Biventricular Physiology of Iatrogenic Atrial Septal Defects Following Transcatheter Mitral Valve Edge-to-Edge Repair.


Journal

JACC. Cardiovascular interventions
ISSN: 1876-7605
Titre abrégé: JACC Cardiovasc Interv
Pays: United States
ID NLM: 101467004

Informations de publication

Date de publication:
11 01 2021
Historique:
received: 12 08 2020
revised: 09 10 2020
accepted: 20 10 2020
entrez: 8 1 2021
pubmed: 9 1 2021
medline: 28 7 2021
Statut: ppublish

Résumé

The study sought to assess the acute hemodynamic effects of iatrogenic atrial septal defect (iASD) closure following transcatheter mitral valve edge-to-edge repair (TMVR). The potential hemodynamic and clinical consequences of an iASD following TMVR are currently subject to controversial debates. In 21 patients with relevant left-to-right shunt flow (50% [IQR: 38% to 60%] of systemic perfusion volume) across an iASD following TMVR, interventional closure was performed with recordings of left ventricular (LV) and right ventricular (RV) pressure-volume loops during iASD occlusion. iASD occlusion led to a volume shift from the RV (RV end-diastolic volume index: pre 102 [IQR: 80 to 120] ml/m iASD closure following TMVR leads to a volume shift from the RV to the LV with reduced pulmonary but increased systemic cardiac index and with favorable biventricular interaction at maintained LV filling pressure, resulting in a decline in heart failure symptoms at 1-month follow-up.

Sections du résumé

OBJECTIVES
The study sought to assess the acute hemodynamic effects of iatrogenic atrial septal defect (iASD) closure following transcatheter mitral valve edge-to-edge repair (TMVR).
BACKGROUND
The potential hemodynamic and clinical consequences of an iASD following TMVR are currently subject to controversial debates.
METHODS
In 21 patients with relevant left-to-right shunt flow (50% [IQR: 38% to 60%] of systemic perfusion volume) across an iASD following TMVR, interventional closure was performed with recordings of left ventricular (LV) and right ventricular (RV) pressure-volume loops during iASD occlusion.
RESULTS
iASD occlusion led to a volume shift from the RV (RV end-diastolic volume index: pre 102 [IQR: 80 to 120] ml/m
CONCLUSIONS
iASD closure following TMVR leads to a volume shift from the RV to the LV with reduced pulmonary but increased systemic cardiac index and with favorable biventricular interaction at maintained LV filling pressure, resulting in a decline in heart failure symptoms at 1-month follow-up.

Identifiants

pubmed: 33413865
pii: S1936-8798(20)32164-6
doi: 10.1016/j.jcin.2020.10.032
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

54-66

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Author Disclosures Dr. Lurz has received institutional fees and research grants from Abbott Vascular, Edwards, Lifesciences, Medtronic, ReCor, and Occlutech. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Stephan Blazek (S)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University of Leipzig and Leipzig Heart Institute, Leipzig, Germany.

Matthias Unterhuber (M)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University of Leipzig and Leipzig Heart Institute, Leipzig, Germany.

Karl-Philipp Rommel (KP)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University of Leipzig and Leipzig Heart Institute, Leipzig, Germany.

Maximilian von Roeder (M)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University of Leipzig and Leipzig Heart Institute, Leipzig, Germany.

Karl-Patrik Kresoja (KP)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University of Leipzig and Leipzig Heart Institute, Leipzig, Germany.

Tobias Kister (T)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University of Leipzig and Leipzig Heart Institute, Leipzig, Germany.

Christian Besler (C)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University of Leipzig and Leipzig Heart Institute, Leipzig, Germany.

Karl Fengler (K)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University of Leipzig and Leipzig Heart Institute, Leipzig, Germany.

Marcus Sandri (M)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University of Leipzig and Leipzig Heart Institute, Leipzig, Germany.

Ingo Daehnert (I)

Department of Pediatric Cardiology, Heart Center Leipzig, University of Leipzig, Leipzig, Germany.

Holger Thiele (H)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University of Leipzig and Leipzig Heart Institute, Leipzig, Germany.

Philipp Lurz (P)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University of Leipzig and Leipzig Heart Institute, Leipzig, Germany. Electronic address: philipp.lurz@medizin.uni-leipzig.de.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH