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European Society of Hypertension position paper on renal denervation 2021.

Authors :
UCL - SSS/IREC/CARD - Pôle de recherche cardiovasculaire
UCL - (SLuc) Département cardiovasculaire
Schmieder, Roland E
Mahfoud, Felix
Mancia, Giuseppe
Azizi, Michael
Böhm, Michael
Dimitriadis, Kyriakos
Kario, Kazuomi
Kroon, Abraham A
D Lobo, Melvin
Ott, Christian
Pathak, Atul
Persu, Alexandre
Scalise, Filippo
Schlaich, Markus
Kreutz, Reinhold
Tsioufis, Costas
members of the ESH Working Group on Device-Based Treatment of Hypertension
UCL - SSS/IREC/CARD - Pôle de recherche cardiovasculaire
UCL - (SLuc) Département cardiovasculaire
Schmieder, Roland E
Mahfoud, Felix
Mancia, Giuseppe
Azizi, Michael
Böhm, Michael
Dimitriadis, Kyriakos
Kario, Kazuomi
Kroon, Abraham A
D Lobo, Melvin
Ott, Christian
Pathak, Atul
Persu, Alexandre
Scalise, Filippo
Schlaich, Markus
Kreutz, Reinhold
Tsioufis, Costas
members of the ESH Working Group on Device-Based Treatment of Hypertension
Source :
Journal of hypertension, Vol. 39, no.9, p. 1733-1741 (2021)
Publication Year :
2021

Abstract

This ESH Position Paper 2021 with updated proposed recommendations was deemed necessary after the publication of a set of new pivotal sham-controlled randomized clinical trials (RCTs), which provided important information about the efficacy and safety of endovascular device-based renal denervation (RDN) for hypertension treatment. RDN is effective in reducing or interrupting the sympathetic signals to the kidneys and decreasing whole body sympathetic activity. Five independent, fully completed, sham-controlled RCTs provide conclusive evidence that RDN lowers ambulatory and office blood pressure (BP) to a significantly greater extent than sham treatment. BP-lowering efficacy is evident both in patients with and without concomitant antihypertensive medication. The average decrease of 10 mmHg in office BP is estimated to lower the incidence of cardiovascular events by 25-30%, based on meta-analyses of RCTs using pharmacological treatment. Neither peri-procedural, nor short-term or long-term adverse events or safety signals (available up to 3 years) have been observed. Implementing RDN as an innovative third option in the armamentarium of antihypertensive treatment requires a structured process that ensures the appropriate performance of the endovascular RDN procedure and adequate selection of hypertensive patients. The latter should also incorporate patients' perspective and preference that needs to be respected in a shared decision-making process.

Details

Database :
OAIster
Journal :
Journal of hypertension, Vol. 39, no.9, p. 1733-1741 (2021)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1372962742
Document Type :
Electronic Resource