Integration of pharmacotherapy for opioid addiction into HIV primary care for HIV/hepatitis C virus-co-infected patients

被引:163
作者
Kresina, TF
Eldred, L
Bruce, RD
Francis, H
机构
[1] Natl Inst Drug Abuse, Ctr AIDS & Other Med Consequence Drug Abuse, NIH, Bethesda, MD 20892 USA
[2] US Hlth Resources & Serv Adm, HIV AIDS Bur, Dept Hlth & Human Serv, Bethesda, MD USA
[3] Yale Univ, Sch Med, Yale AIDS Program, New Haven, CT USA
关键词
substance abuse treatment; HIV primary care; buprenorphine; HIV/HCV co-infection;
D O I
10.1097/01.aids.0000192093.46506.e5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pharmacotherapy for substance abuse is a rapidly evolving field comprising both old and new effective treatments for substance use. Opiate agonist therapy has been shown to diminish and often eliminate opiate use. This behavior change has resulted in the reduced transmission of many infections, including HIV, hepatitis C virus (HCV), and an enhanced quality of life. For the past 35 years, the provision of opioid agonist therapy has been limited to opioid treatment programmes. Opioid treatment programmes treat approximately 200 000 of the estimated million opiate-addicted individuals in the United States. With the need to increase the number of treatment opportunities available for opioid-dependent patients, Congress passed the Drug Addiction Treatment Act of 2000, which allows for the treatment of opioid dependence using buprenorphine by a properly licensed physician, including HIV primary care physicians. The integration of buprenorphine treatment for opioid addiction into HIV primary care thus provides a new treatment paradigm to address substance abuse in patients with HIV and HCV infections. (c) 2005 Lippincott Williams & Wilkins.
引用
收藏
页码:S221 / S226
页数:6
相关论文
共 34 条
[1]   Developing a directly administered antiretroviral therapy intervention for HIV-infected drug users: Implications for program replication [J].
Altice, FL ;
Mezger, JA ;
Hodges, J ;
Bruce, RD ;
Marinovich, A ;
Walton, M ;
Springer, SA ;
Friedland, GH .
CLINICAL INFECTIOUS DISEASES, 2004, 38 :S376-S387
[2]   Adherence to protease inhibitors, HIV-1 viral load, and development of drug resistance in an indigent population [J].
Bangsberg, DR ;
Hecht, FM ;
Charlebois, ED ;
Zolopa, AR ;
Holodniy, M ;
Sheiner, L ;
Bamberger, JD ;
Chesney, MA ;
Moss, A .
AIDS, 2000, 14 (04) :357-366
[3]  
*CDCP, TABL 1 EST NUMB DIAG
[4]   Self-reported antiretroviral therapy in injection drug users [J].
Celentano, DD ;
Vlahov, D ;
Cohn, S ;
Shadle, VM ;
Obasanjo, O ;
Moore, RD .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 280 (06) :544-546
[5]   Reinstatement of ethanol-seeking behavior by drug cues following single versus multiple ethanol intoxication in the rat: effects of naltrexone [J].
Ciccocioppo, R ;
Lin, D ;
Martin-Fardon, R ;
Weiss, F .
PSYCHOPHARMACOLOGY, 2003, 168 (1-2) :208-215
[6]   Personality, substance of choice, and polysubstance involvement among substance dependent patients [J].
Conway, KP ;
Kane, RJ ;
Ball, SA ;
Poling, JC ;
Rounsaville, BJ .
DRUG AND ALCOHOL DEPENDENCE, 2003, 71 (01) :65-75
[7]  
Fiellin David A, 2004, Top HIV Med, V12, P77
[8]   Office-based treatment of opiate addiction with a sublingual-tablet formulation of buprenorphine and naloxone [J].
Fudala, PJ ;
Bridge, TP ;
Herbert, S ;
Williford, WO ;
Chiang, CN ;
Jones, K ;
Collins, J ;
Raisch, D ;
Casadonte, P ;
Goldsmith, RJ ;
Ling, W ;
Malkerneker, U ;
McNicholas, L ;
Renner, J ;
Stine, S ;
Tusel, D .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (10) :949-958
[9]   Racial and gender disparities in receipt of highly active antiretroviral therapy persist in a multistate sample of HIV patients in 2001 [J].
Gebo, KA ;
Fleishman, JA ;
Conviser, R ;
Reilly, ED ;
Korthuis, PT ;
Moore, RD ;
Hellinger, J ;
Keiser, P ;
Rubin, HR ;
Crane, L ;
Hellinger, FJ ;
Mathews, WC .
JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2005, 38 (01) :96-103
[10]  
Gonzales RA, 1998, J NEUROSCI, V18, P10663