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Initial combination therapy reduces the risk of cardiovascular events in hypertensive patients: a matched cohort
Alan H Gradman1, Hélène Parisé, Patrick Lefebvre
1Temple University School of Medicine, 1239 Shady Ave, Pittsburgh, PA 15232, USA. gradmana@temple.edu
Insights
Starting combination therapy for hypertension early significantly reduces cardiovascular events. Rapidly achieving target blood pressure is key to this risk reduction, improving patient outcomes.
Area of Science:
- Cardiology
- Pharmacology
- Public Health
Background:
- Time to blood pressure (BP) control impacts long-term cardiovascular (CV) outcomes in hypertension.
- Real-world evidence on initial versus delayed combination therapy for hypertension is limited.
Purpose of the Study:
- To evaluate the impact of initial versus delayed combination therapy on BP control and CV event risk in hypertensive patients.
- To assess the association between rapid BP control and reduced CV event risk.
Main Methods:
- Retrospective analysis of 1762 adult hypertensive patients using electronic medical charts (2005-2009).
- Comparison of patients initiating immediate combination therapy versus those initially on monotherapy then switched.
- Utilized incidence rate ratios, Kaplan-Meier analysis, and time-varying Cox proportional hazard models.
Main Results:
- Initial combination therapy significantly reduced the risk of CV events or death by 34% (IRR, 0.66; P=0.0008).
- 40.3% of patients on initial combination therapy achieved BP control within 6 months versus 32.6% on delayed therapy.
- Achieving target BP significantly reduced CV event/death risk by 23% (HR, 0.77; P=0.0223).
Conclusions:
- Initial combination therapy for hypertension is associated with a significant reduction in cardiovascular events.
- Faster achievement of target blood pressure is the primary driver of the observed risk reduction with early combination therapy.
Abstract:
This study evaluated the effects of initial versus delayed treatment with a drug combination on blood pressure (BP) control and the risk of cardiovascular (CV) events in hypertensive patients. Clinical trials suggest that the time to BP control is an important determinant of long-term outcomes, but real-world evidence is scarce. Using electronic medical charts (2005-2009), we retrospectively analyzed 1762 adult patients with BP elevation initiating combination therapy matched 1:1 with similar patients initiating monotherapy and later switched to combination therapy. Incidence rate ratios of CV events (myocardial infarction, stroke/transient ischemic attack, or hospitalization for heart failure) or all-cause death and Kaplan-Meier analyses of time to BP control were compared between cohorts. Hazard ratios indicating the effects of initial treatment on CV events and BP control were estimated using time-varying Cox proportional hazard models. Initial combination therapy was associated with a significant reduction in the risk of CV events or death (incidence rate ratio, 0.66 [95% confidence interval, 0.52-0.84]; P=0.0008). After 6 months of therapy, 40.3% and 32.6% of patients with initial versus delayed combination treatment reached BP control, respectively. Achieving target BP was associated with a statistically significant risk reduction of 23% for CV events or death (hazard ratio, 0.77 [95% confidence interval, 0.61-0.96]; P=0.0223); the residual effect of initial combination therapy did not reach statistical significance (hazard ratio, 0.84 [95% confidence interval, 0.68-1.03]; P=0.0935). Initial combination therapy was associated with a significant risk reduction of cardiovascular events. More rapid achievement of target BP was found to be the main contributor to the estimated risk reduction.
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