Alcohol-mediated renal denervation in patients with hypertension in the absence of antihypertensive medications.


Journal

EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology
ISSN: 1969-6213
Titre abrégé: EuroIntervention
Pays: France
ID NLM: 101251040

Informations de publication

Date de publication:
18 Sep 2023
Historique:
pmc-release: 18 09 2024
medline: 19 9 2023
pubmed: 10 7 2023
entrez: 10 7 2023
Statut: ppublish

Résumé

Ultrasound and radiofrequency renal denervation (RDN) have been shown to safely lower blood pressure (BP) in hypertension. The TARGET BP OFF-MED trial investigated the efficacy and safety of alcohol-mediated renal denervation (RDN) in the absence of antihypertensive medications. This randomised, blinded, sham-controlled trial was conducted in 25 centres in Europe and the USA. Patients with a 24-hour systolic BP of 135-170 mmHg, an office systolic BP 140-180 mmHg and diastolic BP ≥90 mmHg on 0-2 antihypertensive medications were enrolled. The primary efficacy endpoint was the change in mean 24-hour systolic BP at 8 weeks. Safety endpoints included major adverse events up to 30 days. A total of 106 patients were randomised; the baseline mean office BP following medication washout was 159.4/100.4±10.9/7.0 mmHg (RDN) and 160.1/98.3±11.0/6.1 mmHg (sham), respectively. At 8 weeks post-procedure, the mean (±standard deviation) 24-hour systolic BP change was â2.9±7.4 mmHg (p=0.009) versus â1.4±8.6 mmHg (p=0.25) in the RDN and sham groups, respectively (mean between-group difference: 1.5 mmHg; p=0.27). There were no differences in safety events between groups. After 12 months of blinded follow-up, with medication escalation, patients achieved similar office systolic BP (RDN: 147.9±18.5 mmHg; sham: 147.8±15.1 mmHg; p=0.68) with a significantly lower medication burden in the RDN group (mean daily defined dose: 1.5±1.5 vs 2.3±1.7; p=0.017). In this trial, alcohol-mediated RDN was delivered safely but was not associated with significant BP differences between groups. Medication burden was lower in the RDN group up to 12 months.

Sections du résumé

BACKGROUND BACKGROUND
Ultrasound and radiofrequency renal denervation (RDN) have been shown to safely lower blood pressure (BP) in hypertension.
AIMS OBJECTIVE
The TARGET BP OFF-MED trial investigated the efficacy and safety of alcohol-mediated renal denervation (RDN) in the absence of antihypertensive medications.
METHODS METHODS
This randomised, blinded, sham-controlled trial was conducted in 25 centres in Europe and the USA. Patients with a 24-hour systolic BP of 135-170 mmHg, an office systolic BP 140-180 mmHg and diastolic BP ≥90 mmHg on 0-2 antihypertensive medications were enrolled. The primary efficacy endpoint was the change in mean 24-hour systolic BP at 8 weeks. Safety endpoints included major adverse events up to 30 days.
RESULTS RESULTS
A total of 106 patients were randomised; the baseline mean office BP following medication washout was 159.4/100.4±10.9/7.0 mmHg (RDN) and 160.1/98.3±11.0/6.1 mmHg (sham), respectively. At 8 weeks post-procedure, the mean (±standard deviation) 24-hour systolic BP change was â2.9±7.4 mmHg (p=0.009) versus â1.4±8.6 mmHg (p=0.25) in the RDN and sham groups, respectively (mean between-group difference: 1.5 mmHg; p=0.27). There were no differences in safety events between groups. After 12 months of blinded follow-up, with medication escalation, patients achieved similar office systolic BP (RDN: 147.9±18.5 mmHg; sham: 147.8±15.1 mmHg; p=0.68) with a significantly lower medication burden in the RDN group (mean daily defined dose: 1.5±1.5 vs 2.3±1.7; p=0.017).
CONCLUSIONS CONCLUSIONS
In this trial, alcohol-mediated RDN was delivered safely but was not associated with significant BP differences between groups. Medication burden was lower in the RDN group up to 12 months.

Identifiants

pubmed: 37427416
pii: EIJ-D-23-00088
doi: 10.4244/EIJ-D-23-00088
pmc: PMC10493775
pii:
doi:

Substances chimiques

Antihypertensive Agents 0
Ethanol 3K9958V90M

Types de publication

Randomized Controlled Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

602-611

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Auteurs

Atul Pathak (A)

Department of Cardiovascular Medicine, Princess Grace Hospital, Principality of Monaco.

Ulrike M Rudolph (UM)

Klinik und Poliklinik für Kardiologie, Universitätsklinikum Leipzig, Universität Leipzig, Leipzig, Germany.

Manish Saxena (M)

Barts NIHR Biomedical Research Centre, William Harvey Research Institute, Queen Mary University of London, London, UK.

Thomas Zeller (T)

Universitäts-Herzzentrum Bad Krozingen, Bad Krozingen, Germany.

Jochen Müller-Ehmsen (J)

Asklepios Klinik Altona, Hamburg, Germany.

Erik Lipsic (E)

Department of Cardiology, University Medical Center Groningen, Groningen, the Netherlands.

Roland E Schmieder (RE)

Universitätsklinikum Erlangen, Erlangen, Germany and Friedrich Alexander University Erlangen/Nürnberg, Erlangen, Germany.

Horst Sievert (H)

CardioVasculäres Centrum (CVC) Frankfurt, Frankfurt, Germany.

Marcel Halbach (M)

University of Cologne, Faculty of Medicine and University Hospital Cologne, Clinic III for Internal Medicine, Cologne, Germany and Herzzentrum der Uniklinik Koln, Koln, Germany.

Faisal Sharif (F)

Saolta University Healthcare Group, University Hospital Galway, Galway, Ireland.

Helen Parise (H)

Yale University School of Medicine, New Haven, CT, USA.

Tim A Fischell (TA)

Ablative Solutions Inc., Wakefield, MA, USA.

Michael A Weber (MA)

Division of Cardiovascular Medicine, State University of New York (SUNY), New York, NY, USA.

David E Kandzari (DE)

Department of Interventional Cardiology, Piedmont Heart Institute, Atlanta, GA, USA.

Felix Mahfoud (F)

Department of Internal Medicine III - cardiology, angiology and internal intensive care medicine, Saarland University Medical Center, Homburg, Germany.
Institute for Medical Engineering and Science, Massachusetts Institute of Technology, Cambridge, MA, USA.

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Classifications MeSH