Case Report Onventricular Septal Defect (VSD) with Pulmonary Hypertention (Eisenmenger Syndrome) with LSCS

Author(s):  
Bali Thool ◽  
Shalini Lokhande

Background: A ventricular septal defect is a defect of the ventricular septal wall where the abnormal opening is present in between the two ventricles. Eisenmenger syndrome is a condition it may develop due to unrepaired heart defect and complication of unrepaired heart defect who is born congenitally. The congenital heart defects lead to Eisenmenger syndrome it developed due to abnormal blood circulate throughout the heart and lungs. Case Report: The 23-year-old female was admitted to AVBRH with the chief complaints of a history of amenorrhoea since 8 months, complaints of breathlessness during exertion since the 7th month of pregnancy and she was referred to AVBRH from Amravati on date 27/1/2021. At the age of 14 years, she had a history of cyanosis at the time of fever and had recurrent episodes of fever for 2-3 yrs, lasting for 2-3 weeks. She is primigravida and had undergone LSCS on date 3/2/2021. She delivered a male child on date 3/2/2021 of birth weight 1.9kg at 12:15 pm. Discussion: Patient with pulmonary hypertension and Eisenmenger syndrome where the surgery is contraindicated because in Eisenmenger syndrome surgery is life-threatening. Only medical management is available to treat Eisenmenger syndrome. Conclusion: Ventricular septal defect in adult females where the pregnancy is contraindicated. Epidural anesthesia should be preferred while the patient undergoes the lower segment cesarean section. This case report concludes that in this condition emergency LSCS is the first choice of treatment and oxygen therapy.

2016 ◽  
Vol 84 (3) ◽  
pp. 178-180 ◽  
Author(s):  
Vishal Walasangikar ◽  
Amit Kumar Dey ◽  
Rajaram Sharma ◽  
Vivek Murumkar ◽  
Rohit Gadewar ◽  
...  

2020 ◽  
Vol 3 (1) ◽  
pp. 62-66
Author(s):  
Akinlade OM ◽  
Ogunmodede JA ◽  
Adeyemi OA ◽  
Yusuf WO ◽  
Awodun RO ◽  
...  

Pentalogy of Fallot is a congenital cardiac defect comprising infundibular stenosis of the pulmonary artery, overriding aorta, ventricular septal defect, right ventricular hypertrophy and atrial septal defect. It is one of the most common cyanotic congenital heart defects with detrimental consequences if left untreated. We present the case of a 25-year-old female artisan and stroke survivor who was admitted with episodes of recurrent dizziness. She was diagnosed with the pentalogy of Fallot after echocardiography and awaiting cardiac repair surgery.


1970 ◽  
Vol 25 (3) ◽  
pp. 161-163
Author(s):  
Nurun Nahar Fatema ◽  
Mamunur Rahman ◽  
Mujubul Haque

A four year old girl was diagnosed as a case of mid muscular Ventricular Septal Defect (VSD) since early infancy. She had history of failure to thrive (FTT) and recurrent chest infection or pneumonia. As her pulmonary artery pressure was almost normal she was planned for device closure on elective basis once device and technology would be available in cardiac centre of combined Military Hospital (CMH) Dhaka. Finally it was done on 21st August 2005 and patient was discharged after 72 hours observation period. Echocardiography on next morning showed complete occlusion of defect with no residual shunt. (J Bangladesh Coll Phys Surg 2007; 25 : 161-163)


Author(s):  
Bahram Alamdary Badlou

We report a rare case of unrepaired Tetralogy_Pantalogy of Fallot (TOF_POF) in a 20 years old Persian girl Mrs Zeynab S., who presented with cyanotic finger tops appearance, ongoing chronic thrombolytic destruction processes, and remarkable thrombocytopenia [1,2], heart ventricular septal defect (VSD), and might atrial septal defect (ASD), anxiety, sleep disorders, nightmares, and limited social life. Additionally, the relationship between underlying mechanisms, possible treatments of the thrombocytopenia, erythrocytosis, and unrepaired cardiovascular leakages remains unknown.


1984 ◽  
Vol 108 (5) ◽  
pp. 1312-1317 ◽  
Author(s):  
Kazuo Momma ◽  
Kan Toyama ◽  
Atsuyoshi Takao ◽  
Masahiko Ando ◽  
Makoto Nakazawa ◽  
...  

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