162
Views
0
CrossRef citations to date
0
Altmetric
Special Report

Evidence-based Management of Arrhythmogenic Right Ventricular Cardiomyopathy in Pregnancy

ORCID Icon, , , , , & show all
Pages 693-703 | Received 10 Aug 2020, Accepted 16 Sep 2020, Published online: 22 Oct 2020

References

  • Basso C , CorradoD, MarcusFI, NavaA, ThieneG. Arrhythmogenic right ventricular cardiomyopathy. Lancet, 373(9671), 1289–1300 (2009).
  • Jarcho JA , CorradoD, LinkMS, CalkinsH. Arrhythmogenic right ventricular cardiomyopathy. N. Engl. J. Med., 376(1), 61–72 (2017).
  • Ackerman M , AtkinsDL, TriedmanJK. Sudden cardiac death in the young. Circulation, 133(10), 1006–1026 (2016).
  • Luo FY , ChadhaR, OsborneC, KealeyA. Arrhythmogenic right ventricular cardiomyopathy (ARVC) in pregnancy: a case series of nine patients and review of literature. J. Matern. Fetal. Neonatal Med. doi: https://doi.org/10.1080/14767058.2020.1745176 ( Epub ahead of print).
  • Akdis D , BrunckhorstC, DuruF, SagunerAM. Arrhythmogenic Cardiomyopathy: Electrical and Structural Phenotypes. Arrhythmia Electrophysiol. Rev., 5(2), 90 (2016).
  • Corrado D , Van TintelenPJ, McKennaWJet al. Arrhythmogenic right ventricular cardiomyopathy: evaluation of the current diagnostic criteria and differential diagnosis. Eur. Heart J., 41(14), 1414–1427b (2020).
  • McKoy G , ProtonotariosN, CrosbyAet al. Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease). Lancet, 355(9221), 2119–2124 (2000).
  • Norgett EE . Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma. Hum. Mol. Genet., 9(18), 2761–2766 (2000).
  • Que D , YangP, SongX, LiuL. Traditional vs. genetic pathogenesis of arrhythmogenic right ventricular cardiomyopathy. Europace, 17(12), 1770–1776 (2015).
  • Kirchhof P , FabritzL, ZwienerMet al. Age- and training-dependent development of arrhythmogenic right ventricular cardiomyopathy in heterozygous plakoglobin-deficient mice. Circulation, 114(17), 1799–1806 (2006).
  • James CA , BhonsaleA, TichnellCet al. Exercise increases age-related penetrance and arrhythmic risk in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers. J. Am. Coll. Cardiol., 62(14), 1290–1297 (2013).
  • Saberniak J , HasselbergNE, BorgquistRet al. Vigorous physical activity impairs myocardial function in patients with arrhythmogenic right ventricular cardiomyopathy and in mutation positive family members. Eur. J. Heart Fail., 16(12), 1337–1344 (2014).
  • Ducas RA , ElliottJE, MelnykSFet al. Cardiovascular magnetic resonance in pregnancy: insights from the cardiac hemodynamic imaging and remodeling in pregnancy (CHIRP) study. J. Cardiovasc. Magn. Reson., 16(1), 1 (2014).
  • Iorga A , CunninghamCM, MoazeniS, RuffenachG, UmarS, EghbaliM. The protective role of estrogen and estrogen receptors in cardiovascular disease and the controversial use of estrogen therapy. Biol. Sex Differ., 8(1), 33 (2017).
  • Metra M , CotterG, DavisonBAet al. Effect of serelaxin on cardiac, renal, and hepatic biomarkers in the relaxin in acute heart failure (RELAX-AHF) development program. J. Am. Coll. Cardiol., 61(2), 196–206 (2013).
  • Leo CH , JelinicM, NgHHet al. Vascular actions of relaxin: nitric oxide and beyond. Br. J. Pharmacol., 174(10), 1002–1014 (2017).
  • Dalal D , NasirK, BommaCet al. Arrhythmogenic right ventricular dysplasia. Circulation, 112(25), 3823–3832 (2005).
  • Hulot JS , JouvenX, EmpanaJP, FrankR, FontaineG. Natural history and risk stratification of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circulation, 110(14), 1879–1884 (2004).
  • Hodes AR , TichnellC, TeRiele ASJMet al. Pregnancy course and outcomes in women with arrhythmogenic right ventricular cardiomyopathy. Heart, 102(4), 303–312 (2016).
  • Gandjbakhch E , VarletE, DuthoitGet al. Pregnancy and newborn outcomes in arrhythmogenic right ventricular cardiomyopathy/dysplasia. Int. J. Cardiol., 258, 172–178 (2018).
  • Wu L , LiangE, FanSet al. Effect of pregnancy in arrhythmogenic right ventricular cardiomyopathy. Am. J. Cardiol., 125(4), 613–617 (2020).
  • Marcus FI , McKennaWJ, SherrillDet al. Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia. Circulation, 121(13), 1533–1541 (2010).
  • Krul SPJ , vander Smagt JJ, vanden Berg MP, SollieKM, PieperPG, van Spaendonck-ZwartsKY. Systematic review of pregnancy in women with inherited cardiomyopathies. Eur. J. Heart Fail., 13(6), 584–594 (2011).
  • Bauce B , DalientoL, FrigoG, RussoG, NavaA. Pregnancy in women with arrhythmogenic right ventricular cardiomyopathy/dysplasia. Eur. J. Obstet. Gynecol. Reprod. Biol., 127(2), 186–189 (2006).
  • Castrini AI , LieØH, LerenISet al. Number of pregnancies and subsequent phenotype in a cross-sectional cohort of women with arrhythmogenic cardiomyopathy. Eur. Heart J. Cardiovasc. Imaging, 20(2), 192–198 (2019).
  • Billebeau G , EtienneM, Cheikh-KhelifaRet al. Pregnancy in women with a cardiomyopathy: outcomes and predictors from a retrospective cohort. Arch. Cardiovasc. Dis., 111(3), 199–209 (2018).
  • Corrado D , WichterT, LinkMSet al. Treatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: an international task force consensus statement. Circulation, 132(5), 441–453 (2015).
  • Calkins H , CorradoD, MarcusF. Risk stratification in arrhythmogenic right ventricular cardiomyopathy. Circulation, 136(21), 2068–2082 (2017).
  • Agir AA , BozyelS, CelikyurtUet al. Arrhythmogenic right ventricular cardiomyopathy in pregnancy: a case report and review of the literature. Int. Heart J., 55(4), 372–376 (2014).
  • Lee LC , BathgateSL, MacriCJ. Arrhythmogenic right ventricular dysplasia in pregnancy: a case report. J. Reprod. Med. Obstet. Gynecol., 51(9), 725–728 (2006).
  • Towbin JA , McKennaWJ, AbramsDJet al. 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy. Hear. Rhythm, 16(11), e301–e372 (2019).
  • Stadiotti I , PompilioG, MaioneAS, PilatoCA, D’AlessandraY, SommarivaE. Arrhythmogenic cardiomyopathy: what blood can reveal?Hear. Rhythm, 16(3), 470–477 (2019).
  • Grewal J , SilversidesCK, ColmanJM. Pregnancy in Women with Heart Disease. Heart Fail. Clin., 10(1), 117–129 (2014).
  • Tanous D , SiuSC, MasonJet al. B-type natriuretic peptide in pregnant women with heart disease. J. Am. Coll. Cardiol., 56(15), 1247–1253 (2010).
  • Yancy CW , JessupM, BozkurtBet al. 2017 ACC/AHA/HFSA Focused Update of the 2013 ACCF/AHA Guideline for the management of heart failure: a report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Failure Society of America. J. Am. Coll. Cardiol., 70(6), 776–803 (2017).
  • Schaefer C . Angiotensin II-receptor-antagonists: further evidence of fetotoxicity but not teratogenicity. Birth Defects Res. Part A - Clin. Mol. Teratol., 67(8), 591–594 (2003).
  • Cooper WO , Hernandez-DiazS, ArbogastPGet al. Major congenital malformations after first-trimester exposure to ACE inhibitors. N. Engl. J. Med., 354(23), 2443–2451 (2006).
  • Lydakis C , LipGYH, BeeversM, BeeversDG. Atenolol and fetal growth in pregnancies complicated by hypertension. Am. J. Hypertens., 12(6), 541–547 (1999).
  • Sliwa K , FettJ, ElkayamU. Peripartum cardiomyopathy. Lancet, 368(9536), 687–693 (2006).
  • McNamara DM , ElkayamU, AlharethiRet al. Clinical outcomes for peripartum cardiomyopathy in North America: results of the IPAC study (Investigations of Pregnancy-Associated Cardiomyopathy). J. Am. Coll. Cardiol., 66(8), 905–914 (2015).
  • Riester A , ReinckeM. Progress in primary aldosteronism: Mineralocorticoid receptor antagonists and management of primary aldosteronism in pregnancy. Eur. J. Endocrinol., 172(1), R23–R30 (2015).
  • Elkayam U . Risk of Subsequent Pregnancy in Women With a History of Peripartum Cardiomyopathy. J. Am. Coll. Cardiol., 64(15), 1629–1636 (2014).
  • Iriyama T , KameiY, KozumaS, TaketaniY. Management of patient with arrhythmogenic right ventricular cardiomyopathy during pregnancy. J. Obstet. Gynaecol. Res., 39(1), 390–394 (2013).
  • Güdücü N , KutaySS, ÖzençE, ÇiftçiÇ, YiğiterAB, İşçiH. Management of a rare case of arrhythmogenic right ventricular dysplasia in pregnancy: a case report. J. Med. Case Rep., 5(1), 300 (2011).
  • Meidahl Petersen K , Jimenez-SolemE, AndersenJTet al. β-Blocker treatment during pregnancy and adverse pregnancy outcomes: a nationwide population-based cohort study. BMJ Open, 2(4), e001185 (2012).
  • Bateman BT , PatornoE, DesaiRJet al. Late Pregnancy Blocker Exposure and Risks of Neonatal Hypoglycemia and Bradycardia. Pediatrics, 138(3), e20160731–e20160731 (2016).
  • Enriquez AD , EconomyKE, TedrowUB. Contemporary management of arrhythmias during pregnancy. Circ. Arrhythmia Electrophysiol., 7(5), 961–967 (2014).
  • Basso C , CorradoD, BauceB, ThieneG. Arrhythmogenic right ventricular cardiomyopathy. Circ. Arrhythmia Electrophysiol., 5(6), 1233–1246 (2012).
  • Regitz-Zagrosek V , Roos-HesselinkJW, BauersachsJet al. 2018 ESC guidelines for the management of cardiovascular diseases during pregnancy. Eur. Heart J., 39(34), 3165–3241 (2018).
  • Limongelli G , RubinoM, EspositoA, RussoM, PacileoG. The challenge of cardiomyopathies and heart failure in pregnancy. Curr. Opin. Obstet. Gynecol., 30(6), 378–384 (2018).
  • Goland S , ElkayamU. Peripartum cardiomyopathy. Curr. Opin. Cardiol., 33(3), 347–353 (2018).
  • Podymow T , AugustP. Update on the Use of Antihypertensive Drugs in Pregnancy. Hypertension, 51(4), 960–969 (2008).

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.