Effectiveness of Amlodipine-Valsartan Single-Pill Combinations: Hierarchical Modeling of Blood Pressure and Total Cardiovascular Disease Risk Outcomes (the EXCELLENT Study)

Author:

Lins Robert1,Aerts Ann2,Coen Nicolas3,Hermans Christine4,MacDonald Karen5,Brié Heidi6,Lee Christopher7,Shen Yu-Ming8,Vancayzeele Stefaan9,Mecum Natalie10,Abraham Ivo11

Affiliation:

1. Robert Lins MD PhD, Professor, Faculty of Medicine, University of Antwerp and Clinician, Division of Nephrology and Hypertension, ZNA Stuivenberg, Antwerpen, Belgium; Managing Director, SGS Life Science Services, Mechelen, Belgium

2. Ann Aerts MD, Medical Advisor, Novartis Pharma, Vilvoorde, Belgium

3. Nicolas Coen MD, Medical Advisor, Novartis Pharma

4. Christine Hermans PharmD, Project Manager, Novartis Pharma

5. Karen MacDonald PhD, Chief Executive, Matrix45, Tucson, AZ

6. Heidi Brié MD, Therapeutic Area Head, Novartis Pharma

7. Christopher Lee PhD, Research Scientist, Matrix45; Assistant Professor, School of Nursing, Oregon Health and Science University, Portland, OR

8. Yu-Ming Shen PhD, Research Scientist, Matrix45

9. Stefaan Vancayzeele MD MSc, Chief Scientific Officer and Medical Director, Novartis Pharma

10. Natalie Mecum MS, Research Associate, Matrix45

11. Ivo Abraham PhD, Chief Scientist, Matrix45; Professor and Investigator, Center for Health Outcomes and Pharmacoeconomic Research, College of Pharmacy, University of Arizona, Tucson, AZ

Abstract

BACKGROUND: Both patient- and physician-related factors have been shown to explain variability in the outcomes of antihypertensive treatment. Total cardiovascular risk (TCVR) is increasingly used as a determinant of treatment effectiveness but has also been proposed as a treatment outcome. To our knowledge, no studies have reported how antihypertensive treatment impacts blood pressure and TCVR outcomes. OBJECTIVE: To examine in patients treated with a regimen including single-pill combinations (SPCs) of amlodipine/valsartan (1) blood pressure (BP) reduction and control, total cardiovascular risk (TCVR) change, and TCVR reduction of 1 class or more; (2) hierarchical patient- and physician-level determinants of these outcomes; and (3) predictors of uncontrolled BP and improved TCVR classification. METHODS: A prospective (90 days), multicenter, multilevel pharmacoepidemiologic study was conducted in 3546 patients with hypertension treated with SPC amlodipine/valsartan by 698 general practitioners. Statistical analysis included hierarchical linear and logistic modeling of BP and TCVR outcomes. RESULTS: Mean (SD) systolic BP (SBP) reductions were 20.1 (15.5) mm Hg and diastolic BP (DBP) reductions were 9.8 (10.3) mm Hg, with higher reductions among high-risk patients. SBP, DBP, and SBP/DBP control rates were 33.3%, 45.3%, and 25.5%, respectively, with lower rates among high-risk patients. Mean TCVR improvement was a reduction of 0.73 (0.96) classes (-4 [best] to +4 [worst]), with higher reductions for high-risk patients; 58.2% of patients achieved a TCVR reduction of 1 or more classes, with lower percentages for high-risk patients. Twenty-two percent of systolic variability and 26% of diastolic variability in 90-day BP values were attributable to a physician class effect, as was 16% of TCVR change. CONCLUSIONS: Regimens that include SPC amlodipine/valsartan formulations are effective in reducing BP and TCVR in a real-world observational setting. Hierarchical modeling identified patient- and physician-related determinants of BP values and TCVR change, as well as independent predictors of uncontrolled BP and reduced TCVR. TCVR is a scientifically feasible and clinically relevant effectiveness outcome of antihypertensive treatment.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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