Schaff E A, Eisinger S H, Franks P, Kim S S
Department of Family Medicine, University of Rochester (NY), USA.
Arch Fam Med. 1995 Sep;4(9):774-9. doi: 10.1001/archfami.4.9.774.
To determine the effectiveness and side effects of and subject satisfaction with an induced abortion by administration of methotrexate and intravaginal misoprostol.
Prospective trial of 100 consecutive pregnant women aged 18 years or older at 8 weeks' gestation or less and wanting an abortion.
Intramuscular administration of 50 mg of methotrexate per square meter of body surface area on day 1 and a misoprostol 800-micrograms vaginal suppository on day 3. Administration of misoprostol was repeated the following day if no bleeding occurred after the first dose.
After pregnancy dating by clinical criteria, subjects were followed up with serum beta-human chorionic gonadotropin (beta-hCG) determinations on days 1, 7, and 14 and a high-sensitivity urine hCG test every 2 weeks until the value was less than 10 IU/L. Subjects completed a daily symptom log and satisfaction questionnaire on day 14.
Complete abortion as defined by vaginal bleeding and a beta-hCG value of less than 10 IU/L without surgical intervention, complications and side effects, and patient satisfaction.
Ninety-seven subjects had a complete abortion and one subject had vaginal bleeding and a 94% decrease of her beta-hCG value on day 7 but was subsequently unavailable for follow-up. Two subjects required surgical procedures: one with a continued pregnancy and one for excessive bleeding. No failures or complications occurred in early gestations prior to 45 days from the last menstrual period. Seventy-three percent responded to misoprostol treatment with bleeding within 12 hours and had a mean decrease of 90% in their beta-hCG value on day 7. Twenty-seven percent had no immediate bleeding response to misoprostol administration, began bleeding on day 10 (SD, 8 days), and had a mean decrease of 10% in their beta-hCG value on day 7. Seventy percent reported nausea; 46%, diarrhea; and 23%, vomiting. Ninety-three percent agreed that the procedure was acceptable and 95% would recommend the procedure.
Methotrexate and misoprostol were effective in inducing an abortion up to 8 weeks. Home administration of a compounded misoprostol vaginal suppository was successful. Although gastrointestinal tract side effects were common, women found the procedure and its side effects acceptable.
确定甲氨蝶呤与阴道用米索前列醇用于人工流产的有效性、副作用及受术者满意度。
对100例连续入选的、年龄18岁及以上、妊娠8周及以内且要求终止妊娠的孕妇进行前瞻性试验。
第1天按每平方米体表面积肌肉注射50mg甲氨蝶呤,第3天放置800μg米索前列醇阴道栓。若首剂用药后未出现阴道流血,则于次日重复使用米索前列醇。
经临床标准确定孕周后,于第1、7和14天测定血清β-人绒毛膜促性腺激素(β-hCG),并每2周进行1次高灵敏度尿hCG检测,直至其值低于10IU/L,以此对受试者进行随访。受试者于第14天完成每日症状记录及满意度问卷调查。
经阴道流血及β-hCG值低于10IU/L定义的完全流产(无需手术干预)、并发症和副作用以及患者满意度。
97例受试者完全流产,1例受试者于第7天出现阴道流血且β-hCG值下降94%,但随后失访。2例受试者需接受手术治疗:1例为持续性妊娠,1例为出血过多。末次月经后45天内的早期妊娠未出现流产失败或并发症。73%的受试者在米索前列醇治疗后12小时内出现阴道流血,且第7天β-hCG值平均下降90%。27%的受试者在使用米索前列醇后未立即出现阴道流血反应,于第10天(标准差8天)开始出血,且第7天β-hCG值平均下降10%。70%的受试者报告有恶心症状;46%有腹泻;23%有呕吐。93%的受试者认为该操作可接受,95%会推荐该操作。
甲氨蝶呤和米索前列醇在妊娠8周内引产有效。自行在家使用复方米索前列醇阴道栓引产成功。虽然胃肠道副作用常见,但女性认为该操作及其副作用可接受。