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采用6个月疗程的利巴韦林治疗慢性乙型肝炎。

Therapy of chronic hepatitis B with a 6-month course of ribavirin.

作者信息

Fried M W, Fong T L, Swain M G, Park Y, Beames M P, Banks S M, Hoofnagle J H, Di Bisceglie A M

机构信息

National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

J Hepatol. 1994 Aug;21(2):145-50. doi: 10.1016/s0168-8278(05)80387-3.

Abstract

Ribavirin is a nucleoside analogue with broad spectrum antiviral activity that has been shown to inhibit viral replication in the woodchuck model of hepatitis B virus infection. We studied the effect of ribavirin on viral replication in 18 patients with chronic hepatitis B who were positive for hepatitis B e antigen. Patients were randomized to receive a 24-week course of oral ribavirin at a dose of either 800, 1000, or 1200 mg/kg per day. All patients completed 24 weeks of treatment and an additional 24 weeks of follow up without significant side effects except for mild, reversible hemolytic anemia. Response to ribavirin was similar among all three dosage groups (p > 0.5); hence the data were pooled and analyzed together. Mean hepatitis B virus DNA levels decreased from 162.7 (95% confidence interval, 106 to 219) pg/ml before treatment to its lowest level of 114.3 (95% confidence interval, 53 to 175) pg/ml at week 20 (p < 0.05). Two patients became negative for HBV DNA and lost hepatitis B e antigen. Mean serum alanine aminotransferase activity decreased markedly from 131.1 (95% confidence interval, 84 to 178) U/l before treatment to 62.4 (95% confidence interval, 48 to 77) U/l at the end of 24 weeks of ribavirin (p < 0.05) and became normal in four patients (22%). Aminotransferase levels returned to baseline within 4 weeks once ribavirin was discontinued, while HBV DNA concentrations remained below baseline even at the end of 24 weeks of follow up.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

利巴韦林是一种具有广谱抗病毒活性的核苷类似物,已证实在乙肝病毒感染的土拨鼠模型中能抑制病毒复制。我们研究了利巴韦林对18例乙肝e抗原阳性的慢性乙型肝炎患者病毒复制的影响。患者被随机分为接受为期24周的口服利巴韦林治疗,剂量分别为每天800、1000或1200mg/kg。所有患者均完成了24周的治疗及额外24周的随访,除了轻度、可逆的溶血性贫血外,无明显副作用。三个剂量组对利巴韦林的反应相似(p>0.5);因此将数据合并并一起分析。乙肝病毒DNA平均水平从治疗前的162.7(95%置信区间,106至219)pg/ml降至第20周时的最低水平114.3(95%置信区间,53至175)pg/ml(p<0.05)。两名患者乙肝病毒DNA转阴并失去乙肝e抗原。血清丙氨酸氨基转移酶平均活性从治疗前的131.1(95%置信区间,84至178)U/l显著降至利巴韦林治疗24周结束时的62.4(95%置信区间,48至77)U/l(p<0.05),4例患者(22%)恢复正常。一旦停用利巴韦林,转氨酶水平在4周内恢复至基线,而即使在随访24周结束时,乙肝病毒DNA浓度仍低于基线。(摘要截选至250字)

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