Rationale and Design of the Pharmacist Intervention for Low Literacy in Cardiovascular Disease (PILL-CVD) Study
Autor: | Jeffrey L, Schnipper, Christianne L, Roumie, Courtney, Cawthon, Alexandra, Businger, Anuj K, Dalal, Ileko, Mugalla, Svetlana, Eden, Terry A, Jacobson, Kimberly J, Rask, Viola, Vaccarino, Tejal K, Gandhi, David W, Bates, Daniel C, Johnson, Stephanie, Labonville, David, Gregory, Sunil, Kripalani, Daniel J, Cobaugh |
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Rok vydání: | 2010 |
Předmět: |
Counseling
Health Knowledge Attitudes Practice medicine.medical_specialty Time Factors Cost-Benefit Analysis Psychological intervention Pharmacist Pharmacists Article Medication Adherence law.invention Professional Role Quality of life (healthcare) Patient Education as Topic Randomized controlled trial law Intervention (counseling) Health care medicine Humans Medication Errors Drug Interactions Acute Coronary Syndrome Heart Failure Academic Medical Centers business.industry Cardiovascular Agents Health Care Costs Patient Discharge United States Clinical trial Research Design Cardiovascular agent Emergency medicine Quality of Life Physical therapy Educational Status Cardiology and Cardiovascular Medicine business Delivery of Health Care |
Zdroj: | Circulation: Cardiovascular Quality and Outcomes. 3:212-219 |
ISSN: | 1941-7705 1941-7713 |
DOI: | 10.1161/circoutcomes.109.921833 |
Popis: | Background— Medication errors and adverse drug events are common after hospital discharge due to changes in medication regimens, suboptimal discharge instructions, and prolonged time to follow-up. Pharmacist-based interventions may be effective in promoting the safe and effective use of medications, especially among high-risk patients such as those with low health literacy. Methods and Results— The Pharmacist Intervention for Low Literacy in Cardiovascular Disease (PILL-CVD) study is a randomized controlled trial conducted at 2 academic centers—Vanderbilt University Hospital and Brigham and Women’s Hospital. Patients admitted with acute coronary syndrome or acute decompensated heart failure were randomly assigned to usual care or intervention. The intervention consisted of pharmacist-assisted medication reconciliation, inpatient pharmacist counseling, low-literacy adherence aids, and tailored telephone follow-up after discharge. The primary outcome is the occurrence of serious medication errors in the first 30 days after hospital discharge. Secondary outcomes are health care utilization, disease-specific quality of life, and cost-effectiveness. Enrollment was completed September 2009. A total of 862 patients were enrolled, and 430 patients were randomly assigned to receive the intervention. Analyses will determine whether the intervention was effective in reducing serious medication errors, particularly in patients with low health literacy. Conclusions— The PILL-CVD study was designed to reduce serious medication errors after hospitalization through a pharmacist-based intervention. The intervention, if effective, will inform health care facilities on the use of pharmacist-assisted medication reconciliation, inpatient counseling, low-literacy adherence aids, and patient follow-up after discharge. Clinical Trial Registration— clinicaltrials.gov. Identifier: NCT00632021. |
Databáze: | OpenAIRE |
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