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血浆肾素活性可预测托伐普坦治疗腹水肝硬化患者的预后和与肝脏疾病相关的事件。

Plasma Renin Activity Predicts Prognosis and Liver Disease-Related Events in Liver Cirrhosis Patients with Ascites Treated by Tolvaptan.

机构信息

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

First Department of Internal Medicine, Faculty of Medicine, University of Yamanashi, Kofu, Japan.

出版信息

Dig Dis. 2022;40(4):479-488. doi: 10.1159/000518099. Epub 2021 Jul 30.

Abstract

BACKGROUND AND AIMS

A retrospective study was to analyze the association of plasma renin activity (PRA) with overall survival and liver disease-related events in decompensated liver cirrhosis with ascites treated by tolvaptan.

METHODS

We included 196 patients with decompensated cirrhosis treated with tolvaptan and for whom hepatic ascites had remained uncontrolled by conventional diuretics. Factors associated with prognosis and appearance of liver disease-related events were investigated, including vasopressin, sympathetic nervous system hormones (adrenaline, noradrenaline, and dopamine), and the renin-angiotensin system (PRA and aldosterone) at the beginning of tolvaptan treatment.

RESULTS

Age, history of hepatocellular carcinoma (HCC), and PRA were identified as independent factors for prognosis after tolvaptan treatment. The median survival time in patients with PRA ≥9.5 ng/mL/h at the beginning of tolvaptan treatment was significantly shorter than in patients with PRA <9.5 ng/mL/h (193 vs. 893 days, p < 0.001). PRA and a history of HCC were independent factors for the occurrence of liver disease-related events. The median event-free period in patients with PRA ≥3.2 ng/mL/h was significantly shorter than that of patients with PRA <3.2 ng/mL/h (89 vs. 222 days, p < 0.001).

CONCLUSIONS

PRA is an independent predictor of prognosis and appearance of liver disease-related events in patients with decompensated cirrhosis who have started tolvaptan treatment.

摘要

背景与目的

本回顾性研究旨在分析血浆肾素活性(PRA)与托伐普坦治疗伴腹水失代偿性肝硬化患者的总生存期和肝脏疾病相关事件的关系。

方法

我们纳入了 196 例接受托伐普坦治疗且常规利尿剂未能控制肝性腹水的失代偿性肝硬化患者。研究调查了与预后和肝脏疾病相关事件发生相关的因素,包括血管加压素、交感神经系统激素(肾上腺素、去甲肾上腺素和多巴胺)以及托伐普坦治疗开始时的肾素-血管紧张素系统(PRA 和醛固酮)。

结果

年龄、肝细胞癌(HCC)病史和 PRA 被确定为托伐普坦治疗后预后的独立因素。托伐普坦治疗开始时 PRA≥9.5ng/ml/h 的患者中位生存时间明显短于 PRA<9.5ng/ml/h 的患者(193 与 893 天,p<0.001)。PRA 和 HCC 病史是发生肝脏疾病相关事件的独立因素。PRA≥3.2ng/ml/h 的患者中位无事件生存时间明显短于 PRA<3.2ng/ml/h 的患者(89 与 222 天,p<0.001)。

结论

PRA 是接受托伐普坦治疗的失代偿性肝硬化患者预后和发生肝脏疾病相关事件的独立预测因素。

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