Villiet Maxime, Laureau Marion, Perier Damien, Pinzani Véronique, Giraud Isabelle, Lohan Laura, Bobbia Xavier, Mercier Grégoire, Jaussent Audrey, Macioce Valérie, Sebbane Mustapha, Faucanié Marie, Breuker Cyril
Clinical Pharmacy Department, CHU Montpellier, University of Montpellier, Montpellier, France.
Emergency Medicine Department, CHU Montpellier, University of Montpellier, Montpellier, France.
JAMA Intern Med. 2025 Apr 28. doi: 10.1001/jamainternmed.2025.0640.
Medication-related events (MREs) are a frequent cause of emergency department (ED) visits and patient harm.
To assess the efficacy of a pharmacist-led transition of care program in reducing ED visits related to the same MRE at 6 months compared with usual care.
DESIGN, SETTING, AND PARTICIPANTS: This prospective, open-label, parallel-group randomized clinical trial was conducted from November 2018 to July 2021 at the ED of Montpellier University Hospital, Montpellier, France, with a 6-month follow-up period. Adult patients with an MRE detected at ED admission were included. MREs included adverse drug events with or without misuse and medication nonadherence with unfavorable clinical evolution. End points were assessed blindly from the randomization arm. Data were analyzed from January 2022 to March 2024.
Participants were randomized to a pharmacist-led transition of care program or usual care. Usual care included the ED pharmacist carrying out a medication history. In the transition of care group, ED pharmacists additionally made a postdischarge telephone call to the general practitioner (GP) and community pharmacist, along with a letter, notifying them about MRE type, suspected medication, and management recommendations.
The primary outcome was the proportion of patients with an ED visit for the same MRE at 6 months (same symptom and medication involved). Secondary outcomes included proportions of all-cause and MRE-related ED visits, hospitalizations, deaths, and medical office visits.
Among 330 patients analyzed, 187 (56.7%) were female, the median (IQR) age was 71 (50-83) years, and the median (IQR) home medications count was 6 (3-10). A total of 167 patients were randomized to the transition of care group and 163 to the control group. At 6 months, fewer participants in the transition of care group had ED visits related to the same MRE (5 [3.0%] vs 36 [22.1%]; risk difference [RD], -19.1 percentage points; 95% CI, -26.0 to -12.2; P < .001), all-cause ED visits (35 [21.0%] vs 57 [35.0%]; RD, -14.0 percentage points; 95% CI, -23.6 to -4.4), hospitalization related to the same MRE (3 [1.8%] vs 29 [17.8%]; RD, -16.0 percentage points; 95% CI, -22.2 to -9.8), and more GP office visits (88 of 158 [55.7%] vs 26 of 146 [17.8%]; RD, 37.9 percentage points; 95% CI, 28.0 to 47.8) and specialist office visits (67 of 158 [42.4%] vs 35 of 146 [24.0%]; RD, 18.4 percentage points; 95% CI, 8.1 to 28.8) related to the same MRE. All-cause hospitalization and death were similar between groups.
In this randomized clinical trial, a pharmacist-led transitional care intervention in the ED among patients with MRE significantly reduced ED visits and hospitalizations for the same MRE. If replicated in subsequent trials, this strategy offers a novel approach for reducing drug-related harms.
ClinicalTrials.gov Identifier: NCT03725046.
与药物相关的事件(MREs)是急诊科(ED)就诊和患者伤害的常见原因。
评估由药剂师主导的护理过渡计划在减少与相同MRE相关的急诊科就诊方面的效果,与常规护理相比,随访6个月。
设计、地点和参与者:这项前瞻性、开放标签、平行组随机临床试验于2018年11月至2021年7月在法国蒙彼利埃大学医院急诊科进行,随访期为6个月。纳入在急诊科入院时检测到MRE的成年患者。MRE包括有或无药物滥用的药物不良事件以及临床进展不利的药物治疗不依从。终点由随机分组组进行盲法评估。数据于2022年1月至2024年3月进行分析。
参与者被随机分配到由药剂师主导的护理过渡计划或常规护理组。常规护理包括急诊科药剂师进行用药史调查。在护理过渡组中,急诊科药剂师还会在出院后给全科医生(GP)和社区药剂师打电话,并附上一封信,通知他们MRE类型、疑似药物和管理建议。
主要结局是6个月时因相同MRE再次到急诊科就诊的患者比例(涉及相同症状和药物)。次要结局包括全因和与MRE相关的急诊科就诊、住院、死亡以及门诊就诊的比例。
在分析的330例患者中,187例(56.7%)为女性,年龄中位数(四分位间距)为71(50 - 83)岁,家庭用药数量中位数(四分位间距)为6(3 - 10)种。共有167例患者被随机分配到护理过渡组,163例被分配到对照组。在6个月时,护理过渡组中因相同MRE到急诊科就诊的参与者较少(5例[3.0%]对36例[22.1%];风险差异[RD],-19.1个百分点;95%置信区间,-26.0至-12.2;P <.001),全因急诊科就诊(35例[21.0%]对57例[35.0%];RD,-14.0个百分点;95%置信区间,-23.6至-4.4),因相同MRE住院(3例[1.8%]对29例[17.8%];RD,-16.0个百分点;95%置信区间,-22.2至-9.8),并且与相同MRE相关的全科医生门诊就诊更多(158例中的88例[55.7%]对146例中的26例[17.8%];RD,37.9个百分点;95%置信区间,28.0至47.8)以及专科医生门诊就诊更多(158例中的67例[42.4%]对146例中的35例[24.0%];RD,18.4个百分点;95%置信区间,8.1至28.8)。两组间全因住院和死亡情况相似。
在这项随机临床试验中,对患有MRE的患者在急诊科进行由药剂师主导的过渡性护理干预显著减少了因相同MRE导致的急诊科就诊和住院。如果在后续试验中得到重复验证,该策略为减少药物相关伤害提供了一种新方法。
ClinicalTrials.gov标识符:NCT03725046。