Pacemaker-Based Cardiac Neuromodulation Therapy in Patients With Hypertension: A Pilot Study
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, multicentrická studie, randomizované kontrolované studie, práce podpořená grantem
PubMed
34387126
PubMed Central
PMC8475046
DOI
10.1161/jaha.120.020492
Knihovny.cz E-zdroje
- Klíčová slova
- atrioventricular interval, hypertension, left ventricular function, pacemaker,
- MeSH
- časové faktory MeSH
- dvojitá slepá metoda MeSH
- funkce levé komory srdeční MeSH
- hypertenze diagnóza patofyziologie terapie MeSH
- kardiostimulace umělá * škodlivé účinky MeSH
- kardiostimulátor * MeSH
- krevní tlak * MeSH
- lidé MeSH
- pilotní projekty MeSH
- prospektivní studie MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- srdce inervace MeSH
- srdeční frekvence * MeSH
- výsledek terapie MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
- Geografické názvy
- Evropa MeSH
Background In prior unblinded studies, cardiac neuromodulation therapy (CNT) employing a sequence of variably timed short and longer atrioventricular intervals yielded sustained reductions of systolic blood pressure (SBP) in patients with hypertension. The effects of CNT on SBP were investigated in this double-blind randomized pilot study. Methods and Results Eligible patients had daytime ambulatory SBP (aSBP) ≥130 mm Hg and office SBP ≥140 mm Hg despite taking ≥1 antihypertensive medication, and an indication for a dual-chamber pacemaker. Patients underwent Moderato device implantation, which was programmed as a standard pacemaker during a 1-month run-in phase. Patients whose daytime aSBP was ≥125 mm Hg at the end of this period were randomized (1:1, double blind) to treatment (CNT) or control (CNT inactive). The primary efficacy end point was the between-group difference of the change in 24-hour aSBP at 6 months. Of 68 patients initially enrolled and who underwent implantation with the Moderato system, 47 met criteria for study continuation and were randomized (26 treatment, 21 control). The mean age was 74.0±8.7 years, 64% were men, left ventricular ejection fraction was 59.2%±5.7%, and aSBP averaged 141.0±10.8 mm Hg despite the use of 3.3±1.5 antihypertensive medications; 81% had isolated systolic hypertension. Six months after randomization, aSBP was 11.1±10.5 mm Hg (95% CI, -15.2 to -8.1 mm Hg) lower than prerandomization in the treatment group compared with 3.1±9.5 mm Hg (-7.4 to 1.2 mm Hg) lower in controls, yielding a net treatment effect of 8.1±10.1 mm Hg (-14.2 to -1.9 mm Hg) (P=0.012). There were no Moderato device- or CNT-related adverse events. Conclusions CNT significantly reduced 24-hour aSBP in patients with hypertension with a clinical indication for a pacemaker. The majority of patients had isolated systolic hypertension, a particularly difficult group of patients to treat. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT02837445.
1st Chair and Department of Cardiology Medical University of Warsaw Poland
1st Department of Cardiology Karol Marcinkowski University of Medical Sciences Poznań Poland
Cardiovascular Research Foundation New York NY
Department of Cardiology DMS in ZabrzeMedical University of Silesia Katowice Poland
Department of Cardiology Na Homolce Hospital Prague Czech Republic
Department of Cardiology Pomeranian Medical University Szczecin Poland
Department of Physics and Astronomy Hofstra University Hempstead NY
Division of Science Mathematics and Computing Bard College at Simon's Rock Great Barrington MA
Heart and Vascular Center Semmelweis University Budapest Hungary
Pauls Stradins Clinical University Hospital University of Latvia Riga Latvia
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ClinicalTrials.gov
NCT02837445