A Cluster-Randomized Trial of a Centralized Clinical Pharmacy Cardiovascular Risk Service to Improve Guideline Adherence

被引:11
作者
Carter, Barry L. [1 ,2 ]
Coffey, Christopher S. [3 ]
Chrischilles, Elizabeth A. [4 ]
Ardery, Gail [1 ]
Ecklund, Dixie [3 ]
Gryzlak, Brian [1 ,4 ]
Vander Weg, Mark W. [5 ,6 ,7 ]
James, Paul A. [2 ]
Christensen, Alan J. [6 ,7 ]
Parker, Christopher P. [1 ]
Gums, Tyler [1 ]
Finkelstein, Rachel J. [1 ]
Uribe, Liz [3 ]
Polgreen, Linnea A. [1 ]
机构
[1] Univ Iowa, Coll Pharm, Dept Pharm Practice & Sci, Iowa City, IA 52242 USA
[2] Roy J & Lucille A Carver Coll Med, Dept Family Med, Iowa City, IA USA
[3] Coll Publ Hlth, Dept Biostat, Iowa City, IA USA
[4] Coll Publ Hlth, Dept Epidemiol, Iowa City, IA USA
[5] Iowa City Vet Adm, Iowa City, IA USA
[6] Carver Coll Med, Dept Internal Med, Iowa City, IA USA
[7] Univ Iowa, Dept Psychol, Coll Liberal Arts, Iowa City, IA 52242 USA
来源
PHARMACOTHERAPY | 2015年 / 35卷 / 07期
关键词
cardiovascular disease; diabetes; clinical trial; pharmacist management; guideline adherence; PRINTED EDUCATIONAL MESSAGE; VITAL SIGNS PREVALENCE; OF-NEUROLOGY AFFIRMS; SECONDARY PREVENTION; ISCHEMIC-STROKE; PRIMARY-CARE; COLLABORATIVE MODEL; VASCULAR-DISEASE; UNITED-STATES; PHYSICIAN;
D O I
10.1002/phar.1603
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BackgroundNumerous studies have demonstrated the value of including pharmacists in team-based care to improve adherence to cardiovascular (CV) guidelines, medication adherence, and risk factor control. However, there is limited information on whether these models can be successfully implemented more widely in diverse settings and populations. The purpose of this study is to evaluate whether a centralized, web-based cardiovascular risk service (CVRS) managed by clinical pharmacists will improve guideline adherence in multiple primary care medical offices with diverse geographic and patient characteristics. MethodsThis study is a prospective trial in 20 primary care offices stratified by the percent of under-represented minorities and then randomized to either the CVRS intervention or usual care. The intervention will last for 12months and all subjects will have research visits at baseline and 12months. The primary outcome is the difference in guideline adherence between groups. Data will also be abstracted from the medical record at 24months to determine if the intervention effect is sustained after it is discontinued. ConclusionsPatient enrollment will continue through 2016, with results expected in 2019. This study will provide information on whether a distant, centralized CVRS can be implemented in large numbers of medical offices, if it is effective in diverse populations, and if there is a long-term sustained effect.
引用
收藏
页码:653 / 662
页数:10
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