Open AccessClinical presentation and outcomes of peripartum cardiomyopathy in the Middle East: a cohort from seven Arab countries
Author(s) -
Salam Amar M.,
Ahmed Mohamed Badie,
Sulaiman Kadhim,
Singh Rajvir,
Alhashemi Mohammed,
Carr Alison S.,
AlsheikhAli Alawi A.,
AlHabib Khalid F.,
AlZakwani Ibrahim,
Panduranga Prashanth,
Asaad Nidal,
Shehab Abdulla,
AlMahmeed Wael,
Al Suwaidi Jassim
Publication year - 2020
Publication title -
esc heart failure
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.787
H-Index - 25
ISSN - 2055-5822
DOI - 10.1002/ehf2.13030
Subject(s) - medicine , peripartum cardiomyopathy , heart failure , cohort , cardiomyopathy , pediatrics , presentation (obstetrics) , surgery
Aims Published data on the clinical presentation of peripartum cardiomyopathy (PPCM) are very limited particularly from the Middle East. The aim of this study was to examine the clinical presentation, management, and outcomes of patients with PPCM using data from a large multicentre heart failure (HF) registry from the Middle East. Methods and results From February to November 2012, a total of 5005 consecutive patients with HF were enrolled from 47 hospitals in 7 Middle East countries. From this cohort, patients with PPCM were identified and included in this study. Clinical features, in‐hospital, and 12 months outcomes were examined. During the study period, 64 patients with PPCM were enrolled with a mean age of 32.5 ± 5.8 years. Family history was identified in 11 patients (17.2%) and hypertension in 7 patients (10.9%). The predominant presenting symptom was dyspnoea New York Heart Association class IV in 51.6%, class III in 31.3%, and class II in 17.2%. Basal lung crepitations and peripheral oedema were the predominant signs on clinical examination (98.2% and 84.4%, respectively). Most patients received evidence‐based HF therapies. Inotropic support and mechanical ventilation were required in 16% and 5% of patients, respectively. There was one in‐hospital death (1.6%), and after 1 year of follow‐up, nine patients were rehospitalized with HF (15%), and one patient died (1.6%). Conclusions A high index of suspicion of PPCM is required to make the diagnosis especially in the presence of family history of HF or cardiomyopathy. Further studies are warranted on the genetic basis of PPCM.