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Erschienen in: Journal of Genetic Counseling 4/2017

10.03.2017 | Review Paper

At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease

verfasst von: Ana Morales, Dawn C. Allain, Patricia Arscott, Emily James, Gretchen MacCarrick, Brittney Murray, Crystal Tichnell, Amy R. Shikany, Sara Spencer, Sara M. Fitzgerald-Butt, Jessica D. Kushner, Christi Munn, Emily Smith, Katherine G. Spoonamore, Harikrishna S. Tandri, W. Aaron Kay

Erschienen in: Journal of Genetic Counseling | Ausgabe 4/2017

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Abstract

In the last decade, an increasing number of cardiac conditions have been shown to have a genetic basis. Cardiovascular genetic counseling has emerged as a subspecialty aiming to identify unaffected at-risk individuals. An important sector of this at-risk population also includes expectant mothers, in whom unique clinical challenges may arise. Genetic counselors, especially those in cardiovascular and prenatal settings, have an opportunity to identify and assist women who may benefit from cardiovascular care during pregnancy. This paper provides basic management and genetic evaluation principles for affected women, as well as guidance on identifying those who are at risk. We provide considerations for cardiac surveillance in pregnancy and the post-partum period. Finally, key psychosocial issues that appraise how to best provide support to at risk women as they make informed decisions are discussed. We propose that a team approach including cardiology, maternal fetal medicine, and genetic counseling best serves this patient population. Ongoing questions addressing an evidence based approach to cardiovascular genetic conditions in pregnancy still remain. Thus, well-designed research protocols are essential to mark progress in this area.
Literatur
Zurück zum Zitat Ackerman, M. J., Priori, S. G., Willems, S., Berul, C., Brugada, R., Calkins, H., et al. (2011). HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European heart rhythm association (EHRA). Heart Rhythm, 8, 1308–1339.PubMedCrossRef Ackerman, M. J., Priori, S. G., Willems, S., Berul, C., Brugada, R., Calkins, H., et al. (2011). HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European heart rhythm association (EHRA). Heart Rhythm, 8, 1308–1339.PubMedCrossRef
Zurück zum Zitat Ackerman, M. J., Marcou, C. A., & Tester, D. J. (2013). Personalized medicine: Genetic diagnosis for inherited cardiomyopathies/channelopathies. Reviews Espanolas Cardiology (Engl Ed), 66, 298–307.CrossRef Ackerman, M. J., Marcou, C. A., & Tester, D. J. (2013). Personalized medicine: Genetic diagnosis for inherited cardiomyopathies/channelopathies. Reviews Espanolas Cardiology (Engl Ed), 66, 298–307.CrossRef
Zurück zum Zitat ACOG Practice Bulletin No. 88. (2007). Invasive prenatal testing for aneuploidy. American College of Obstetricians and Gynecologists. Obstetrics and Gynecology, 110, 1459–1467.CrossRef ACOG Practice Bulletin No. 88. (2007). Invasive prenatal testing for aneuploidy. American College of Obstetricians and Gynecologists. Obstetrics and Gynecology, 110, 1459–1467.CrossRef
Zurück zum Zitat Allison, S. J., Stafford, J., & Anumba, D. O. (2011). The effect of stress and anxiety associated with maternal prenatal diagnosis on feto-maternal attachment. BMC Womens Health, 11, 33.PubMedPubMedCentralCrossRef Allison, S. J., Stafford, J., & Anumba, D. O. (2011). The effect of stress and anxiety associated with maternal prenatal diagnosis on feto-maternal attachment. BMC Womens Health, 11, 33.PubMedPubMedCentralCrossRef
Zurück zum Zitat Bauce, B., Daliento, L., Frigo, G., Russo, G., & Nava, A. (2006). Pregnancy in women with arrhythmogenic right ventricular cardiomyopathy/dysplasia. European Journal of Obstetrics, Gynecology, and Reproductive Biology, 127, 186–189.PubMedCrossRef Bauce, B., Daliento, L., Frigo, G., Russo, G., & Nava, A. (2006). Pregnancy in women with arrhythmogenic right ventricular cardiomyopathy/dysplasia. European Journal of Obstetrics, Gynecology, and Reproductive Biology, 127, 186–189.PubMedCrossRef
Zurück zum Zitat Bedard, E., Dimopoulos, K., & Gatzoulis, M. A. (2009). Has there been any progress made on pregnancy outcomes among women with pulmonary arterial hypertension? European Heart Journal, 30, 256–265.PubMedCrossRef Bedard, E., Dimopoulos, K., & Gatzoulis, M. A. (2009). Has there been any progress made on pregnancy outcomes among women with pulmonary arterial hypertension? European Heart Journal, 30, 256–265.PubMedCrossRef
Zurück zum Zitat Beighton, P., De Paepe, A., Steinmann, B., Tsipouras, P., & Wenstrup, R. J. (1998). Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos support group (UK). American Journal of Medical Genetics, 77, 31–37.PubMedCrossRef Beighton, P., De Paepe, A., Steinmann, B., Tsipouras, P., & Wenstrup, R. J. (1998). Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos support group (UK). American Journal of Medical Genetics, 77, 31–37.PubMedCrossRef
Zurück zum Zitat Bendszus, M., Koltzenburg, M., Bartsch, A. J., Goldbrunner, R., Gunthner-Lengsfeld, T., Weilbach, F. X., et al. (2004). Heparin and air filters reduce embolic events caused by intra-arterial cerebral angiography: A prospective, randomized trial. Circulation, 110, 2210–2215.PubMedCrossRef Bendszus, M., Koltzenburg, M., Bartsch, A. J., Goldbrunner, R., Gunthner-Lengsfeld, T., Weilbach, F. X., et al. (2004). Heparin and air filters reduce embolic events caused by intra-arterial cerebral angiography: A prospective, randomized trial. Circulation, 110, 2210–2215.PubMedCrossRef
Zurück zum Zitat Bergeron, M. E., Child, T., & Fatum, M. (2014). In vitro maturation and surrogacy in patients with vascular-type Ehlers-Danlos syndrome--a safe assisted reproductive technology approach. Human Fertility (Cambridge, England), 17, 141–144.CrossRef Bergeron, M. E., Child, T., & Fatum, M. (2014). In vitro maturation and surrogacy in patients with vascular-type Ehlers-Danlos syndrome--a safe assisted reproductive technology approach. Human Fertility (Cambridge, England), 17, 141–144.CrossRef
Zurück zum Zitat Bieskeker, B. B. (2001). Goals of genetic counseling. Clinical Genetics, 60, 323–330.CrossRef Bieskeker, B. B. (2001). Goals of genetic counseling. Clinical Genetics, 60, 323–330.CrossRef
Zurück zum Zitat Blomstrom-Lundqvist, C., Scheinman, M. M., Aliot, E. M., Alpert, J. S., Calkins, H., Camm, A. J., et al. (2003). ACC/AHA/ESC guidelines for the management of patients with supraventricular arrhythmias--executive summary. a report of the American college of cardiology/American heart association task force on practice guidelines and the European society of cardiology committee for practice guidelines (writing committee to develop guidelines for the management of patients with supraventricular arrhythmias) developed in collaboration with NASPE-Heart Rhythm Society. Journal of the American College of Cardiology, 42, 1493–1531.PubMedCrossRef Blomstrom-Lundqvist, C., Scheinman, M. M., Aliot, E. M., Alpert, J. S., Calkins, H., Camm, A. J., et al. (2003). ACC/AHA/ESC guidelines for the management of patients with supraventricular arrhythmias--executive summary. a report of the American college of cardiology/American heart association task force on practice guidelines and the European society of cardiology committee for practice guidelines (writing committee to develop guidelines for the management of patients with supraventricular arrhythmias) developed in collaboration with NASPE-Heart Rhythm Society. Journal of the American College of Cardiology, 42, 1493–1531.PubMedCrossRef
Zurück zum Zitat Bons, L. R., & Roos-Hesselink, J. W. (2016). Aortic disease and pregnancy. Current Opinion in Cardiology, 31, 611.PubMedCrossRef Bons, L. R., & Roos-Hesselink, J. W. (2016). Aortic disease and pregnancy. Current Opinion in Cardiology, 31, 611.PubMedCrossRef
Zurück zum Zitat Briggs, G.G. (2011). Drugs in pregnancy and lactation: a reference guide to fetal and neonatal risk (9th ed. 2011 ed.). Philadelphia: Wolter Kluwer Health/Lippincott Williams & Wilkins. Briggs, G.G. (2011). Drugs in pregnancy and lactation: a reference guide to fetal and neonatal risk (9th ed. 2011 ed.). Philadelphia: Wolter Kluwer Health/Lippincott Williams & Wilkins.
Zurück zum Zitat Burkett, E. L., & Hershberger, R. E. (2005). Clinical and genetic issues in familial dilated cardiomyopathy. Journal of the American College of Cardiology, 45, 969–981.PubMedCrossRef Burkett, E. L., & Hershberger, R. E. (2005). Clinical and genetic issues in familial dilated cardiomyopathy. Journal of the American College of Cardiology, 45, 969–981.PubMedCrossRef
Zurück zum Zitat Chaix, M. A., Andelfinger, G., & Khairy, P. (2016). Genetic testing in congenital heart disease: A clinical approach. World Journal of Cardiology, 8, 180–191.PubMedPubMedCentralCrossRef Chaix, M. A., Andelfinger, G., & Khairy, P. (2016). Genetic testing in congenital heart disease: A clinical approach. World Journal of Cardiology, 8, 180–191.PubMedPubMedCentralCrossRef
Zurück zum Zitat Chandra, N. C., Gates, E. A., & Thamer, M. (1991). Conservative treatment of paroxysmal ventricular tachycardia during pregnancy. Clinical Cardiology, 14, 347–350.PubMedCrossRef Chandra, N. C., Gates, E. A., & Thamer, M. (1991). Conservative treatment of paroxysmal ventricular tachycardia during pregnancy. Clinical Cardiology, 14, 347–350.PubMedCrossRef
Zurück zum Zitat Cowan, J. R., & Ware, S. M. (2015). Genetics and genetic testing in congenital heart disease. Clinics in Perinatology, 42, 373–393.PubMedCrossRef Cowan, J. R., & Ware, S. M. (2015). Genetics and genetic testing in congenital heart disease. Clinics in Perinatology, 42, 373–393.PubMedCrossRef
Zurück zum Zitat Cox, S., O'Donoghue, A. C., McKenna, W. J., & Steptoe, A. (1997). Health related quality of life and psychological wellbeing in patients with hypertrophic cardiomyopathy. Heart, 78, 182–187.PubMedPubMedCentralCrossRef Cox, S., O'Donoghue, A. C., McKenna, W. J., & Steptoe, A. (1997). Health related quality of life and psychological wellbeing in patients with hypertrophic cardiomyopathy. Heart, 78, 182–187.PubMedPubMedCentralCrossRef
Zurück zum Zitat Cuneo, B. F., Etheridge, S. P., Horigome, H., Sallee, D., Moon-Grady, A., Weng, H. Y., et al. (2013). Arrhythmia phenotype during fetal life suggests long-QT syndrome genotype: Risk stratification of perinatal long-QT syndrome. Circulation. Arrhythmia and Electrophysiology, 6, 946–951.PubMedPubMedCentralCrossRef Cuneo, B. F., Etheridge, S. P., Horigome, H., Sallee, D., Moon-Grady, A., Weng, H. Y., et al. (2013). Arrhythmia phenotype during fetal life suggests long-QT syndrome genotype: Risk stratification of perinatal long-QT syndrome. Circulation. Arrhythmia and Electrophysiology, 6, 946–951.PubMedPubMedCentralCrossRef
Zurück zum Zitat Danielsson, B. R., Skold, A. C., & Azarbayjani, F. (2001). Class III antiarrhythmics and phenytoin: Teratogenicity due to embryonic cardiac dysrhythmia and reoxygenation damage. Current Pharmaceutical Design, 7, 787–802.PubMedCrossRef Danielsson, B. R., Skold, A. C., & Azarbayjani, F. (2001). Class III antiarrhythmics and phenytoin: Teratogenicity due to embryonic cardiac dysrhythmia and reoxygenation damage. Current Pharmaceutical Design, 7, 787–802.PubMedCrossRef
Zurück zum Zitat Dolgin, M. (1994). The Criteria Committee of the New York Heart Association. In 9th ed (Ed.), Nomenclature and Criteria for Diagnosis of Diseases of the Heart and Great Vessels (pp. 253–256). Boston: Little, Brown & Co. Dolgin, M. (1994). The Criteria Committee of the New York Heart Association. In 9th ed (Ed.), Nomenclature and Criteria for Diagnosis of Diseases of the Heart and Great Vessels (pp. 253–256). Boston: Little, Brown & Co.
Zurück zum Zitat Drenthen, W., Boersma, E., Balci, A., Moons, P., Roos-Hesselink, J. W., Mulder, B. J., et al. (2010). Predictors of pregnancy complications in women with congenital heart disease. European Heart Journal, 31, 2124–2132.PubMedCrossRef Drenthen, W., Boersma, E., Balci, A., Moons, P., Roos-Hesselink, J. W., Mulder, B. J., et al. (2010). Predictors of pregnancy complications in women with congenital heart disease. European Heart Journal, 31, 2124–2132.PubMedCrossRef
Zurück zum Zitat Ekholm, E. M., Piha, S. J., Erkkola, R. U., & Antila, K. J. (1994). Autonomic cardiovascular reflexes in pregnancy. A longitudinal study. Clinical Autonomous Research, 4, 161–165.CrossRef Ekholm, E. M., Piha, S. J., Erkkola, R. U., & Antila, K. J. (1994). Autonomic cardiovascular reflexes in pregnancy. A longitudinal study. Clinical Autonomous Research, 4, 161–165.CrossRef
Zurück zum Zitat El-Hamamsy, I., & Yacoub, M. H. (2009). Cellular and molecular mechanisms of thoracic aortic aneurysms. Nature Reviews. Cardiology, 6, 771–786.PubMedCrossRef El-Hamamsy, I., & Yacoub, M. H. (2009). Cellular and molecular mechanisms of thoracic aortic aneurysms. Nature Reviews. Cardiology, 6, 771–786.PubMedCrossRef
Zurück zum Zitat Elkayam, U., & Bitar, F. (2005a). Valvular heart disease and pregnancy part I: Native valves. Journal of the American College of Cardiology, 46, 223–230.PubMedCrossRef Elkayam, U., & Bitar, F. (2005a). Valvular heart disease and pregnancy part I: Native valves. Journal of the American College of Cardiology, 46, 223–230.PubMedCrossRef
Zurück zum Zitat Elkayam, U., & Bitar, F. (2005b). Valvular heart disease and pregnancy: Part II: Prosthetic valves. Journal of the American College of Cardiology, 46, 403–410.PubMedCrossRef Elkayam, U., & Bitar, F. (2005b). Valvular heart disease and pregnancy: Part II: Prosthetic valves. Journal of the American College of Cardiology, 46, 403–410.PubMedCrossRef
Zurück zum Zitat Elkayam, U., Tummala, P. P., Rao, K., Akhter, M. W., Karaalp, I. S., Wani, O. R., et al. (2001). Maternal and fetal outcomes of subsequent pregnancies in women with peripartum cardiomyopathy. The New England Journal of Medicine, 344, 1567–1571.PubMedCrossRef Elkayam, U., Tummala, P. P., Rao, K., Akhter, M. W., Karaalp, I. S., Wani, O. R., et al. (2001). Maternal and fetal outcomes of subsequent pregnancies in women with peripartum cardiomyopathy. The New England Journal of Medicine, 344, 1567–1571.PubMedCrossRef
Zurück zum Zitat Elkayam, U., Goland, S., Pieper, P. G., & Silverside, C. K. (2016). High-risk cardiac disease in pregnancy: Part I. Journal of the American College of Cardiology, 68, 396–410.PubMedCrossRef Elkayam, U., Goland, S., Pieper, P. G., & Silverside, C. K. (2016). High-risk cardiac disease in pregnancy: Part I. Journal of the American College of Cardiology, 68, 396–410.PubMedCrossRef
Zurück zum Zitat Elliott, P., Andersson, B., Arbustini, E., Bilinska, Z., Cecchi, F., Charron, P., et al. (2008). Classification of the cardiomyopathies: A position statement from the European Society of Cardiology working group on myocardial and pericardial diseases. European Heart Journal, 29, 270–276.PubMedCrossRef Elliott, P., Andersson, B., Arbustini, E., Bilinska, Z., Cecchi, F., Charron, P., et al. (2008). Classification of the cardiomyopathies: A position statement from the European Society of Cardiology working group on myocardial and pericardial diseases. European Heart Journal, 29, 270–276.PubMedCrossRef
Zurück zum Zitat Ferrero, S., Colombo, B. M., & Ragni, N. (2004). Maternal arrhythmias during pregnancy. Archives of Gynecology and Obstetrics, 269, 244–253.PubMedCrossRef Ferrero, S., Colombo, B. M., & Ragni, N. (2004). Maternal arrhythmias during pregnancy. Archives of Gynecology and Obstetrics, 269, 244–253.PubMedCrossRef
Zurück zum Zitat Fett, J. D. (2011). Validation of a self-test for early diagnosis of heart failure in peripartum cardiomyopathy. Critical Pathways in Cardiology, 10, 44–45.PubMedCrossRef Fett, J. D. (2011). Validation of a self-test for early diagnosis of heart failure in peripartum cardiomyopathy. Critical Pathways in Cardiology, 10, 44–45.PubMedCrossRef
Zurück zum Zitat Fett, J. D., Shah, T. P., & McNamara, D. M. (2015). Why do some recovered peripartum cardiomyopathy mothers experience heart failure with a subsequent pregnancy? Current Treatment Options in Cardiovascular Medicine, 17, 354.PubMedCrossRef Fett, J. D., Shah, T. P., & McNamara, D. M. (2015). Why do some recovered peripartum cardiomyopathy mothers experience heart failure with a subsequent pregnancy? Current Treatment Options in Cardiovascular Medicine, 17, 354.PubMedCrossRef
Zurück zum Zitat GeneTests Medical Genetics Information Resource (database online). (1993). Copyright. Seattle: University of Washington Available at http://www.genetests.org Accessed 11 Jan 2016. GeneTests Medical Genetics Information Resource (database online). (1993). Copyright. Seattle: University of Washington Available at http://​www.​genetests.​org Accessed 11 Jan 2016.
Zurück zum Zitat Gill, H. K., Splitt, M., Sharland, G. K., & Simpson, J. M. (2003). Patterns of recurrence of congenital heart disease: An analysis of 6,640 consecutive pregnancies evaluated by detailed fetal echocardiography. Journal of the American College of Cardiology, 42, 923–929.PubMedCrossRef Gill, H. K., Splitt, M., Sharland, G. K., & Simpson, J. M. (2003). Patterns of recurrence of congenital heart disease: An analysis of 6,640 consecutive pregnancies evaluated by detailed fetal echocardiography. Journal of the American College of Cardiology, 42, 923–929.PubMedCrossRef
Zurück zum Zitat Goel, K., Tweet, M., & Olson, T. M. (2015). Familial spontaneous coronary artery dissection: Evidence for genetic susceptiblity. JAMA Internal Medicine, 175, 821–826.PubMedCrossRef Goel, K., Tweet, M., & Olson, T. M. (2015). Familial spontaneous coronary artery dissection: Evidence for genetic susceptiblity. JAMA Internal Medicine, 175, 821–826.PubMedCrossRef
Zurück zum Zitat Gollob, M. H., Blier, L., Brugada, R., Champagne, J., Chauhan, V., Connors, S., et al. (2011). Recommendations for the use of genetic testing in the clinical evaluation of inherited cardiac arrhythmias associated with sudden cardiac death: Canadian cardiovascular society/Canadian Heart Rhythm Society joint position paper. The Canadian Journal of Cardiology, 27, 232–245.PubMedCrossRef Gollob, M. H., Blier, L., Brugada, R., Champagne, J., Chauhan, V., Connors, S., et al. (2011). Recommendations for the use of genetic testing in the clinical evaluation of inherited cardiac arrhythmias associated with sudden cardiac death: Canadian cardiovascular society/Canadian Heart Rhythm Society joint position paper. The Canadian Journal of Cardiology, 27, 232–245.PubMedCrossRef
Zurück zum Zitat Gowda, R. M., Khan, I. A., Mehta, N. J., Vasavada, B. C., & Sacchi, T. J. (2003). Cardiac arrhythmias in pregnancy: Clinical and therapeutic considerations. International Journal of Cardiology, 88, 129–133.PubMedCrossRef Gowda, R. M., Khan, I. A., Mehta, N. J., Vasavada, B. C., & Sacchi, T. J. (2003). Cardiac arrhythmias in pregnancy: Clinical and therapeutic considerations. International Journal of Cardiology, 88, 129–133.PubMedCrossRef
Zurück zum Zitat Grobstein, R. (1979). Amniocentesis counseling. In genetic counseling psychological dimensions. New York: Academic Press. Grobstein, R. (1979). Amniocentesis counseling. In genetic counseling psychological dimensions. New York: Academic Press.
Zurück zum Zitat Groeneweg, J. A., Bhonsale, A., James, C. A., te Riele, A. S., Dooijes, D., Tichnell, C., et al. (2015). Clinical presentation, long-term follow-up, and outcomes of 1001 arrhythmogenic right ventricular dysplasia/cardiomyopathy patients and family members. Circulation. Cardiovascular Genetics, 8(3), 437–446. doi:10.1161/CIRCGENETICS.114.001003.PubMedCrossRef Groeneweg, J. A., Bhonsale, A., James, C. A., te Riele, A. S., Dooijes, D., Tichnell, C., et al. (2015). Clinical presentation, long-term follow-up, and outcomes of 1001 arrhythmogenic right ventricular dysplasia/cardiomyopathy patients and family members. Circulation. Cardiovascular Genetics, 8(3), 437–446. doi:10.​1161/​CIRCGENETICS.​114.​001003.PubMedCrossRef
Zurück zum Zitat Hameed, A., Karaalp, I. S., Tummala, P. P., Wani, O. R., Canetti, M., Akhter, M. W., et al. (2001). The effect of valvular heart disease on maternal and fetal outcome of pregnancy. Journal of the American College of Cardiology, 37, 893–899.PubMedCrossRef Hameed, A., Karaalp, I. S., Tummala, P. P., Wani, O. R., Canetti, M., Akhter, M. W., et al. (2001). The effect of valvular heart disease on maternal and fetal outcome of pregnancy. Journal of the American College of Cardiology, 37, 893–899.PubMedCrossRef
Zurück zum Zitat Hassan, N., Patenaude, V., Oddy, L., & Abenhaim, H. A. (2015). Pregnancy outcomes in Marfan syndrome: A retrospective cohort study. American Journal of Perinatology, 30, 123–130.PubMedCrossRef Hassan, N., Patenaude, V., Oddy, L., & Abenhaim, H. A. (2015). Pregnancy outcomes in Marfan syndrome: A retrospective cohort study. American Journal of Perinatology, 30, 123–130.PubMedCrossRef
Zurück zum Zitat Helbig, K. L., Bernhardt, B. A., Conway, L. J., Valverde, K. D., Helbig, I., & Sperling, M. R. (2010). Genetic risk perception and reproductive decision making among people with epilepsy. Epilepsia, 51, 1874–1877.PubMedCrossRef Helbig, K. L., Bernhardt, B. A., Conway, L. J., Valverde, K. D., Helbig, I., & Sperling, M. R. (2010). Genetic risk perception and reproductive decision making among people with epilepsy. Epilepsia, 51, 1874–1877.PubMedCrossRef
Zurück zum Zitat Hershberger, R. E., Hedges, D. J., & Morales, A. (2013). Dilated cardiomyopathy: The complexity of a diverse genetic architecture. Nature Reviews. Cardiology, 10, 531–547.PubMedCrossRef Hershberger, R. E., Hedges, D. J., & Morales, A. (2013). Dilated cardiomyopathy: The complexity of a diverse genetic architecture. Nature Reviews. Cardiology, 10, 531–547.PubMedCrossRef
Zurück zum Zitat Hess, R. F., & Weinland, J. A. (2012). The life-changing impact of peripartum cardiomyopathy: An analysis of online postings. MCN: American Journal of Maternal Child Nursing, 37, 241–246.PubMed Hess, R. F., & Weinland, J. A. (2012). The life-changing impact of peripartum cardiomyopathy: An analysis of online postings. MCN: American Journal of Maternal Child Nursing, 37, 241–246.PubMed
Zurück zum Zitat Hess, R. F., Weinland, J. A., & Beebe, K. (2010). "I am not alone": A survey of women with peripartum cardiomyopathy and their participation in an online support group. Computers, Informatics, Nursing, 28, 215–221.PubMedCrossRef Hess, R. F., Weinland, J. A., & Beebe, K. (2010). "I am not alone": A survey of women with peripartum cardiomyopathy and their participation in an online support group. Computers, Informatics, Nursing, 28, 215–221.PubMedCrossRef
Zurück zum Zitat Hidayatallah, N., Silverstein, L. B., Stolerman, M., McDonald, T., Walsh, C. A., Paljevic, E., et al. (2014). Psychological stress associated with cardiogenetic conditions. Personalized Medicine, 11, 631–640.PubMedPubMedCentralCrossRef Hidayatallah, N., Silverstein, L. B., Stolerman, M., McDonald, T., Walsh, C. A., Paljevic, E., et al. (2014). Psychological stress associated with cardiogenetic conditions. Personalized Medicine, 11, 631–640.PubMedPubMedCentralCrossRef
Zurück zum Zitat Higgins, R. O., Murphy, B., Nicholas, A., Worcester, M., & Lindner, H. (2007). Emotional and adjustment issues faced by cardiac patients seen in clinical practice: A qualitative survey of experienced clinicians. Journal of Cardiopulmonary Rehabilitation and Prevention, 27, 291–297.PubMedCrossRef Higgins, R. O., Murphy, B., Nicholas, A., Worcester, M., & Lindner, H. (2007). Emotional and adjustment issues faced by cardiac patients seen in clinical practice: A qualitative survey of experienced clinicians. Journal of Cardiopulmonary Rehabilitation and Prevention, 27, 291–297.PubMedCrossRef
Zurück zum Zitat Immer, F. F., Bansi, A. G., Immer-Bansi, A. S., McDougall, J., Zehr, K. J., Schaff, H. V., et al. (2003). Aortic dissection in pregnancy: Analysis of risk factors and outcome. The Annals of Thoracic Surgery, 76, 309–314.PubMedCrossRef Immer, F. F., Bansi, A. G., Immer-Bansi, A. S., McDougall, J., Zehr, K. J., Schaff, H. V., et al. (2003). Aortic dissection in pregnancy: Analysis of risk factors and outcome. The Annals of Thoracic Surgery, 76, 309–314.PubMedCrossRef
Zurück zum Zitat Ingles, J., Lind, J., Phongsavan, P., & Semsarian, C. (2008). Psychosocial impact of specialized cardiac genetic clinics for hypertrophic cardiomyopathy. Genetics in Medicine, 10, 117–120.PubMedCrossRef Ingles, J., Lind, J., Phongsavan, P., & Semsarian, C. (2008). Psychosocial impact of specialized cardiac genetic clinics for hypertrophic cardiomyopathy. Genetics in Medicine, 10, 117–120.PubMedCrossRef
Zurück zum Zitat Jacobs, K., Giacobbe, L., Aguilera, M., Ramin, K., & Sivanandam, S. (2014). A case of fetal diagnosis of noncompaction cardiomyopathy and coarctation of the aorta. AJP Report, 4, 45–48.CrossRef Jacobs, K., Giacobbe, L., Aguilera, M., Ramin, K., & Sivanandam, S. (2014). A case of fetal diagnosis of noncompaction cardiomyopathy and coarctation of the aorta. AJP Report, 4, 45–48.CrossRef
Zurück zum Zitat Joglar, J. A., & Page, R. L. (2014). Management of arrhythmia syndromes during pregnancy. Current Opinion in Cardiology, 29, 36–44.PubMedCrossRef Joglar, J. A., & Page, R. L. (2014). Management of arrhythmia syndromes during pregnancy. Current Opinion in Cardiology, 29, 36–44.PubMedCrossRef
Zurück zum Zitat Kanal, E., Barkovich, A. J., Bell, C., Borgstede, J. P., Bradley Jr., W. G., Froelich, J. W., et al. (2013). ACR guidance document on MR safe practices: 2013. Journal of Magnetic Resonance Imaging, 37, 501–530.PubMedCrossRef Kanal, E., Barkovich, A. J., Bell, C., Borgstede, J. P., Bradley Jr., W. G., Froelich, J. W., et al. (2013). ACR guidance document on MR safe practices: 2013. Journal of Magnetic Resonance Imaging, 37, 501–530.PubMedCrossRef
Zurück zum Zitat Kerstjens-Frederikse, W. S., Du Marchie Sarvaas, G. J., Ruiter, J. S., Van Den Akker, P. C., Temmerman, A. M., Van Melle, J. P., et al. (2011). Left ventricular outflow tract obstruction: Should cardiac screening be offered to first-degree relatives? Heart, 97, 1228–1232.PubMedCrossRef Kerstjens-Frederikse, W. S., Du Marchie Sarvaas, G. J., Ruiter, J. S., Van Den Akker, P. C., Temmerman, A. M., Van Melle, J. P., et al. (2011). Left ventricular outflow tract obstruction: Should cardiac screening be offered to first-degree relatives? Heart, 97, 1228–1232.PubMedCrossRef
Zurück zum Zitat Klitzman, R., Thorne, D., Williamson, J., Chung, W., & Marder, K. (2007). Decision-making about reproductive choices among individuals at-risk for Huntington's disease. Journal of Genetic Counseling, 16, 347–362.PubMedCrossRef Klitzman, R., Thorne, D., Williamson, J., Chung, W., & Marder, K. (2007). Decision-making about reproductive choices among individuals at-risk for Huntington's disease. Journal of Genetic Counseling, 16, 347–362.PubMedCrossRef
Zurück zum Zitat Kuliev, A., Pomerantseva, E., Polling, D., Verlinsky, O., & Rechitsky, S. (2012). PGD for inherited cardiac diseases. Reproductive Biomedicine Online, 24, 443–453.PubMedCrossRef Kuliev, A., Pomerantseva, E., Polling, D., Verlinsky, O., & Rechitsky, S. (2012). PGD for inherited cardiac diseases. Reproductive Biomedicine Online, 24, 443–453.PubMedCrossRef
Zurück zum Zitat Lima, F. V., Parikh, P. B., Zhu, J., Yang, J., & Stergiopoulos, K. (2015). Association of cardiomyopathy with adverse cardiac events in pregnant women at the time of delivery. JACC Heart Fail, 3, 257–266.PubMedCrossRef Lima, F. V., Parikh, P. B., Zhu, J., Yang, J., & Stergiopoulos, K. (2015). Association of cardiomyopathy with adverse cardiac events in pregnant women at the time of delivery. JACC Heart Fail, 3, 257–266.PubMedCrossRef
Zurück zum Zitat Lind, J., & Wallenburg, H. C. (2001). The Marfan syndrome and pregnancy: A retrospective study in a Dutch population. European Journal of Obstetrics, Gynecology, and Reproductive Biology, 98, 28–35.PubMedCrossRef Lind, J., & Wallenburg, H. C. (2001). The Marfan syndrome and pregnancy: A retrospective study in a Dutch population. European Journal of Obstetrics, Gynecology, and Reproductive Biology, 98, 28–35.PubMedCrossRef
Zurück zum Zitat Loeys, B. L., Dietz, H. C., Braverman, A. C., Callewaert, B. L., De Backer, J., Devereux, R. B., et al. (2010). The revised Ghent nosology for the Marfan syndrome. Journal of Medical Genetics, 47, 476–485.PubMedCrossRef Loeys, B. L., Dietz, H. C., Braverman, A. C., Callewaert, B. L., De Backer, J., Devereux, R. B., et al. (2010). The revised Ghent nosology for the Marfan syndrome. Journal of Medical Genetics, 47, 476–485.PubMedCrossRef
Zurück zum Zitat Lu, C. W., Shih, J. C., Chen, S. Y., Chiu, H. H., Wang, J. K., Chen, C. A., et al. (2015). Comparison of 3 risk estimation methods for predicting cardiac outcomes in pregnant women with congenital heart disease. Circulation Journal, 79, 1609–1617.PubMedCrossRef Lu, C. W., Shih, J. C., Chen, S. Y., Chiu, H. H., Wang, J. K., Chen, C. A., et al. (2015). Comparison of 3 risk estimation methods for predicting cardiac outcomes in pregnant women with congenital heart disease. Circulation Journal, 79, 1609–1617.PubMedCrossRef
Zurück zum Zitat Malfait, F., Wenstrup, R., De Paepe, A. (1997-2013). Ehlers-Danlos Syndrome, Classic Type. In: GeneReviews at GeneTests Medical Genetics Information Resource (database online). Retrieved 23 Apr 2016 http://www.genetests.org. Malfait, F., Wenstrup, R., De Paepe, A. (1997-2013). Ehlers-Danlos Syndrome, Classic Type. In: GeneReviews at GeneTests Medical Genetics Information Resource (database online). Retrieved 23 Apr 2016 http://​www.​genetests.​org.
Zurück zum Zitat Malfait, F., Wenstrup, R. J., & De Paepe, A. (2010). Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type. Genetics in Medicine, 12, 597–605.PubMedCrossRef Malfait, F., Wenstrup, R. J., & De Paepe, A. (2010). Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type. Genetics in Medicine, 12, 597–605.PubMedCrossRef
Zurück zum Zitat Meijboom, L. J., Vos, F. E., Timmermans, J., Boers, G. H., Zwinderman, A. H., & Mulder, B. J. (2005). Pregnancy and aortic root growth in the Marfan syndrome: A prospective study. European Heart Journal, 26, 914–920.PubMedCrossRef Meijboom, L. J., Vos, F. E., Timmermans, J., Boers, G. H., Zwinderman, A. H., & Mulder, B. J. (2005). Pregnancy and aortic root growth in the Marfan syndrome: A prospective study. European Heart Journal, 26, 914–920.PubMedCrossRef
Zurück zum Zitat Morales, A., Cowan, J., Dagua, J., & Hershberger, R. E. (2008). Family history: An essential tool for cardiovascular genetic medicine. Congestive Heart Failure, 14(1), 37–45.PubMedCrossRef Morales, A., Cowan, J., Dagua, J., & Hershberger, R. E. (2008). Family history: An essential tool for cardiovascular genetic medicine. Congestive Heart Failure, 14(1), 37–45.PubMedCrossRef
Zurück zum Zitat Morales, A., Painter, T., Li, R., Siegfried, J. D., Li, D., Norton, N., et al. (2010). Rare variant mutations in pregnancy-associated or peripartum cardiomyopathy. Circulation, 121, 2176–2182.PubMedPubMedCentralCrossRef Morales, A., Painter, T., Li, R., Siegfried, J. D., Li, D., Norton, N., et al. (2010). Rare variant mutations in pregnancy-associated or peripartum cardiomyopathy. Circulation, 121, 2176–2182.PubMedPubMedCentralCrossRef
Zurück zum Zitat Morgan, J. F., O'Donoghue, A. C., McKenna, W. J., & Schmidt, M. M. (2008). Psychiatric disorders in hypertrophic cardiomyopathy. General Hospital Psychiatry, 30, 49–54.PubMedCrossRef Morgan, J. F., O'Donoghue, A. C., McKenna, W. J., & Schmidt, M. M. (2008). Psychiatric disorders in hypertrophic cardiomyopathy. General Hospital Psychiatry, 30, 49–54.PubMedCrossRef
Zurück zum Zitat Mozaffarian, D., Benjamin, E. J., Go, A. S., Arnett, D. K., Blaha, M. J., Cushman, M., et al. (2015). Heart disease and stroke statistics--2015 update: A report from the American Heart Association. Circulation, 131, e29–322.PubMedCrossRef Mozaffarian, D., Benjamin, E. J., Go, A. S., Arnett, D. K., Blaha, M. J., Cushman, M., et al. (2015). Heart disease and stroke statistics--2015 update: A report from the American Heart Association. Circulation, 131, e29–322.PubMedCrossRef
Zurück zum Zitat Murray, M. L., Pepin, M., Peterson, S., & Byers, P. H. (2014). Pregnancy-related deaths and complications in women with vascular Ehlers-Danlos syndrome. Genetics in Medicine, 16, 874–880.PubMedCrossRef Murray, M. L., Pepin, M., Peterson, S., & Byers, P. H. (2014). Pregnancy-related deaths and complications in women with vascular Ehlers-Danlos syndrome. Genetics in Medicine, 16, 874–880.PubMedCrossRef
Zurück zum Zitat Nakagawa, M., Katou, S., Ichinose, M., Nobe, S., Yonemochi, H., Miyakawa, I., et al. (2004). Characteristics of new-onset ventricular arrhythmias in pregnancy. Journal of Electrocardiology, 37, 47–53.PubMedCrossRef Nakagawa, M., Katou, S., Ichinose, M., Nobe, S., Yonemochi, H., Miyakawa, I., et al. (2004). Characteristics of new-onset ventricular arrhythmias in pregnancy. Journal of Electrocardiology, 37, 47–53.PubMedCrossRef
Zurück zum Zitat Napolitano, C., Priori, S.G., Bloise, R. (2004-2016). Catecholaminergic Polymorphic Ventricular Tachycardia. In GeneReviews at GeneTests Medical Genetics Information Resource (database online). Retrieved 20 Oct 2016 http://www.genetests.org. Napolitano, C., Priori, S.G., Bloise, R. (2004-2016). Catecholaminergic Polymorphic Ventricular Tachycardia. In GeneReviews at GeneTests Medical Genetics Information Resource (database online). Retrieved 20 Oct 2016 http://​www.​genetests.​org.
Zurück zum Zitat Naqvi, T. Z. (2014). Challenges in cardiology research in pregnancy. Future Cardiology, 10, 759–768.PubMedCrossRef Naqvi, T. Z. (2014). Challenges in cardiology research in pregnancy. Future Cardiology, 10, 759–768.PubMedCrossRef
Zurück zum Zitat National Institutes of Health Genetic Testing Registry (database online). (2013). Copyright, National Center for biotechnology information. Bethesda, Maryland: U.S. National Library of Medicine Available at http://www.ncbi.nlm.nih.gov/gtr/ Accessed 11 Jan 2016. National Institutes of Health Genetic Testing Registry (database online). (2013). Copyright, National Center for biotechnology information. Bethesda, Maryland: U.S. National Library of Medicine Available at http://​www.​ncbi.​nlm.​nih.​gov/​gtr/​ Accessed 11 Jan 2016.
Zurück zum Zitat Nizamuddin, S. L., Broderick, D. K., Minehart, R. D., & Kamdar, B. B. (2015). Spontaneous coronary artery dissection in a parturient with nail-patella syndrome. International Journal of Obstetric Anesthesia, 24, 69–73.PubMedCrossRef Nizamuddin, S. L., Broderick, D. K., Minehart, R. D., & Kamdar, B. B. (2015). Spontaneous coronary artery dissection in a parturient with nail-patella syndrome. International Journal of Obstetric Anesthesia, 24, 69–73.PubMedCrossRef
Zurück zum Zitat Omnes, S., Jondeau, G., Detaint, D., Dumont, A., Yazbeck, C., Guglielminotti, J., et al. (2013). Pregnancy outcomes among women with Marfan syndrome. International Journal of Gynaecology and Obstetrics, 122, 219–223.PubMedCrossRef Omnes, S., Jondeau, G., Detaint, D., Dumont, A., Yazbeck, C., Guglielminotti, J., et al. (2013). Pregnancy outcomes among women with Marfan syndrome. International Journal of Gynaecology and Obstetrics, 122, 219–223.PubMedCrossRef
Zurück zum Zitat Palmer, D. G. (2006). Peripartum cardiomyopathy. The Journal of Perinatal & Neonatal Nursing, 20, 324–332.CrossRef Palmer, D. G. (2006). Peripartum cardiomyopathy. The Journal of Perinatal & Neonatal Nursing, 20, 324–332.CrossRef
Zurück zum Zitat Palmquist, M., Pappas, J. G., Petrikovsky, B., Blakemore, K., & Roshan, D. (2009). Successful pregnancy outcome in Ehlers-Danlos syndrome, vascular type. The Journal of Maternal-Fetal & Neonatal Medicine, 22, 924–927.CrossRef Palmquist, M., Pappas, J. G., Petrikovsky, B., Blakemore, K., & Roshan, D. (2009). Successful pregnancy outcome in Ehlers-Danlos syndrome, vascular type. The Journal of Maternal-Fetal & Neonatal Medicine, 22, 924–927.CrossRef
Zurück zum Zitat Panayotova, R., Macnab, A., & Waterworth, P. D. (2013). A pilot project of familial screening in patients with bicuspid aortic valve disease. The Journal of Heart Valve Disease, 22, 150–155.PubMed Panayotova, R., Macnab, A., & Waterworth, P. D. (2013). A pilot project of familial screening in patients with bicuspid aortic valve disease. The Journal of Heart Valve Disease, 22, 150–155.PubMed
Zurück zum Zitat Pedra, S. R., Smallhorn, J. F., Ryan, G., Chitayat, D., Taylor, G. P., Khan, R., et al. (2002). Fetal cardiomyopathies: Pathogenic mechanisms, hemodynamic findings, and clinical outcome. Circulation, 106, 585–591.PubMedCrossRef Pedra, S. R., Smallhorn, J. F., Ryan, G., Chitayat, D., Taylor, G. P., Khan, R., et al. (2002). Fetal cardiomyopathies: Pathogenic mechanisms, hemodynamic findings, and clinical outcome. Circulation, 106, 585–591.PubMedCrossRef
Zurück zum Zitat Pepin, M., Murray, M.L., Byers, B.H. (1997-2013). Vascular Ehlers Danlos. In GeneReviews at GeneTests Medical Genetics Information Resource (database online). Retrieved 23 Apr 2016 http://www.genetests.org. Pepin, M., Murray, M.L., Byers, B.H. (1997-2013). Vascular Ehlers Danlos. In GeneReviews at GeneTests Medical Genetics Information Resource (database online). Retrieved 23 Apr 2016 http://​www.​genetests.​org.
Zurück zum Zitat Pepin, M. G., Schwarze, U., Rice, K. M., Liu, M., Leistritz, D., & Byers, P. H. (2014). Survival is affected by mutation type and molecular mechanism in vascular Ehlers-Danlos syndrome (EDS type IV). Genetics in Medicine, 16, 881–888.PubMedCrossRef Pepin, M. G., Schwarze, U., Rice, K. M., Liu, M., Leistritz, D., & Byers, P. H. (2014). Survival is affected by mutation type and molecular mechanism in vascular Ehlers-Danlos syndrome (EDS type IV). Genetics in Medicine, 16, 881–888.PubMedCrossRef
Zurück zum Zitat Pierpont, M. E., Basson, C. T., Benson, D. W., Gelb, B. D., Giglia, T. M., Goldmuntz, E., McGee, G., Sable, C. A., Srivastava, D., & Webb, C. L. (2007). Genetic basis for congenital heart defects: Current knowledge: A scientific statement from the American Heart Association congenital cardiac defects committee, council on cardiovascular disease in the young: Endorsed by the American Academy of Pediatrics. Circulation, 115, 3015–3038.PubMedCrossRef Pierpont, M. E., Basson, C. T., Benson, D. W., Gelb, B. D., Giglia, T. M., Goldmuntz, E., McGee, G., Sable, C. A., Srivastava, D., & Webb, C. L. (2007). Genetic basis for congenital heart defects: Current knowledge: A scientific statement from the American Heart Association congenital cardiac defects committee, council on cardiovascular disease in the young: Endorsed by the American Academy of Pediatrics. Circulation, 115, 3015–3038.PubMedCrossRef
Zurück zum Zitat Pijuan-Domenech, A., Galian, L., Goya, M., Casellas, M., Merced, C., Ferreira-Gonzalez, I., et al. (2015). Cardiac complications during pregnancy are better predicted with the modified WHO risk score. International Journal of Cardiology, 195, 149–154.PubMedCrossRef Pijuan-Domenech, A., Galian, L., Goya, M., Casellas, M., Merced, C., Ferreira-Gonzalez, I., et al. (2015). Cardiac complications during pregnancy are better predicted with the modified WHO risk score. International Journal of Cardiology, 195, 149–154.PubMedCrossRef
Zurück zum Zitat Poole, N. A., & Morgan, J. F. (2006). Validity and reliability of the hospital anxiety and depression scale in a hypertrophic cardiomyopathy clinic: The HADS in a cardiomyopathy population. General Hospital Psychiatry, 28, 55–58.PubMedCrossRef Poole, N. A., & Morgan, J. F. (2006). Validity and reliability of the hospital anxiety and depression scale in a hypertrophic cardiomyopathy clinic: The HADS in a cardiomyopathy population. General Hospital Psychiatry, 28, 55–58.PubMedCrossRef
Zurück zum Zitat Postma, A. V., Denjoy, I., Kamblock, J., Alders, M., Lupoglazoff, J. M., Vaksmann, G., et al. (2005). Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients. Journal of Medical Genetics, 42(11), 863–870. doi:10.1136/jmg.2004.028993.PubMedPubMedCentralCrossRef Postma, A. V., Denjoy, I., Kamblock, J., Alders, M., Lupoglazoff, J. M., Vaksmann, G., et al. (2005). Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients. Journal of Medical Genetics, 42(11), 863–870. doi:10.​1136/​jmg.​2004.​028993.PubMedPubMedCentralCrossRef
Zurück zum Zitat Priori, S. G., Wilde, A. A., Horie, M., Cho, Y., Behr, E. R., Berul, C., et al. (2013). HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: Document endorsed by HRS, EHRA, and APHRS in may 2013 and by ACCF, AHA, PACES, and AEPC in June 2013. Heart Rhythm, 10, 1932–1963.PubMedCrossRef Priori, S. G., Wilde, A. A., Horie, M., Cho, Y., Behr, E. R., Berul, C., et al. (2013). HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: Document endorsed by HRS, EHRA, and APHRS in may 2013 and by ACCF, AHA, PACES, and AEPC in June 2013. Heart Rhythm, 10, 1932–1963.PubMedCrossRef
Zurück zum Zitat Rashba, E. J., Zareba, W., Moss, A. J., Hall, W. J., Robinson, J., Locati, E. H., et al. (1998). Influence of pregnancy on the risk for cardiac events in patients with hereditary long QT syndrome. LQTS Investigators. Circulation, 97, 451–456.PubMedCrossRef Rashba, E. J., Zareba, W., Moss, A. J., Hall, W. J., Robinson, J., Locati, E. H., et al. (1998). Influence of pregnancy on the risk for cardiac events in patients with hereditary long QT syndrome. LQTS Investigators. Circulation, 97, 451–456.PubMedCrossRef
Zurück zum Zitat Regitz-Zagrosek, V., Blomstrom Lundqvist, C., Borghi, C., Cifkova, R., Ferreira, R., Foidart, J. M., et al. (2011). 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). European Heart Journal, 32, 3147–3197.PubMedCrossRef Regitz-Zagrosek, V., Blomstrom Lundqvist, C., Borghi, C., Cifkova, R., Ferreira, R., Foidart, J. M., et al. (2011). 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). European Heart Journal, 32, 3147–3197.PubMedCrossRef
Zurück zum Zitat Regitz-Zagrosek, V., Gohlke-Barwolf, C., Iung, B., & Pieper, P. G. (2014). Management of cardiovascular diseases during pregnancy. Current Problems in Cardiology, 39, 85–151.PubMedCrossRef Regitz-Zagrosek, V., Gohlke-Barwolf, C., Iung, B., & Pieper, P. G. (2014). Management of cardiovascular diseases during pregnancy. Current Problems in Cardiology, 39, 85–151.PubMedCrossRef
Zurück zum Zitat Rychik, J., Donaghue, D. D., Levy, S., Fajardo, C., Combs, J., Zhang, X., et al. (2013). Maternal psychological stress after prenatal diagnosis of congenital heart disease. The Journal of Pediatrics, 162(302–307), e301. Rychik, J., Donaghue, D. D., Levy, S., Fajardo, C., Combs, J., Zhang, X., et al. (2013). Maternal psychological stress after prenatal diagnosis of congenital heart disease. The Journal of Pediatrics, 162(302–307), e301.
Zurück zum Zitat Seth, R., Moss, A. J., McNitt, S., Zareba, W., Andrews, M. L., Qi, M., et al. (2007). Long QT syndrome and pregnancy. Journal of the American College of Cardiology, 49, 1092–1098.PubMedCrossRef Seth, R., Moss, A. J., McNitt, S., Zareba, W., Andrews, M. L., Qi, M., et al. (2007). Long QT syndrome and pregnancy. Journal of the American College of Cardiology, 49, 1092–1098.PubMedCrossRef
Zurück zum Zitat Siu, S. C., Sermer, M., Colman, J. M., Alvarez, A. N., Mercier, L. A., Morton, B. C., et al. (2001). Prospective multicenter study of pregnancy outcomes in women with heart disease. Circulation, 104, 515–521.PubMedCrossRef Siu, S. C., Sermer, M., Colman, J. M., Alvarez, A. N., Mercier, L. A., Morton, B. C., et al. (2001). Prospective multicenter study of pregnancy outcomes in women with heart disease. Circulation, 104, 515–521.PubMedCrossRef
Zurück zum Zitat Sliwa, K., van Hagen, I. M., Budts, W., Swan, L., Sinagra, G., Caruana, M., et al. (2016). Pulmonary hypertension and pregnancy outcomes: Data from the registry of pregnancy and cardiac disease (ROPAC) of the European Society of Cardiology. European Journal of Heart Failure, 18, 1119–1128.PubMedCrossRef Sliwa, K., van Hagen, I. M., Budts, W., Swan, L., Sinagra, G., Caruana, M., et al. (2016). Pulmonary hypertension and pregnancy outcomes: Data from the registry of pregnancy and cardiac disease (ROPAC) of the European Society of Cardiology. European Journal of Heart Failure, 18, 1119–1128.PubMedCrossRef
Zurück zum Zitat Tanaka, K., Tanaka, H., Kamiya, C., Katsuragi, S., Sawada, M., Tsuritani, M., et al. (2016). Beta-blockers and fetal growth restriction in pregnant women with cardiovascular disease. Circulation Journal, 80, 2221–2226.PubMedCrossRef Tanaka, K., Tanaka, H., Kamiya, C., Katsuragi, S., Sawada, M., Tsuritani, M., et al. (2016). Beta-blockers and fetal growth restriction in pregnant women with cardiovascular disease. Circulation Journal, 80, 2221–2226.PubMedCrossRef
Zurück zum Zitat Tarani, L., Lampariello, S., Raguso, G., Colloridi, F., Pucarelli, I., Pasquino, A. M., et al. (1998). Pregnancy in patients with Turner's syndrome: Six new cases and review of literature. Gynecological Endocrinology, 12, 83–87.PubMedCrossRef Tarani, L., Lampariello, S., Raguso, G., Colloridi, F., Pucarelli, I., Pasquino, A. M., et al. (1998). Pregnancy in patients with Turner's syndrome: Six new cases and review of literature. Gynecological Endocrinology, 12, 83–87.PubMedCrossRef
Zurück zum Zitat Teekakirikul, P., Kelly, M. A., Rehm, H. L., Lakdawala, N. K., & Funke, B. H. (2013). Inherited cardiomyopathies: Molecular genetics and clinical genetic testing in the postgenomic era. The Journal of Molecular Diagnostics, 15, 158–170.PubMedCrossRef Teekakirikul, P., Kelly, M. A., Rehm, H. L., Lakdawala, N. K., & Funke, B. H. (2013). Inherited cardiomyopathies: Molecular genetics and clinical genetic testing in the postgenomic era. The Journal of Molecular Diagnostics, 15, 158–170.PubMedCrossRef
Zurück zum Zitat Tsiaras, S., & Poppas, A. (2009). Mitral valve disease in pregnancy: Outcomes and management. Obstetrics Medicine, 2, 6–10.CrossRef Tsiaras, S., & Poppas, A. (2009). Mitral valve disease in pregnancy: Outcomes and management. Obstetrics Medicine, 2, 6–10.CrossRef
Zurück zum Zitat van Spaendonck-Zwarts, K. Y., Posafalvi, A., van den Berg, M. P., Hilfiker-Kleiner, D., Bollen, I. A., Sliwa, K., et al. (2014). Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy. European Heart Journal, 35, 2165–2173.PubMedCrossRef van Spaendonck-Zwarts, K. Y., Posafalvi, A., van den Berg, M. P., Hilfiker-Kleiner, D., Bollen, I. A., Sliwa, K., et al. (2014). Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy. European Heart Journal, 35, 2165–2173.PubMedCrossRef
Zurück zum Zitat Van Tintelen, J. P., Pieper, P. G., Van Spaendonck-Zwarts, K. Y., & Van Den Berg, M. P. (2014). Pregnancy, cardiomyopathies, and genetics. Cardiovascular Research, 101, 571–578.PubMedCrossRef Van Tintelen, J. P., Pieper, P. G., Van Spaendonck-Zwarts, K. Y., & Van Den Berg, M. P. (2014). Pregnancy, cardiomyopathies, and genetics. Cardiovascular Research, 101, 571–578.PubMedCrossRef
Zurück zum Zitat Vohnout, B., Gabcova, D., Huckova, M., Klimes, I., Gasperikova, D., & Raslova, K. (2016). Genetic testing of familial hypercholesterolemia in a real clinical setting. Wien Klin Wochenschr. Epub. doi:10.1007/s00508-016-1053-2. Vohnout, B., Gabcova, D., Huckova, M., Klimes, I., Gasperikova, D., & Raslova, K. (2016). Genetic testing of familial hypercholesterolemia in a real clinical setting. Wien Klin Wochenschr. Epub. doi:10.​1007/​s00508-016-1053-2.
Zurück zum Zitat Wanga, S., Silversides, C., Dore, A., de Waard, V., & Mulder, B. (2016). Pregnancy and thoracic aortic disease: Managing the risks. The Canadian Journal of Cardiology, 32, 78–85.PubMedCrossRef Wanga, S., Silversides, C., Dore, A., de Waard, V., & Mulder, B. (2016). Pregnancy and thoracic aortic disease: Managing the risks. The Canadian Journal of Cardiology, 32, 78–85.PubMedCrossRef
Zurück zum Zitat Webb, G., & Gatzoulis, M. A. (2006). Atrial septal defects in the adult: Recent progress and overview. Circulation, 114, 1645–1653.PubMedCrossRef Webb, G., & Gatzoulis, M. A. (2006). Atrial septal defects in the adult: Recent progress and overview. Circulation, 114, 1645–1653.PubMedCrossRef
Zurück zum Zitat Webb, G., & Williams, R. (2001). 32nd Bethesda conference: ‘care of the adult with congenital heart disease’. Journal of the American College of Cardiology, 37, 1162–1198.CrossRef Webb, G., & Williams, R. (2001). 32nd Bethesda conference: ‘care of the adult with congenital heart disease’. Journal of the American College of Cardiology, 37, 1162–1198.CrossRef
Zurück zum Zitat Weil, J. (2000). Psychosocial genetic counseling (pp. 155). New York: Oxford University Press. Weil, J. (2000). Psychosocial genetic counseling (pp. 155). New York: Oxford University Press.
Zurück zum Zitat Wilkins, R. G., & Unverdorben, M. (2012). Accidental intravenous infusion of air: A concise review. Journal of Infusion Nursing, 35, 404–408.PubMedCrossRef Wilkins, R. G., & Unverdorben, M. (2012). Accidental intravenous infusion of air: A concise review. Journal of Infusion Nursing, 35, 404–408.PubMedCrossRef
Zurück zum Zitat Yuan, S. M. (2013). Postpartum aortic dissection. Taiwanese Journal of Obstetrics & Gynecology, 52, 318–322.CrossRef Yuan, S. M. (2013). Postpartum aortic dissection. Taiwanese Journal of Obstetrics & Gynecology, 52, 318–322.CrossRef
Metadaten
Titel
At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease
verfasst von
Ana Morales
Dawn C. Allain
Patricia Arscott
Emily James
Gretchen MacCarrick
Brittney Murray
Crystal Tichnell
Amy R. Shikany
Sara Spencer
Sara M. Fitzgerald-Butt
Jessica D. Kushner
Christi Munn
Emily Smith
Katherine G. Spoonamore
Harikrishna S. Tandri
W. Aaron Kay
Publikationsdatum
10.03.2017
Verlag
Springer US
Erschienen in
Journal of Genetic Counseling / Ausgabe 4/2017
Print ISSN: 1059-7700
Elektronische ISSN: 1573-3599
DOI
https://doi.org/10.1007/s10897-017-0081-z

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