Mitral valve prolapse: arrhythmic risk during pregnancy and postpartum.

Arrhythmic mitral valve prolapse Cardiomyopathy Mitral annular disjunction Pregnancy Ventricular arrhythmia

Journal

European heart journal
ISSN: 1522-9645
Titre abrégé: Eur Heart J
Pays: England
ID NLM: 8006263

Informations de publication

Date de publication:
14 May 2024
Historique:
received: 17 08 2023
revised: 02 02 2024
accepted: 26 03 2024
medline: 14 5 2024
pubmed: 14 5 2024
entrez: 13 5 2024
Statut: aheadofprint

Résumé

Arrhythmic mitral valve prolapse (AMVP) is linked to life-threatening ventricular arrhythmias (VAs), and young women are considered at high risk. Cases of AMVP in women with malignant VA during pregnancy have emerged, but the arrhythmic risk during pregnancy is unknown. The authors aimed to describe features of women with high-risk AMVP who developed malignant VA during the perinatal period and to assess if pregnancy and the postpartum period were associated with a higher risk of malignant VA. This retrospective international multi-centre case series included high-risk women with AMVP who experienced malignant VA and at least one pregnancy. Malignant VA included ventricular fibrillation, sustained ventricular tachycardia, or appropriate shock from an implantable cardioverter defibrillator. The authors compared the incidence of malignant VA in non-pregnant periods and perinatal period; the latter defined as occurring during pregnancy and within 6 months after delivery. The authors included 18 women with AMVP from 11 centres. During 7.5 (interquartile range 5.8-16.6) years of follow-up, 37 malignant VAs occurred, of which 18 were pregnancy related occurring in 13 (72%) unique patients. Pregnancy and 6 months after delivery showed increased incidence rate of malignant VA compared to the non-pregnancy period (univariate incidence rate ratio 2.66, 95% confidence interval 1.23-5.76). The perinatal period could impose increased risk of malignant VA in women with high-risk AMVP. The data may provide general guidance for pre-conception counselling and for nuanced shared decision-making between patients and clinicians.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Arrhythmic mitral valve prolapse (AMVP) is linked to life-threatening ventricular arrhythmias (VAs), and young women are considered at high risk. Cases of AMVP in women with malignant VA during pregnancy have emerged, but the arrhythmic risk during pregnancy is unknown. The authors aimed to describe features of women with high-risk AMVP who developed malignant VA during the perinatal period and to assess if pregnancy and the postpartum period were associated with a higher risk of malignant VA.
METHODS METHODS
This retrospective international multi-centre case series included high-risk women with AMVP who experienced malignant VA and at least one pregnancy. Malignant VA included ventricular fibrillation, sustained ventricular tachycardia, or appropriate shock from an implantable cardioverter defibrillator. The authors compared the incidence of malignant VA in non-pregnant periods and perinatal period; the latter defined as occurring during pregnancy and within 6 months after delivery.
RESULTS RESULTS
The authors included 18 women with AMVP from 11 centres. During 7.5 (interquartile range 5.8-16.6) years of follow-up, 37 malignant VAs occurred, of which 18 were pregnancy related occurring in 13 (72%) unique patients. Pregnancy and 6 months after delivery showed increased incidence rate of malignant VA compared to the non-pregnancy period (univariate incidence rate ratio 2.66, 95% confidence interval 1.23-5.76).
CONCLUSIONS CONCLUSIONS
The perinatal period could impose increased risk of malignant VA in women with high-risk AMVP. The data may provide general guidance for pre-conception counselling and for nuanced shared decision-making between patients and clinicians.

Identifiants

pubmed: 38740526
pii: 7671160
doi: 10.1093/eurheartj/ehae224
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Slezak fund
Organisme : Norwegian Research Council
ID : 288438 and #309762

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology.

Auteurs

Avi Sabbag (A)

Sheba Medical Centre, Ramat-Gan, affiliated with the School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Eivind W Aabel (EW)

ProCardio Center for Research Based Innovation, Department of Cardiology, Oslo University Hospital, Rikshospitalet, and University of Oslo, Sognsvannsveien 20, 0372 Oslo, Norway.

Anna Isotta Castrini (AI)

ProCardio Center for Research Based Innovation, Department of Cardiology, Oslo University Hospital, Rikshospitalet, and University of Oslo, Sognsvannsveien 20, 0372 Oslo, Norway.

Konstantinos C Siontis (KC)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.

Mikael Laredo (M)

Sorbonne Université, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.

Jacky Nizard (J)

Sorbonne Université, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.

Guillaume Duthoit (G)

Sorbonne Université, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.

Samuel Asirvatham (S)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.

Ojasay Sehrawat (O)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.

Feddo P Kirkels (FP)

Department of Cardiology, University Medical Centre Utrecht, Utrecht, The Netherlands.

Philippe J van Rosendael (PJ)

Department of Cardiology, University Medical Centre Utrecht, Utrecht, The Netherlands.

Roy Beinart (R)

Sheba Medical Centre, Ramat-Gan, affiliated with the School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Moshe Rav Acha (MR)

Jesselson Integrated Heart Center, Shaare Zedek Medical Center, Jerusalem, Israel.

Petr Peichl (P)

Department of Cardiology, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

Han S Lim (HS)

Austin and Northern Health, University of Melbourne, Melbourne, Australia.

Christian Sohns (C)

Clinic for Electrophysiology, Herz- und Diabeteszentrum NRW, Ruhr-Universität Bochum, Bad Oeynhausen, Germany.

Raphael Martins (R)

LTSI, Rennes University Hospital, Rennes, France.

Jonaz Font (J)

LTSI, Rennes University Hospital, Rennes, France.

Nguyen N K Truong (NNK)

Department of Interventional Cardiology, Medical University Center of Ho Chi Minh City, Ho Chi Minh, Vietnam.

Mette Estensen (M)

ProCardio Center for Research Based Innovation, Department of Cardiology, Oslo University Hospital, Rikshospitalet, and University of Oslo, Sognsvannsveien 20, 0372 Oslo, Norway.

Kristina H Haugaa (KH)

ProCardio Center for Research Based Innovation, Department of Cardiology, Oslo University Hospital, Rikshospitalet, and University of Oslo, Sognsvannsveien 20, 0372 Oslo, Norway.
Department of Cardiology, Karolinska University Hospital, Stockholm, Sweden.

Classifications MeSH