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Mitral valve prolapse: arrhythmic risk during pregnancy and postpartum.
Sabbag, Avi; Aabel, Eivind W; Castrini, Anna Isotta; Siontis, Konstantinos C; Laredo, Mikael; Nizard, Jacky; Duthoit, Guillaume; Asirvatham, Samuel; Sehrawat, Ojasay; Kirkels, Feddo P; van Rosendael, Philippe J; Beinart, Roy; Acha, Moshe Rav; Peichl, Petr; Lim, Han S; Sohns, Christian; Martins, Raphael; Font, Jonaz; Truong, Nguyen N K; Estensen, Mette; Haugaa, Kristina H.
Affiliation
  • Sabbag A; Sheba Medical Centre, Ramat-Gan, affiliated with the School of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Aabel EW; ProCardio Center for Research Based Innovation, Department of Cardiology, Oslo University Hospital, Rikshospitalet, and University of Oslo, Sognsvannsveien 20, 0372 Oslo, Norway.
  • Castrini AI; ProCardio Center for Research Based Innovation, Department of Cardiology, Oslo University Hospital, Rikshospitalet, and University of Oslo, Sognsvannsveien 20, 0372 Oslo, Norway.
  • Siontis KC; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.
  • Laredo M; Sorbonne Université, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.
  • Nizard J; Sorbonne Université, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.
  • Duthoit G; Sorbonne Université, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.
  • Asirvatham S; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.
  • Sehrawat O; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.
  • Kirkels FP; Department of Cardiology, University Medical Centre Utrecht, Utrecht, The Netherlands.
  • van Rosendael PJ; Department of Cardiology, University Medical Centre Utrecht, Utrecht, The Netherlands.
  • Beinart R; Sheba Medical Centre, Ramat-Gan, affiliated with the School of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Acha MR; Jesselson Integrated Heart Center, Shaare Zedek Medical Center, Jerusalem, Israel.
  • Peichl P; Department of Cardiology, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
  • Lim HS; Austin and Northern Health, University of Melbourne, Melbourne, Australia.
  • Sohns C; Clinic for Electrophysiology, Herz- und Diabeteszentrum NRW, Ruhr-Universität Bochum, Bad Oeynhausen, Germany.
  • Martins R; LTSI, Rennes University Hospital, Rennes, France.
  • Font J; LTSI, Rennes University Hospital, Rennes, France.
  • Truong NNK; Department of Interventional Cardiology, Medical University Center of Ho Chi Minh City, Ho Chi Minh, Vietnam.
  • Estensen M; ProCardio Center for Research Based Innovation, Department of Cardiology, Oslo University Hospital, Rikshospitalet, and University of Oslo, Sognsvannsveien 20, 0372 Oslo, Norway.
  • Haugaa KH; ProCardio Center for Research Based Innovation, Department of Cardiology, Oslo University Hospital, Rikshospitalet, and University of Oslo, Sognsvannsveien 20, 0372 Oslo, Norway.
Eur Heart J ; 45(20): 1831-1839, 2024 May 27.
Article in En | MEDLINE | ID: mdl-38740526
ABSTRACT
BACKGROUND AND

AIMS:

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:

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:

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:

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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pregnancy Complications, Cardiovascular / Mitral Valve Prolapse Limits: Adult / Female / Humans / Pregnancy Language: En Journal: Eur Heart J Year: 2024 Document type: Article Affiliation country: Israel Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pregnancy Complications, Cardiovascular / Mitral Valve Prolapse Limits: Adult / Female / Humans / Pregnancy Language: En Journal: Eur Heart J Year: 2024 Document type: Article Affiliation country: Israel Country of publication: United kingdom