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药剂师干预改善心力衰竭患者药物依从性:一项随机试验。

Pharmacist intervention to improve medication adherence in heart failure: a randomized trial.

作者信息

Murray Michael D, Young James, Hoke Shawn, Tu Wanzhu, Weiner Michael, Morrow Daniel, Stroupe Kevin T, Wu Jingwei, Clark Daniel, Smith Faye, Gradus-Pizlo Irmina, Weinberger Morris, Brater D Craig

机构信息

Center for Pharmaceutical Outcomes and Policy, University of North Carolina School of Pharmacy, Chapel Hill, North Carolina 27599-7360, USA.

出版信息

Ann Intern Med. 2007 May 15;146(10):714-25. doi: 10.7326/0003-4819-146-10-200705150-00005.

Abstract

BACKGROUND

Patients with heart failure who take several prescription medications sometimes have poor adherence to their treatment regimens. Few interventions designed to improve adherence to therapy have been rigorously tested.

OBJECTIVE

To determine whether a pharmacist intervention improves medication adherence and health outcomes compared with usual care for low-income patients with heart failure.

DESIGN

Randomized, controlled trial conducted from February 2001 to June 2004.

SETTING

University-affiliated, inner-city, ambulatory care practice.

PATIENTS

314 low-income patients 50 years of age or older with heart failure confirmed by their primary care physician.

INTERVENTION

Patients were randomly assigned to intervention (39% [n = 122]) or usual care (61% [n = 192]) groups and were followed for 12 months. A pharmacist provided a 9-month multilevel intervention, with a 3-month poststudy phase. An interdisciplinary team of investigators designed the intervention to support medication management by patients who have low health literacy and limited resources.

MEASUREMENTS

Primary outcomes were adherence, as measured by using electronic prescription monitors, and exacerbations requiring emergency department care or hospital admission. Secondary outcomes included health-related quality of life, patient satisfaction with pharmacy services, and total direct costs.

RESULTS

During the 9-month intervention period, medication adherence was 67.9% and 78.8% in the usual care and intervention groups, respectively (difference, 10.9 percentage points [95% CI, 5.0 to 16.7 percentage points]). However, these salutary effects dissipated in the 3-month postintervention follow-up period, in which adherence was 66.7% and 70.6%, respectively (difference, 3.9 percentage points [CI, -5.9 to 6.5 percentage points]). Medications were taken on schedule 47.2% of the time in the usual care group and 53.1% of the time in the intervention group (difference, 5.9 percentage points [CI, 0.4 to 11.5 percentage points]), but this effect also dissipated at the end of the intervention (48.9% vs. 48.6%, respectively; difference, 0.3 percentage point [CI, -5.9 to 6.5 percentage points]). Emergency department visits and hospital admissions were 19.4% less (incidence rate ratio, 0.82 [CI, 0.73 to 0.93]) and annual direct health care costs were lower ($-2960 [CI, $-7603 to $1338]) in the intervention group.

LIMITATIONS

Because electronic monitors were used to ascertain adherence, patients were not permitted to use medication container adherence aids. The intervention involved 1 pharmacist and a single study site that served a large, indigent, inner-city population of patients. Because the intervention had several components, intervention effects could not be attributed to a single component.

CONCLUSIONS

A pharmacist intervention for outpatients with heart failure can improve adherence to cardiovascular medications and decrease health care use and costs, but the benefit probably requires constant intervention because the effect dissipates when the intervention ceases. ClinicalTrials.gov registration number: NCT00388622.

摘要

背景

服用多种处方药的心力衰竭患者有时对其治疗方案的依从性较差。很少有旨在提高治疗依从性的干预措施经过严格测试。

目的

确定与针对低收入心力衰竭患者的常规护理相比,药剂师干预是否能提高用药依从性和健康结局。

设计

2001年2月至2004年6月进行的随机对照试验。

地点

大学附属医院的市中心门诊护理机构。

患者

314名50岁及以上的低收入心力衰竭患者,由其初级保健医生确诊。

干预措施

患者被随机分配到干预组(39%[n = 122])或常规护理组(61%[n = 192]),并随访12个月。一名药剂师提供为期9个月的多层面干预,并设3个月的研究后阶段。一个跨学科研究团队设计了该干预措施,以支持健康素养低且资源有限的患者进行药物管理。

测量指标

主要结局是使用电子处方监测仪测量的依从性,以及需要急诊科护理或住院治疗的病情加重情况。次要结局包括与健康相关的生活质量、患者对药房服务的满意度以及总直接费用。

结果

在9个月的干预期内,常规护理组和干预组的用药依从性分别为67.9%和78.8%(差异为10.9个百分点[95%CI,5.0至16.7个百分点])。然而,这些有益效果在干预后3个月的随访期内消失,此时依从性分别为66.7%和70.6%(差异为3.9个百分点[CI,-5.9至6.5个百分点])。常规护理组按时服药的时间为47.2%,干预组为53.1%(差异为5.9个百分点[CI,0.4至11.5个百分点]),但这种效果在干预结束时也消失了(分别为48.9%和48.6%;差异为0.3个百分点[CI,-5.9至6.5个百分点])。干预组的急诊科就诊和住院次数减少了19.4%(发病率比,0.82[CI,0.73至0.93]),年度直接医疗费用更低(-2960美元[CI,-7603至1338美元])。

局限性

由于使用电子监测仪来确定依从性,患者不允许使用药盒依从性辅助工具。该干预由一名药剂师和一个单一研究地点实施,该研究地点服务于大量贫困的市中心患者群体。由于干预措施有多个组成部分,干预效果不能归因于单个组成部分。

结论

对心力衰竭门诊患者的药剂师干预可以提高心血管药物治疗的依从性,并减少医疗保健的使用和费用,但这种益处可能需要持续干预,因为干预停止后效果会消失。ClinicalTrials.gov注册号:NCT00388622。

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