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Mitral valve prolapse: arrhythmic risk during pregnancy and postpartum
A. Sabbag, EW. Aabel, AI. Castrini, KC. Siontis, M. Laredo, J. Nizard, G. Duthoit, S. Asirvatham, O. Sehrawat, FP. Kirkels, PJ. van Rosendael, R. Beinart, MR. Acha, P. Peichl, HS. Lim, C. Sohns, R. Martins, J. Font, NNK. Truong, M. Estensen, KH. Haugaa
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, multicentrická studie
Grantová podpora
Slezak fund
288438 and #309762
Norwegian Research Council
NLK
Free Medical Journals
od 1996 do Před 1 rokem
Open Access Digital Library
od 1996-01-01
- MeSH
- defibrilátory implantabilní MeSH
- dospělí MeSH
- fibrilace komor epidemiologie etiologie MeSH
- incidence MeSH
- kardiovaskulární komplikace v těhotenství * epidemiologie MeSH
- komorová tachykardie epidemiologie etiologie MeSH
- lidé MeSH
- poporodní období MeSH
- poruchy v puerperiu epidemiologie etiologie MeSH
- prolaps mitrální chlopně * komplikace epidemiologie MeSH
- retrospektivní studie MeSH
- rizikové faktory MeSH
- srdeční arytmie epidemiologie etiologie MeSH
- těhotenství MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
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.
Austin and Northern Health University of Melbourne Melbourne Australia
Department of Cardiology Institute for Clinical and Experimental Medicine Prague Czech Republic
Department of Cardiology Karolinska University Hospital Stockholm Sweden
Department of Cardiology University Medical Centre Utrecht Utrecht The Netherlands
Department of Cardiovascular Medicine Mayo Clinic Rochester MN USA
Jesselson Integrated Heart Center Shaare Zedek Medical Center Jerusalem Israel
LTSI Rennes University Hospital Rennes France
Sorbonne Université AP HP Groupe Hospitalier Pitié Salpêtrière Paris France
Citace poskytuje Crossref.org
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