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1.
JPMA-Journal of Pakistan Medical Association. 2015; 65 (1): 81-83
in English | IMEMR | ID: emr-153795

ABSTRACT

We planned to investigate the rates of Caesarean Section [CS], potential Vaginal Births After previous Caesarean Section [VBAC], and successful VBAC in a secondary care hospital. We conducted an analytical retrospective study at Aga Khan Hospital for Women, Karimabad, Karachi, from October 2011 to September 2012. Data related to total deliveries, Lower Segment CS [LSCS], attempted VBAC and successful VBAC was retrieved from medical records. Total number of deliveries were 3266. Of these, 1021[31.26%] deliveries were conducted by CS. A total of 365[11.1%] had a previous history of one CS and VBAC trial was given to 33[9%] of these pregnancies. The success rate of VBAC was 21[63.6%]. Our results highlight that despite having limited resources, our rates of CS, VBAC trials and successful VBACs were within reasonable limits when compared with international rates


Subject(s)
Humans , Female , Pregnancy , Vaginal Birth after Cesarean , Secondary Care Centers , Retrospective Studies
2.
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2013; 23 (6): 432-433
in English | IMEMR | ID: emr-142571

ABSTRACT

We report a case of gastroschisis which was not diagnosed antenatally and was delivered through lower segment caesarean section due to non-reassuring cardiotocograph and small for gestational age fetus in a 21-year old mother. It was associated with oligohydramnios and partial extension of wrist joint in the neonate. After delivery, baby was referred to tertiary care for specialized care by paediatric surgeon and neonatologist where he had silo reduction and surgical repair. Postnatally, the baby is in healthy condition till now


Subject(s)
Humans , Female , Gastroschisis/surgery , Oligohydramnios/etiology , Gestational Age , Cesarean Section , Delivery, Obstetric , Infant, Newborn
4.
Pakistan Journal of Medical Sciences. 2013; 29 (1): 234-236
in English | IMEMR | ID: emr-127077

ABSTRACT

Meckel-Gruber Syndrome [MKS] is a rare, autosomal recessive genetic disorder, incompatible with life. It is characterized by enlarged polycystic kidneys and post axial polydactyly. Foetal or neonatal death is caused by pulmonary hypoplasia. We report a case of a 35 year old woman who presented at 7 weeks of gestation of her sixth pregnancy. A transabdominal anomaly ultrasound performed for her current pregnancy at 18 weeks of gestation showed features consistent with MKS. The termination of pregnancy was declined and a live newborn female was delivered via an emergency caeserean section at 34 weeks of gestation due to previous history of lower segment caesarean section [LSCS] and leaking. Physical examination of the neonate confirmed the features of MKS. The neonate died within 4-5 hours of birth. This case represented a second trimester diagnosis of a recurrent case of MKS in a non-consanguineous marriage


Subject(s)
Humans , Female , Encephalocele/diagnosis , Polycystic Kidney Diseases/diagnosis , Pregnancy Trimester, Second , Consanguinity
5.
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2012; 22 (9): 613-614
in English | IMEMR | ID: emr-153047
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