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慢性、高剂量阿片类药物使用非癌症患者不良事件风险增加——一项健康保险理赔分析。

Increased risk of adverse events in non-cancer patients with chronic and high-dose opioid use-A health insurance claims analysis.

机构信息

Department of Internal Medicine, Horten Center for Patient Oriented Research and Knowledge Transfer, University of Zurich, Zurich, Switzerland.

Institute of Primary Care, University and University Hospital Zürich, Zürich, Switzerland.

出版信息

PLoS One. 2020 Sep 14;15(9):e0238285. doi: 10.1371/journal.pone.0238285. eCollection 2020.

Abstract

BACKGROUND

Chronic and high dose opioid use may result in adverse events. We analyzed the risk associated with chronic and high dose opioid prescription in a Swiss population.

METHODS

Using insurance claims data covering one-sixth of the Swiss population, we analyzed recurrent opioid prescriptions (≥2 opioid claims with at least 1 strong opioid claim) between 2006 and 2014. We calculated the cumulative dose in milligrams morphine equivalents (MED) and treatment duration. Excluded were single opioid claims, opioid use that was cancer treatment related, and opioid use in substitution programs. We assessed the association between the duration of opioid use, prescribed opioid dose, and benzodiazepine use with emergency department (ED) visits, urogenital and pulmonary infections, acute care hospitalization, and death at the end of the episode.

RESULTS

In 63,642 recurrent opioid prescription episodes (acute 38%, subacute 7%, chronic 25.8%, very chronic (>360 days) episodes 29%) 18,336 ED visits, 30,209 infections, 19,375 hospitalizations, and 9,662 deaths occurred. The maximum daily MED dose was <20 mg in 15.8%, 20-<50 mg in 16.6%, 50-<100 mg in 21.6%, and ≥100 mg in 46%. Compared to acute episodes (<90 days), episode duration was an independent predictor of ED visits (chronic OR 1.09 (95% CI 1.03-1.15), very chronic (>360 days) OR 1.76 (1.67-1.86)) for adverse effects; infections (chronic OR 1.74 (1.66-1.82), very chronic 4.16 (3.95-4.37)), and hospitalization (chronic: OR 1.22 (1.16-1.29), very chronic OR 1.82 (1.73-1.93)). The risk of death decreased over time (very chronic OR 0.46 (0.43-0.50)). A dose dependent increased risk was observed for ED visits, hospitalization, and death (≥100mg daily MED OR 1.21 (1.13-1.29), OR 1.29 (1.21-1.38), and OR 1.67, 1.50-1.85, respectively). A concomitant use of benzodiazepines increased the odds for ED visits by 46% (OR 1.46, 1.41-1.52), infections by 44% (OR 1.44, 1.41-1.52), hospitalization by 12% (OR 1.12, 1.07-1.1), and death by 45% (OR 1.45, 1.37-1.53).

CONCLUSION

The length of opioid use and higher prescribed morphine equivalent dose were independently associated with an increased risk for ED visits and hospitalizations. The risk for infections, ED visits, hospitalizations, and death also increased with concomitant benzodiazepine use.

摘要

背景

慢性和大剂量使用阿片类药物可能导致不良事件。我们分析了瑞士人群中慢性和大剂量阿片类药物处方相关的风险。

方法

利用涵盖瑞士六分之一人口的保险索赔数据,我们分析了 2006 年至 2014 年期间的复发性阿片类药物处方(≥2 次阿片类药物索赔,至少有 1 次强阿片类药物索赔)。我们计算了以毫克吗啡当量(MED)表示的累积剂量和治疗持续时间。排除单次阿片类药物索赔、与癌症治疗相关的阿片类药物使用以及替代方案中的阿片类药物使用。我们评估了阿片类药物使用时间、处方阿片类药物剂量和苯二氮䓬类药物使用与急诊科(ED)就诊、泌尿生殖和肺部感染、急性护理住院以及治疗结束时死亡之间的关联。

结果

在 63642 例复发性阿片类药物处方(急性 38%,亚急性 7%,慢性 25.8%,非常慢性(>360 天)29%)中,发生了 18336 次 ED 就诊、30209 次感染、19375 次住院和 9662 例死亡。最大日 MED 剂量<20mg 占 15.8%,20-<50mg 占 16.6%,50-<100mg 占 21.6%,≥100mg 占 46%。与急性发作(<90 天)相比,发作持续时间是 ED 就诊的独立预测因素(慢性 OR 1.09(95%CI 1.03-1.15),非常慢性(>360 天)OR 1.76(1.67-1.86));感染(慢性 OR 1.74(1.66-1.82),非常慢性 4.16(3.95-4.37))和住院(慢性:OR 1.22(1.16-1.29),非常慢性 OR 1.82(1.73-1.93))。随着时间的推移,死亡风险降低(非常慢性 OR 0.46(0.43-0.50))。ED 就诊、住院和死亡的风险呈剂量依赖性增加(每日 MED≥100mg OR 1.21(1.13-1.29),OR 1.29(1.21-1.38)和 OR 1.67,1.50-1.85)。苯二氮䓬类药物的同时使用使 ED 就诊的几率增加 46%(OR 1.46,1.41-1.52),感染的几率增加 44%(OR 1.44,1.41-1.52),住院的几率增加 12%(OR 1.12,1.07-1.1),死亡的几率增加 45%(OR 1.45,1.37-1.53)。

结论

阿片类药物使用时间的长短和更高的处方吗啡当量剂量与 ED 就诊和住院的风险增加独立相关。苯二氮䓬类药物的同时使用也会增加感染、ED 就诊、住院和死亡的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47ff/7489518/edd394094cf5/pone.0238285.g001.jpg

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