King's College London, National Addiction Centre, London, UK.
Lancet. 2010 May 29;375(9729):1885-95. doi: 10.1016/S0140-6736(10)60349-2.
Some heroin addicts persistently fail to benefit from conventional treatments. We aimed to compare the effectiveness of supervised injectable treatment with medicinal heroin (diamorphine or diacetylmorphine) or supervised injectable methadone versus optimised oral methadone for chronic heroin addiction.
In this multisite, open-label, randomised controlled trial, we enrolled chronic heroin addicts who were receiving conventional oral treatment (>or=6 months), but continued to inject street heroin regularly (>or=50% of days in preceding 3 months). Randomisation by minimisation was used to assign patients to receive supervised injectable methadone, supervised injectable heroin, or optimised oral methadone. Treatment was provided for 26 weeks in three supervised injecting clinics in England. Primary outcome was 50% or more of negative specimens for street heroin on weekly urinalysis during weeks 14-26. Primary analysis was by intention to treat; data were adjusted for centre, regular crack use at baseline, and treatment with optimised oral methadone at baseline. Percentages were calculated with Rubin's rules and were then used to estimate numbers of patients in the multiple imputed samples. This study is registered, ISRCTN01338071.
Of 301 patients screened, 127 were enrolled and randomly allocated to receive injectable methadone (n=42 patients), injectable heroin (n=43), or oral methadone (n=42); all patients were included in the primary analysis. At 26 weeks, 80% (n=101) patients remained in assigned treatment: 81% (n=34) on injectable methadone, 88% (n=38) on injectable heroin, and 69% (n=29) on oral methadone. Patients on injectable heroin were significantly more likely to have achieved the primary outcome (72% [n=31]) than were those on oral methadone (27% [n=11], OR 7.42, 95% CI 2.69-20.46, p<0.0001; adjusted: 66% [n=28] vs 19% [n=8], 8.17, 2.88-23.16, p<0.0001), with number needed to treat of 2.17 (95% CI 1.60-3.97). For injectable methadone (39% [n=16]; adjusted: 30% [n=14]) versus oral methadone, the difference was not significant (OR 1.74, 95% CI 0.66-4.60, p=0.264; adjusted: 1.79, 0.67-4.82, p=0.249). For injectable heroin versus injectable methadone, a significant difference was recorded (4.26, 1.63-11.14, p=0.003; adjusted: 4.57, 1.71-12.19, p=0.002), but the study was not powered for this comparison. Differences were evident within the first 6 weeks of treatment.
Treatment with supervised injectable heroin leads to significantly lower use of street heroin than does supervised injectable methadone or optimised oral methadone. UK Government proposals should be rolled out to support the positive response that can be achieved with heroin maintenance treatment for previously unresponsive chronic heroin addicts.
Community Fund (Big Lottery) Research section, through Action on Addiction.
一些海洛因成瘾者持续无法从常规治疗中获益。我们旨在比较监督注射治疗与药用海洛因(吗啡或二乙酰吗啡)或监督注射美沙酮与优化口服美沙酮治疗慢性海洛因成瘾的效果。
在这项多中心、开放标签、随机对照试验中,我们招募了正在接受常规口服治疗(> 6 个月)但仍持续定期注射街头海洛因(> 3 个月前的 50% 以上天数)的慢性海洛因成瘾者。通过最小化分配患者接受监督注射美沙酮、监督注射海洛因或优化口服美沙酮。在英格兰的三个监督注射诊所提供 26 周的治疗。主要结局是在第 14-26 周的每周尿液分析中,有 50%或更多的街头海洛因呈阴性。主要分析为意向治疗;数据根据中心、基线时定期使用快克和基线时接受优化口服美沙酮进行了调整。用鲁宾的规则计算了百分比,然后用这些百分比估计了多个插补样本中的患者人数。这项研究已注册,ISRCTN01338071。
在筛选的 301 名患者中,有 127 名符合条件并被随机分配接受注射美沙酮(n=42 名患者)、注射海洛因(n=43 名患者)或口服美沙酮(n=42 名患者);所有患者均纳入主要分析。在 26 周时,80%(n=101)的患者仍在接受指定的治疗:81%(n=34)接受注射美沙酮,88%(n=38)接受注射海洛因,69%(n=29)接受口服美沙酮。接受注射海洛因的患者达到主要结局的可能性显著高于接受口服美沙酮的患者(72%[n=31]比 27%[n=11],OR 7.42,95%CI 2.69-20.46,p<0.0001;调整后:66%[n=28]比 19%[n=8],8.17,2.88-23.16,p<0.0001),需要治疗的人数为 2.17(95%CI 1.60-3.97)。对于注射美沙酮(39%[n=16];调整后:30%[n=14])与口服美沙酮相比,差异无统计学意义(OR 1.74,95%CI 0.66-4.60,p=0.264;调整后:1.79,0.67-4.82,p=0.249)。对于注射海洛因与注射美沙酮,记录到显著差异(4.26,1.63-11.14,p=0.003;调整后:4.57,1.71-12.19,p=0.002),但这项研究对此比较没有足够的效力。差异在治疗的前 6 周内就显现出来了。
监督注射海洛因治疗可显著降低街头海洛因的使用量,优于监督注射美沙酮或优化口服美沙酮治疗。英国政府的提议应得到实施,以支持对以前对常规治疗无反应的慢性海洛因成瘾者进行海洛因维持治疗所取得的积极反应。
社区基金(大彩票)研究部分,通过成瘾行动提供。