Abstract
Peripartum cardiomyopathy (PPCM) is a specific cardiomyopathy in which heart failure develops during pregnancy or in the postpartum period in women without a history of heart disease, and reduced myocardial contraction is found on examination. The frequency of this condition is low in routine medical practice, but it should be included in differential diagnosis for pregnant and postpartum women who complain of dyspnea and excessive edema because it may lead to maternal death in severe cases. Advanced age, grand multipara, multiple conception, hypertensive disorders in pregnancy (HDP), and use of tocolytic agents are known risk factors. Especially, HDP is the strongest risk factor and complicates in about 40% of PPCM patients. A Japanese survey found that PPCM patients with HDP tended to have better long-term outcomes than those without. In contrast, PPCM patients with truncating variants associated with dilated cardiomyopathy (DCM) tended to have lower cardiac function in long-term than those without. Basic studies in animals and genetic analyses have recently been reported, and an association between vascular disorder such as HDP cardiomyopathy is currently attracting attention. Since “peripartum cardiomyopathy” is a diagnosis of exclusion, it indicates that PPCM is a group of heterogeneous conditions.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Demakis JG, Rahimtoola SH (1971) Peripartum cardiomyopathy. Circulation 44:964–968
Sliwa K, Hilfiker-Kleiner D, Petrie MC et al (2010) Current state of knowledge on aetiology, diagnosis, management, and therapy of peripartum cardiomyopathy: a position statement from the Heart Failure Association of the European Society of Cardiology Working Group on peripartum cardiomyopathy. Eur J Heart Fail 12:767–778
Tomoike H, Izumi T, Imaizumi T et al (2016) Guidelines for management of dilated cardiomyopathy and secondary cardiomyopathy (JCS 2011). Circ J 80:753–774. http://www.j-circ.or.jp/form/kankoubutsu/guuideline_index.htm
Elkayam U, Akhter MW, Singh H et al (2005) Pregnancy-associated cardiomyopathy: clinical characteristics and a comparison between early and late presentation. Circulation 111(16):2050–2055
Halkein J, Tabruyn SP, Ricke-Hoch M et al (2013) MicroRNA-146a is a therapeutic target and biomarker for peripartum cardiomyopathy. J Clin Invest 123:2143–2154
Kamiya CA, Kitakaze M, Ishibashi-Ueda H et al (2011) Different characteristics of peripartum cardiomyopathy between patients complicated with and without hypertensive disorders. Results from the Japanese Nationwide survey of peripartum cardiomyopathy. Circ J 75:1975–1981
Haghikia A, Podewski E, Libhaber E et al (2013) Phenotyping and outcome on contemporary management in a German cohort of patients with peripartum cardiomyopathy. Basic Res Cardiol 108:366
McNamara DM, Elkayam U, Alharethi R, Damp J, Hsich E, Ewald G et al (2015) Clinical outcomes for peripartum cardiomyopathy in North America: results of the IPAC Study (Investigations of Pregnancy-Associated Cardiomyopathy). J Am Coll Cardiol 66:905–914
Sliwa K, Fett J, Elkayam U (2006) Peripartum cardiomyopathy. Lancet 368:687–693
Sliwa K, Forster O, Libhaber E, Fett JD, Sundstrom JB, Hilfiker-Kleiner D, Ansari AA (2006) Peripartum cardiomyopathy: inflammatory markers as predictors of outcome in 100 prospectively studied patients. Eur Heart J 27:441–446
Kamiya CA, Yoshimatsu J, Ikeda T (2016) Peripartum cardiomyopathy from a genetic perspective. Circ J 80:1684–1688
Pearson GD, Veille JC, Rahimtoola S et al (2000) Peripartum cardiomyopathy: National Heart, Lung, and Blood Institute and Office of Rare Diseases (National Institutes of Health) workshop recommendations and review. JAMA 283:1183–1188
Hilfiker-Kleiner D, Kaminski K, Podewski E et al (2007) A cathepsin D-cleaved 16 kDa form of prolactin mediates postpartum cardiomyopathy. Cell 128:589–600
Patten IS, Rana S, Shahul S et al (2012) Cardiac angiogenic imbalance leads to peripartum cardiomyopathy. Nature 485:333–338
Morales A et al (2010) Rare variant mutations in pregnancy-associated or peripartum cardiomyopathy. Criculation 121:2176–2182
van Spaendonck-Zwarts KY, van Tintelen JP, van Veldhuisen DJ et al (2010) Peripartum cardiomyopathy as a part of familial dilated cardiomyopathy. Circulation 121:2169–2175
Ware JS, Li J, Mazaika E et al (2016) Shared genetic predisposition in peripartum and dilated cardiomyopathies. N Engl J Med 374:233–241
Sliwa K, Blauwet L, Tibazarwa K et al (2010) Evaluation of bromocriptine in the treatment of acute severe peripartum cardiomyopathy: a proof-of-concept pilot study. Circulation 121:1465–1473
Arrigo M, Blet A, Mebazaa A (2017) Bromocriptine for the treatment of peripartum cardiomyopathy: welcome on BOARD. Eur Heart J 38(35):2680–2682
Demakis JG, Rahimtoola SH, Sutton GC et al (1971) Natural course of peripartum cardiomyopathy. Circulation 44:1053–1061
van Spaendonck-Zwarts KY, Posafalvi A, van den Berg MP et al (2014) Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy. Eur Heart J 35:2165–2173
Elkayam U (2014) Risk of subsequent pregnancy in women with a history of peripartum cardiomyopathy. J Am Coll Cardiol 64:1629–1636
Regitz-Zagrosek V, Lundqvist CB, Borghi C et al (2011) ESC guidelines on the management of cardiovascular diseases during pregnancy. Eur Heart J 32:3147–3197
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2019 Springer Science+Business Media Singapore
About this chapter
Cite this chapter
Aoki-Kamiya, C. (2019). Peripartum Cardiomyopathy. In: Ikeda, T., Aoki-Kamiya, C. (eds) Maternal and Fetal Cardiovascular Disease. Springer, Singapore. https://doi.org/10.1007/978-981-10-1993-7_11
Download citation
DOI: https://doi.org/10.1007/978-981-10-1993-7_11
Published:
Publisher Name: Springer, Singapore
Print ISBN: 978-981-10-1991-3
Online ISBN: 978-981-10-1993-7
eBook Packages: MedicineMedicine (R0)