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首页> 外文期刊>Implementation Science >An integrated general practice and pharmacy-based intervention to promote the use of appropriate preventive medications among individuals at high cardiovascular disease risk: protocol for a cluster randomized controlled trial
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An integrated general practice and pharmacy-based intervention to promote the use of appropriate preventive medications among individuals at high cardiovascular disease risk: protocol for a cluster randomized controlled trial

机译:基于综合的一般实践和基于药房的干预,以促进在高心血管疾病风险中使用适当预防性药物的使用:集群随机对照试验的议定书

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Background Cardiovascular diseases (CVD) are responsible for significant morbidity, premature mortality, and economic burden. Despite established evidence that supports the use of preventive medications among patients at high CVD risk, treatment gaps remain. Building on prior evidence and a theoretical framework, a complex intervention has been designed to address these gaps among high-risk, under-treated patients in the Australian primary care setting. This intervention comprises a general practice quality improvement tool incorporating clinical decision support and audit/feedback capabilities; availability of a range of CVD polypills (fixed-dose combinations of two blood pressure lowering agents, a statin ± aspirin) for prescription when appropriate; and access to a pharmacy-based program to support long-term medication adherence and lifestyle modification. Methods Following a systematic development process, the intervention will be evaluated in a pragmatic cluster randomized controlled trial including 70 general practices for a median period of 18?months. The 35 general practices in the intervention group will work with a nominated partner pharmacy, whereas those in the control group will provide usual care without access to the intervention tools. The primary outcome is the proportion of patients at high CVD risk who were inadequately treated at baseline who achieve target blood pressure (BP) and low-density lipoprotein cholesterol (LDL-C) levels at the study end. The outcomes will be analyzed using data from electronic medical records, utilizing a validated extraction tool. Detailed process and economic evaluations will also be performed. Discussion The study intends to establish evidence about an intervention that combines technological innovation with team collaboration between patients, pharmacists, and general practitioners (GPs) for CVD prevention. Trial registration Australian New Zealand Clinical Trials Registry ACTRN12616000233426
机译:背景技术心血管疾病(CVD)负责显着的发病率,过早死亡率和经济负担。尽管具有在高CVD风险的患者中使用预防性药物的既定证据,但仍然存在治疗差距。在现有证据和理论框架上建立一个复杂的干预,旨在解决澳大利亚初级护理环境中的高风险,患者的高风险。该干预包括临床决策支持和审计/反馈能力的一般实践质量改进工具;适当时,一系列CVD滤波器(两种血压降低剂的固定剂量组合,Satin±Aspirin)适当时;并访问基于药房的计划,以支持长期用药依从性和生活方式修改。方法在系统的开发过程之后,将在务实的集群随机对照试验中进行干预,包括70个月期间的70个月的一般惯例。干预组的35项一般行为将与提名的合作伙伴药房合作,而控制小组的普通伙伴则将提供通常的护理,而无需进入干预工具。主要结果是高CVD风险的患者的比例,该患者在基线上不充分处理,在基线上达到靶血压(BP)和低密度脂蛋白胆固醇(LDL-C)水平在研究端。利用验证的提取工具,将使用来自电子医疗记录的数据进行分析的结果。还将进行详细的流程和经济评估。讨论该研究打算建立有关干预的证据,这些干预将技术创新与患者,药剂师和全科医生(GPS)之间的团队合作结合在一起进行CVD预防。试用注册澳大利亚新西兰临床试验登记处ACRRN12616000233426

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