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Chapter 12 - Management of aortopathies, including Marfan syndrome and coarctation, in pregnancy

from Section 4 - Antenatal Care: Specific Maternal Conditions

Published online by Cambridge University Press:  05 March 2016

Philip J. Steer
Affiliation:
Chelsea and Westminster Hospital, London
Michael A. Gatzoulis
Affiliation:
Royal Brompton Hospital, London
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Publisher: Cambridge University Press
Print publication year: 2016

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References

Huisman, CM, Zwart, JJ, Roos-Hesselink, JW et al. Incidence and predictors of maternal cardiovascular mortality and severe morbidity in the Netherlands: A prospective cohort study. PLoS ONE 2013;8:e56494.Google Scholar
Cantwell, R, Clutton-Brock, T, Cooper, G. Saving Mothers’ Lives. Reviewing maternal death to make motherhood safer 2006–2008. BJOG 2011;118(Supp.1):1203.Google Scholar
Mabie, WC, DiSessa, TG, Crocker, LG, et al. A longitudinal study of cardiac output in normal human pregnancy. Am J Obstet Gynecol 1994;170:849–56.Google Scholar
Robson, SC, Hunter, S, Boys, RJ. et al. Serial study of factors influencing changes in cardiac output during pregnancy. Am J Physiol 1989;256:H1060–5.Google Scholar
Poppas, A, Shroff, SG, Korcarz, CE et al. Serial assessment of the cardiovascular system in normal pregnancy. Role of arterial compliance and pulsatile arterial load. Circulation 1997;95:2407–15.Google Scholar
Gutin, LS, Merz, AE, Bakalov, VK et al. Parity and aortic dimensions in healthy women. Int J Cardiol 2013;165(2):383–4.CrossRefGoogle ScholarPubMed
Campisi, D, Cutolo, M, Carruba, G et al. Evidence for soluble and nuclear site I binding of estrogens in human aorta. Atherosclerosis 1993;103:267–77.CrossRefGoogle ScholarPubMed
Wingrove, CS, Garr, E, Godsland, IF et al. 17-beta-oestradiol enhances release of matrix metalloproteinase-2 from human vascular smooth muscle cells. Biochim Biophys Acta 1998;1406:169–74.Google Scholar
Manallo-Estrella, P, Barker, AE. Histopathologic findings in human aortic media associated with pregnancy. Arch Path 1967;83:336–41.Google Scholar
Pedowitz, P, Perell, A. Aneurysms complicated by pregnancy. I. Aneurysms of the aorta and its major branches. Am J Obstet Gynecol 1957;73(4):720–35.CrossRefGoogle ScholarPubMed
Pyeritz, RE. Disorders of fibrillins and microfibrilogenesis: Marfan syndrome, MASS phenotype, contractural arachnodactyly and related conditions. In: Principles and Practice of Medical Genetics, 3rd edn. New York: Churchill Livingstone; 1996.Google Scholar
Lind, J, Wallenburg, HC. The Marfan syndrome and pregnancy: A retrospective study in a Dutch population. Eur J Obstet Gynecol Reprod Biol 2001;98(1):2835.Google Scholar
Meijboom, LJ, Drenthen, W, Pieper, PG et al. Obstetric complications in Marfan syndrome. Int J Cardiol 2006;110:53–9.CrossRefGoogle ScholarPubMed
Pini, R, Roman, MJ, Kramer-Fox, R et al. Mitral valve dimensions and motion in Marfan patients with and without mitral valve prolapse. Comparison to primary mitral valve prolapse and normal subjects. Circulation 1989;80:915–24.CrossRefGoogle ScholarPubMed
Schnitker, MA, Bayer, CA. Dissection aneurysm of the aorta in young individuals, particularly in association with pregnancy. Ann Intern Med 1944;29:486511.Google Scholar
Williams, GM, Gott, VL, Brawley, RK. et al. Aortic disease associated with pregnancy. J Vasc Surg 1988;8:470–5.Google Scholar
Hirst, AE, Johns, VJ, Kime, SW. Dissecting aneurysm of the aorta: A review of 505 cases. Medicine (Baltimore) 1958;37:217–79.Google Scholar
Oskoui, R, Lindsay, J. Aortic dissection in women < 40 years of age and the unimportance of pregnancy. Am J Cardiol 1994;73(11):821–3.CrossRefGoogle ScholarPubMed
Meijboom, LJ, Vos, FE, Timmermans, J et al. Pregnancy and aortic root growth in the Marfan syndrome: A prospective study. Eur Heart J 2005:26(9):914–20.Google Scholar
European Society of Gynecology (ESG), Association for European Paediatric Cardiology (AEPC), German Society for Gender Medicine (DGesGM), et al. ESC Guidelines on the management of cardiovascular diseases during pregnancy: The Task Force on the Management of Cardiovascular Diseases during Pregnancy of the European Society of Cardiology (ESC). Eur Heart J 2011;32:3147–97.Google Scholar
Hiratzka, LF, Bakris, GL, Beckman, JA et al. 2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM Guidelines for the diagnosis and management of patients with thoracic aortic disease. A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, American Association for Thoracic Surgery, American College of Radiology, American Stroke Association, Society of Cardiovascular Anesthesiologists, Society for Cardiovascular Angiography and Interventions, Society of Interventional Radiology, Society of Thoracic Surgeons, and Society for Vascular Medicine. J Am Coll Cardiol 2010;55(14):e27–e129.CrossRefGoogle Scholar
Groenink, M, Lohuis, TAJ, Tijssen, JGP et al. Survival and complication free survival in Marfan syndrome: Implications of current guidelines. Heart 1999;82:499504.CrossRefGoogle ScholarPubMed
Silverman, DI, Gray, J, Roman, MJ et al. Family history of severe cardiovascular disease in Marfan syndrome is associated with increased aortic diameter and decreased survival. J Am Coll Cardiol 1995;26(4):1062–7.CrossRefGoogle ScholarPubMed
Immer, FF, Bansi, AG, Immer-Bansi, AS. et al. Aortic dissection in pregnancy: Analysis of risk factors and outcome. Ann Thorac Surg 2003;76(1):309–14.Google Scholar
Williams, A, Child, A, Rowntree, J et al. Marfan syndrome: Successful pregnancy after aortic root and arch replacement. BJOG 2002;109(10):1187–8.Google Scholar
Shores, J, Berger, KR, Murphy, EA et al. Progression of aortic dilatation and the benefit of long-term beta-adrenergic blockade in Marfan syndrome. N Engl J Med 1994;330(19):1335–41.CrossRefGoogle Scholar
Groenink, M, de Roos, A, Mulder, BJ et al.Changes in aortic distensibility and pulse wave velocity assessed with magnetic resonance imaging following beta-blocker therapy in the Marfan syndrome. Am J Cardiol 1998;82(2):203–8.Google Scholar
Gao, L, Mao, Q, Wen, D et al. The effect of beta-blocker therapy on progressive aortic dilatation in children and adolescents with Marfan syndrome: A meta-analysis. Acta Paediatr 2011;100(9):e101–5.Google Scholar
Groenink, M, den Hartog, AW, Franken, R et al. Losartan reduces aortic dilatation rate in adults with Marfan syndrome: A randomized controlled trial. Eur Heart J 2013;34(45):3491–500.Google Scholar
Harton, GL, Tsipouras, P, Sisson, ME. et al. Preimplantation genetic testing for Marfan syndrome. Mol Hum Reprod 1996;2(9):713–5.CrossRefGoogle ScholarPubMed
Regalado, ES, Guo, DC, Estrera, AL et al. Acute aortic dissections with pregnancy in women with ACTA2 mutations. Am J Med Genet A 2014;164:106–12.Google Scholar
Rossiter, JP, Repke, JT, Morales, AJ et al. A prospective longitudinal evaluation of pregnancy in the Marfan syndrome. Am J Obstet Gynecol 1995;173(5):1599–606.Google Scholar
Zeebregts, CJ, Schepens, MA, Hameeteman, TM et al. Acute aortic dissection complicating pregnancy. Ann Thorac Surg 1997;64:1345–8.CrossRefGoogle ScholarPubMed
Parry, AJ, Westaby, S. Cardiopulmonary bypass during pregnancy. Ann Thorac Surg 1996;61(6):1865–9.CrossRefGoogle ScholarPubMed
Mahli, A, Izdes, S, Coskun, D. Cardiac operations during pregnancy: Review of factors influencing fetal outcome. Ann Thorac Surg 2000;69:1622–6.CrossRefGoogle ScholarPubMed
Lacassie, HJ, Millar, S, Leithe, LG et al. Dural ectasia: A likely cause of inadequate spinal anaesthesia in two parturients with Marfan syndrome. Br J Anaesth 2005;94(4):500–4.Google Scholar
Beauchesne, LM, Connolly, HM, Ammash, NM et al. Coarctation of the aorta: Outcome of pregnancy. J Am Coll Cardiol 2001;38(6):1728–33.CrossRefGoogle ScholarPubMed
Stern, HC, Locher, D, Wallnofer, K et al. Noninvasive assessment of coarctation of the aorta: Comparative measurements by two-dimensional echocardiography, magnetic resonance, and angiography. Pediatr Cardiol 1991;12(1):15.CrossRefGoogle ScholarPubMed
Stewart, AB, Ahmed, R, Travill, CM et al. Coarctation of the aorta life and health 20–44 years after surgical repair. Br Heart J 1993;69(1):6570.Google Scholar
Siu, SC, Sermer, M, Colman, JM et al. Prospective multicenter study of pregnancy outcomes in women with heart disease. Circulation 2001;104(5):515–21.Google Scholar
Kupferminc, MJ, Lessing, JB, Jaffa, A et al. Fetomaternal blood flow measurements and management of combined coarctation and aneurysm of the thoracic aorta in pregnancy. Acta Obstet Gynecol Scand 1993;72(5):398402.CrossRefGoogle ScholarPubMed
Knyshov, GV, Sitar, LL, Glagola, MD et al. Aortic aneurysms at the site of the repair of coarctation of the aorta: A review of 48 patients. Ann Thorac Surg 1996;61(3):935–9.CrossRefGoogle ScholarPubMed
Rose, V, Gold, RJM, Lindsay, G et al. A possible increase in the incidence of congenital heart defects among the offspring of affected parents. JACC 1985;6:376–82.CrossRefGoogle ScholarPubMed
Cecconi, M, Manfrin, M, Moraca, A et al. Aortic dimensions in patients with bicuspid aortic valve without significant valve dysfunction. Am J Cardiol 2005;95(2):292–4.CrossRefGoogle ScholarPubMed
Oliver, JM, Alonso-Gonzalez, R, Gonzalez, AE et al. Risk of aortic root or ascending aorta complications in patients with bicuspid aortic valve with and without coarctation of the aorta. Am J Cardiol 2009;104(7):1001–6.CrossRefGoogle ScholarPubMed
McKellar, SH, MacDonald, RJ, Michelena, HI et al. Frequency of cardiovascular events in women with a congenitally bicuspid aortic valve in a single community and effect of pregnancy on events. Am J Cardiol 2011;107:96–9.CrossRefGoogle Scholar
Ostberg, JE, Brookes, JA, McCarthy, C et al. A comparison of echocardiography and magnetic resonance imaging in cardiovascular screening of adults with Turner syndrome. J Clin Endocrinol Metab 2004;89(12):5966–71.CrossRefGoogle ScholarPubMed
Hagman, A, Loft, A, Wennerholm, UB et al. Obstetric and neonatal outcome after oocyte donation in 106 women with Turner syndrome: A Nordic cohort study. Hum Reprod 2013;28(6):1598–609.CrossRefGoogle ScholarPubMed
Lurie, S, Manor, M, Hagay, ZJ. The threat of type IV Ehlers-Danlos syndrome on maternal well-being during pregnancy: Early delivery may make the difference. J Obstet Gynaecol 1998;18(3):245–8.Google Scholar
Hauenstein, E, Frank, H, Bauer, JS. et al. Takayasu’s arteritis in pregnancy: Review of literature and discussion. J Perinat Med 2010;38:5562.Google Scholar

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