Fournier's gangrene is a rare infection of the perianal and genital area. Despite advances in its etiology, diagnosis, and intensive care techniques, the mortality rate in Fournier's gangrene remains high. Due to the high mortality rates, the scoring systems used to predict mortality in these patients are of great importance. It has been demonstrated in previous studies that conditions such as diabetes mellitus, coagulopathy, severe sepsis, advanced age, prolonged hospital stay, malignancy, multiple organ failure, and alcoholism increase mortality in FG patients [8–10]. Despite advances in follow-up and medical treatment in modern intensive care units, mortality rates have been reported in the range of 30-50% [2]. The mortality rate in our study was 20.7%.
Existing studies have indicated that advanced age increases mortality [11–13]. The most important reason regarding this condition seems to be related to the increasing number of predisposing diseases and the incidence of FG with aging. However, it was found that advanced age is not a direct factor affecting survival [14]. The mean age of the survivors in our study was 49.64±15.26 years, while the mean age of those who died was 68.91±15.96 years, and advanced age was found to impact mortality.
Diabetes mellitus is an important risk factor for necrotizing infections involving the lower extremities, perineum, head, and neck region [15, 16]. The patients included in our study had cardiovascular disease, DM, hematological diseases, and malignancies. DM, which is frequently involved in the etiology of FG, was determined in approximately 25% of the patients included in the study. The rate of diagnosis of DM in patients who died was 53.85%, and it was not statistically significant. In our study, high creatinine, one of the daily routine blood biochemistry tests, was another factor that increased mortality and was statistically significant. However, serum sodium, potassium, calcium, and hematocrit values were not statistically significant. Likewise, in the study of Tenorio (N) and Mangwiron [11], it was revealed that high serum creatinine is a risk factor for mortality.
FGSI is a scoring developed by Laor et al. [4] using vital signs and some laboratory data to determine the severity and prognosis of FG in patients. FGSI is a modification of the APACHE II score. FGSI scores of 9 and above were found to be associated with mortality. However, Yılmazlar et al. [5] reported that this scoring system had some drawbacks in estimating prognosis and mortality, and the UFGSI scoring system was developed by adding age and extent of disease spread to this system. Both of these systems are frequently used to predict the prognosis and mortality of FG. In a study, both systems gave 100% sensitivity in sensitivity and specificity analysis. Specificity was 78% for FGSI and 73% for UFGSI [17]. While Czymek et al. reported 87% sensitivity and 77% specificity for FGSI in their study [18], in the study of Roghmann et al., these figures were reported as 85% and 67% for UFGSI [19]. In another study conducted by Yılmazlar et al. [20] in a series of 120 cases, no survivors were reported in patients with a UFGSI score of ≥9. Threshold values for FGSI and UFGSI were 7 and 9, respectively. In this study, the FGSI score was 2 in the survivors and 5 in the deceased. While the UGFSI score was 5 in the survivors, it was 10 in the deceased. These scores were considered to be directly related to mortality and statistically significant. Besides, in the ROC analysis used for mortality-based sensitivity and specificity, the cut-off values for FGSI and UFGSI were 3 and 4, respectively, the sensitivity was 81% and 54%, and the specificity was 90% and 90%, respectively. The AUC value was 0.859 for FGSI and 0.785 for UGFSI. We found that both scoring systems are practical markers in predicting mortality in parallel with the literature.
This study also used SOFA and ACCI scoring systems, which we assumed to affect mortality. The SOFA score is a scoring system used to calculate organ systems' defect status by grading from 1 to 4. Few studies have been performed in the literature on predicting prognosis and mortality in this scoring system FG. In a recent study in our country, the SOFA score was 1 in the survivors and 4 in the deceased, and it was found to be directly related to mortality and statistically significant. Also, in the ROC analysis used, the cut-off value was 4, while the sensitivity and specificity rates were 90% and 88%, respectively [21]. In another study, it was reported that low mean SOFA scores were significantly associated with the probability of primary wound closure. In the study, the SOFA score was also 1.8 for those who survived and 3.8 for those who died [6]. In this study, we found the SOFA score to be 1 in the survivors and 3 in the deceased, and we found that it was directly related to mortality and was statistically significant. Also, in the ROC analysis used, the cut-off value was 4, while the sensitivity and specificity rates were 81% and 88%, respectively.
On the other hand, the ACCI score is a scoring system calculated in the range from 1 to 6, evaluating the presence of 19 medical conditions into account. In two studies, the ACCI score was 3 and 3, respectively, in the survivors, and 5 and 6, in the deceased. In both studies, the ACCI score was found to be statistically significant in predicting mortality [22–23]. In a recent study of Usta et al. [21] with 60 patients, the ACCI score was found to be 3 in the survivors and 5 in the deceased, and the difference was found to be statistically significant. In the same study, the cut-off value was 5 in the ROC analysis used for ACCI, while the sensitivity and specificity rates were 30% and 98%, respectively [21]. Our study determined the ACCI score to be 2 in the survivors and 4 in the deceased. The difference was statistically significant. In the ROC analysis used, the cut-off value was 8, while the sensitivity and specificity rates were 100% and 88%, respectively.
The retrospective nature of our study and the relatively low number of patients were the major limitations of our study. However, the inclusion of SOFA and ACCI as a scoring system for FG was the biggest challenge.
In conclusion, FG is a type of necrotizing fasciitis that affects the perianal and genitourinary regions, accompanied by thrombosis of the feeding arteries. Mortality rates still range between 30-50%. There is still no standard parameter or scoring system to predict prognosis and mortality in the follow-up. In this study, we revealed that advanced age and high creatinine are significant parameters in predicting mortality. Also, we found that the FGSI, UFGSI, SOFA, and ACCI scoring systems used in our study were associated with mortality for FG. ACCI had the highest diagnostic confirmation value. This was followed by SOFA, FGSI, and UFGSI, respectively. We recommend that these scoring systems be used to predict mortality for FG.