Skip to content
Review Open access

Favorable maternal and neonatal outcomes in probable Eisenmenger physiology with suspected DORV: a case report and literature review

Sep 2026 · Egyptian Heart Journal · Vol 78 · 0 citations · 23 references
Medicine

TL;DR

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.

Read PDF

Similar papers

Case report Open access Sep 2026

Dual clinical dilemmas in late pregnancy: A multidisciplinary conservative approach to high-risk pulmonary embolism with persistent category III fetal status

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 · 0 citations
Open access Sep 2026

Perioperative anesthetic management of perforated appendicitis in a pregnant patient with severe pulmonary hypertension: a rare case report

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. · 0 citations
Case report Open access Aug 2026

Pulmonary artery dissection with patent ductus arteriosus presenting with differential cyanosis: a case report and review of literature

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 · 0 citations
Review Open access Sep 2026

The Eye That Revealed the Hidden Storm: A Neonatal Vein of Galen Aneurysmal Malformation—A Case Report and Comprehensive Literature Review

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 · 0 citations
Open access Sep 2026

Challenges in anesthetic management of an obstetric patient with dilated cardiomyopathy and multiple organ dysfunction posted for emergency cesarean section: A case report

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 · 0 citations
Open access Oct 2026

Prenatal Identification, Transitional Hemodynamic Remodeling, and Multidisciplinary Management of Ebstein's Anomaly with Coexistent Urogenital Malformations: An Observational Analytic Case Study

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...

Nugrahanti Prasetyorini, Qonita Prasta Agustia, Dyahris Koentartiwi et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.