4.5 Article

Telemedicine cardiovascular risk reduction in veterans: The CITIES trial

期刊

AMERICAN HEART JOURNAL
卷 199, 期 -, 页码 122-129

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MOSBY-ELSEVIER
DOI: 10.1016/j.ahj.2018.02.002

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资金

  1. Durham Center of Innovation for Health Services Research in Primary Care [CIN 13-410]
  2. VA Health Service Research and Development [VA HSRD IIR 08-297, VA HSRD 08-027]
  3. HSRD CDA award [13-261, 13-025, 13-263]

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Background: Comprehensive programs addressing tailored patient self-management and pharmacotherapymay reduce barriers to cardiovascular disease (CVD) risk reduction. Methods: This is a 2-arm (clinical pharmacist specialist-delivered, telehealth intervention and education control) randomized controlled trial including Veterans with poorly controlled hypertension and/or hypercholesterolemia. Primary outcome was Framingham CVD risk score at 6 and 12 months, with systolic blood pressure; diastolic blood pressure; total cholesterol; low-density lipoprotein; high- density lipoprotein; body mass index; and, for those with diabetes, HbA1c as secondary outcomes. Results: Among 428 Veterans, 50% were African American, 85% were men, and 33% had limited health literacy. Relative to the education control group, the clinical pharmacist specialist-delivered intervention did not show a reduction in CVD risk score at 6 months (-1.8, 95% CI -3.9 to 0.3; P =.10) or 12 months (-0.3, 95% CI -2.4 to 1.7; P =.74). No differences were seen in systolic blood pressure, diastolic blood pressure, or lowdensity lipoprotein at 6 or 12 months. We did observe a significant decline in total cholesterol at 6 months (-7.0, 95% CI-13.4 to-0.6; P=. 03) in the intervention relative to education control group. Among patients in the intervention group, 34% received at least 5 of the 12 planned intervention calls and were considered compliers. A sensitivity analysis of the complier average causal effect of intervention compared to control showed a mean difference in CVD risk score reduction of 5.7 (95% CI-12.0 to 0.7) at 6 months and-1.7 (95% CI-7.6 to 4.8) at 12 months. Conclusions: Despite increased access to pharmacist resources, we did not observe significant improvements in CVD risk for patients randomized to the intervention compared to education control over 12 months. However, the intervention may have positive impact among those who actively participate, particularly in the short term. (c) 2018 Elsevier Inc. All rights reserved.

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