Aggressive BP lowering may prevent LV conduction disease: Sprint

Written By :  Dr. Kamal Kant Kohli
Published On 2022-05-03 05:21 GMT   |   Update On 2022-05-03 05:21 GMT

Aggressive blood pressure (BP) control reduced the risk of left-ventricular conduction disease, finds a new clinical trial. The study is the first to provide causal evidence that cardiac conduction disease is preventable, according to researchers. The findings of the study were presented as a late-breaking clinical trial at the Heart Rhythm Society's annual Heart Rhythm meeting (HRS 2022,...

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Aggressive blood pressure (BP) control reduced the risk of left-ventricular conduction disease, finds a new clinical trial. The study is the first to provide causal evidence that cardiac conduction disease is preventable, according to researchers.

The findings of the study were presented as a late-breaking clinical trial at the Heart Rhythm Society's annual Heart Rhythm meeting (HRS 2022, 29 April–1 May, San Francisco, USA).

Conduction diseases are heart rhythm disorders that impact how electrical impulses travel through the heart. Left-ventricular conduction disease, which can appear as left bundle branch block (LBBB) or fascicular block, is a common disorder detected by routine EKG that can lead to heart failure, complete heart block and the need for a permanent pacemaker. Today, no strategies exist to help prevent the risk of left ventricular conduction disease. This trial sought to determine whether aggressive BP control could potentially serve as a preventative strategy and reduce patient risk for incident left ventricular conduction disease.

The study used the Systolic Blood Pressure Intervention Trial (SPRINT) and randomized 3,918 hypertensive patients to standard BP treatment (target systolic BP < 140 mm Hg) and 3,956 participants to intensive BP treatment (target systolic BP < 120 mm Hg). The mean age was 67.6 ± 9.2 years and patients were observed for an average 3.5 years. Researchers used serial 12- lead electrocardiograms to track the development of left ventricular conduction disease and new ventricular pacing, examining the incidence of right bundle branch as a negative control.

Among all of the participants, 203 developed left-ventricular conduction disease. Random assignment to intensive BP control was associated with a 26% lower risk of left-ventricular conduction disease (HR 0.74, 95% CI 0.56-0.98, P=0.038). Additionally, older age (HR 1.04, 95% CI 1.02-1.05, p=0.001), male sex (HR 2.31, 95% CI 1.63-3.32, p=0.001), and cardiovascular disease (HR 1.46, 95% CI 1.06-2.00, p=0.02) were associated with a heightened risk of developing LBBB or fascicular block. The statistically significant results persisted when incident ventricular pacing was included in the outcome. No relationship between randomization assignment and a negative control, right ventricular conduction disease, was observed (HR 0.95, 95% CI 0.71-1.27, p=0.75).

"Patient questions around how and why they were diagnosed with left ventricular conduction disease and the need to offer better answers inspired this study. We sought to uncover a prevention strategy for this common disorder," said senior author, Gregory Marcus, MD, MAS, University of California, San Francisco. "Before our trial, earlier studies were strictly observational. We hope these results will drive even more research dedicated to identifying modifiable characteristics of conduction disease and studying interventions that could help reduce patient risk."

The authors of this trial believe that future efforts to mitigate the development and progression of conduction disease could change guidelines around diagnosis and treatment of the condition as well as the clinical perception of the disease. They also call for additional studies to further understand how a reduction in conduction disease could impact the need for antihypertensive medications and other therapies.

Reference: Marcus GM. Effect of intensive versus standard blood pressure treatment on incident left ventricular conduction disease. Presented at: HRS 2022. April 29, 2022. San Francisco, CA.

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