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篇名 Efficacy of Peginterferon Alfa Plus Ribavirin Treatment for Chronic Hepatitis C Virus Infection in Cirrhotic Patients
卷期 17:2
並列篇名 合併長效型干擾素及RIBAVIRIN治療肝硬化患者之慢性C型肝炎的療效評估
作者 林恭弘許秉毅蔡維倫陳文誌黎國洪余憲忠
頁次 053-062
關鍵字 C型肝炎病毒長效型干擾素雷巴威林肝硬化HCVpeginterferon-αribavirincirrhosis
出刊日期 201106

中文摘要

腹直肌血腫是一種罕見引起急性腹痛的急症,目的:慢性C型肝炎所致肝硬化患者之預後不佳,每年約有5%發生肝失償。根除C型肝炎病毒可以避免這些患者之疾病惡化。本回溯性研究之目的在於探討肝硬化患者接受長效型α-干擾素加雷巴威林(ribavirin)治療慢性C型肝炎感染之效果,並比較此合併療法於肝硬化及非肝硬化患者之療效。方法:本研究將2003年9月至2009年11月間,接受長效型α-干擾素加雷巴威林治療慢性C型肝炎之肝硬化與非肝硬化患者納入,比較肝硬化與非肝硬化患者之基本特徵、病毒學反應、與不良作用之發生率。結果:本研究共納入15位肝硬化及121位非肝硬化,接受長效型α-干擾素加雷巴威林治療之患者。兩組患者治療前之病毒量、基因型、年紀、及性別皆近似。於治療過程中,肝硬化患者有快速病毒學反應之比率較非肝硬化組為低(57.1%與92.5%, P=0.035)。肝硬化組之治療終反應率及持續性病毒學反應率(分別為86.7%與60.0%)較非肝硬化組(89.8%與68.6%)略低,但兩者之差距皆未達統計學差異(P值分別為0.659與0.562)。此外,肝硬化組與非肝硬化組之不良作用發生頻率亦無明顯差別。結論:肝硬化及非肝硬化之C 型肝炎患者接受長效型α-干擾素加雷巴威林治療可以達到不錯的療效。

英文摘要

Objective: Hepatitis C virus (HCV)-related cirrhotic patients have a poor prognosis with 5% annual risk of hepatic decompensation. Eradicating HCV may prevent disease progression of cirrhotic patients. The aims of this retrospective study were to investigate the efficacy of peginterferon-α plus ribavirin treatment for chronic HCV infection in cirrhotic patients and to compare the efficacies of the combined therapy between patients with and without cirrhosis. Method: From September 2003 to November 2009, cirrhotic and non-cirrhotic HCV-infected patients receiving ribavirin plus peginterferon-α therapy were included. The baseline characteristics, virological response and incidence of adverse events were compared between the patients with and without cirrhosis. Results: Fifteen cirrhotic and 121 non-cirrhotic patients receiving ribavirin plus peginterferon-α therapy were included. The baseline HCV RNA levels, genotype, age, and gender were comparable between groups. Cirrhotic patients had a lower rapid virological response (RVR) rate than non-cirrhotic patients (57.1% vs. 92.5%, P=0.035). The end-of-treatment response (ETR) rate and sustained virological response (SVR) in cirrhotic patients (86.7% and 60.0%, respectively) were slightly lower than those in non-cirrhotic patients (89.8% and 68.6%) but both differences didn’t reach statistic significance (P = 0.659 and 0.562, respectively). Additionally, there were no significant differences in the frequencies of adverse events between cirrhotic and non-cirrhotic patients. Conclusions: Those cirrhotic patients who received standard treatment with ribavirin plus peginterferon-α might achieved an acceptable SVR rate in Taiwan.

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