| Literature DB >> 33609068 |
Karen Sliwa1, Peter van der Meer2, Mark C Petrie3, Alexandra Frogoudaki4, Mark R Johnson5, Denise Hilfiker-Kleiner6, Righab Hamdan7, Alice M Jackson3, Bassem Ibrahim8, Amam Mbakwem9, Carsten Tschöpe10, Vera Regitz-Zagrosek11, Elmir Omerovic12, Jolien Roos-Hesselink13, Michael Gatzoulis14, Oktay Tutarel15, Susanna Price16, Stephane Heymans17,18, Andrew J S Coats19, Christian Müller20, Ovidiu Chioncel21, Thomas Thum22, Rudolf A de Boer2, Ewa Jankowska23, Piotr Ponikowski23, Alexander R Lyon24, Giuseppe Rosano18,25, Petar M Seferovic26,27, Johann Bauersachs6.
Abstract
This position paper focusses on the pathophysiology, diagnosis and management of women diagnosed with a cardiomyopathy, or at risk of heart failure (HF), who are planning to conceive or present with (de novo or previously unknown) HF during or after pregnancy. This includes the heterogeneous group of heart muscle diseases such as hypertrophic, dilated, arrhythmogenic right ventricular and non-classified cardiomyopathies, left ventricular non-compaction, peripartum cardiomyopathy, Takotsubo syndrome, adult congenital heart disease with HF, and patients with right HF. Also, patients with a history of chemo-/radiotherapy for cancer or haematological malignancies need specific pre-, during and post-pregnancy assessment and counselling. We summarize the current knowledge about pathophysiological mechanisms, including gene mutations, clinical presentation, diagnosis, and medical and device management, as well as risk stratification. Women with a known diagnosis of a cardiomyopathy will often require continuation of drug therapy, which has the potential to exert negative effects on the foetus. This position paper assists in balancing benefits and detrimental effects.Entities:
Keywords: Cancer; Heart failure; Pregnancy
Mesh:
Year: 2021 PMID: 33609068 DOI: 10.1002/ejhf.2133
Source DB: PubMed Journal: Eur J Heart Fail ISSN: 1388-9842 Impact factor: 15.534