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Investigation of Motivational Interviewing and Prevention Consults to Achieve Cardiovascular Targets (IMPACT) trial - 12/05/18

Doi : 10.1016/j.ahj.2017.12.019 
Eugenia Gianos, MD a, , Antoinette Schoenthaler, EdD, MA c, Yu Guo, MA c, Judy Zhong, PhD c, Howard Weintraub, MD a, Arthur Schwartzbard, MD a, James Underberg, MD a, Michael Schloss, MD a, Jonathan D. Newman, MD, MPH a, Sean Heffron, MD, MS a, b, Edward A. Fisher, MD, PhD a, b, Jeffrey S. Berger, MD, MS a, b
a Department of Medicine, Division of Cardiology, Center for the Prevention of Cardiovascular Disease, New York University School of Medicine, New York, NY 
b Marc and Ruti Bell Program in Vascular Biology, New York University School of Medicine, New York, NY 
c Department of Population Health, Center for Healthful Behavioral Change, New York University School of Medicine, New York, NY 

Reprint requests: Eugenia Gianos, MD, Associate Professor of Medicine, Co-Clinical Director, Center for the Prevention of Cardiovascular Disease, Director, Preventive Cardiology Fellowship, 530 First Ave Schwartz HCC 4F, New York University Langone Medical Center, New York, NY 10016.Associate Professor of Medicine, Co-Clinical Director, Center for the Prevention of Cardiovascular Disease, Director, Preventive Cardiology FellowshipNew York University Langone Medical Center530 First Ave Schwartz HCC 4FNew YorkNY10016

Abstract

Background

Patients undergoing cardiovascular (CV) procedures often have suboptimal CV risk factor control and may benefit from strategies targeting healthy lifestyle behaviors and education. Implementation of prevention strategies may be particularly effective at this point of heightened motivation.

Methods

A prospective, randomized, pilot study was conducted in 400 patients undergoing a nonurgent CV procedure (cardiac catheterization ± revascularization) to evaluate the impact of different prevention strategies. Patients were randomized in a 1:1:1 fashion to usual care (UC; group A, n = 134), in-hospital CV prevention consult (PC; group B, n = 130), or PC plus behavioral intervention program (telephone-based motivational interviewing and optional tailored text messages) (group C, n = 133). The primary end point was the Δ change in non–high-density lipoprotein cholesterol (non–HDL-C) from baseline to 6 month.

Results

The mean age was 64.6 ± 10.8 years, 23.7% were female, and 31.5% were nonwhite. After 6 months, the absolute difference in non–HDL-C for all participants was −19.8 mg/dL (95% CI −24.1 to −15.6, P < .001). There were no between-group differences in the primary end point for the combined PC groups (B and C) versus UC, with a Δ adjusted between group difference of −5.5 mg/dL (95% CI −13.1 to 2.1, P = .16). Patients in the PC groups were more likely to be on high-intensity statins at 6 months (52.9% vs 38.1%, P = .01). After excluding participants with baseline non–HDL-C <100 mg/dL (initial exclusion criterion), Δ non–HDL-C and Δ low-density lipoprotein cholesterol were improved in the PC groups compared to UC (non–HDL-C −8.13 mg/dL [−16.00 to −0.27], P = .04; low-density lipoprotein cholesterol −7.87mg/dL [−15.10 to −0.64], P = .03).

Conclusions

Although non–HDL-C reduction at 6 months following a nonurgent CV procedure was not significant in the overall cohort, an increased uptake in high-potency statins may translate into improved long-term health outcomes and cost reductions.

Le texte complet de cet article est disponible en PDF.

Plan


 Vera Bittner, MD, MSPH, served as guest editor for this article.
 Relationship with industry: none.
 Clinical Trial Unique Identifier: NCT01642355.


© 2018  Publié par Elsevier Masson SAS.
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Vol 199

P. 37-43 - mai 2018 Retour au numéro
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