Ngo Hanh T T, Tait Robert J, Hulse Gary K
School of Psychiatry and Clinical Neurosciences, University of Western Australia, Crawley, Western Australia, Australia.
Arch Gen Psychiatry. 2008 Apr;65(4):457-65. doi: 10.1001/archpsyc.65.4.457.
Most research on heroin dependence treatments assesses short-term changes in patients' self-reported drug use. To our knowledge, long-term sustainability of changes in patients' drug use and associated hospital morbidity posttreatment have not been studied.
To evaluate drug-related hospital morbidity in heroin users at 6 months and 3 1/2 years after receiving naltrexone implant treatment and to compare these results with outcomes from a similar cohort treated with methadone maintenance treatment.
Retrospective longitudinal follow-up, using data prospectively collected via a state hospital (public and private) reporting system.
Perth, Western Australia. Methadone maintenance dosage was generally dispensed daily by registered community pharmacies. Naltrexone implant treatment was performed as a day procedure at a community clinic.
A total of 522 and 314 heroin-dependent persons (according to DSM-IV), first time treated with methadone maintenance or a naltrexone implant, respectively, between January 1, 2001, and December 30, 2002, were identified, using health record linkage.
Planned outcomes included crude hospital admission rates, adjusted changes in risks (odds ratio [OR]), and rates (rate ratio) of "overdose-related" and "non-overdose-related" hospital morbidity associated with opioid vs nonopioid drugs 6 months and 3 1/2 years posttreatment.
Following naltrexone implant treatment, opioid-related risk decreased for overdose (OR, 0.23; 95% confidence interval [CI], 0.11-0.48) and nonoverdose (OR, 0.64; 95% CI, 0.46-0.89) conditions at 3 1/2 years. Such reductions were not observed after methadone treatment. Overdose on nonopioid drugs increased in older patients to 6 months: OR of 16.31 (95% CI, 3.07-86.53) for naltrexone and OR of 5.03 (95% CI, 1.18-21.54) for methadone. Nonoverdose (eg, dependence and withdrawal) associated with nonopioid drugs also increased for patients receiving the naltrexone implant: OR of 1.52 (95% CI, 1.04-2.23) at 3 1/2 years. In addition, there were 6 drug-related deaths: 5 after methadone maintenance and 1 after naltrexone implantation.
Naltrexone implants, but not methadone maintenance, has long-term benefits in reducing opioid-related hospital morbidity. However, long-lasting and increased nonopioid drug-related morbidity following naltrexone implantation is particularly concerning. Similar studies are required to confirm these findings.
大多数关于海洛因依赖治疗的研究评估的是患者自我报告的药物使用情况的短期变化。据我们所知,患者药物使用变化的长期可持续性以及治疗后相关的医院发病率尚未得到研究。
评估接受纳曲酮植入治疗的海洛因使用者在6个月和3年半后的药物相关医院发病率,并将这些结果与接受美沙酮维持治疗的类似队列的结果进行比较。
回顾性纵向随访,使用通过州立医院(公立和私立)报告系统前瞻性收集的数据。
西澳大利亚州珀斯。美沙酮维持剂量通常由注册社区药房每日发放。纳曲酮植入治疗在社区诊所作为日间手术进行。
通过健康记录链接,确定了2001年1月1日至2002年12月30日期间分别首次接受美沙酮维持治疗或纳曲酮植入治疗的总共522名和314名海洛因依赖者(根据《精神疾病诊断与统计手册》第四版)。
计划的结局包括粗住院率、风险的调整变化(比值比[OR])以及治疗后6个月和3年半时与阿片类药物和非阿片类药物相关的“过量相关”和“非过量相关”医院发病率的发生率(率比)。
纳曲酮植入治疗后,在3年半时,与阿片类药物相关的过量风险(OR,0.23;95%置信区间[CI],0.11 - 0.48)和非过量风险(OR,0.64;95%CI,0.46 - 0.89)降低。美沙酮治疗后未观察到此类降低。在6个月时,老年患者非阿片类药物过量情况增加:纳曲酮组的OR为16.31(95%CI,3.07 - 86.53),美沙酮组的OR为5.03(95%CI,1.18 - 21.54)。接受纳曲酮植入的患者与非阿片类药物相关的非过量情况(如依赖和戒断)也增加:在3年半时OR为1.52(95%CI,1.04 - 2.23)。此外,有6例药物相关死亡:美沙酮维持治疗后5例,纳曲酮植入后1例。
纳曲酮植入在降低与阿片类药物相关的医院发病率方面具有长期益处,但美沙酮维持治疗则不然。然而,纳曲酮植入后与非阿片类药物相关的发病率长期持续增加尤其令人担忧。需要进行类似研究以证实这些发现。