Evidence map›Paper›PMID 38740526›Full record

ArticleEuropean heart journal2024

Mitral valve prolapse: arrhythmic risk during pregnancy and postpartum.

Avi Sabbag, Eivind W Aabel, Anna Isotta Castrini, Konstantinos C Siontis, Mikael Laredo, Jacky Nizard, Guillaume Duthoit, Samuel Asirvatham, Ojasay Sehrawat, Feddo P Kirkels and 11 more

Abstract readMulticenter Study
In one paragraph

Article in European heart journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Observational
  2. Review
  3. Interstitial fibrosis and arrhythmic mitral valve prolapse: Unraveling sex-based differences.Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Avi SabbagSheba Medical Centre, Ramat-Gan, affiliated with the School of Medicine, Tel Aviv University, Tel Aviv, Israel.ORCID 0000-0003-4295-6679
Eivind W AabelProCardio Center for Research Based Innovation, Department of Cardiology, Oslo University Hospital, Rikshospitalet, and University of Oslo, Sognsvannsveien 20, 0372 Oslo, Norway.ORCID 0000-0002-2022-4568
Anna Isotta CastriniProCardio Center for Research Based Innovation, Department of Cardiology, Oslo University Hospital, Rikshospitalet, and University of Oslo, Sognsvannsveien 20, 0372 Oslo, Norway.
Konstantinos C SiontisDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.
Mikael LaredoSorbonne Université, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.ORCID 0000-0002-7326-2656
Jacky NizardSorbonne Université, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.
Guillaume DuthoitSorbonne Université, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.ORCID 0000-0002-5730-6946
Samuel AsirvathamDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.
Ojasay SehrawatDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.
Feddo P KirkelsDepartment of Cardiology, University Medical Centre Utrecht, Utrecht, The Netherlands.ORCID 0000-0002-1350-8765
Philippe J van RosendaelDepartment of Cardiology, University Medical Centre Utrecht, Utrecht, The Netherlands.
Roy BeinartSheba Medical Centre, Ramat-Gan, affiliated with the School of Medicine, Tel Aviv University, Tel Aviv, Israel.ORCID 0000-0002-9268-4766
Moshe Rav AchaJesselson Integrated Heart Center, Shaare Zedek Medical Center, Jerusalem, Israel.
Petr PeichlDepartment of Cardiology, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.ORCID 0000-0002-5625-0071
Han S LimAustin and Northern Health, University of Melbourne, Melbourne, Australia.
Christian SohnsClinic for Electrophysiology, Herz- und Diabeteszentrum NRW, Ruhr-Universität Bochum, Bad Oeynhausen, Germany.ORCID 0000-0003-0490-5862
Raphael MartinsLTSI, Rennes University Hospital, Rennes, France.
Jonaz FontLTSI, Rennes University Hospital, Rennes, France.
Nguyen N K TruongDepartment of Interventional Cardiology, Medical University Center of Ho Chi Minh City, Ho Chi Minh, Vietnam.
Mette EstensenProCardio Center for Research Based Innovation, Department of Cardiology, Oslo University Hospital, Rikshospitalet, and University of Oslo, Sognsvannsveien 20, 0372 Oslo, Norway.
Kristina H HaugaaProCardio Center for Research Based Innovation, Department of Cardiology, Oslo University Hospital, Rikshospitalet, and University of Oslo, Sognsvannsveien 20, 0372 Oslo, Norway.ORCID 0000-0002-4900-0453

Funding

Norwegian Research Council 288438 and #309762Slezak fund
6 · The paper itself

Abstract

BACKGROUND AND

aimsArrhythmic 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.

methodsThis 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.

resultsThe 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).

conclusionsThe 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.

Indexed as

Mitral Valve ProlapsePregnancy Complications, CardiovascularAdultArrhythmias, CardiacDefibrillators, ImplantableFemaleHumansIncidencePostpartum PeriodPregnancyPuerperal DisordersRetrospective StudiesRisk FactorsTachycardia, VentricularVentricular FibrillationArrhythmic mitral valve prolapseCardiomyopathyMitral annular disjunctionPregnancyVentricular arrhythmia

Identifiers

PMID38740526
PMCPMC11129793

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.