Fifth
Annual Grant Winners 2004-2005
Deborah H. Kennedy, Pharm.D., HPD -
College of Pharmacy
Ceressa T. Ward, Pharm.D., HPD - College
of Pharmacy
Brent Salvig, Pharm.D., West Palm Beach
Veterans Affairs Medical Center
Timothy Kelley, MSW, West Palm Beach Veterans
Affairs Medical Center
Shashi Bhandari-Gadson, ARNP, West Palm
Beach Veterans Affairs Medical Center
Wallace Marsh, Ph.D., HPD - College
of Pharmacy
Christine M. Ruby, Pharm.D., BCPS, Duke
University Division of Geriatric Medicine Durham Veterans
Affairs Medical Center
Dean William Hardigan, HPD – College of Pharmacy
Title: Impact
of a Clinical Pharmacist on Medication Appropriateness
for Elderly Veterans Residing in Assisted Living
Facilities
Abstract:
The primary objective of this research study is
to demonstrate that clinical pharmacist review of medication
therapy improves medication prescribing. Secondary objectives
are to determine changes in adverse drug events and/or
healthcare resource utilization for elderly veterans
residing in Assisted Living Facilities (ALFs) after a clinical
pharmacist intervention. The literature has assessed medication
appropriateness and the impact of a clinical pharmacist for
elderly residing in community and inpatient settings. There
is very little literature describing medication appropriateness
and there are no studies documenting the impact of a clinical
pharmacist in the ALF environment. This research will provide
new information about clinical pharmacists’ impact
in ALFs.
One-hundred and two patients greater than 65 years old
residing in ALFs and cared for by the Community Residential
Care (CRC) team will be randomly selected for inclusion.
Before randomization, a retrospective chart review will
be conducted to determine a baseline Medication Appropriateness
Index (MAI) score and develop written pharmacotherapy
recommendations. Only patients randomized to clinical pharmacist
intervention will have their written pharmacotherapy recommendations
forwarded to their Primary Care provider and have a clinical
pharmacist join the CRC team to address all medication-related
issues during the 6 month intervention period. After
6 months or close-out, another MAI score, adverse drug events,
and healthcare resource utilization (emergency room visits,
unscheduled hospital admissions and/or unscheduled outpatient
clinic visits) will be recorded.
Descriptive statistics will be reported for all continuous
variables. Differences between groups at baseline will
be determined using the Student’s t-test for continuous
data and the Chi-square test for nominal data. Differences
between MAI scores at baseline and follow-up for each group
and between groups, adverse drug events, and healthcare
resource utilization between the groups and the association
between MAI score and healthcare utilization will be determined
using appropriate regression, ANOVA, and ANCOVA techniques.