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High risk of complications and acute-on-chronic liver failure in cirrhosis patients with acute pancreatitis

医学 急性胰腺炎 肝硬化 胰腺炎 内科学 失代偿 胃肠病学 并发症 肝病 不利影响 慢性肝病
作者
M. Vogel,Hanno Ehlken,Stefan Kluge,Thomas Röesch,Ansgar W. Lohse,Samuel Huber,Martina Sterneck,Peter Huebener
出处
期刊:European Journal of Internal Medicine [Elsevier BV]
卷期号:102: 54-62 被引量:4
标识
DOI:10.1016/j.ejim.2022.05.034
摘要

Background & aims Acute pancreatitis (AP) is a frequent indication for hospitalization and may present with varying degrees of severity. AP often coincides with hepatic disease, yet the impact of liver cirrhosis (LC) on the course of AP is uncertain, and early identification of patients at risk for complications remains challenging. We aimed to assess the impact of LC on the development of pancreatic and extra-pancreatic complications of AP, and to identify predictors of adverse outcomes in cirrhotic patients. Methods All adult patients with LC and AP (LC-AP, n = 52) admitted to our institution between 01/2011–03/2020 were subjected to a 1:2 matched-pair analysis with patients with AP but without LC (NLC-AP, n = 104). Results At hospital admission, Glasgow-Imrie and Ranson scores as well as markers of systemic inflammation were comparable in LC-AP and NLC-AP patients, and both groups had similar rates of necrotizing AP. Infectious complications were more prevalent, and medical interventions were performed more often and with higher complication rates in LC-AP patients. While only 12.5% of NLC-AP patients developed organ failures, 48% of LC-AP patients developed single (7.7%) or multiple organ failure (40.4%), resulting in 44% of LC-AP patients with acute-on-chronic liver failure (ACLF). Patients with overt portal hypertension were particularly prone for decompensation. Mortality was higher among LC-AP compared to NLC-AP patients (6-month mortality 25% vs. 1.9%, p < 0.001), and SOFA and MELD scores at admission most accurately predicted outcomes in LC-AP. Conclusion Among AP patients, concomitant cirrhosis substantially increases the risk for infections, periprocedural complications, multiorgan failure and death.
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