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Postpartum rectal misoprostol in addition to intra - operative IV oxytocin Vs Intra - operative IV oxytocin alone to reduce intra - operative and post - operative blood loss / Sally Alaa Eldien Ibrahim Mohamed Elattar ; Supervised Ehab Mohamed Soliman , Abdalla Yehia Elkateb , Heba Wageih Saeid

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Sally Alaa Eldien Ibrahim Mohamed Elattar , 2015Description: 77 P. : charts ; 25cmOther title:
  • ميزوبروستول الشرجى بعد الولادة القيصرية بالإضافة إلى الأوكسيتوسين الوريدى أثناء العملية مقابل الأوكسيتوسين الوريدى أثناء العملية فقط فى تقليل فقد الدم أثناء و بعد العملية [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Gynecology and Obstetrics Summary: The current study is designed to compare the efficacy of post partum rectal misoprostol in addition to intra operative IV oxytocin to intra-operative IV oxytocin alone during cesarean delivery to reduce intra - operative and post operative blood loss. This is an interventional prospective controlled study assessing the use of postpartum rectal misoprostol in addition to intraoperative IV oxytocin during cesarean delivery to reduce intra operative and postoperative blood loss in comparison with routinely used intra operative intravenous oxytocin injection alone. The Study is composed of 150 women undergoing elective or emergency cesarean delivery under general or spinal anaesthesia, subjects included in the study will be randomized into 2 groups: First group (75 women): will receive post-partum misoprostol 800 ug, administered rectally in addition to intra operative 5 IU of IV oxytocin. Second group (75 women): will receive intra operative 5 IU of oxytocin after the delivery of the neonate as slow IV dose. In our study, differences in the age, parity and gestational age were statistically insignificant among the two groups. In our study, 32 % among the first group patients needed further uterotonic agents compared to 26% of the patients in the other group, also 14.7 % out of the first group needed blood transfusion, compared to 12 % of the second group, which is statistically insignificant
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Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.15.M.Sc.2015.Sa.P (Browse shelf(Opens below)) Not for loan 01010110068362000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.15.M.Sc.2015.Sa.P (Browse shelf(Opens below)) 68362.CD Not for loan 01020110068362000

Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Gynecology and Obstetrics

The current study is designed to compare the efficacy of post partum rectal misoprostol in addition to intra operative IV oxytocin to intra-operative IV oxytocin alone during cesarean delivery to reduce intra - operative and post operative blood loss. This is an interventional prospective controlled study assessing the use of postpartum rectal misoprostol in addition to intraoperative IV oxytocin during cesarean delivery to reduce intra operative and postoperative blood loss in comparison with routinely used intra operative intravenous oxytocin injection alone. The Study is composed of 150 women undergoing elective or emergency cesarean delivery under general or spinal anaesthesia, subjects included in the study will be randomized into 2 groups: First group (75 women): will receive post-partum misoprostol 800 ug, administered rectally in addition to intra operative 5 IU of IV oxytocin. Second group (75 women): will receive intra operative 5 IU of oxytocin after the delivery of the neonate as slow IV dose. In our study, differences in the age, parity and gestational age were statistically insignificant among the two groups. In our study, 32 % among the first group patients needed further uterotonic agents compared to 26% of the patients in the other group, also 14.7 % out of the first group needed blood transfusion, compared to 12 % of the second group, which is statistically insignificant

Issued also as CD

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