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一项量身定制的项目对基层医疗实践中患有多种疾病且使用多种药物的患者实施循证推荐的影响——一项整群随机对照试验的结果

Impact of a tailored program on the implementation of evidence-based recommendations for multimorbid patients with polypharmacy in primary care practices-results of a cluster-randomized controlled trial.

作者信息

Jäger Cornelia, Freund Tobias, Steinhäuser Jost, Stock Christian, Krisam Johannes, Kaufmann-Kolle Petra, Wensing Michel, Szecsenyi Joachim

机构信息

Department of General Practice and Health Services Research, University Hospital Heidelberg, Im Neuenheimer Feld 130.3, Turm West, 4.OG, 69120, Heidelberg, Germany.

Institute of Family Medicine, UniversityHospital Schleswig-Holstein, Campus Lübeck, Ratzburger Allee 160, Haus 50, 23538, Lübeck, Germany.

出版信息

Implement Sci. 2017 Jan 13;12(1):8. doi: 10.1186/s13012-016-0535-y.

Abstract

BACKGROUND

Multimorbid patients receiving polypharmacy represent a growing population at high risk for negative health outcomes. Tailoring is an approach of systematic intervention development taking account of previously identified determinants of practice. The aim of this study was to assess the effect of a tailored program to improve the implementation of three important processes of care for this patient group: (a) structured medication counseling including brown bag reviews, (b) the use of medication lists, and (c) structured medication reviews to reduce potentially inappropriate medication.

METHODS

We conducted a cluster-randomized controlled trial with a follow-up time of 9 months. Participants were general practitioners (GPs) organized in quality circles and participating in a GP-centered care contract of a German health insurance. Patients aged >50 years, suffering from at least 3 chronic diseases, receiving more than 4 drugs, and being at high risk for medication-related events according to the assessment of the treating GP were enrolled. The tailored program consisted of a workshop for GPs and health care assistants, educational materials and reminders for patients, and the elaboration of implementation action plans. The primary outcome was the change in the degree of implementation between baseline and follow-up, measured by a summary score of 10 indicators. The indicators were based on structured surveys with patients and GPs.

RESULTS

We analyzed the data of 21 GPs (10 - intervention group, 11 - control group) and 273 patients (130 - intervention group, 143 - control group). The increase in the degree of implementation was 4.2 percentage points (95% confidence interval: -0.3, 8.6) higher in the intervention group compared to the control group (p = 0.1). Two of the 10 indicators were significantly improved in the intervention group: medication counseling (p = 0.017) and brown bag review (p = 0.012). Secondary outcomes showed an effect on patients' self-reported use of medication lists when buying drugs in the pharmacy (p = 0.03).

CONCLUSIONS

The tailored program may improve implementation of medication counseling and brown bag review whereas the use of medication lists and medication reviews did not improve. No effect of the tailored program on the combined primary outcome could be substantiated. Due to limitations of the study, results have to be interpreted carefully. The factors facilitating and hindering successful implementation will be examined in a comprehensive process evaluation.

TRIAL REGISTRATION NUMBER

ISRCTN34664024 , assigned 14/08/2013.

摘要

背景

接受多种药物治疗的多病患者群体日益庞大,面临不良健康结局的高风险。量身定制是一种系统干预开发方法,需考虑先前确定的实践决定因素。本研究旨在评估一项量身定制的项目对改善该患者群体三项重要护理流程实施情况的效果:(a)包括药袋核查在内的结构化药物咨询,(b)用药清单的使用,以及(c)结构化药物审查以减少潜在不适当用药。

方法

我们进行了一项整群随机对照试验,随访时间为9个月。参与者为以质量改进小组形式组织并参与德国医疗保险以全科医生为中心护理合同的全科医生(GP)。纳入年龄>50岁、患有至少3种慢性病、服用超过4种药物且经主治全科医生评估有药物相关事件高风险的患者。量身定制的项目包括为全科医生和医护助理举办的研讨会、给患者的教育材料和提醒,以及制定实施行动计划。主要结局是基线和随访之间实施程度的变化,通过10项指标的汇总评分来衡量。这些指标基于对患者和全科医生的结构化调查。

结果

我们分析了21名全科医生(10名在干预组,11名在对照组)和273名患者(130名在干预组,143名在对照组)的数据。与对照组相比,干预组实施程度的增加高出4.2个百分点(95%置信区间:-0.3,8.6)(p = 0.1)。干预组10项指标中有2项显著改善:药物咨询(p = 0.017)和药袋核查(p = 0.012)。次要结局显示,对患者在药店购药时自我报告的用药清单使用情况有影响(p = 0.03)。

结论

量身定制的项目可能改善药物咨询和药袋核查的实施情况,而用药清单的使用和药物审查并未改善。无法证实量身定制的项目对综合主要结局有影响。由于研究的局限性,结果必须谨慎解读。将在全面的过程评估中研究促进和阻碍成功实施的因素。

试验注册号

ISRCTN34664024,于2013年8月14日分配。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e089/5237147/05ba78ddcd86/13012_2016_535_Fig1_HTML.jpg

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