammation for identification of pressure ulcer risk. J Clin Pathol 2006,59(3):308–310.PubMedView Article
      30. Naber HJ, de Bree A, Schermer TRJ, et al.: Specificity of indexes of malnutrition when applied to apparently healthy people: the effect of age. Am J Clin Nutr 1997, 65:1721–1725.PubMed
      31. Bouillanne O, Morineau G, Dupont C, Coulombel I, Vincent J-P, Nicolis I, Benazeth S, Cynober L, Aussel Ch: Geriatric Nutritional Risk Index: a new index for evaluating at-risk elderly medical patients. Am J Clin Nutr 2005, 82:777–783.PubMed
      32. Carson JL, Noveck H, Berlin JA, Gould SA: Mortality and morbidity in patients with very low postoperative Hb levels who decline blood transfusion. Transfusion 2002,42(7):812–818.PubMedView Article
      33. Garson JL, Duff A, Poses RM, Berlin JA, Spence RK, Trout R, Noveck H, Strom BL: Effect of anaemia and cardiovascular disease on surgical mortality and morbidity. Lancet 1996, 348:1055–1060.View Article
      34. Welch HG, Mehan KR, Goodnough LT: Prudent strategies for elective red blood cell transfusion. Ann Intern Med 1992, 116:393–402.PubMed
      35. American College of Chest Physicians/Society of Critical Care Medicine Consensus Conference: definitions for sepsis and organ failure and guidelines on the use of innovative therapies in sepsis-Members of the American College of Chest Physicians/Society of Critical Care Medicine Consensus Conference Committee. Crit Care Med 1992, 20:864–874.View Article
      36. Weitzman M: Diagnostic utility of white blood cell and differential cell counts. Am J Dis Child 1975, 129:1183–1189.PubMed
      37. Okamura JM, Miyagi JM, Terada K, Hokama Y: Potential clinical applications of C-reactive protein. J Clin Lab Anal 1990, 4:231–235.PubMedView Article
      38. Clark BA, Mayhew JL: An inexpensive method of determining body composition by underwater weighing. Br J Nutr 1979, 42:173–183.View Article
      39. Balkwill F, Mantovani A: Inflammation and cancer: back to Virchow? Lancet 2001, 357:539–545.PubMedView Article
      40. Matson A, Soni N, Sheldon J: C-reactive protein as a diagnostic test of sepsis in the critically ill. Anaesth Intensive Care 1991, 19:182–186.PubMed
      41. Warren S: The immediate causes of death in cancer. Am J Med Sciences 1932, 184:610–615.View Article
      42. Brunkhorst FM, Wegscheider K, Forycki ZF, Brunkhorst R: Procalcitonin for early diagnosis and differentiation of SIRS, sepsis, severe sepsis, and septic shock. Intensive Care Med 2000,26(Suppl 2):148–252.
      43. Bertsch T, Richter A, Hofheinz H, Bohm C, Hartel M, Aufenanger J: Procalcitonin.A new marker for acute phase reaction in acute pancreatitis. Langenbecks Arch Chir 1997, 382:367–372.PubMed
      44. de Werra I, Jaccard C, Corradin SB, et al.: Cytokines, nitrite/nitrate, soluble tumour necrosis factor receptors, and procalcitonin concentrations: comparisons in patients with septic shock, cardiogenic shock, and bacterial pneumonia. Crit Care Med 1997, 25:607–613.PubMedView Article
      45. Dalton H: Procalticonin: a predictor of lung injury attributable to sepsis. Crit Care Med 1999, 25:2304–2308.View Article
      46. Whang KT, Vath SD, Becker KL, et al.: Procalticonin and proinflamatory cytokine interactions in sepsis. Shock 2000, 4:73–78.View Article
      47. Perier C, Granouillet R, Chamson A, Gonthier R, Frey J: Nutritional markers, acute phase reactants and tissue inhibitor of matrix metalloproteinase 1 in elderly patients with pressure sores. Gerontology 2002, 48:298–301.PubMedView Article
      48. Gottschlich MM, Baumer T, Jenkins M, Khoury J, Warden GD: The prognostic value of nutritional and inflammatory indices in patients with burns. J Burn Care Rehabil 1992, 13:105–113.PubMedView Article
      49. Bonnefoy M, Ayzac L, Ingenbleek Y, Kostka T, Boisson RC, Bienvenu J: Usefulness of the prognostic inflammatory and nutritional index (PINI) in hospitalized elderly patients. Int J Vitam Nutr Res 1998, 68:189–195.PubMed
      50. Walsh D, Mahmoud F, Barna B: Assessment of nutritional status and prognosis in advanced cancer: interleukin-6, C-reactive protein, and the prognostic and inflammatory nutritional index. Support Care Cancer 2003, 11:60–62.PubMedView Article
      51. Slaviero KA, Clarke SJ, Rivory LP: Inflammatory response: an nrecognized sourceof variability in the pharmacokinetics and pharmacodynamics of cancer chemotherapy. Lancet Oncol 2003, 4:224–232.PubMedView Article
      52. Rivory LP, Slaviero K, Clarke SJ: Hepatic cytochrome P450 3A drug metabolism isreduced in cancer patients with an acute-phase response. Br J Cancer 2002, 87:277–280.PubMedView Article
      53. Wunder C, Eichelbronner O, Roewer N: Are IL-6, IL-10 and PCT plasma concentrations reliable for outcome prediction in severe sepsis? A comparison with APACHE III and SAPS II. Inflamm Res 2004, 53:158–163.PubMedView Article
      54. Novotny A, Emanuel K, Matevossian E, Kriner M, Ulm K, Bartels H, Holzmann B, Weighardt H, Siwert J-R: Use of procalcitonin for early prediction of lethal outcome of postoperative sepsis. Am J Surg 2007, 194:35–39.PubMedView Article

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      © Jablonski and Kozakiewicz; licensee BioMed Central Ltd. 2012

      This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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