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Rectal administration of misoprostol to prevent hemorrhage after cesarean section observation.doc

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Rectal administration of misoprostol to prevent hemorrhage after cesarean section observation

 PAGE \* MERGEFORMAT 7 Rectal administration of misoprostol to prevent hemorrhage after cesarean section observation [Abstract] Objective To observe the misoprostol to prevent hemorrhage after cesarean section. Methods 206 cases of cesarean section were selected randomly divided into experimental group and control group of 103 cases. Test group after cesarean section in the clean-up hemorrhage after vaginal misoprostol 0.4 mg into the rectum through the anus at .6 ~ 7 cm. control group misoprostol, respectively, were observed 2 h and 24 h post-partum bleeding difference. Results 2 h and 24 h blood loss, the experimental group compared with the control group, the difference was significant (P lt;0.05). Conclusion Rectal administration of misoprostol can be effective in promoting contraction of the uterus, hemorrhage after cesarean section with satisfactory result. [Keywords:] misoprostol; cesarean section; prevention; postpartum hemorrhage Postpartum hemorrhage is one of obstetric complications, maternal causes of postpartum hemorrhage in the first place [1]. Prevention of postpartum hemorrhage is to reduce the incidence of postpartum hemorrhage, an important part. In order to explore a safe, effective, simple convenient method for prevention of postpartum hemorrhage, cesarean section in our hospital in rectal misoprostol 0.4 mg, by increasing uterine contractions and reduce postpartum bleeding, with good results. are as follows. 1 Materials and Methods 1.1 General information select from January 2005 to January 2007 in our hospital obstetric maternal cesarean section a total of 206 cases. Cesarean section indications, including fetal distress, cephalopelvic disproportion, a huge children, breech presentation, severe child preeclampsia, elderly primiparous precious children, and other .206 uterine scar were randomly divided into test group and control group of 103 cases. the two groups in age, gestational age, parity, and pregnancy complications a

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