Effect of tricuspid regurgitation and right ventricular dysfunction on long-term mortality in patients undergoing cardiac devices implantation: >10-year follow-up study.


Journal

International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291

Informations de publication

Date de publication:
15 Nov 2020
Historique:
received: 26 01 2020
revised: 13 05 2020
accepted: 19 05 2020
pubmed: 30 5 2020
medline: 29 4 2021
entrez: 30 5 2020
Statut: ppublish

Résumé

The long-term effect of tricuspid regurgitation (TR) after device implantation on long-term mortality remains unknown. In the present study, we sought to examine whether patients undergoing an implantable cardiac device procedure (pacemaker, cardiac defibrillator or cardiac resynchronisation therapy) have an increased risk of TR and to determine the effect of this on long-term survival. A total of 304 patients who underwent device implant and had pre- and post-implant transthoracic echocardiogram were included in the analysis. All-cause mortality was the study endpoint over a follow-up period of median 11.6 years. New ≥ moderate tricuspid regurgitation post-device implantation developed in 66/304 (21.7%) patients. New right ventricular dysfunction post-device implantation occurred in 59/304 (19.4%) patients. Independent predictors of new RV dysfunction were ischaemic heart disease (OR 4.23, 95% CI 1.58 - 11.33, p = 0.004), left ventricular impairment (OR 2.74, 95% CI 5.41 - 30.00, p < 0.0001) and new ≥ moderate TR (OR 7.72, 95% CI 3.27 - 18.23, p < 0.001). Independent predictors of mortality were new ≥ moderate TR [HR: 3.14 (95% CI 1.29 - 7.63) p = 0.01] and new RV impairment [HR: 2.82 (95% CI 1.33 - 5.98) p = 0.01. Worsening TR and RV dysfunction post-device implantation is common. New post-implant ≥ moderate TR is associated with increased risk of new RV impairment and poor long term (>10 years) survival.

Sections du résumé

BACKGROUND BACKGROUND
The long-term effect of tricuspid regurgitation (TR) after device implantation on long-term mortality remains unknown. In the present study, we sought to examine whether patients undergoing an implantable cardiac device procedure (pacemaker, cardiac defibrillator or cardiac resynchronisation therapy) have an increased risk of TR and to determine the effect of this on long-term survival.
METHODS METHODS
A total of 304 patients who underwent device implant and had pre- and post-implant transthoracic echocardiogram were included in the analysis. All-cause mortality was the study endpoint over a follow-up period of median 11.6 years.
RESULTS RESULTS
New ≥ moderate tricuspid regurgitation post-device implantation developed in 66/304 (21.7%) patients. New right ventricular dysfunction post-device implantation occurred in 59/304 (19.4%) patients. Independent predictors of new RV dysfunction were ischaemic heart disease (OR 4.23, 95% CI 1.58 - 11.33, p = 0.004), left ventricular impairment (OR 2.74, 95% CI 5.41 - 30.00, p < 0.0001) and new ≥ moderate TR (OR 7.72, 95% CI 3.27 - 18.23, p < 0.001). Independent predictors of mortality were new ≥ moderate TR [HR: 3.14 (95% CI 1.29 - 7.63) p = 0.01] and new RV impairment [HR: 2.82 (95% CI 1.33 - 5.98) p = 0.01.
CONCLUSIONS CONCLUSIONS
Worsening TR and RV dysfunction post-device implantation is common. New post-implant ≥ moderate TR is associated with increased risk of new RV impairment and poor long term (>10 years) survival.

Identifiants

pubmed: 32470533
pii: S0167-5273(20)30403-4
doi: 10.1016/j.ijcard.2020.05.062
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

52-56

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Nikolaos Papageorgiou (N)

Echocardiography Laboratory, Barts Heart Centre, St Bartholomew's Hospital, London, UK; Electrophysiology Department, Barts Heart Centre, St. Bartholomew's Hospital, London, UK; Institute of Cardiovascular Science, UCL, London, UK.

Debbie Falconer (D)

University College London Hospitals NHS Trust, London, UK.

Nikolas Wyeth (N)

University College London Hospitals NHS Trust, London, UK.

Guy Lloyd (G)

Echocardiography Laboratory, Barts Heart Centre, St Bartholomew's Hospital, London, UK; University College London Hospitals NHS Trust, London, UK; Institute of Cardiovascular Science, UCL, London, UK; William Harvey Research Institute, Queen Mary University of London, London, UK.

Denis Pellerin (D)

Echocardiography Laboratory, Barts Heart Centre, St Bartholomew's Hospital, London, UK.

Elsya Speechly-Dick (E)

University College London Hospitals NHS Trust, London, UK; Institute of Cardiovascular Science, UCL, London, UK.

Oliver R Segal (OR)

Electrophysiology Department, Barts Heart Centre, St. Bartholomew's Hospital, London, UK.

Martin Lowe (M)

Electrophysiology Department, Barts Heart Centre, St. Bartholomew's Hospital, London, UK.

Edward Rowland (E)

Electrophysiology Department, Barts Heart Centre, St. Bartholomew's Hospital, London, UK.

Pier D Lambiase (PD)

Electrophysiology Department, Barts Heart Centre, St. Bartholomew's Hospital, London, UK; Institute of Cardiovascular Science, UCL, London, UK.

Anthony W Chow (AW)

Electrophysiology Department, Barts Heart Centre, St. Bartholomew's Hospital, London, UK.

Sanjeev Bhattacharyya (S)

Echocardiography Laboratory, Barts Heart Centre, St Bartholomew's Hospital, London, UK; University College London Hospitals NHS Trust, London, UK; Institute of Cardiovascular Science, UCL, London, UK; William Harvey Research Institute, Queen Mary University of London, London, UK. Electronic address: Sanjeev.Bhattacharyya@bartshealth.nhs.uk.

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Classifications MeSH