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Mifepristone on termination of ethacridine 105 cases of mid-pregnancy
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Mifepristone on termination of ethacridine 105 cases of mid-pregnancy
Keywords:] Mifepristone ethacridine trimester termination
In recent years, application of mid-pregnancy induction Ethacridine their safety range, induction of labor success rate, but higher residual placental membranes, curettage rate. In this paper, ethacridine intra-amniotic injection of mifepristone for mid-pregnancy induction, effectively reducing the placenta, fetal membrane residues, reducing the Qing rate, effectively shortening the induction of labor and total labor time, achieved good results, reported below.
Subjects and methods
1. PARTICIPANTS: January 2000 to December 2006 in our hospital and because of fetal malformations, unwanted pregnancy and other reasons to terminate a voluntary 16 to 26 weeks of pregnancy of 105 cases of pregnant women as mifepristone plus Ethacridine study group, compared to the same reason to terminate pregnancy in 100 cases of pregnant women with gestational age ethacridine as the control group, 2 groups of pregnant women without pregnancy complications and complications and there were no ethacridine and mifepristone medication contraindications . Primipara study group, 23 cases 82 cases by maternal age (26.35 ± 2.54) years, mean gestational age (24.38 + -1.33) weeks, height (160.00 + -3.26) cm, body weight (60.0 + -4.54) Kg, control Initial maternal in 20 cases, 80 cases by maternal age (25.78 + -2.53) years, mean gestational age (24.70 ± 1.32) weeks, height (160.0 + -3.25) cm, body weight (60.0 + -4.53) Kg, the factors the difference was not statistically significant (Pgt; 0.05).
2. Methods: The study group through the abdominal wall to intra-amniotic injection of ethacridine 100 mg, then oral mifepristone 50 mg, service interval of 12 h and then 50 mg, such as application Ethacridine not after 24 h if the fetus was delivered and then oral mifepristone 50 mg, the maximum drug mifepristone total 150 mg. 2 h fasting
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