Introduction
Fournier fasciitis (FF) is a serious infectious and life-threatening disease of rapid dissemination. Therefore, it is actually worth of early diagnosis and timely management. A polymicrobial pathology affects the genital, perineal, and perianal region1. It is named after Jean Alfred Fournier, a French dermatologist, who presented the case of a young man with perineal gangrene in 18832. Due to its acute and rapid progression and polymicrobial involvement, Fournier's gangrene continues to represent high mortality rates despite advances in surgical techniques, critical care, and the development of new antibiotics. Most studies report mortality rates between 20% and 40%, with a range of 4-88%3.
Different scoring systems and prognostic factors have been proposed in an effort to predict FF survival and prognosis. The Fournier gangrene severity index (FGSI) Table 1, first described in 1995, is a scoring system that consists of some clinical and laboratory parameters that help predict prognosis and survival4.
Variables/assigned points | High | Normal | Low | ||||||
---|---|---|---|---|---|---|---|---|---|
+ 4 | + 3 | + 2 | + 1 | 0 | + 1 | + 2 | + 3 | + 4 | |
Temp. °C | > 41 | 39-40.9 | - | 38.5-38.9 | 36-38.4 | 34-35.9 | 32-33.9 | 30-31.9 | < 39.9 |
Heart rate | > 180 | 140-179 | 110-139 | - | 70-109 | - | 55-69 | 40-54 | < 39 |
Respiratory rate | > 50 | 35-49 | - | 25-34 | 12-24 | 10-11 | 6-9 | - | < 5 |
Serum sodium mmol/l | > 180 | 160-179 | 155-159 | 150-154 | 130-149 | - | 120-129 | 111-119 | < 110 |
Serum potassium mmol/l | > 7 | 6-6.9 | - | 5.5-5.9 | 3.5-5.4 | 3-3.4 | 2.5-2.9 | - | < 2.5 |
Serum creatinine mg/100 ml | > 3.5 | 2-3.4 | 1.5-1.9 | - | 0.6-1.4 | - | < 0.6 | - | - |
Hematocrit (HT) | > 60 | - | 50-59.9 | 46-49.9 | 30-45.9 | - | 20-29.9 | - | < 20 |
Leukocytes total/mm3 × 1000 | > 40 | - | 20-39.9 | 15-19.9 | 3-14.9 | - | 1-2.9 | - | < 1 |
Venous serum bicarbonate mmol/l | > 52 | 41-51.9 | - | 32-40.9 | 22-31.9 | - | 18-21.9 | 15-17.9 | < 15 |
FF severity is traditionally evaluated by means of the FGSI scale, which is an internationally accredited index, and requires hematic biometrics, blood chemistry, serum electrolytes and blood gas test, neutrophil-to-lymphocyte ratio (NLR), and platelet-to-lymphocyte ratio (PLR) for its application. These items have proven to be useful as predictors of severity in different septic and ischemic processes; in addition, hematic biometrics may be the only requirement for its application5,6.
Given the simplicity of determining these ratios, their utility to measure FF severity should be evaluated by comparing them against the usual FGSI measurement.
Materials and methods
A retrospective, observational, analytical study of patients diagnosed with FF was performed to determine if the severity measured by the FGSI scale is associated with the severity measured by the NLR and PLR ratios. Patients diagnosed with FF and treated at the Hospital General de México "Dr. Eduardo Liceaga" from 2010 to 2016 were included in the study.
Results
A sample of 45 cases was included from 2010 to 2016, 40 (88.8%) were male and 5 of them (11.2%) were female. The average age of the sample was 50.6 years. In 40 cases, the FF origin was anorectal and in five cases, the origin was urological.
Regarding the severity scales under evaluation, a mean score for the FGSI sample of 7.7 (SD 3.8) was found. A mean NLR score of 13.3 (SD 10.4) and a PLR of 215 points (SD 170) were obtained, as shown in table 2
Index | Mean | SD ± |
---|---|---|
FGSI | 7.7 | 3.8 |
NLR | 13.3 | 10.4 |
PLR | 215 | 170 |
FGSI: Fournier gangrene severity index; NLR: neutrophil-to-lymphocyte ratio; PLR: platelet-to-lymphocyte ratio.
The severity assessment scale was set for FGSI values at 9 points, NLR at 7 points, and PLR at 140, which are the values referred to in literature7-9. By categorizing the severity, the values were obtained, which are shown in (table 3).
Variable | Mild | Severe |
---|---|---|
FGSI | < 9 (66.7%) | 10 (33.3%) |
NLR | < 7 (22.2%) | 8 (77.8%) |
PLR | < 140 (44.4) | 141 (56.6%) |
FGSI: Fournier gangrene severity index; NLR: neutrophil-to-lymphocyte ratio; PLR: platelet-to-lymphocyte ratio.
About 40% of cases deemed severe by the NLR were also considered severe by the FGSI, while 60% of cases diagnosed as severe by the NLR resulted in an FGSI score lower than 9. When applying Fisher's exact test, a statistically non-significant p = 0.077 was obtained. By submitting these differences to statistical hypothesis testing, using Mann-Whitney U-test, for independent samples, we obtained p = 0.547, without statistical significance (Table 4). When comparing the severity determined by the PLR with the severity determined by FGSI, it is observed that 28% of the cases diagnosed as severe by the PLR corresponded to an FGSI score > 10, while 72% diagnosed as severe by the PLR, yielded an FGSI score lower than 9. While applying the Chi-square test as a test statistic, p = 0.396 was obtained, without statistical significance. By submitting these differences to the Mann-Whitney U-test, we obtained p = 0.613, without statistical significance (Table 5).
Discussion
FF management is complex and requires a timely evaluation in the emergency services to apply the appropriate treatment as soon as possible. The systematic use of prediction scales overtime has allowed to improve the prognosis of patients by making a prediction of severity and mortality and based thereon, to establish the ideal treatment. The clearest example is the FGSI scale, which is accepted in multiple studies. The FGSI scale requires the calculation of numerous variables, which are not always accessible in all media. In an attempt to simplify the initial evaluation, studies have been conducted using scales such as LRINEC, UFGSI, sAPGAR, and Charlson Comorbidity Index. The NLR and PLR are two markers that have been tested in different pathologies, including FF, and which have yielded very variable results. Studies conducted for this pathology have attempted to simplify the way to assess the clinical stage of the disease with a single laboratory study. No previous studies were found in Mexico. Kahramanaca reports in a study with 68 patients that high NLR and PLR are associated with the need for more debridement, higher hospitalization costs, and higher mortality rates7. Manu in a study with 24 patients reported higher morbidity and mortality rates with high FGSI, NLR, and PLR values8.
Yim et al. also reported NLR and PLR as independent prognostic factors that are associated with increased mortality from FF9.
In this study, there was no statistically significant relationship while comparing NLR and PLR values with the FGSI scale, which correlated the severity measured between the different means to determine the severity of FF. It is worth noting that in the present sample obtained for convenience, there were no mortality cases. The reference values for NLR and PLR have not been established uniformly and do not allow establishing a position to determine the ideal treatment at the time of diagnosis.