Impact of selected comorbidities on the presentation and management of aortic stenosis.


Journal

Open heart
ISSN: 2053-3624
Titre abrégé: Open Heart
Pays: England
ID NLM: 101631219

Informations de publication

Date de publication:
07 2020
Historique:
received: 19 02 2020
revised: 26 03 2020
accepted: 02 06 2020
entrez: 26 7 2020
pubmed: 28 7 2020
medline: 22 12 2020
Statut: ppublish

Résumé

Contemporary data regarding the impact of comorbidities on the clinical presentation and management of patients with severe aortic stenosis (AS) are scarce. Prospective registry of severe patients with AS across 23 centres in nine European countries. Of the 2171 patients, chronic kidney disease (CKD 27.3%), left ventricular ejection fraction (LVEF) <50% (22.0%), atrial fibrillation (15.9%) and chronic obstructive pulmonary disease (11.4%) were the most prevalent comorbidities (49.3% none, 33.9% one and 16.8% ≥2 of these). The decision to perform aortic valve replacement (AVR) was taken in a comparable proportion (67%, 72% and 69%, in patients with 0, 1 and ≥2 comorbidities; p=0.186). However, the decision for TAVI was more common with more comorbidities (35.4%, 54.0% and 57.0% for no, 1 and ≥2; p<0.001), while the decision for surgical AVR (SAVR) was decreased with increasing comorbidity burden (31.9%, 17.4% and 12.3%; p<0.001). The proportion of patients with planned AVRs that were performed within 3 months was significantly higher in patients with 1 or ≥2 comorbidities than in those without (8.7%, 10.0% and 15.7%; p<0.001). Furthermore, the mean time to AVR was significantly shorter in patients with one (30.5 days) or ≥2 comorbidities (30.8 days) than in those without (35.7 days; p=0.012). Patients with reduced LVEF tended to be offered an AVR more frequently and with a shorter delay while patients with CKD were less frequently treated. Comorbidities in severe patients with AS affect the presentation and management of patients with severe AS. TAVI was offered more often than SAVR and performed within a shorter time period.

Sections du résumé

BACKGROUND
Contemporary data regarding the impact of comorbidities on the clinical presentation and management of patients with severe aortic stenosis (AS) are scarce.
METHODS
Prospective registry of severe patients with AS across 23 centres in nine European countries.
RESULTS
Of the 2171 patients, chronic kidney disease (CKD 27.3%), left ventricular ejection fraction (LVEF) <50% (22.0%), atrial fibrillation (15.9%) and chronic obstructive pulmonary disease (11.4%) were the most prevalent comorbidities (49.3% none, 33.9% one and 16.8% ≥2 of these). The decision to perform aortic valve replacement (AVR) was taken in a comparable proportion (67%, 72% and 69%, in patients with 0, 1 and ≥2 comorbidities; p=0.186). However, the decision for TAVI was more common with more comorbidities (35.4%, 54.0% and 57.0% for no, 1 and ≥2; p<0.001), while the decision for surgical AVR (SAVR) was decreased with increasing comorbidity burden (31.9%, 17.4% and 12.3%; p<0.001). The proportion of patients with planned AVRs that were performed within 3 months was significantly higher in patients with 1 or ≥2 comorbidities than in those without (8.7%, 10.0% and 15.7%; p<0.001). Furthermore, the mean time to AVR was significantly shorter in patients with one (30.5 days) or ≥2 comorbidities (30.8 days) than in those without (35.7 days; p=0.012). Patients with reduced LVEF tended to be offered an AVR more frequently and with a shorter delay while patients with CKD were less frequently treated.
CONCLUSIONS
Comorbidities in severe patients with AS affect the presentation and management of patients with severe AS. TAVI was offered more often than SAVR and performed within a shorter time period.

Identifiants

pubmed: 32709699
pii: openhrt-2020-001271
doi: 10.1136/openhrt-2020-001271
pmc: PMC7380845
pii:
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: PB is the representative of the IPPMed, Cloppenburg, Germany. NF, RPS, DM-Z and TKR are consultants to Edwards Lifesciences. The institutions of these three and those of the remaining authors representing study centres have received funding for employing a study nurse.

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Auteurs

Tanja K Rudolph (TK)

Department of Cardiology, Heart and Diabetes Center Bad Oeynhausen, Ruhr-University of Bochum, Bad Oeynhausen, Germany tk.rudolph@me.com.

David Messika-Zeitoun (D)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Norbert Frey (N)

Department of Cardiology and Angiology, University of Kiel, Kiel, Germany.

Jeetendra Thambyrajah (J)

James Cook University Hospital, Middlesbrough, Middlesbrough, UK.

Antonio Serra (A)

Interventional Cardiology Unit, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Eberhard Schulz (E)

Cardiology Department, AKH Celle, Celle, Germany.

Jiri Maly (J)

Department of Cardiovascular Surgery, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Department of Cardiovascular Surgery, Second Faculty of Medicine, Charles University, Prague, Czech Republic.

Marco Aiello (M)

Department of Cardiothoracic Surgery, Foundation IRCCS Policlinico S.Matteo, Pavia, Italy.

Guy Lloyd (G)

St Bartholomew's Hospital, London, UK.

Alessandro Santo Bortone (AS)

University of Bari, Bari, Italy.

Alberto Clerici (A)

University of Turin, Turin, Italy.

Georg Delle-Karth (G)

4th Medical Department, Hietzing Hospital, Vienna, Austria.

Johannes Rieber (J)

Herzkatheterlabor Nymphenburg and Department of Cardiology, University of Munich, Munich, Germany.

Ciro Indolfi (C)

Division of Cardiology and URT CNR of IFC, Magna Graecia University, Catanzaro, Italy.

Massimo Mancone (M)

Sapienza University of Rome, Rome, Italy.

Loic Belle (L)

Centre Hospital d'Annecy, Annecy, France.

Alexander Lauten (A)

German Centre for Cardiovascular Research (DZHK), University Heart Center & Charité, Berlin, Germany.

Martin Arnold (M)

Department of Cardiology, University of Erlangen, Erlangen, Germany.

Berto J Bouma (BJ)

University of Amsterdam, Amsterdam, Netherlands.

Matthias Lutz (M)

Department of Cardiology and Angiology, University of Kiel, Kiel, Germany.

Cornelia Deutsch (C)

Institute for Pharmacology and Preventive Medicine, Cloppenburg, Germany.

Jana Kurucova (J)

Edwards Lifesciences, Prague, Czech Republic.

Martin Thoenes (M)

Edwards Lifesciences, Nyon, Switzerland.

Peter Bramlage (P)

Institute for Pharmacology and Preventive Medicine, Cloppenburg, Germany.

Richard P Steeds (RP)

Queen Elizabeth Hospital & Institute of Cardiovascular Sciences, University of Birmingham, Birmingham, UK.

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