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本文引用的文献

1
Curtailing diversion and abuse of opioid analgesics without jeopardizing pain treatment.在不危及疼痛治疗的前提下减少阿片类镇痛药的转移和滥用。
JAMA. 2011 Apr 6;305(13):1346-7. doi: 10.1001/jama.2011.369.
2
Effects of buprenorphine and hepatitis C on liver enzymes in adolescents and young adults.丁丙诺啡和丙型肝炎对青少年和年轻成年人肝酶的影响。
J Addict Med. 2010 Dec;4(4):211-6. doi: 10.1097/ADM.0b013e3181c4e27e.
3
Neonatal abstinence syndrome after methadone or buprenorphine exposure.美沙酮或丁丙诺啡暴露后的新生儿戒断综合征。
N Engl J Med. 2010 Dec 9;363(24):2320-31. doi: 10.1056/NEJMoa1005359.
4
Buprenorphine maintenance versus placebo or methadone maintenance for opioid dependence.丁丙诺啡维持治疗与安慰剂或美沙酮维持治疗用于阿片类物质依赖的比较
Cochrane Database Syst Rev. 2008 Apr 16(2):CD002207. doi: 10.1002/14651858.CD002207.pub3.
5
Acute liver and renal failure during treatment with buprenorphine at therapeutic dose.治疗剂量丁丙诺啡治疗期间出现急性肝肾功能衰竭。
Dig Liver Dis. 2009 Jul;41(7):e8-e10. doi: 10.1016/j.dld.2007.12.014. Epub 2008 Feb 21.
6
A stepped care strategy using buprenorphine and methadone versus conventional methadone maintenance in heroin dependence: a randomized controlled trial.一项使用丁丙诺啡和美沙酮的阶梯式护理策略与传统美沙酮维持治疗对海洛因依赖的疗效比较:一项随机对照试验。
Am J Psychiatry. 2007 May;164(5):797-803. doi: 10.1176/ajp.2007.164.5.797.
7
Acute hepatitis due to buprenorphine administration.因使用丁丙诺啡导致的急性肝炎。
Eur J Gastroenterol Hepatol. 2004 Oct;16(10):1033-7. doi: 10.1097/00042737-200410000-00013.
8
The Clinical Opiate Withdrawal Scale (COWS).临床阿片戒断量表(COWS)。
J Psychoactive Drugs. 2003 Apr-Jun;35(2):253-9. doi: 10.1080/02791072.2003.10400007.
9
Hepatitis after intravenous buprenorphine misuse in heroin addicts.海洛因成瘾者静脉滥用丁丙诺啡后出现的肝炎。
J Hepatol. 2001 Feb;34(2):346-50. doi: 10.1016/s0168-8278(00)00049-0.
10
Mechanisms for experimental buprenorphine hepatotoxicity: major role of mitochondrial dysfunction versus metabolic activation.实验性丁丙诺啡肝毒性的机制:线粒体功能障碍与代谢活化的主要作用
J Hepatol. 2001 Feb;34(2):261-9. doi: 10.1016/s0168-8278(00)00050-7.

丁丙诺啡/纳洛酮和美沙酮对肝脏健康实验室指标的影响:一项随机试验。

Buprenorphine/Naloxone and methadone effects on laboratory indices of liver health: a randomized trial.

机构信息

Veteran's Affairs Puget Sound Health Care System, 1660 South Columbian Way, Room 116 ATC, Seattle, WA 98108, USA.

出版信息

Drug Alcohol Depend. 2013 Feb 1;128(1-2):71-6. doi: 10.1016/j.drugalcdep.2012.08.002. Epub 2012 Aug 22.

DOI:10.1016/j.drugalcdep.2012.08.002
PMID:22921476
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3543467/
Abstract

BACKGROUND

Buprenorphine/naloxone (BUP) and methadone (MET) are efficacious treatments for opioid dependence, although concerns about a link between BUP and drug-induced hepatitis have been raised. This study compares the effects of BUP and MET on liver health in opioid-dependent participants.

METHODS

This was a randomized controlled trial of 1269 opioid-dependent participants seeking treatment at 8 federally licensed opioid treatment programs and followed for up to 32 weeks between May 2006 and August 2010; 731 participants met "evaluable" criteria defined as completing 24 weeks of medication and providing at least 4 blood samples for transaminase testing. Participants were randomly assigned to receive BUP or MET for 24 weeks. Shift table analysis determined how many evaluable participants moved between categories of low and elevated transaminase levels. Predictors of moving from low to high transaminase levels were identified.

RESULTS

Changes in transaminase levels did not differ by medication condition. Baseline infection with hepatitis C or B was the only significant predictor of moving from low to elevated transaminase levels; 9 BUP and 15 MET participants showed extreme liver test elevations and were more likely than those without extreme elevations to have seroconverted to both hepatitis B and C during the study, or to use illicit drugs during the first 8 weeks of treatment. MET participants were retained longer in treatment than BUP participants.

CONCLUSIONS

This study demonstrated no evidence of liver damage during the initial 6 months of treatment in either condition. Physicians can prescribe either medication without major concern for liver injury.

摘要

背景

丁丙诺啡/纳洛酮(BUP)和美沙酮(MET)是治疗阿片类药物依赖的有效方法,尽管人们对 BUP 与药物性肝炎之间的联系存在担忧。本研究比较了 BUP 和 MET 对阿片类药物依赖者肝脏健康的影响。

方法

这是一项在 2006 年 5 月至 2010 年 8 月期间,在 8 家联邦许可的阿片类药物治疗机构寻求治疗的 1269 名阿片类药物依赖者中进行的随机对照试验;731 名参与者符合“可评估”标准,定义为完成 24 周的药物治疗,并至少提供 4 份用于转氨酶检测的血液样本。参与者被随机分配接受 BUP 或 MET 治疗 24 周。移位表分析确定了多少可评估参与者在低和高转氨酶水平之间移动。确定了从低到高转氨酶水平转移的预测因素。

结果

药物治疗条件并未改变转氨酶水平的变化。丙型或乙型肝炎感染是从低到高转氨酶水平转移的唯一显著预测因素;9 名 BUP 和 15 名 MET 参与者的肝试验值升高明显,与没有明显升高的参与者相比,他们在研究期间更有可能同时对乙型和丙型肝炎血清转化,或在治疗的前 8 周内使用非法药物。MET 参与者比 BUP 参与者在治疗中保留时间更长。

结论

本研究在两种情况下均未发现治疗最初 6 个月期间有肝损伤的证据。医生可以开这两种药物而不必担心肝损伤。