University Hospitals of Leicester, Leicester, UK.
BJU Int. 2020 Apr;125(4):610-616. doi: 10.1111/bju.14998. Epub 2020 Feb 17.
To report a case series of Fournier's gangrene (FG) from our institution, and to investigate its mortality over the past 25 years.
Case notes of men presenting to our institution from 2013 to 2016 with FG were reviewed. As well as age, diabetic history, length of stay, length of stay in critical care, and mortality; we calculated (where possible) the Uludag Fournier's Gangrene Severity Index (UFGSI). Published studies and cases series reporting the mortality rates for FG were reviewed from 1993 to 2018. The size of the study, country of origin, average age and gender ratio were collected, alongside mortality.
Two of the 11 patients treated for FG at out institution died within 90 days of admission, a mortality rate of 18%. Predicted mortality was significantly higher. A total of 173 publications were identified from the Medical Literature Analysis and Retrieval System Online (MEDLINE) database published between 1993 and 2018, reporting data from 1975 to 2018. Analysis of heterogeneity, by both time and precision, supported exclusion of four retrospective coded database-driven studies from the analysis. From the remaining studies, mortality ranged from 0% to 42%. Of the 6152 reported cases, there were 1220 deaths, giving an overall mortality rate of 19.8%. There was no evidence of a significant change in the mortality rate for FG over time (P = 0.996).
In our case series, the mortality rate for FG was 18%, despite a higher predicated mortality (based on UFGSI scores). The treatment of FG remains appropriate resuscitation, aggressive surgical debridement, and critical care management. Perceived high risk of mortality should not deter aggressive management. Mortality due to FG does not appear to have changed over the past 25 years, and is estimated at 19.8%. In studies identifying cases of FG, careful attention should be paid to case definition, particularly when cases are being abstracted retrospectively from large coded databases.
报告我院发生的一系列坏疽性脓皮病(FG)病例,并研究过去 25 年来 FG 的死亡率。
回顾了我院 2013 年至 2016 年 FG 患者的病例资料。记录患者的年龄、糖尿病史、住院时间、重症监护室住院时间和死亡率;并尽可能计算乌卢达格 FG 严重程度指数(UFGSI)。回顾了 1993 年至 2018 年期间发表的报告 FG 死亡率的研究和病例系列。收集了研究的规模、来源国、平均年龄和性别比例以及死亡率。
我院收治的 11 例 FG 患者中,有 2 例在入院后 90 天内死亡,死亡率为 18%。预计死亡率明显更高。通过 MEDLINE 数据库共确定了 1993 年至 2018 年期间发表的 173 篇文献,这些文献报告的数据时间范围为 1975 年至 2018 年。通过时间和精度的异质性分析,支持将四项回顾性编码数据库驱动研究排除在分析之外。在剩余的研究中,死亡率范围为 0%至 42%。在报告的 6152 例病例中,有 1220 例死亡,总死亡率为 19.8%。过去 25 年来,FG 的死亡率没有明显变化(P=0.996)。
在我们的病例系列中,FG 的死亡率为 18%,尽管预测死亡率更高(基于 UFGSI 评分)。FG 的治疗仍然是适当的复苏、积极的手术清创和重症监护管理。高死亡率不应阻止积极治疗。过去 25 年来,FG 的死亡率似乎没有变化,估计为 19.8%。在确定 FG 病例的研究中,应特别注意病例定义,特别是当病例是从大型编码数据库中回顾性提取时。