Whiston Hospital, Prescot, Merseyside and Academic Unit of Medical Education, The Medical School, University of Sheffield, Sheffield, UK.
The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
Intensive Care Med. 2014 Feb;40(2):202-210. doi: 10.1007/s00134-013-3158-7. Epub 2013 Dec 4.
Faecal peritonitis (FP) is a common cause of sepsis and admission to the intensive care unit (ICU). The Genetics of Sepsis and Septic Shock in Europe (GenOSept) project is investigating the influence of genetic variation on the host response and outcomes in a large cohort of patients with sepsis admitted to ICUs across Europe. Here we report an epidemiological survey of the subset of patients with FP.
To define the clinical characteristics, outcomes and risk factors for mortality in patients with FP admitted to ICUs across Europe.
Data was extracted from electronic case report forms. Phenotypic data was recorded using a detailed, quality-assured clinical database. The primary outcome measure was 6-month mortality. Patients were followed for 6 months. Kaplan-Meier analysis was used to determine mortality rates. Cox proportional hazards regression analysis was employed to identify independent risk factors for mortality.
Data for 977 FP patients admitted to 102 centres across 16 countries between 29 September 2005 and 5 January 2011 was extracted. The median age was 69.2 years (IQR 58.3-77.1), with a male preponderance (54.3%). The most common causes of FP were perforated diverticular disease (32.1%) and surgical anastomotic breakdown (31.1%). The ICU mortality rate at 28 days was 19.1%, increasing to 31.6% at 6 months. The cause of FP, pre-existing co-morbidities and time from estimated onset of symptoms to surgery did not impact on survival. The strongest independent risk factors associated with an increased rate of death at 6 months included age, higher APACHE II score, acute renal and cardiovascular dysfunction within 1 week of admission to ICU, hypothermia, lower haematocrit and bradycardia on day 1 of ICU stay.
In this large cohort of patients admitted to European ICUs with FP the 6 month mortality was 31.6%. The most consistent predictors of mortality across all time points were increased age, development of acute renal dysfunction during the first week of admission, lower haematocrit and hypothermia on day 1 of ICU admission.
粪便性腹膜炎(FP)是导致脓毒症和入住重症监护病房(ICU)的常见原因。欧洲脓毒症和感染性休克遗传学(GenOSept)项目正在研究遗传变异对欧洲 ICU 收治的大量脓毒症患者的宿主反应和结局的影响。在此,我们报告了 FP 患者亚组的流行病学调查结果。
确定欧洲 ICU 收治的 FP 患者的临床特征、结局和死亡风险因素。
从电子病历报告表中提取数据。使用详细的、经过质量保证的临床数据库记录表型数据。主要结局测量指标为 6 个月死亡率。患者随访 6 个月。采用 Kaplan-Meier 分析确定死亡率。采用 Cox 比例风险回归分析确定死亡的独立风险因素。
2005 年 9 月 29 日至 2011 年 1 月 5 日期间,从 16 个国家的 102 个中心共提取了 977 例 FP 患者的数据。中位年龄为 69.2 岁(IQR 58.3-77.1),男性居多(54.3%)。FP 的最常见原因是穿孔性憩室疾病(32.1%)和手术吻合口破裂(31.1%)。28 天 ICU 死亡率为 19.1%,6 个月时增至 31.6%。FP 的病因、既往合并症以及从症状估计发作到手术的时间均未影响生存。与 6 个月死亡率增加相关的最强独立风险因素包括年龄、APACHE II 评分较高、入住 ICU 后 1 周内急性肾功能和心血管功能障碍、低体温、入住 ICU 第 1 天的血细胞比容和心动过缓。
在这一大批入住欧洲 ICU 的 FP 患者中,6 个月的死亡率为 31.6%。所有时间点死亡率的最一致预测因素是年龄增加、入院后第 1 周内急性肾功能障碍、入住 ICU 第 1 天的血细胞比容和低体温。