Berk Steven I, Litwin Alain H, Arnsten Julia H, Du Evelyn, Soloway Irene, Gourevitch Marc N
Division of General Internal Medicine, Department of Medicine, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, New York 10461, USA.
Clin Ther. 2007 Jan;29(1):131-8. doi: 10.1016/j.clinthera.2007.01.009.
Hepatitis C virus (HCV) infection is common among methadone-maintained HIV-positive individuals. Pegylated interferon (pegIFN) used in combination with ribavirin is conventional treatment for HCV. However, pegIFN has been associated with adverse effects (AEs) that may simulate opioid withdrawal and be confused with insufficient methadone dosage.
The aim of this study was to determine, using methadone pharmacokinetic properties, whether methadone dosage adjustments are needed on initiation of treatment with pegIFN alfa-2b for HCV in methadone-maintained HIV-positive patients.
This prospective, nonrandomized, crossover study was conducted at the Albert Einstein College of Medicine and Montefiore Medical Center (Bronx, New York). Patients who were aged > or =18 years, coinfected with chronic HCV and HIV, and had been receiving methadone maintenance treatment (dosage, 40-200 mg/d PO) for at least 8 weeks prior to enrollment were eligible. We determined mean methadone C(max), T(max), Cn,in, AUC, and oral clearance (CL/F) values over a 24-hour period before (baseline) and after the administration of pegIFN alfa-2b 1.5 microg/kg SC (2 doses given 1 week apart). To determine differences in opiate withdrawal symptoms, one of the primary investigators administered the Subjective Opiate Withdrawal Scale (SOWS) and Objective Opiate Withdrawal Scale (OOWS) at baseline and 7, 14, and 21 days after the administration of the first dose. Study participants underwent weekly clinical evaluation for signs and symptoms of methadone withdrawal and for AEs of pegIFN.
Nine patients were included in the study (7 men, 2 women; 7 Hispanic, 2 black; mean [SD] age, 41 [8.3] years; mean [SD] weight, 75.0 [12.3] kg). We did not observe any significant changes from baseline in mean C(max), T(max), C(min), AUC, and CL/F values despite 80% power to detect a 30% change in either direction. Changes from baseline in SOWS and OOWS scores were not statistically significant. The only AEs reported were mild and consistent with those expected after pegIFN alfa-2b administration, such as inflammation at the injection site and mild, brief, flu-like symptoms.
Based on the results of this small, prospective, nonrandomized study, pegIFN alfa-2b did not appear to precipitate opioid withdrawal in this sample of methadone-maintained persons with HIV and chronic HCV coinfection; methadone dosage adjustments were unlikely to be needed.
丙型肝炎病毒(HCV)感染在接受美沙酮维持治疗的HIV阳性个体中很常见。聚乙二醇化干扰素(pegIFN)联合利巴韦林是HCV的传统治疗方法。然而,pegIFN与不良反应(AEs)相关,这些不良反应可能模拟阿片类药物戒断反应,并与美沙酮剂量不足相混淆。
本研究的目的是利用美沙酮的药代动力学特性,确定在接受美沙酮维持治疗的HIV阳性患者开始使用pegIFN alfa-2b治疗HCV时是否需要调整美沙酮剂量。
这项前瞻性、非随机、交叉研究在阿尔伯特爱因斯坦医学院和蒙特菲奥里医疗中心(纽约州布朗克斯)进行。年龄≥18岁、合并慢性HCV和HIV感染、且在入组前至少8周接受美沙酮维持治疗(剂量为40 - 200 mg/d口服)的患者符合条件。我们在给予pegIFN alfa-2b 1.5 μg/kg皮下注射(分2剂,间隔1周给药)之前(基线)和之后的24小时内测定美沙酮的平均C(max)、T(max)、Cn,in、AUC和口服清除率(CL/F)值。为了确定阿片类药物戒断症状的差异,一名主要研究者在基线以及首次给药后的第7、14和21天使用主观阿片类药物戒断量表(SOWS)和客观阿片类药物戒断量表(OOWS)进行评估。研究参与者每周接受一次临床评估,以检查美沙酮戒断的体征和症状以及pegIFN的不良反应。
9名患者纳入本研究(7名男性,2名女性;7名西班牙裔,2名黑人;平均[标准差]年龄41[8.3]岁;平均[标准差]体重75.0[12.3]kg)。尽管有80%的把握度检测到任一方向30%的变化,但我们未观察到平均C(max)、T(max)、C(min)、AUC和CL/F值相对于基线有任何显著变化。SOWS和OOWS评分相对于基线的变化无统计学意义。报告的唯一不良反应较轻,且与给予pegIFN alfa-2b后预期出现的不良反应一致,如注射部位炎症以及轻微、短暂的流感样症状。
基于这项小型、前瞻性、非随机研究的结果,在该组接受美沙酮维持治疗的HIV和慢性HCV合并感染患者中,pegIFN alfa-2b似乎不会引发阿片类药物戒断反应;不太可能需要调整美沙酮剂量。