Suppr超能文献

解决低剂量可待因在复方镇痛药中的有效性和安全性问题:一项系统评价

Resolving Issues About Efficacy and Safety of Low-Dose Codeine in Combination Analgesic Drugs: A Systematic Review.

作者信息

Ćelić Ivan, Bach-Rojecky Lidija, Merćep Iveta, Soldo Ana, Petrak Anja Kos, Bučan Ana

机构信息

Department of Dual Diagnosis, University Psychiatric Hospital Vrapče, Bolnička Cesta 32, 10000, Zagreb, Croatia.

Department of Pharmacology, University of Zagreb Faculty of Pharmacy and Biochemistry, Domagojeva 2, 10000, Zagreb, Croatia.

出版信息

Pain Ther. 2020 Jun;9(1):171-194. doi: 10.1007/s40122-020-00162-8. Epub 2020 Mar 14.

Abstract

INTRODUCTION

The objective of this systematic review is to reflect on assumptions in relation to codeine use in combination with other analgesics.

METHODS

MEDLINE was searched according to the predetermined keywords and criteria. Only English language studies were taken into consideration and the outcome data of the final studies were extracted by two reviewers independently from each other and were checked by the third reviewer. Additionally, the available codeine-related Individual Case Safety Reports (ICSRs) retrieved from EudraVigilance were reviewed.

RESULTS

Sixteen placebo-controlled studies that involved 3378 subjects suffering from acute pain were analyzed for the efficacy of low-dose codeine (≤ 30 mg) combination products. Twelve of them found low-dose codeine combinations more efficient in relieving pain than the assigned comparator. According to 20 randomized clinical trials which included at least one dose of codeine (from 30 to 240 mg daily), the vast majority of reported side-effects were mild or moderate in severity. A total of 20 ICSRs for dependence were identified in the EudraVigilance database with codeine as a suspect drug for the 10-year time period for the European region.

CONCLUSIONS

Low-dose codeine combinations are effective after a single application in treating acute pain. Codeine in doses ≤ 30 mg and higher was considered safe since only mild to moderate side-effects were observed. There is no indication in the available sources which clearly links low doses of codeine to substance use disorder in non-dependent subjects.

摘要

引言

本系统评价的目的是反思与可待因与其他镇痛药联合使用相关的假设。

方法

根据预先确定的关键词和标准检索MEDLINE。仅纳入英文研究,最终研究的结果数据由两名审阅者相互独立提取,并由第三名审阅者进行核对。此外,还对从欧洲药品不良反应数据库(EudraVigilance)中检索到的可用的与可待因相关的个体病例安全报告(ICSR)进行了审查。

结果

对16项涉及3378名急性疼痛患者的安慰剂对照研究进行了分析,以评估低剂量可待因(≤30mg)复方制剂的疗效。其中12项研究发现低剂量可待因复方制剂在缓解疼痛方面比指定的对照药物更有效。根据20项至少包含一剂可待因(每日30至240mg)的随机临床试验,报告的绝大多数副作用严重程度为轻度或中度。在欧洲药品不良反应数据库中,共识别出20份关于成瘾性的个体病例安全报告,在10年时间内可待因被列为可疑药物。

结论

低剂量可待因复方制剂单次应用治疗急性疼痛有效。由于仅观察到轻度至中度副作用,≤30mg及更高剂量的可待因被认为是安全的。现有资料中没有明确表明低剂量可待因与非成瘾者的物质使用障碍有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecce/7203384/aa871512715a/40122_2020_162_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验