Nachar Carole, Lamy Olivier, Sadeghipour Farshid, Garnier Antoine, Voirol Pierre
Service of Pharmacy, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
Service of Internal Medicine, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
Eur J Hosp Pharm. 2019 May;26(3):129-134. doi: 10.1136/ejhpharm-2017-001358. Epub 2018 Jan 30.
To assess the feasibility and main obstacles to the implementation of a medication reconciliation (MR) process in a Swiss hospital and to develop a standardised method which can be used in similar healthcare systems.
For this prospective, observational single-centre and single-ward study, a best possible medication history (BPMH) was established by a clinical pharmacist for 147 patients with heart failure based on two sources and a patient interview for each case. Identified discrepancies with medication histories established during emergency service were conveyed to the ward physician. At the end of each hospital stay, the planned discharge treatments were compared with the BPMHs to identify discrepancies and to propose modifications. After a final validation, the comparative treatment plans were distributed.
MR was conducted for 120 (82%) patients and the mean time needed was 74 min/patient. At least one discrepancy was identified among 94% of the patients on admission, with 4.1 discrepancies found per patient (mainly omissions). At discharge, 83% of the patients had at least one discrepancy, with 2.3 discrepancies found per patient (mainly unintentional substitutions). The majority (86%) of pharmaceutical interventions to adjust the discharge prescriptions were accepted by the physician.
A standardised method of MR which offers precise definitions of discrepancies and key tools for the process was developed. This method was applicable to most of our cohort and it effectively identified medication discrepancies. Two potential obstacles for its implementation are the time needed for MR and the questionable impact of pharmaceutical interventions on discrepancies.
评估在一家瑞士医院实施用药核对(MR)流程的可行性和主要障碍,并开发一种可用于类似医疗系统的标准化方法。
在这项前瞻性、观察性单中心单病房研究中,临床药师基于两个来源并对每个病例进行患者访谈,为147例心力衰竭患者建立了尽可能完善的用药史(BPMH)。将识别出的与急诊服务期间建立的用药史的差异告知病房医生。在每次住院结束时,将计划的出院治疗与BPMH进行比较,以识别差异并提出修改建议。经过最终验证后,分发比较治疗计划。
对120例(82%)患者进行了MR,平均每位患者所需时间为74分钟。入院时94%的患者至少发现一处差异,每位患者发现4.1处差异(主要是遗漏)。出院时,83%的患者至少有一处差异,每位患者发现2.3处差异(主要是无意的替换)。调整出院处方的大多数(86%)药学干预措施被医生接受。
开发了一种标准化的MR方法,该方法为该流程提供了差异的精确定义及关键工具。该方法适用于我们队列中的大多数患者,并且有效地识别了用药差异。其实施的两个潜在障碍是MR所需的时间以及药学干预对差异的影响存疑。