Office-based treatment of opiate addiction with a sublingual-tablet formulation of buprenorphine and naloxone

被引:436
作者
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
机构
[1] Univ Penn, Sch Med, Vet Affairs Med Ctr, Philadelphia, PA 19104 USA
[2] NIDA, Div Treatment Res & Dev, NIH, Bethesda, MD 20892 USA
[3] VA Cooperat Studies Program, Coordinating Ctr, Perry Point, MD USA
[4] Univ Maryland, Sch Med, Dept Epidemiol & Prevent Med, Baltimore, MD 21201 USA
[5] Univ New Mexico, VA Cooperat Studies Program, Clin Res Pharm Coordinating Ctr, Albuquerque, NM 87131 USA
[6] NYU, Sch Med, New York Harbor Hlth Care Syst, VA Med Ctr, New York, NY USA
[7] VA Med Ctr, Cincinnati, OH USA
[8] VA Med Ctr, Los Angeles, CA USA
[9] VA Med Ctr, Hines, IL USA
[10] Boston Univ, Sch Med, VA Boston Healthcare Syst, Boston, MA 02118 USA
[11] VA Med Ctr, West Haven, CT USA
[12] Univ Calif San Francisco, VA Med Ctr, San Francisco, CA 94143 USA
关键词
D O I
10.1056/NEJMoa022164
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Office-based treatment of opiate addiction with a sublingual-tablet formulation of buprenorphine and naloxone has been proposed, but its efficacy and safety have not been well studied. Methods: We conducted a multicenter, randomized, placebo-controlled trial involving 326 opiate-addicted persons who were assigned to office-based treatment with sublingual tablets consisting of buprenorphine (16 mg) in combination with naloxone (4 mg), buprenorphine alone (16 mg), or placebo given daily for four weeks. The primary outcome measures were the percentage of urine samples negative for opiates and the subjects' self-reported craving for opiates. Safety data were obtained on 461 opiate-addicted persons who participated in an open-label study of buprenorphine and naloxone (at daily doses of up to 24 mg and 6 mg, respectively) and another 11 persons who received this combination only during the trial. Results: The double-blind trial was terminated early because buprenorphine and naloxone in combination and buprenorphine alone were found to have greater efficacy than placebo. The proportion of urine samples that were negative for opiates was greater in the combined-treatment and buprenorphine groups (17.8 percent and 20.7 percent, respectively) than in the placebo group (5.8 percent, P<0.001 for both comparisons); the active-treatment groups also reported less opiate craving (P<0.001 for both comparisons with placebo). Rates of adverse events were similar in the active-treatment and placebo groups. During the open-label phase, the percentage of urine samples negative for opiates ranged from 35.2 percent to 67.4 percent. Results from the open-label follow-up study indicated that the combined treatment was safe and well tolerated. Conclusions: Buprenorphine and naloxone in combination and buprenorphine alone are safe and reduce the use of opiates and the craving for opiates among opiate-addicted persons who receive these medications in an office-based setting.
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收藏
页码:949 / 958
页数:10
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