肝硬化患者ercp后肝功能失代偿的预测因素:一项回顾性病例对照研究。

IF 2.5 4区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Mohammed Abusuliman, Sanad Dawod, Faisal Nimri, Taher Jamali, Gordon Jacobsen, Muhammad Zarrar Khan, Remy Arwani, Omar Shamaa, Suhaib Alhaj Ali, Spandana Alluri, Rami Youssef, Abdulmalik Saleem, Ahmad Alomari, Muhammad Saad Faisal, Haya Omeish, Muhammad Salman Faisal, Amr Abusuliman, Sumit Singla, Cyrus Piraka, Mazen Elatrache, Tobias Zuchelli
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引用次数: 0

摘要

背景与目的:内窥镜逆行胰胆管造影(ERCP)是肝硬化患者诊断和治疗的重要手段;然而,它有术后肝功能失代偿的风险。本研究旨在确定与ercp后肝硬化患者肝功能失代偿相关的预测因素,以便更好地为临床决策提供信息,并最大限度地减少不良后果。方法:对肝硬化行ERCP患者进行回顾性分析。评估临床、生化和程序变量以确定它们与肝失代偿的关系。进行多变量分析以确定独立预测因子。结果:共纳入了277例接受ERCP的肝硬化患者。该队列的平均年龄为63.4岁,男性占多数(65.3%),肝硬化的病因多种多样,包括酒精相关(39.3%)和丙型肝炎(11.4%)。ercp术后并发症发生率为26.7%。最常见的并发症是肝功能失代偿事件(18.4%)、败血症(10.8%)和胆管炎(6.1%)。并发症患者的基线MELD评分、INR、慢性肾脏疾病(CKD)以及腹水、肝性脑病和肝肾综合征(HRS)病史均显著较高。一项多因素分析显示,MELD评分较高、腹水、肝性脑病和支架置入等因素与ercp后并发症相关。亚组分析表明,发生肝失代偿事件(腹水、收缩压或HRS)的患者在基线时具有更严重的肝功能障碍,这反映在较高的MELD评分和INR以及先前的腹水和肝性脑病发作中。结论:手术前肝功能参数和手术因素是ercp术后肝硬化患者肝功能失代偿的重要预测因素。主要危险因素包括较高的MELD评分、CKD、腹水史和肝性脑病。谨慎的程序前评估和管理对于减少这些风险至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predictive Factors of Post-ERCP Hepatic Decompensation in Patients with Cirrhosis: A Retrospective Case-Control Study.

Background and aim: Endoscopic retrograde cholangiopancreatography (ERCP) is a crucial diagnostic and therapeutic procedure in patients with cirrhosis; however, it carries the risk of post-procedural hepatic decompensation. This study aims to identify predictive factors associated with post-ERCP hepatic decompensation in patients with cirrhosis to better inform clinical decision-making and minimize adverse outcomes.

Methods: A retrospective analysis was conducted on patients with cirrhosis undergoing ERCP. Clinical, biochemical, and procedural variables were evaluated to determine their association with hepatic decompensation. Multivariate analysis was performed to identify independent predictors.

Results: A total of 277 patients with cirrhosis who underwent an ERCP were included. The cohort had a mean age of 63.4 years, with a male predominance (65.3%) and various etiologies of cirrhosis, including alcohol-related (39.3%) and hepatitis C (11.4%). Post-ERCP complications occurred in 26.7% of patients. The most common complications were hepatic decompensation events (18.4%), sepsis (10.8%), and cholangitis (6.1%). Patients with complications had significantly higher baseline MELD scores, INR, chronic kidney disease (CKD) and history of ascites, hepatic encephalopathy, and hepatorenal syndrome (HRS). A Multivariate analysis revealed that factors such as higher MELD score, ascites, hepatic encephalopathy, and stent placement were associated with post-ERCP complications. Subgroup analyses indicated that patients who developed hepatic decompensation events (ascites, SBP, or HRS) had a more severe liver dysfunction at baseline, as reflected by a higher MELD score and INR, and prior episodes of ascites and hepatic encephalopathy.

Conclusion: Pre-procedural liver function parameters and procedural factors are crucial predictors of post-ERCP hepatic decompensation in patients with cirrhosis. Key risk factors include higher MELD score, CKD, history of ascites, and hepatic encephalopathy. Careful pre-procedural evaluation and management are essential to reduce these risks.

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来源期刊
Digestive Diseases and Sciences
Digestive Diseases and Sciences 医学-胃肠肝病学
CiteScore
6.40
自引率
3.20%
发文量
420
审稿时长
1 months
期刊介绍: Digestive Diseases and Sciences publishes high-quality, peer-reviewed, original papers addressing aspects of basic/translational and clinical research in gastroenterology, hepatology, and related fields. This well-illustrated journal features comprehensive coverage of basic pathophysiology, new technological advances, and clinical breakthroughs; insights from prominent academicians and practitioners concerning new scientific developments and practical medical issues; and discussions focusing on the latest changes in local and worldwide social, economic, and governmental policies that affect the delivery of care within the disciplines of gastroenterology and hepatology.
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