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1.
ScientificWorldJournal ; 2014: 270120, 2014.
Article in English | MEDLINE | ID: mdl-25478587

ABSTRACT

AIM: To examine the factors associated with placenta praevia in primigravidas and also compare the pregnancy outcomes between primigravidas and nonprimigravidas. METHOD: A retrospective cohort study was conducted in women who underwent caesarean section for major placenta praevia in a tertiary university hospital from January 2007 till December 2013. Medical records were reviewed. RESULT: Among 243 with major placenta praevia, 56 (23.0%) were primigravidas and 187 (77.0%) were nonprimigravidas. Factors associated with placenta praevia in the primigravidas were history of assisted conception (P = 0.02) and history of endometriosis (P = 0.01). For maternal outcomes, the nonprimigravidas required earlier delivery than primigravidas (35.76 ± 2.54 weeks versus 36.52 ± 1.95 weeks, P = 0.03) and had greater blood loss (P = 0.04). A vast majority of the primigravidas had either posterior type II or type III placenta praevia. As for neonatal outcomes, the Apgar score at 1 minute was significantly lower for the nonprimigravidas (7.89 ± 1.72 versus 8.39 ± 1.288.39 ± 1.28, P = 0.02). CONCLUSION: This study highlighted that endometriosis and assisted conception were highly associated with placenta praevia in primigravida. Understanding the pregnancy outcomes of women with placenta praevia can assist clinicians in identifying patients who are at higher risk of mortality and morbidity. Identifying potential risk factors in primigravida may assist in counseling and management of such patients.


Subject(s)
Gravidity , Placenta Previa/surgery , Pregnancy Outcome , Adult , Cesarean Section , Cohort Studies , Female , Humans , Placenta Previa/pathology , Pregnancy , Risk Factors
2.
Arch Gynecol Obstet ; 284(5): 1073-9, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21136267

ABSTRACT

PURPOSE: Retained placenta is potentially life threatening due to possible complications associated with manual removal. Our aim was to determine whether umbilical vein injection of oxytocin in saline reduces the need for manual removal of placenta. METHODS: This was a randomised controlled trial conducted at a tertiary hospital from December 2002 to March 2004. A total of 61 women delivering singletons, who had no sign of placental separation 20 min after vaginal delivery, were randomised to receive either intra-umbilical oxytocin 100 IU diluted in 30 ml of saline or controlled cord traction only. Manual removal was done if the placenta was not expelled in another 30 min in both arms. RESULTS: There was a significant reduction in the rate of subsequent manual removal of placenta (30 vs. 67.7%, p < 0.05), incidence of uterine atony (3.3 vs. 25.8%, p < 0.05) and the need for uterotonic agents (33.3 vs. 64.5%, p < 0.05) in the oxytocin group when compared with the control group. No significant differences were found in the need for blood transfusion, uterine curettage, incidence of postpartum haemorrhage and haemoglobin level reduction. CONCLUSION: Intra-umbilical vein oxytocin injection is clinically effective for the management of a retained placenta.


Subject(s)
Oxytocin/therapeutic use , Placenta, Retained/drug therapy , Placenta, Retained/surgery , Adult , Female , Humans , Injections, Intravenous , Postpartum Hemorrhage/prevention & control , Pregnancy , Treatment Outcome , Umbilical Veins/drug effects , Uterine Inertia/drug therapy
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