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首页> 外文期刊>The American Journal of Gastroenterology >Efficacy and safety of peginterferon alfa-2a/ribavirin in methadone maintenance patients: randomized comparison of direct observed therapy and self-administration.
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Efficacy and safety of peginterferon alfa-2a/ribavirin in methadone maintenance patients: randomized comparison of direct observed therapy and self-administration.

机译:聚乙二醇干扰素α-2a/利巴韦林在美沙酮维持患者中的疗效和安全性:直接观察到的治疗和自我给药的随机比较。

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BACKGROUND: Adherence to chronic hepatitis C (CHC) treatment may be particularly challenging in methadone maintenance patients. We assessed the safety, tolerability, and efficacy of peginterferon alfa-2a/ribavirin treatment in methadone maintenance patients previously untreated for CHC. METHODS: Patients were randomized 1:1 to direct observed therapy (DOT) or self-administration (SA) of peginterferon alfa-2a. DOT patients were seen weekly at methadone clinics; SA patients were seen less frequently, only at investigative sites. Genotype 1-infected patients were treated for 48 wk with peginterferon alfa-2a (180 microg/wk)/ribavirin (1,000/1,200 mg/day); genotypes 2- and 3-infected patients were treated for 24 wk with peginterferon alfa-2a (180 microg/wk)/ribavirin (800 mg/day). RESULTS: Based on defined efficacy stopping rules, 77% (37/48) completed their targeted length of treatment, and 44% (21/48) achieved sustained virologic response (SVR). Two DOT and 3 SA patients were withdrawn for safety reasons and 6 and 9, respectively, for nonsafety reasons. Over 60% and 50% of each group were >80% compliant with the planned cumulative doses of peginterferon alfa-2a and ribavirin, respectively, and over 60% with overall treatment duration. SVR rates were 54% (13/24) for DOT and 33% (8/24) for SA; 23% (3/13) and 38% (6/16), respectively, for genotype 1 and 91% (10/11) and 25% (2/8), respectively, for genotypes 2 and 3. Stepwise logistic regression analysis, showed that DOT (vs SA; OR 3.27, 95% CI 0.90-11.91, P = 0.073) and Caucasian race (vs Other; OR 13.31, 95% CI 1.42-124.71, P = 0.023) were predictors of SVR. CONCLUSION: Peginterferon alfa-2a/ribavirin can be used safely and successfully in CHC patients receiving methadone maintenance.
机译:背景:在美沙酮维持治疗患者中,坚持慢性丙型肝炎(CHC)治疗可能特别具有挑战性。我们评估了聚乙二醇干扰素α-2a/利巴韦林治疗以前未经CHC治疗的美沙酮维持患者的安全性,耐受性和疗效。方法:将患者以1:1的比例随机分配到聚乙二醇干扰素alfa-2a的直接观察疗法(DOT)或自我给药(SA)。每周在美沙酮诊所看望DOT患者;仅在研究地点,SA患者的出现频率较低。用聚乙二醇干扰素α-2a(180 microg / wk)/利巴韦林(1,000 / 1,200 mg / day)治疗感染基因型1的患者48周。基因型2和3感染的患者用聚乙二醇干扰素alfa-2a(180 microg / wk)/利巴韦林(800 mg / day)治疗24周。结果:根据明确的疗效停止规则,有77%(37/48)完成了目标治疗时间,有44%(21/48)实现了持续病毒学应答(SVR)。出于安全原因,分别撤回了2名DOT和3名SA患者,出于非安全原因,分别撤回了6和9人。每组分别有超过60%和50%的患者接受聚乙二醇干扰素α-2a和利巴韦林的计划累积剂量分别> 80%的顺应性,而在总体治疗期间超过60%的顺应性。 DOT的SVR率为54%(13/24),SA的SVR率为33%(8/24)。基因型1分别为23%(3/13)和38%(6/16),基因型2和3分别为91%(10/11)和25%(2/8)。 ,表明DOT(vs SA; OR 3.27,95%CI 0.90-11.91,P = 0.073)和白种人(vs Other; OR 13.31,95%CI 1.42-124.71,P = 0.023)是SVR的预测指标。结论:聚乙二醇干扰素α-2a/利巴韦林可安全,成功地用于接受美沙酮维持治疗的CHC患者。

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