Pregnancy and newborn outcomes in arrhythmogenic right ventricular cardiomyopathy/dysplasia. (1st May 2018)
- Record Type:
- Journal Article
- Title:
- Pregnancy and newborn outcomes in arrhythmogenic right ventricular cardiomyopathy/dysplasia. (1st May 2018)
- Main Title:
- Pregnancy and newborn outcomes in arrhythmogenic right ventricular cardiomyopathy/dysplasia
- Authors:
- Gandjbakhch, E.
Varlet, E.
Duthoit, G.
Fressart, V.
Charron, P.
Himbert, C.
Maupain, C.
Bordet, C.
Hidden-Lucet, F.
Nizard, J. - Abstract:
- Abstract: Introduction: The prognosis of pregnancy in patients with Arrhythmogenic Right Ventricular Cardiomyopathy/dysplasia (ARVC/D) is poorly documented. The aim of this study is to assess the cardiac risks during pregnancy and the impact of ARVC/D on fetuses/neonates/children. Methods: We included all ARVC/D women with a history of pregnancy from the ARVC/D Pitié-Salpêtrière registry. Cardiac and obstetrical events having occurred during pregnancy/delivery/post-partum periods and neonatal data/follow-up were collected. Results: Sixty pregnancies in twenty-three patients were identified between 1968 and 2016. Only two major non-fatal cardiac events (one sustained non-documented tachycardia and one ventricular tachycardia) were recorded during pregnancy in two different mothers (3% of pregnancies, 9% of mothers). None occurred during delivery or in the postpartum period. No mother developed heart failure. Beta-blocker therapy during pregnancy ( n = 15) was associated with lower birthweight (2730 vs 3400 g, p = 0.004). Only two preterm deliveries occurred, unrelated to cardiac condition. Caesarean section was performed in 13% of cases. Premature sudden-death occurred in 10% ( n = 5) of children before 25 years-old including two in the first year of life. Conclusion: ARVC/D is associated with a low rate of major cardiac events during pregnancy and vaginal delivery appears safe. The risk of sustained ventricular arrhythmia seems poorly predictable and supports theAbstract: Introduction: The prognosis of pregnancy in patients with Arrhythmogenic Right Ventricular Cardiomyopathy/dysplasia (ARVC/D) is poorly documented. The aim of this study is to assess the cardiac risks during pregnancy and the impact of ARVC/D on fetuses/neonates/children. Methods: We included all ARVC/D women with a history of pregnancy from the ARVC/D Pitié-Salpêtrière registry. Cardiac and obstetrical events having occurred during pregnancy/delivery/post-partum periods and neonatal data/follow-up were collected. Results: Sixty pregnancies in twenty-three patients were identified between 1968 and 2016. Only two major non-fatal cardiac events (one sustained non-documented tachycardia and one ventricular tachycardia) were recorded during pregnancy in two different mothers (3% of pregnancies, 9% of mothers). None occurred during delivery or in the postpartum period. No mother developed heart failure. Beta-blocker therapy during pregnancy ( n = 15) was associated with lower birthweight (2730 vs 3400 g, p = 0.004). Only two preterm deliveries occurred, unrelated to cardiac condition. Caesarean section was performed in 13% of cases. Premature sudden-death occurred in 10% ( n = 5) of children before 25 years-old including two in the first year of life. Conclusion: ARVC/D is associated with a low rate of major cardiac events during pregnancy and vaginal delivery appears safe. The risk of sustained ventricular arrhythmia seems poorly predictable and supports the continuation of beta-blockers during pregnancy. Major cardiac events were frequent in childhood, justifying close cardiac monitoring. Highlights: ARVC/D is associated with a low rate of major cardiac events during pregnancy and vaginal delivery appears safe. No haemodynamic compromise was observed during pregnancy or post-partum period. The risk of sustained ventricular arrhythmia seems poorly predictable and supports the continuation of beta-blockers during pregnancy. We recommend a multidisciplinary care with obstetricians, cardiologists, anaesthesiologist, and paediatricians. The follow-up of children revealed frequent major cardiac events including SCD in 10%, justifying close cardiac monitoring. … (more)
- Is Part Of:
- International journal of cardiology. Volume 258(2018)
- Journal:
- International journal of cardiology
- Issue:
- Volume 258(2018)
- Issue Display:
- Volume 258, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 258
- Issue:
- 2018
- Issue Sort Value:
- 2018-0258-2018-0000
- Page Start:
- 172
- Page End:
- 178
- Publication Date:
- 2018-05-01
- Subjects:
- ARVC -- ARVD -- Pregnancy -- Cardiomyopathy -- Ventricular arrhythmias
Cardiology -- Periodicals
Electronic journals
616.12 - Journal URLs:
- http://www.clinicalkey.com/dura/browse/journalIssue/01675273 ↗
http://www.sciencedirect.com/science/journal/01675273 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.ijcard.2017.11.067 ↗
- Languages:
- English
- ISSNs:
- 0167-5273
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.158000
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