Improving Quality Through Decision Support for Evidence-Based Pharmacotherapy
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 5,000
- 试验地点
- 2
- 主要终点
- Rates of aggregate adherence by study group to all applicable pharmacotherapy rules during the study period.
研究概览
简要总结
This three-year, grant funded project will be conducted by the Division of Clinical Informatics in the Department of Community and Family Medicine at Duke University Medical Center. The project seeks to improve care quality and safety in an ambulatory care setting through clinical decision support for evidence-based (EB) pharmacotherapy delivered as point-of-care reports to clinic-based practitioners and as population health-based alerts to care managers.
This project will build upon a regional Health Information Exchange (HIE) network created to connect providers serving 37,000 Medicaid beneficiaries from both rural and urban settings in a 5 county region in the Northern Piedmont of North Carolina. This network includes 16 private practices, 3 federally qualified health centers, 5 rural health centers, 3 urgent care facilities, 10 government agencies, 5 hospitals, and 2 cross-disciplinary care management teams.
The proposed information system will be based on an emerging standard for decision support and will utilize routinely available claims and scheduling data in order to serve as a replicable model for broader use of decision support for medication management. Increased availability and use of decision support tools for medication management can be expected to reduce medication errors, improve health care quality at an acceptable cost, and augment disease management for patients and populations.
详细描述
The study will be conducted in accordance with the following four specific aims:
Aim 1: Expand the functionality of an existing decision support system in use within a regional HIE network to incorporate EB pharmacotherapy guidelines and to promote medication adherence. Primary care clinicians will receive EB pharmacotherapy suggestions and a patient-specific summary of prescription claims data delivered to the point-of-care via fax. Care managers will receive alerts delivered via email to encourage patients to arrange follow-up clinic appointments because of possible medication non-adherence.
Aim 2: Implement and evaluate the impact of the two interventions on adherence to EB pharmacotherapy recommendations among Medicaid patients with high priority conditions as designated by the Institute of Medicine (IOM) in ambulatory care settings through a three-arm randomized controlled trial.
Aim 3: Compare resource utilization and assess the economic attractiveness (cost-savings or cost-effectiveness) of the interventions to promote medication adherence and EB pharmacotherapy.
Aim 4: Disseminate information regarding the development and impact of the interventions through Web teleconferences, professional meetings, educational lectures, and peer review journals.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Health Services Research
- 盲法
- None
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Carolina Access Medicaid patients continuously enrolled for 10 of 12 months prior to August 2009
- •Patients assigned to one of 14 participating primary care clinics within the Northern Piedmont Community Care Network
- •At least one of six IOM priority conditions: hypertension, diabetes mellitus, stroke, ischemic heart disease, heart failure, or persistent asthma
排除标准
- •Patient opted-out
研究组 & 干预措施
Control
Medication report
Medication reports delivered to providers at the point of care
干预措施: Medication Management report (Other)
Med. report plus care manager notices
Medication reports delivered to providers at the point of care and notices sent electronically to care managers
干预措施: Medication Management report (Other)
Med. report plus care manager notices
Medication reports delivered to providers at the point of care and notices sent electronically to care managers
干预措施: Care manager email notices (Other)
结局指标
主要结局
Rates of aggregate adherence by study group to all applicable pharmacotherapy rules during the study period.
时间窗: Baseline, 12 months
次要结局
- Provider satisfaction measured using standard usability survey instruments.(12 months)
- Rates of adherence to pharmacotherapy rules for a specific IOM priority condition.(Baseline, 12 months)
- Rates of adherence by IOM condition to applicable pharmacotherapy rules 6 months after an intervention was first initiated or could have been initiated for the control arm.(Baseline, 6 months)
- Outpatient encounter rates.(Baseline, 12 months)
- Rates of adherence by drug class to applicable pharmacotherapy rules 6 months after an intervention was first initiated or could have been initiated for the control arm.(Baseline, 6 months)
- Resource use and medical costs associated with the interventions and their delivery, as well as direct healthcare costs (inpatient and outpatient).(12 months)
- Rates of adherence to pharmacotherapy rules for a specific therapeutic drug class(Baseline, 12 months)
- The proportion of email notices that were followed up by a completed clinic encounter within 60 days.(12 months)
- Rates of adherence to applicable pharmacotherapy rules 6 months after an intervention was first initiated or could have been initiated for the control arm.(Baseline, 6 months)
- The proportion of email notices that were followed up by a documented care management encounter within 30 days.(12 months)
- Emergency department encounter rates.(Baseline, 12 months)
- Inpatient hospitalization rates.(Baseline, 12 months)