Bowel Colonization With Carbapenem‐Resistant Bacteria Is Associated With Short‐Term Outcomes in Patients With Acute‐On‐Chronic Liver Failure

医学 内科学 胃肠病学 肝硬化 肺炎克雷伯菌 抗生素 粪便 病因学 自发性细菌性腹膜炎 肺炎 乳果糖 微生物学 大肠杆菌 生物化学 化学 基因 生物
作者
Satender Pal Singh,Vikram Bhatia,Pratibha Kale,Guresh Kumar,Vikas Khillan,Rajan Vijayaraghavan
出处
期刊:Journal of Gastroenterology and Hepatology [Wiley]
卷期号:40 (2): 528-536 被引量:3
标识
DOI:10.1111/jgh.16830
摘要

BACKGROUND: Bowel colonization with antimicrobial-resistant bacteria has been associated with worse clinical outcomes in patients with cirrhosis; however, it has not been studied in patients with acute-on-chronic liver failure (ACLF). We evaluated whether fecal isolation of carbapenem-resistant gram-negative bacteria (CR-GNB) among patients with ACLF affects short-term outcomes. METHODS: Patients of APASL-ACLF (n = 339) were screened between June 2020 and December 2021, and 150 were included. Stool cultures were carried out at baseline and every 5 days thereafter until discharge or death. All surviving patients were followed until 60 days after discharge. RESULTS: Mean age was 44.8 (8.8) years, with 86% males and alcohol as etiology in 66%. CR-GNB organisms were isolated from stool in 42% of hospitalized ACLF patients, with E. coli and Klebsiella pneumoniae as the most common species. Patients with CR-GNB fecal carriage were associated with higher CTP, MELD, and DF scores but not with recent antibiotics, proton pump inhibitors, or lactulose use. Extraintestinal infections developed in 59.3% overall, most commonly UTI, pneumonia, and SBP. Infectious complications developed in 57.3% and 19.7% with and without CR-GNB in the stool (RR: 5.5; p < 0.001). Peripheral cultures were positive in 60.7% with infections, with species concordant with the fecal isolates found in 90.7%. Isolation of CR-GNB from stool and high bilirubin were independently associated with both in-hospital mortality and 60-day mortality (p = 0.05). CONCLUSIONS: Hospitalized ACLF patients with CR-GNB in the stool have a significantly higher risk of extraintestinal infections, in-hospital mortality, and short-term mortality up to 60 days. TRIAL NUMBER: [NCT04383106].
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