Suppr超能文献

电子健康记录中阿片类药物不良反应的文档记录。

Documentation of adverse drug reactions to opioids in an electronic health record.

机构信息

Department of Clinical Pharmacology, Royal Adelaide Hospital, Adelaide, South Australia, Australia.

Adelaide Medical School, Faculty of Health and Medical Sciences, University of Adelaide, Adelaide, South Australia, Australia.

出版信息

Intern Med J. 2021 Sep;51(9):1490-1496. doi: 10.1111/imj.15209.

Abstract

BACKGROUND

Allergy to opioids is the second most common drug allergy label in electronic health records (EHR). Adverse drug reactions (ADR) to opioids cause significant morbidity and contribute to healthcare costs, while incorrect opioid allergy labels may unnecessarily complicate patient management.

AIMS

To examine the documentation of opioid ADR in a large-scale hospital-based EHR.

METHODS

A cross-sectional retrospective review of EHR documentation of opioid ADR at four public hospitals in South Australia was conducted. Data were extracted from all ADR entries including the reported allergen, ADR category (allergy or intolerance) and reaction details. Expert criteria were used to determine consistency of ADR categorisation as allergy or intolerance.

RESULTS

Of 86 727 unique ADR reports, there were 13 781 ADR to opioids with most being entered as allergy (n = 8913, 64.7%) rather than intolerance (n = 4868, 35.3%). The most commonly documented reactions were nausea/vomiting (n = 3912, 28%), rash (n = 647, 5%), itch (n = 642, 5%) and hallucinations (n = 527, 4%). There were 362 (3%) ADR labels of anaphylaxis. Of those ADR containing a reaction description (n = 11 868), 89% of reports entered as allergy had a reaction description that was consistent with intolerance and 8% of the entered intolerances had descriptions consistent with allergy when assessed using predefined criteria.

CONCLUSIONS

This large EHR-based study demonstrates the high rate of opioid ADR labels in EHR. The majority of these labels were for symptoms suggestive of pharmacological intolerance. Reactions consistent with true allergy were uncommon. Systematic review of ADR by a dedicated clinical service would improve the accuracy of documentation.

摘要

背景

在电子健康记录(EHR)中,对阿片类药物的过敏是第二常见的药物过敏标签。阿片类药物的不良反应(ADR)会导致严重的发病率,并导致医疗保健费用增加,而不正确的阿片类药物过敏标签可能会不必要地使患者的管理复杂化。

目的

检查大型基于医院的 EHR 中阿片类药物 ADR 的记录情况。

方法

对南澳大利亚州四家公立医院的 EHR 中阿片类药物 ADR 记录进行了横断面回顾性研究。从所有 ADR 条目(包括报告的过敏原、ADR 类别(过敏或不耐受)和反应细节)中提取数据。使用专家标准来确定 ADR 分类为过敏或不耐受的一致性。

结果

在 86727 个独特的 ADR 报告中,有 13781 个阿片类药物 ADR,其中大多数被记录为过敏(n=8913,64.7%)而不是不耐受(n=4868,35.3%)。记录最常见的反应是恶心/呕吐(n=3912,28%)、皮疹(n=647,5%)、瘙痒(n=642,5%)和幻觉(n=527,4%)。有 362(3%)个 ADR 标签为过敏反应。在包含反应描述的 ADR 中(n=11868),89%的记录为过敏的报告有与不耐受一致的反应描述,而使用预定义标准评估时,8%的记录不耐受有与过敏一致的描述。

结论

这项基于大型 EHR 的研究表明,EHR 中阿片类药物 ADR 标签的比例很高。这些标签中的大多数是对药理学不耐受的症状提示。与真正过敏一致的反应并不常见。由专门的临床服务对 ADR 进行系统审查将提高文档的准确性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验