急诊科就诊的老年患者服用苯二氮卓类药物与短期预后的关系:EDEN 项目的结果。

IF 2.4 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pharmacoepidemiology and Drug Safety Pub Date : 2024-11-01 DOI:10.1002/pds.70044
Jesus Ruiz-Ramos, Aitor Alquézar-Arbé, Ana Juanes-Borrego, Juan González-Del-Castillo, Javier Jacob, Guillermo Burillo, Sira Aguiló, Cesáreo Fernandez, Adrián Plaza-Díaz, Javier Millán-Soria, Gema Jara-Torres, Nieves López-Delmas, Esperanza Muñoz-Triano, Cristina Martín-Durán, Violeta Delgado-Sardina, Blanca Andrea Gallardo-Sánchez, Ivet Gina Osorio-Quispe, Antonio Real-López, Susana Gordo-Remartinez, Lucía González-Ferreira, Alberto Álvarez-Madrigal, Julia Martínez-Ibarreta-Zorita, María Sánchez-Moreno, Maite Sanchez-Moreno, Jesús Ángel Sánchez-Serrano, Raquel Hernando-Fernández, Jennifer Turcios-Torres, Paola Ponte-Márquez, Òscar Miró
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引用次数: 0

摘要

目的:在老年人口中,苯二氮卓类药物的处方越来越多。然而,有关老年人在急诊科(ED)就诊时使用这些药物的频率及其对预后影响的信息却很少。本研究旨在评估苯二氮卓类药物处方的使用率,并分析其与急诊科就诊的老年患者短期预后的关系:方法:对 EDEN(急诊科贫困老人)队列进行回顾性分析。该登记册包括2019年4月1日至7日期间在西班牙52家急诊室就诊的所有老年患者。社会人口学数据、合并症和用药情况均通过查阅患者的电子健康记录记录在案。评估的结果包括首次急诊就诊后30天内的新急诊就诊、住院和死亡率,与基线使用苯二氮卓类药物和未处方苯二氮卓类药物进行比较。我们进行了包括患者合并症在内的粗略和调整后逻辑回归分析。结果:共评估了 25 557 名患者(平均年龄 78 岁 [IQR:71-84])。7865(30.8%)名患者在入院时服用了苯二氮卓类药物。在对合并症和其他中枢神经系统药物进行调整后,苯二氮卓类药物处方与急诊室复诊相关[OR:1.10 (95%CI:1.03-1.18)]。剔除使用中枢神经抑制剂的患者[OR:1.11 (1.03-1.25)]和出院回家的患者[OR:1.13 (1.04-1.23)]后,敏感性分析也发现了类似的结果。使用这些药物与新的住院治疗[OR:0.90 (0.77-1.05)]或出院后 30 天的死亡率[OR:1.01 (0.88-1.18)]之间没有关联。在敏感性分析中,这三个结果均成立:结论:在急诊室就诊的老年人中,苯二氮卓类药物的使用是一种常见现象,它与急诊室新就诊风险的增加有关,但与 30 天住院风险或死亡率的增加无关。
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Association of Benzodiazepine Prescription With Short-Term Prognosis in Elderly Patients Attended in Emergency Department: Results From the EDEN PROJECT.

Aim: Benzodiazepine prescription is a growing phenomenon among the elderly population. However, information related to the frequency of these drugs among the elderly population attending in emergency departments (ED) and its impact over prognosis is scarce. The aim of this study is to assess the prevalence of benzodiazepine prescription and to analyze its association with short-term prognosis in elderly patients attended in ED.

Methods: A retrospective analysis of the EDEN (Emergency Department Elderly in Need) cohort was conducted. This registry included all elderly patients attending in 52 Spanish EDs for any condition, between April 1st and 7th in 2019. Socio-demographic data, comorbidities, and medication were recorded by consulting the patient's electronic health records. The assessed outcomes consisted on new ED visit, hospitalization, and mortality at 30 days after the first ED visit, associated with the use of benzodiazepines at baseline in comparison with no prescription of benzodiazepines. Crude and adjusted logistic regression analyses including patient's comorbidities were performed. Two sensitivity analyses were performed considering concomitant prescription of other central nervous system depressants as well as direct discharge from the ED.

Results: 25 557 patients were evaluated (mean age 78 [IQR: 71-84]). 7865 (30.8%) patients were taken benzodiazepines at admission. After adjustment for comorbidities and other central nervous system drugs, benzodiazepine prescription was associated with ED revisit [OR: 1.10 (95%CI: 1.03-1.18)]. Similar results were found in the sensitivity analysis, eliminating patients with central nervous depressors [OR: 1.11 (1.03-1.25)] and patients discharged to home [OR: 1.13 (1.04-1.23)]. No association was found between the use of these drugs and new hospitalizations [OR: 0.90 (0.77-1.05)] or mortality 30 days after discharge [OR: 1.01 (0.88-1.18)]. The results held for all three outcomes in the sensitivity analyses.

Conclusion: The use of benzodiazepines is a frequent phenomenon among the elderly population attended in the ED, being associated with an increased risk of new visits to the emergency room, but not with an increased risk of 30-day hospitalization or mortality.

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来源期刊
CiteScore
4.80
自引率
7.70%
发文量
173
审稿时长
3 months
期刊介绍: The aim of Pharmacoepidemiology and Drug Safety is to provide an international forum for the communication and evaluation of data, methods and opinion in the discipline of pharmacoepidemiology. The Journal publishes peer-reviewed reports of original research, invited reviews and a variety of guest editorials and commentaries embracing scientific, medical, statistical, legal and economic aspects of pharmacoepidemiology and post-marketing surveillance of drug safety. Appropriate material in these categories may also be considered for publication as a Brief Report. Particular areas of interest include: design, analysis, results, and interpretation of studies looking at the benefit or safety of specific pharmaceuticals, biologics, or medical devices, including studies in pharmacovigilance, postmarketing surveillance, pharmacoeconomics, patient safety, molecular pharmacoepidemiology, or any other study within the broad field of pharmacoepidemiology; comparative effectiveness research relating to pharmaceuticals, biologics, and medical devices. Comparative effectiveness research is the generation and synthesis of evidence that compares the benefits and harms of alternative methods to prevent, diagnose, treat, and monitor a clinical condition, as these methods are truly used in the real world; methodologic contributions of relevance to pharmacoepidemiology, whether original contributions, reviews of existing methods, or tutorials for how to apply the methods of pharmacoepidemiology; assessments of harm versus benefit in drug therapy; patterns of drug utilization; relationships between pharmacoepidemiology and the formulation and interpretation of regulatory guidelines; evaluations of risk management plans and programmes relating to pharmaceuticals, biologics and medical devices.
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