Outcomes in patients with moderate and asymptomatic severe aortic stenosis followed up in heart valve clinics.


Journal

Heart (British Cardiac Society)
ISSN: 1468-201X
Titre abrégé: Heart
Pays: England
ID NLM: 9602087

Informations de publication

Date de publication:
27 03 2023
Historique:
received: 12 09 2022
accepted: 17 11 2022
medline: 9 8 2023
pubmed: 5 1 2023
entrez: 4 1 2023
Statut: epublish

Résumé

Heart valve clinics (HVC) have been introduced to manage patients with valvular heart disease within a multidisciplinary team. To determine the outcome benefit of HVC approach compared with standard of care (SOC) for patients with moderate and asymptomatic severe aortic stenosis (mAS and asAS). Single-centre, observational registry of patients with mAS and asAS with at least one cardiac ambulatory consultation at our Cardiovascular Centre. Based on the outpatient strategy, patients were divided into HVC group, if receiving at least one visit at HVC, and SOC group, if followed by routine cardiac consultations. 2129 patients with mAS and asAS were divided into those followed in HVC (n=251) versus SOC group (n=1878). The mean age was 76.5±12.4 years; 919 (43.2%) had asAS. During a follow-up of 4.8±1.8 years, 822 patients (38.6%) died, 307 (14.4%) were hospitalised for heart failure and 596 (28%) underwent aortic valve replacement (AVR). After propensity score matching, the number of consultations per year, exercise stress tests, brain natriuretic peptide (BNP) determinations and CTs were higher in the HVC cohort (p<0.05 for all). A shorter time between indication of AVR and less advanced New York Heart Association class was reported in the HVC cohort (p<0.001 and p=0.032). Compared with SOC, the HVC approach was associated with reduced all-cause mortality (HR=0.63, 95% CI 0.40 to 0.98, p=0.038) and cardiovascular death (p=0.030). At multivariable analysis, the HVC remained an independent predictor of all-cause mortality (HR=0.54, 95% CI 0.34 to 0.85, p=0.007). In patients with mAS and asAS, the HVC approach was associated with more efficient management and outcome benefit compared with SOC.

Sections du résumé

BACKGROUND
Heart valve clinics (HVC) have been introduced to manage patients with valvular heart disease within a multidisciplinary team.
OBJECTIVE
To determine the outcome benefit of HVC approach compared with standard of care (SOC) for patients with moderate and asymptomatic severe aortic stenosis (mAS and asAS).
METHODS
Single-centre, observational registry of patients with mAS and asAS with at least one cardiac ambulatory consultation at our Cardiovascular Centre. Based on the outpatient strategy, patients were divided into HVC group, if receiving at least one visit at HVC, and SOC group, if followed by routine cardiac consultations.
RESULTS
2129 patients with mAS and asAS were divided into those followed in HVC (n=251) versus SOC group (n=1878). The mean age was 76.5±12.4 years; 919 (43.2%) had asAS. During a follow-up of 4.8±1.8 years, 822 patients (38.6%) died, 307 (14.4%) were hospitalised for heart failure and 596 (28%) underwent aortic valve replacement (AVR). After propensity score matching, the number of consultations per year, exercise stress tests, brain natriuretic peptide (BNP) determinations and CTs were higher in the HVC cohort (p<0.05 for all). A shorter time between indication of AVR and less advanced New York Heart Association class was reported in the HVC cohort (p<0.001 and p=0.032). Compared with SOC, the HVC approach was associated with reduced all-cause mortality (HR=0.63, 95% CI 0.40 to 0.98, p=0.038) and cardiovascular death (p=0.030). At multivariable analysis, the HVC remained an independent predictor of all-cause mortality (HR=0.54, 95% CI 0.34 to 0.85, p=0.007).
CONCLUSIONS
In patients with mAS and asAS, the HVC approach was associated with more efficient management and outcome benefit compared with SOC.

Identifiants

pubmed: 36598073
pii: heartjnl-2022-321874
doi: 10.1136/heartjnl-2022-321874
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

634-642

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

© Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Pasquale Paolisso (P)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium.
Department of Advanced Biomedical Sciences, Federico II University Hospital, Napoli, Campania, Italy.

Monika Beles (M)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium.

Marta Belmonte (M)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium.
Department of Advanced Biomedical Sciences, Federico II University Hospital, Napoli, Campania, Italy.

Emanuele Gallinoro (E)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium.

Cristina De Colle (C)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium.
Department of Advanced Biomedical Sciences, Federico II University Hospital, Napoli, Campania, Italy.

Niya Mileva (N)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium.

Dario Tino Bertolone (DT)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium.
Department of Advanced Biomedical Sciences, Federico II University Hospital, Napoli, Campania, Italy.

Celine Deschepper (C)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium.

Jerrold Spapen (J)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium.

Sofie Brouwers (S)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium.
Department of Experimental Pharmacology, Vrije Universiteit Brussel, Brussel, Belgium.

Ivan Degrieck (I)

Department of Cardiovascular Surgery, Hartcentrum OLV Aalst, Aalst, Belgium.

Filip Casselman (F)

Department of Cardiovascular Surgery, Hartcentrum OLV Aalst, Aalst, Belgium.

Bernard Stockman (B)

Department of Cardiovascular Surgery, Hartcentrum OLV Aalst, Aalst, Belgium.

Frank Van Praet (F)

Department of Cardiovascular Surgery, Hartcentrum OLV Aalst, Aalst, Belgium.

Martin Penicka (M)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium.

Carlos Collet (C)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium.

Eric Wyffels (E)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium.

Marc Vanderheyden (M)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium.

Emanuele Barbato (E)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium.
Department of Advanced Biomedical Sciences, Federico II University Hospital, Napoli, Campania, Italy.

Jozef Bartunek (J)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium.

Guy Van Camp (G)

Cardiology Department, Hartcentrum OLV Aalst, Aalst, Belgium guy_vancamp@outlook.com.

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