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An exploratory propensity score matched comparison of second-generation and first-generation baroreflex activation therapy systems.
- Source :
-
Journal of the American Society of Hypertension : JASH [J Am Soc Hypertens] 2017 Feb; Vol. 11 (2), pp. 81-91. Date of Electronic Publication: 2016 Dec 16. - Publication Year :
- 2017
-
Abstract
- Baroreflex activation therapy (BAT) is a device-based therapy for patients with treatment-resistant hypertension. In a randomized, controlled trial, the first-generation system significantly reduced blood pressure (BP) versus sham. Although an open-label validation study of the second-generation system demonstrated similar BP reductions, controlled data are not presently available. Therefore, this investigation compares results of first- and second-generation BAT systems. Two cohorts of first-generation BAT system patients were generated with propensity matching to compare against the validation group of 30 second-generation subjects. The first cohort was drawn from the first-generation randomized trial sham group and the second cohort from the active therapy group. Safety and efficacy were compared for the second-generation group relative to the first generation. At 6 months, second-generation BAT outperformed first-generation sham systolic BP reduction by 20 ± 28 mm Hg (mean ± standard deviation, P = .008), while BP reduction in first- and second-generation active groups was similar. At 12 months, efficacy was comparable between all three groups after the sham group had received 6 months of therapy; 47% of second-generation patients achieved goal systolic BP of 140 mm Hg or less after 12 months, comparable to 50% of patients at goal in the first-generation group (P > .999). Implant procedure time, system/procedural safety, and pulse generator longevity improved with the second-generation system. Propensity-matched cohort analysis of the first- and second-generation BAT systems suggests similar therapeutic benefit and superior BP reduction of the second-generation system relative to sham control. Implantation procedure duration and perioperative safety were improved with the second-generation device. These findings should be validated in a prospective randomized trial.<br /> (Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Aged
Antihypertensive Agents therapeutic use
Baroreflex physiology
Blood Pressure Determination
Electric Stimulation Therapy adverse effects
Equipment Design
Female
Humans
Male
Middle Aged
Operative Time
Propensity Score
Randomized Controlled Trials as Topic
Retrospective Studies
Treatment Outcome
Coronary Vasospasm therapy
Electric Stimulation Therapy instrumentation
Electric Stimulation Therapy methods
Electrodes, Implanted
Hypertension therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1878-7436
- Volume :
- 11
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Journal of the American Society of Hypertension : JASH
- Publication Type :
- Academic Journal
- Accession number :
- 28065708
- Full Text :
- https://doi.org/10.1016/j.jash.2016.12.003