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双硫仑在当今酒精戒毒治疗中的地位。

Status of disulfiram in present day alcoholic deaddiction therapy.

机构信息

Department of Pharmacology, Fr. Muller Medical College, Mangalore - 575 002, India.

出版信息

Indian J Psychiatry. 2011 Jan;53(1):25-9. doi: 10.4103/0019-5545.75557.

DOI:10.4103/0019-5545.75557
PMID:21431004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3056183/
Abstract

AIM

Assessment of safety and efficacy profile of disulfiram (DSM) in the alcoholic de-addiction regimen.

OBJECTIVES

a. Assessment of Adverse Drug Reaction (ADR) profile; b. Evaluation of effectiveness of various deaddiction regimen; c. Defaulters and dropouts

PATIENTS AND METHODS

Fifty-one patients in a de-addiction center were investigated on 0(th) , 30(th) and 60(th) day along with psychiatric evaluation, ADR surveillance was made. Statistical analysis was done thereafter.

RESULTS

125 mg DSM given OD for 2 months. 76.5% patients had taken full course of treatment, 45% didn't complain of any ADR. Of ADR reported 27.4% had drowsiness, 21.4% tiredness, 7.8% skin manifestation.

CONCLUSION

DSM is the main drug among naltrexone, acamprosate, nalmefene and other drugs used in alcoholic de-addiction. Relative and effectiveness is lost by the degree of dropouts and hence relapses. Low-dose DSM had decreased adverse effects with 76.5% patients taking the full course of treatment. DSM alters liver functions as there were significant changes in the lab parameters of SGPT(P=0.007), SGOT(P=0.001), GGT(P=<0.001) between first and third samples. Occurrence of ADR is not the cause of default; patients find it confusing to differentiate between the symptoms of alcohol withdrawal and those due to ADR of DSM.

摘要

目的

评估双硫仑(DSM)在酒精戒毒方案中的安全性和疗效概况。

目的

a. 评估药物不良反应(ADR)概况;b. 评估各种戒毒方案的有效性;c. 违约者和辍学率。

患者和方法

在戒毒中心对 51 名患者进行了调查,分别在第 0、30 和 60 天进行了精神病学评估和 ADR 监测。随后进行了统计分析。

结果

给予 DSM 125mg ,每天一次,连续 2 个月。76.5%的患者完成了全程治疗,45%的患者没有报告任何不良反应。报告的不良反应中,27.4%有嗜睡,21.4%疲倦,7.8%皮肤表现。

结论

DSM 是纳曲酮、安非他酮、纳美芬和其他用于酒精戒毒药物中的主要药物。由于辍学率和复发率的原因,相对和有效性会降低。低剂量的 DSM 减少了不良反应,76.5%的患者完成了全程治疗。DSM 改变了肝功能,因为 SGPT(P=0.007)、SGOT(P=0.001)和 GGT(P=<0.001)的实验室参数在第一和第三样本之间有显著变化。不良反应的发生不是违约的原因;患者发现难以区分酒精戒断症状和 DSM 不良反应的症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c95b/3056183/595a7d791a5d/IJPsy-53-25-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c95b/3056183/b9826fe51bef/IJPsy-53-25-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c95b/3056183/2013fbdd8493/IJPsy-53-25-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c95b/3056183/96d37a7659bf/IJPsy-53-25-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c95b/3056183/595a7d791a5d/IJPsy-53-25-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c95b/3056183/b9826fe51bef/IJPsy-53-25-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c95b/3056183/de2fc816384d/IJPsy-53-25-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c95b/3056183/7b718e4d06f8/IJPsy-53-25-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c95b/3056183/886ead8ca4c1/IJPsy-53-25-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c95b/3056183/632bd637aab4/IJPsy-53-25-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c95b/3056183/466983387439/IJPsy-53-25-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c95b/3056183/b6a6dd5ac2de/IJPsy-53-25-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c95b/3056183/2013fbdd8493/IJPsy-53-25-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c95b/3056183/96d37a7659bf/IJPsy-53-25-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c95b/3056183/595a7d791a5d/IJPsy-53-25-g010.jpg

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