Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Centre Groningen, PO-Box 30001, HPC AP50, UMCG, Groningen, 9700RB, The Netherlands.
SIR Institute for Pharmacy Practice and Policy, Leiden, The Netherlands.
BMC Prim Care. 2024 Jun 11;25(1):210. doi: 10.1186/s12875-024-02465-7.
BACKGROUND: Deprescribing of medication for cardiovascular risk factors and diabetes has been incorporated in clinical guidelines but proves to be difficult to implement in primary care. Training of healthcare providers is needed to enhance deprescribing in eligible patients. This study will examine the effects of a blended training program aimed at initiating and conducting constructive deprescribing consultations with patients. METHODS: A cluster-randomized trial will be conducted in which local pharmacy-general practice teams in the Netherlands will be randomized to conducting clinical medication reviews with patients as usual (control) or after receiving the CO-DEPRESCRIBE training program (intervention). People of 75 years and older using specific cardiometabolic medication (diabetes drugs, antihypertensives, statins) and eligible for a medication review will be included. The CO-DEPRESCRIBE intervention is based on previous work and applies models for patient-centered communication and shared decision making. It consists of 5 training modules with supportive tools. The primary outcome is the percentage of patients with at least 1 cardiometabolic medication deintensified. Secondary outcomes include patient involvement in decision making, healthcare provider communication skills, health/medication-related outcomes, attitudes towards deprescribing, medication regimen complexity and health-related quality of life. Additional safety and cost parameters will be collected. It is estimated that 167 patients per study arm are needed in the final intention-to-treat analysis using a mixed effects model. Taking loss to follow-up into account, 40 teams are asked to recruit 10 patients each. A baseline and 6-months follow-up assessment, a process evaluation, and a cost-effectiveness analysis will be conducted. DISCUSSION: The hypothesis is that the training program will lead to more proactive and patient-centered deprescribing of cardiometabolic medication. By a comprehensive evaluation, an increase in knowledge needed for sustainable implementation of deprescribing in primary care is expected. TRIAL REGISTRATION: The study is registered at ClinicalTrials.gov (identifier: NCT05507177).
背景:减少心血管风险因素和糖尿病的药物治疗已纳入临床指南,但在基层医疗实践中实施较为困难。需要对医疗保健提供者进行培训,以提高合格患者的药物减量能力。本研究将考察一种混合培训方案对启动和开展与患者进行建设性药物减量咨询的效果。
方法:将在荷兰进行一项群组随机试验,当地的药房-全科医疗团队将被随机分配,按照常规(对照组)或接受 CO-DEPRESCRIBE 培训方案(干预组)为患者进行临床药物评估。将纳入年龄在 75 岁及以上、使用特定心血管代谢药物(糖尿病药物、降压药、他汀类药物)且有药物评估资格的患者。CO-DEPRESCRIBE 干预方案基于先前的工作,并应用了以患者为中心的沟通和共同决策模型。它包括 5 个培训模块和支持工具。主要结局指标是至少有 1 种心血管代谢药物减量的患者比例。次要结局指标包括患者参与决策、医疗保健提供者沟通技巧、健康/药物相关结局、对药物减量的态度、药物治疗方案的复杂性和健康相关生活质量。还将收集其他安全性和成本参数。采用混合效应模型,预计最终意向治疗分析中每组需要 167 例患者。考虑到失访,要求 40 个团队每组招募 10 例患者。将进行基线和 6 个月随访评估、过程评估和成本效益分析。
讨论:假设培训方案将导致更积极主动和以患者为中心的心血管代谢药物减量。通过全面评估,预计将增加在初级保健中可持续实施药物减量所需的知识。
试验注册:该研究在 ClinicalTrials.gov 注册(标识符:NCT05507177)。
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