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Pacemaker-Mediated Programmable Hypertension Control Therapy
P. Neuzil, B. Merkely, A. Erglis, G. Marinskis, JR. de Groot, H. Schmidinger, M. Rodriguez Venegas, M. Voskuil, T. Sturmberger, J. Petru, N. Jongejan, J. Aichinger, G. Kamzola, A. Aidietis, L. Gellér, T. Mraz, I. Osztheimer, Y. Mika, S. Evans, D....
Language English Country England, Great Britain
Document type Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't
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- MeSH
- Blood Pressure Monitoring, Ambulatory methods MeSH
- Hypertension physiopathology therapy MeSH
- Pacemaker, Artificial * MeSH
- Blood Pressure physiology MeSH
- Humans MeSH
- Follow-Up Studies MeSH
- Prospective Studies MeSH
- Aged MeSH
- Heart Rate physiology MeSH
- Treatment Outcome MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Randomized Controlled Trial MeSH
BACKGROUND: Many patients requiring a pacemaker have persistent hypertension with systolic blood pressures above recommended levels. We evaluated a pacemaker-based Programmable Hypertension Control (PHC) therapy that uses a sequence of variably timed shorter and longer atrioventricular intervals. METHODS AND RESULTS: Patients indicated for dual-chamber pacing with office systolic blood pressure (oSBP) >150 mm Hg despite stable medical therapy were implanted with a ModeratoTM pulse generator that delivers PHC therapy. Patients were followed for 1 month (Run-In period) with conventional pacing; those with persistent oSBP >140 mm Hg were included in the study and had PHC therapy activated. The co-primary efficacy end points were changes in 24-hour ambulatory systolic blood pressure and oSBP between baseline and 3 months. Safety was assessed by tracking adverse events. Thirty-five patients met the initial inclusion criteria and underwent Moderato implantation. At 1 month, oSBP was <140 mm Hg in 7 patients who were excluded. PHC was activated in the remaining 27 patients with baseline office blood pressure 166±11/80±10 mm Hg despite an average of 3.2 antihypertensive medications. During the Run-In period, oSBP and 24-hour ambulatory systolic blood pressure decreased by 8±13 and 5±12 mm Hg (P<0.002), respectively. Compared with pre-PHC activation measurements, oSBP decreased by another 16±15 mm Hg and 24-hour ambulatory systolic blood pressure decreased by an additional 10±13 mm Hg (both P<0.01) at 3 months. No device-related serious adverse effects were noted. CONCLUSIONS: In pacemaker patients with persistent hypertension despite medical therapy, oSBP and 24-hour ambulatory systolic blood pressure are decreased by PHC therapy. Initial indications are that this therapy is a safe and promising therapy for such patients. CLINICAL TRIAL REGISTRATION: URL: http://www.clinicaltrials.gov. Unique identifier: NCT02282033.
Asklepios Klinik St Georg Hamburg Germany
Cardiovascular Research Foundation New York City NY
Department of Cardiology Academic Medical Center Amsterdam The Netherlands
Department of Cardiology University Medical Center Utrecht Utrecht The Netherlands
Heart and Vascular Center Semmelweis University Budapest Budapest Hungary
Hospital Dr Sótero del Río Puente Alto Santiago Chile
Latvian Centre of Cardiology Pauls Stradins Clinical University Hospital Riga Latvia
Na Homolce Hospital Prague Czech Republic
Vilnius University Hospital Santariskiu Klinikos Vilnius Lithuania
References provided by Crossref.org
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