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Effects of a pharmaceutical care intervention on clinical outcomes and patient adherence in coronary heart disease: the MIMeRiC randomized controlled trial

机译:药物护理干预对冠心病临床结果和患者粘附的影响:模糊的随机对照试验

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In the treatment of coronary heart disease, secondary prevention goals are still often unmet and poor adherence to prescribed drugs has been suggested as one of the reasons. We aimed to investigate whether pharmaceutical care by a pharmacist at the cardiology clinic trained in motivational interviewing improves clinical outcomes and patient adherence. This was a prospective, randomized, controlled, outcomes-blinded trial designed to compare pharmaceutical care follow-up with standard care. After standard follow-up at the cardiology clinic, patients in the intervention group were seen by a clinical pharmacist two to five times as required over seven months. Pharmacists were trained to use motivational interviewing in the consultations and they tailored their support to each patient’s clinical needs and beliefs about medicines. The primary study end-point was the proportion of patients who reached the treatment goal for low-density lipoprotein cholesterol by 12?months after discharge. The key secondary outcome was patient adherence to lipid-lowering therapy at 15?months after discharge, and other secondary outcomes were the effects on patient adherence to other preventive drugs, systolic blood pressure, disease-specific quality of life, and healthcare use. 316 patients were included. The proportion of patients who reached the target for low-density lipoprotein cholesterol were 37.0% in the intervention group and 44.2% in the control group (P?=?.263). More intervention than control patients were adherent to cholesterol-lowering drugs (88 vs 77%; P?=?.033) and aspirin (97 vs 91%; P?=?.036) but not to beta-blocking agents or renin–angiotensin–aldosterone system inhibitors. Our intervention had no positive effects on risk factors for CHD, but it increased patient adherence. Further investigation of the intervention process is needed to explore the difference in results between patient adherence and medication effects. Longer follow-up of healthcare use and mortality will determine if the increased adherence per se eventually will have a meaningful effect on patient health. Trial registration: ClinicalTrials.gov NCT02102503, 03/04/2014 retrospectively registered.
机译:在治疗冠心病中,二级预防目标仍然是未满足的,并且已经提出了对规定的药物的贫困性,作为其中一个原因。我们旨在调查药剂师在励志面试中训练的药剂师药物护理是否改善了临床结果和患者遵守。这是一项潜在的,随机的,受控,结果盲化试验,旨在与标准护理进行比较药物护理随访。在心脏病学诊所的标准后续后,临床药剂师的患者被临床药剂师看到两到五倍,如七个月超过七个月。药剂师们接受培训以在磋商中使用励志面试,并对每个患者的临床需求和对药物的信仰量身定制了他们的支持。初级研究终点是患者的比例达到低密度脂蛋白胆固醇的治疗目标12?出院后的月份。关键的二次结果是患者在排出后15?几个月患者依赖于降脂治疗,而其他二次结果是对患者粘附对其他预防性药物的影响,收缩压,疾病的生活质量和医疗保健使用。包括316名患者。达到低密度脂蛋白胆固醇靶标的患者的比例在干预组中为37.0%,对照组44.2%(p?= 263)。比对照患者依赖于胆固醇的药物(88 vs 77%; p?=β.033)和阿司匹林(97 vs 91%; p?=β.036),但不是对β-封闭剂或肾素的血管紧张素 - 醛固酮系统抑制剂。我们的干预对CHD的危险因素没有积极影响,但它增加了患者遵守。需要进一步调查干预过程,以探讨患者粘附和药物影响之间的结果差异。较长的医疗保健使用和死亡率的后续行动将决定是否增加了对患者健康的有意义的依从性。审判注册:ClinicalTrials.gov NCT02102503,03/04/2014回顾性注册。

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