Maternal survival through induced vaginal delivery and the first postpartum week, with a live birth is documents, despite late recognition of probable Eisenmenger physiology and suspected complex congenital heart disease.
Abstract
Pregnancy in Eisenmenger syndrome is associated with very high maternal and fetal risk. Complex congenital anatomy further complicates diagnosis and peripartum management, particularly where advanced imaging and pulmonary hypertension therapies are limited. Published evidence specifically addressing pregnancy with uncorrected DORV and Eisenmenger physiology remains sparse. A 25-year-old primigravida at 34 weeks’ gestation presented with progressive dyspnoea and generalized oedema. The available record documented a heart rate of 130 beats/min, respiratory rate of 25 breaths/min, oxygen saturation of 80% despite face-mask oxygen, a loud second heart sound, and a systolic murmur. Echocardiography showed large ventricular and atrial septal defects with colour Doppler flow, severe tricuspid regurgitation, and an estimated systolic pulmonary artery pressure of 85 mmHg. In the setting of marked hypoxaemia, these findings supported probable Eisenmenger physiology, although shunt direction and pulmonary vascular resistance were not documented. The aorta appeared to arise predominantly from the right ventricle, supporting suspected DORV, but the origin of both great arteries, VSD-great-artery relationship, and DORV subtype could not be defined. Following cardiology and obstetric assessment, labour was induced and vaginal delivery occurred four hours later. The liveborn neonate weighed 2.7 kg, had an initial Apgar score of 5, and was admitted to neonatal intensive care for stabilisation and monitoring. Postpartum haemoglobin fell to 7 g/dL and two units of packed red cells were transfused. The mother was monitored in intensive care for three days, transferred to cardiology on day 6, and discharged in stable condition on day 7. This report documents maternal survival through induced vaginal delivery and the first postpartum week, with a live birth, despite late recognition of probable Eisenmenger physiology and suspected complex congenital heart disease. The report does not establish the safety of vaginal delivery in Eisenmenger syndrome, and incomplete haemodynamic, anatomical, anaesthetic, and neonatal data limit causal interpretation.
Pregnancy increases the risk of venous thromboembolism, and pulmonary embolism (PE) remains a leading cause of maternal morbidity and mortality. Diagnosis is challenging due to symptom overlap with normal pregnancy, and management is complex in severe cases without hemodynamic instability. A 32-year-old woman at 32 wee...
Mohammed Y. Abushamma, Omar Marouf, Abdulla M. S. Alawi· Radiology Case Reports· 0 citations
The incidence of severe pulmonary hypertension associated with a valvular heart disease in pregnancy is very rare. This patient may have presented with different defects like Eisenmneger syndrome, systematic- to-pulmonary shunts, and other defects. This case report contributes to the existing literature by providing in...
T. Hordofa, Dinku Urji, Kelil Nerso et al.· Discover medicine· 0 citations
Spontaneous pulmonary artery (PA) dissection is an extremely rare and life-threatening complication of chronic pulmonary hypertension, most commonly associated with congenital heart disease. We report a 54-year-old woman who presented with sharp chest pain, progressive dyspnea, and differential cyanosis between the upp...
Yefu Liu, Dou Yuan· Frontiers in Cardiovascular...· 0 citations
Background: Vein of Galen aneurysmal malformation (VGAM) is a rare congenital cerebrovascular anomaly
that predominantly presents in the neonatal period with cardiovascular compromise rather than primary
neurological deficits. Diagnostic delays are common because initial neurological examinations are typically
reass...
Mohamed Sadik, Ahmed M. El Melhat· SVOA Paediatrics· 0 citations
The prevalence of dilated cardiomyopathy (DCM) is 1:2500 among women of childbearing age. DCM often develops during the second trimester or may be present before pregnancy. We present a 36-year-old gravida (G3, P0+2) coming to the emergency ward with severe breathlessness, pedal edema, oliguria, and absent fetal moveme...
Deepali Chandra· Asian Journal of Medical Sci...· 0 citations
Background: Ebstein’s anomaly is an uncommon congenital heart defect with failed tricuspid delamination, right-ventricular atrialization, and severe regurgitation. Prenatal detection is difficult on routine obstetric ultrasonography, and perinatal hemodynamic transition carries substantial mortality.
Objective: To docu...