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Effectiveness of pharmaceutical care at discharge in the emergency department: study protocol of a randomized controlled trial

机译:急诊科出院时药物治疗的有效性:一项随机对照试验的研究方案

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Background Patient education on pharmacological therapy may increase medication adherence and decrease hospitalizations. Our aim is to evaluate the effectiveness of pharmaceutical care at emergency department discharge in patients with hypertension and/or diabetes. Methods/design This is a randomized controlled trial. Participants will be recruited from a public emergency department at Restinga district in Porto Alegre, southern Brazil. A total of 380 patients will be randomly assigned into 2 groups at the moment of emergency department discharge after receiving medical orientations: an intervention group, consisting of a structured individual counseling session by a pharmacist in addition to written orientations, or a control group, consisting only of written information about the disease. Outcomes will be assessed in an ambulatory visit 2?months after the randomization. The primary outcome is the proportion of patients with high medication adherence assessed using the Morisky-Green Test and the Brief Medication Questionnaire. The secondary outcomes are reduction of blood pressure, glycated hemoglobin, fasting plasma glucose, quality of life and number of visits to the emergency department. Discussion Pharmaceutical care interventions have shown to be feasible and effective in increasing medication adherence in both hospital outpatient and community pharmacy settings. However, there have been no previous assessments of the effectiveness of pharmacy care interventions initiated in patients discharged from emergency departments. Our hypothesis is that pharmaceutical counseling is also effective in this population. Trial registration ClinicalTrials.gov registration number: NCT01978925 (11 November 2013) and Brazilian Registry of Clinical Trials U1111-1149-8922 (5 November 2013).
机译:背景技术对患者进行药理学教育可以增加药物依从性并减少住院。我们的目标是评估高血压和/或糖尿病患者急诊出院时的药物治疗效果。方法/设计这是一项随机对照试验。参与者将从巴西南部阿雷格里港Restinga区的公共紧急部门招募。总共380名患者在接受医疗说明后,在急诊室出院时将被随机分为2组:干预组,除书面说明外,由药剂师进行的结构化个人咨询会议组成,或对照组,包括仅关于疾病的书面信息。结果将在随机分组后2个月的非卧床就诊中进行评估。主要结果是使用Morisky-Green测试和简明药物调查问卷评估的高药物依从性患者的比例。次要结果是血压降低,糖化血红蛋白,空腹血糖,生活质量和就诊次数。讨论在医院的门诊和社区药房,药物护理干预措施已显示出增加药物依从性的可行性和有效性。但是,对于从急诊科出院的患者启动的药房护理干预措施的有效性,以前没有任何评估。我们的假设是药物咨询在该人群中也有效。试验注册ClinicalTrials.gov注册号:NCT01978925(2013年11月11日)和巴西临床试验注册处U1111-1149-8922(2013年11月5日)。

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