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阿片类药物用于非癌症疼痛和成年人心肌梗死风险。

Opioid use for noncancer pain and risk of myocardial infarction amongst adults.

机构信息

Boston Collaborative Drug Surveillance Program, Boston University School of Public Health, Lexington, MA 02421, USA.

出版信息

J Intern Med. 2013 May;273(5):511-26. doi: 10.1111/joim.12035. Epub 2013 Feb 16.

Abstract

BACKGROUNDS

With increasing use of opioids for chronic noncancer pain comes concern about safety of this class of drugs. Opioid-induced hypogonadism, which could increase the risk for myocardial infarction (MI), has recently come to the attention of clinicians. To evaluate this concern we examined the association between opioid use for noncancer pain and risk of MI amongst adults.

METHODS

We conducted a nested case-control study using the UK General Practice Research Database. Amongst 1.7 million opioid users during 1990-2008, we identified 11 693 incident MI cases aged 18-80 years, and randomly selected up to four controls matched by age, gender, index date (date of onset symptoms or diagnosis of first-ever MI) and general practice via risk-set sampling. Cases and controls were required to have no cancer and no major risk factors for MI before the index date. Adjusted odds ratios (ORs) and 95% confidence intervals (CIs) were estimated from conditional logistic regression.

RESULTS

Compared with nonuse, current use of opioids was associated with a 1.28-fold (95% CI 1.19-1.37) risk of MI. Cumulative use of opioids with 11-50 (OR = 1.38, 95% CI: 1.28-1.49) or > 50 (OR = 1.25, 95% CI: 1.11-1.40) prescriptions, was also marginally associated with increased risk of MI. The risk was particularly increased in users of morphine (OR = 1.71, 95% CI: 1.09-2.68), meperidine (OR = 2.15, 95% CI: 1.24-3.74) and polytherapy (OR = 1.46, 95% CI: 1.22-1.76).

CONCLUSIONS

Current use of any opioids and cumulative use of 11 or more prescriptions are associated with a small increased risk for MI compared to nonuse and the risk was greater in morphine, meperidine and polytherapy users. Residual confounding, particularly confounding by indication, should be considered in interpreting our results.

摘要

背景

随着慢性非癌性疼痛中阿片类药物使用的增加,人们对这类药物的安全性产生了担忧。阿片类药物诱导的性腺功能减退症可能会增加心肌梗死(MI)的风险,最近引起了临床医生的关注。为了评估这一担忧,我们研究了非癌性疼痛患者使用阿片类药物与成年人 MI 风险之间的关系。

方法

我们使用英国全科医学研究数据库进行了一项嵌套病例对照研究。在 1990 年至 2008 年间,我们在 170 万例阿片类药物使用者中发现了 11693 例年龄在 18-80 岁的新发 MI 病例,并通过风险集抽样按年龄、性别、指数日期(首发症状或首次 MI 诊断日期)和全科医生随机选择最多 4 名匹配的对照。病例和对照在指数日期前均无癌症和 MI 的主要危险因素。通过条件逻辑回归估计调整后的比值比(OR)和 95%置信区间(CI)。

结果

与不使用相比,当前使用阿片类药物与 MI 的风险增加 1.28 倍(95%CI:1.19-1.37)。使用 11-50 张(OR=1.38,95%CI:1.28-1.49)或>50 张(OR=1.25,95%CI:1.11-1.40)处方的累积阿片类药物使用也与 MI 风险增加相关。吗啡(OR=1.71,95%CI:1.09-2.68)、哌替啶(OR=2.15,95%CI:1.24-3.74)和联合治疗(OR=1.46,95%CI:1.22-1.76)使用者的风险尤其增加。

结论

与不使用相比,目前使用任何阿片类药物以及累积使用 11 张或更多处方与 MI 风险略有增加,而在使用吗啡、哌替啶和联合治疗的患者中风险更大。在解释我们的结果时,应考虑到残余混杂因素,特别是混杂因素。

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