Effects of pegylated interferon alfa-2b on the pharmacokinetic and pharmacodynamic properties of methadone: A prospective, nonrandomized, crossover study in patients coinfected with hepatitis C and HIV receiving methadone maintenance treatment

被引:15
作者
Berk, Steven I.
Litwin, Alain H.
Arnsten, Julia H.
Du, Evelyn
Soloway, Irene
Gourevitch, Marc N.
机构
[1] Albert Einstein Coll Med, Div Gen Internal Med, Dept Med, Bronx, NY 10467 USA
[2] Montefiore Med Ctr, Bronx, NY 10467 USA
[3] Albert Einstein Coll Med, Div Subst Abuse, Dept Psychiat & Behav Sci, Bronx, NY 10467 USA
[4] Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, Bronx, NY 10467 USA
[5] NYU, Sch Med, Dept Med, Div Gen Internal Med, New York, NY USA
关键词
hepatitis C; HIV; pegylated interferon; methadone;
D O I
10.1016/j.clinthera.2007.01.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: 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 opiold withdrawal and be confused with insufficient methadone dosage. Objective: 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. Methods: 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 >= 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 C-min, AUC, and oral clearance (CUF) values over a 24-hour period before (baseline) and after the administration of pegIFN alfa-2b 1.5 mu g/kg SC (2 doses given I 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. Results: 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,C- 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, flulike symptoms. Conclusion: 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.
引用
收藏
页码:131 / 138
页数:8
相关论文
共 44 条
[1]   False reduction in serum methadone concentrations by BD Vacutainer® serum separator tubes (SST™) [J].
Berk, Steven I. ;
Litwin, Alain H. ;
Du, Yunling ;
Cruikshank, Greg ;
Gourevitch, Marc N. ;
Arnsten, Julia H. .
CLINICAL CHEMISTRY, 2006, 52 (10) :1972-1974
[2]   Pharmacokinetic drug interactions between opioid agonist therapy and antiretroviral medications: Implications and management for clinical practice [J].
Bruce, RD ;
Altice, FL ;
Gourevitch, MA ;
Friedland, GH .
JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2006, 41 (05) :563-572
[3]   The effect of fluconazole on the clinical pharmacokinetics of methadone [J].
Cobb, MN ;
Desai, J ;
Brown, LS ;
Zannikos, PN ;
Rainey, PM .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1998, 63 (06) :655-662
[4]  
COVERDALE S, 1995, HEPATOLOGY, V22, P1065, DOI 10.1002/hep.1840220408
[5]   Treatment of chronic hepatitis C in active drug users [J].
Davis, GL ;
Rodrigue, JR .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (03) :215-217
[6]   EFFECTS OF SUBCHRONIC TREATMENT WITH NATURAL HUMAN INTERFERONS ON ANTIPYRINE CLEARANCE AND LIVER-FUNCTION IN PATIENTS WITH CHRONIC HEPATITIS [J].
ECHIZEN, H ;
OHTA, Y ;
SHIRATAKI, H ;
TSUKAMOTO, K ;
UMEDA, N ;
ODA, T ;
ISHIZAKI, T .
JOURNAL OF CLINICAL PHARMACOLOGY, 1990, 30 (06) :562-567
[7]   Is it justifiable to withhold treatment for hepatitis C from illicit-drug users? [J].
Edlin, BR ;
Seal, KH ;
Lorvick, J ;
Kral, AH ;
Ciccarone, DH ;
Moore, LD ;
Lo, B .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (03) :211-214
[8]   Antipyrine as a probe for human oxidative drug metabolism: Identification of the cytochrome P450 enzymes catalyzing 4-hydroxyantipyrine, 3-hydromethylantipyrine, and norantipyrine formation [J].
Engel, G ;
Hofmann, U ;
Heidemann, H ;
Cosme, J ;
Eichelbaum, M .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1996, 59 (06) :613-623
[9]  
European Agency for the Evaluation of Medicinal Products, 2002, INT C HARM WHO GUID
[10]  
Hamilton SP, 2000, AM J ADDICTION, V9, P63