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Design of the Blood Pressure Goals in Dialysis pilot study
Ambreen Gul1, Dana Miskulin, Jennifer Gassman
1Department of Medicine (AG, AH, BH, EB, PZ), University of New Mexico, Albuquerque, New Mexico; Department of Medicine (DM), Tufts University, Boston, Massachusetts; Department of Quantitative Health Sciences (JG), Cleveland Clinic Foundation, Cleveland, Ohio; Department of Medicine (JC), Boston University, Boston, Massachusetts; Dialysis Clinic, Inc (SP, PZ), Quality Management, Albuquerque, New Mexico; National Institutes of Health (JWK), NIDDK, Bethesda, Maryland; and Department of Medicine (MU), University of Pittsburgh, Pittsburgh, Pennsylvania.
Insights
This pilot study investigates optimal blood pressure (BP) targets for hemodialysis (HD) patients to reduce cardiovascular disease (CVD) risk. Findings will inform a larger trial on BP management in HD populations.
Area of Science:
- Nephrology
- Cardiology
- Clinical Trials
Background:
- Cardiovascular disease (CVD) risk is significantly elevated in hemodialysis (HD) patients.
- Current guidelines for predialysis systolic blood pressure (SBP) < 140 mm Hg in HD patients lack robust evidence.
- Existing trials are small and lack prespecified BP targets.
Purpose of the Study:
- To assess the feasibility and safety of targeting different predialysis systolic blood pressure (SBP) levels in hemodialysis patients.
- To inform the design of a larger, powered clinical trial for definitive outcomes.
Main Methods:
- Pilot, multicenter randomized controlled trial (RCT) comparing two predialysis SBP targets: 110-140 mm Hg versus 155-165 mm Hg.
- Primary outcomes: feasibility (recruitment, retention, adherence, target achievement) and safety (hypotension, adverse events).
- Secondary outcomes: preliminary data on left ventricular mass, aortic pulse wave velocity, vascular access thromboses, and quality of life.
Main Results:
- Feasibility and safety data are being collected to evaluate the study's viability.
- Preliminary data on secondary outcomes across study arms are being analyzed.
- The pilot study is designed to determine the parameters for a full-scale trial.
Conclusions:
- Data from this pilot RCT will establish feasibility and safety.
- Findings will guide the design of a full-scale trial, potentially requiring 2000 participants.
- This research aims to optimize blood pressure management in hemodialysis patients to reduce CVD disparities.
Background:
Cardiovascular disease (CVD) is markedly increased among hemodialysis (HD) patients. Optimizing blood pressure (BP) among HD patients may present an important opportunity to reduce the disparity in CVD rates between HD patients and the general population. The optimal target predialysis systolic BP (SBP) among HD patients is unknown. Current international guidelines, calling for a predialysis SBP < 140 mm Hg, are based on the opinion and extrapolation from the general population. Existing randomized controlled trials (RCTs) were small and did not include prespecified BP targets.
Methods:
The authors described the design of the Blood Pressure in Dialysis (BID) Study, a pilot, multicenter RCT where HD patients are randomized to either a target-standardized predialysis SBP of 110 to 140 mm Hg or 155 to 165 mm Hg. This is the first study to randomize HD patients to 2 different SBP targets.
Results:
Primary outcomes are feasibility and safety. Feasibility parameters include recruitment and retention rates, adherence with prescribed BP measurements and achievement and maintenance of selected BP targets. Safety parameters include rates of hypotension and other adverse and serious adverse events. The authors obtained preliminary data on changes in left ventricular mass, aortic pulse wave velocity, vascular access thromboses and health-related quality of life across study arms, which may be the secondary outcomes in the full-scale study.
Conclusions:
The data acquired in the pilot RCT will determine the feasibility and safety and inform the design of a full-scale trial, powered for hard outcomes, which may require 2000 participants.
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