Results 21 to 30 of about 93,056 (192)

Lived experiences of mothers with peripartum cardiomyopathy

open access: yesInternational Journal of Africa Nursing Sciences
Peripartum cardiomyopathy is known to occur more commonly in African women or those of African descent, with potentially devastating consequences. The purpose of this study was to explore the lived experiences of women with post-partum cardiomyopathy.
Doreen Macherera Mukona   +2 more
doaj   +2 more sources

Peripartum dilated cardiomyopathy [PDF]

open access: yesSanamed, 2011
Peripartum cardiomyopathy (PPCM) is a form of dilated cardiomyopathy that is defined as deterioration in cardiac function presenting towards the end of pregnancy or in the months following delivery, where no other cause of HF is found.
Đorđević Spomenka   +3 more
doaj   +1 more source

Peripartum Cardiomyopathy Treatment with Dopamine Agonist and Subsequent Pregnancy with a Satisfactory Outcome [PDF]

open access: yesRevista Brasileira de Ginecologia e Obstetrícia, 2016
Pathophysiological mechanisms of peripartum cardiomyopathy are not yet completely defined, although there is a strong association with various factors that are already known, including pre-eclampsia.
Maria Adélia Medeiros e Melo   +6 more
doaj   +1 more source

Patofisiologi dan Penanganan Kardiomiopati Peripartum

open access: yesJurnal Anestesi Obstetri Indonesia, 2020
Kardiomiopati peripartum adalah salah satu penyebab dari kardiomiopati dilatasi yang timbul pada waktu akhir trimester tiga kehamilan sampai 5 bulan kelahiran.
Dwiana Sulistyanti, Bambang Suryono
doaj   +1 more source

Case Report: Severe Peripartum Cardiac Disease in Myotonic Dystrophy Type 1

open access: yesFrontiers in Cardiovascular Medicine, 2022
BackgroundMyotonic dystrophy type 1 (DM1) is a hereditary muscular dystrophy affecting ∼2.1–14.3/100,000 adults. Cardiac manifestations of DM1 include conduction disorders and rarely cardiomyopathies.
Georgia Besant   +17 more
doaj   +1 more source

Peripartum Cardiomyopathy: A Case Report

open access: yesGynecology Obstetrics & Reproductive Medicine, 2020
Peripartum cardiomyopathy is one of the potentially life-threatening complications of pregnancy. It is characterized by symptoms of heart failure in the last months of gestation or within five months after birth. The objective of this case report was to
Ozlem Ece Basaran   +2 more
doaj   +1 more source

Anesthetic experience using extracorporeal membrane oxygenation for cesarean section in the patient with peripartum cardiomyopathy: a case report [PDF]

open access: yesKorean Journal of Anesthesiology, 2014
Peripartum cardiomyopathy is a rare form of cardiomyopathy that is associated with significant mortality. It can cause a cardiac arrest during cesarean section even though the patient does not have any previous symptom and sign.
Han-Young Kim   +5 more
doaj   +1 more source

Peripartum cardiomyopathy: current theories about etiopathogenesis, potential biomarkers and treatment - a literature review

open access: yesJournal of Education, Health and Sport, 2023
Background: Peripartum cardiomyopathy (PPCM) is a form of an idiopathic systolic heart failure, which occurs the most often in the last weeks of pregnancy or in the early postpartum period. Symptoms of this disease include exertional dyspnea, orthopnoea,
Bartłomiej Zielonka   +9 more
doaj   +1 more source

Recurrent and Life-Threatening Peripartum Cardiomyopathy

open access: yesJACC: Case Reports, 2020
Peripartum cardiomyopathy is an idiopathic reduction in left ventricular systolic function (ejection fraction 
Summer Aldrugh, MD   +4 more
doaj   +1 more source

Peripartum cardiomyopathy and HELLP syndrome in a previously healthy multiparous woman: A case report

open access: yesSAGE Open Medical Case Reports, 2020
Peripartum cardiomyopathy is a type of dilated cardiomyopathy in which the exact etiology is uncertain. HELLP syndrome is characterized by a constellation of different clinical and laboratory findings, including hemolysis, elevated liver enzymes, and low
Shany Quevedo   +7 more
doaj   +1 more source

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