Assadi Seyed Mohammad, Hafezi Mohsen, Mokri Azarakhsh, Razzaghi Emran Mohammad, Ghaeli Padideh
Department of Psychiatry, Tehran University of Medical Sciences, Tehran, Iran.
J Subst Abuse Treat. 2004 Jul;27(1):75-82. doi: 10.1016/j.jsat.2004.05.002.
In recent years, interest in shortening of opioid detoxification has increased with the rising demands to find more cost-effective approaches for treatment of opioid dependence. This study was designed to evaluate the efficacy of administration of high doses of buprenorphine during 24 h in the management of acute opioid withdrawal. A total of 40 treatment-seeking opioid dependents were admitted and randomly assigned to two groups in a double blind, parallel trial. Buprenorphine was administered intramuscularly. Twenty patients received 12 mg buprenorphine in 24 h and the remaining 20 patients treated with conventional doses of buprenorphine tapered down over 5 days. Variables that were assessed included retention in treatment, rates of successful detoxification, the Subjective Opiate Withdrawal Scale (OOWS) scores, the Objective Opiate Withdrawal Scale (SOWS) scores, intensity of craving, drug side effects, and levels of hepatic enzymes (ALT and AST). There was no significant difference between the two groups on most variables. The main difference was in the time that maximal withdrawal symptoms occurred, which in the experimental protocol group appeared early while in the conventional protocol group appeared later during the detoxification period. Moreover, the experimental protocol was not only tolerated well but also accompanied with significantly less elevation in the ALT levels compared to the conventional treatment. However, patients in this group used more indomethacin and trazodone for symptom palliation. This study suggests that administration of high doses of buprenorphine in 24 h may be a reasonable approach for shortening of opioid detoxification. However, a larger study to confirm our results is warranted.
近年来,随着寻找更具成本效益的阿片类药物依赖治疗方法的需求不断增加,人们对缩短阿片类药物脱毒时间的兴趣也日益浓厚。本研究旨在评估24小时内给予高剂量丁丙诺啡在急性阿片类药物戒断管理中的疗效。在一项双盲、平行试验中,共纳入40名寻求治疗的阿片类药物依赖者,并将其随机分为两组。丁丙诺啡采用肌肉注射给药。20名患者在24小时内接受12毫克丁丙诺啡,其余20名患者接受常规剂量的丁丙诺啡,在5天内逐渐减量。评估的变量包括治疗保留率、成功脱毒率、主观阿片类药物戒断量表(OOWS)评分、客观阿片类药物戒断量表(SOWS)评分、渴望强度、药物副作用以及肝酶(ALT和AST)水平。两组在大多数变量上没有显著差异。主要差异在于出现最大戒断症状的时间,在实验方案组中出现较早,而在常规方案组中在脱毒期较晚出现。此外,与传统治疗相比,实验方案不仅耐受性良好,而且ALT水平升高明显较少。然而,该组患者使用更多的吲哚美辛和曲唑酮来缓解症状。本研究表明,24小时内给予高剂量丁丙诺啡可能是缩短阿片类药物脱毒时间的一种合理方法。然而,需要进行更大规模的研究来证实我们的结果。