ABSTRACT
To evaluate the safety, efficacy of two Meth-otrexate [MTX] regimens for treatment of ectopic pregnancy [EP] and determine the future fertility after medical and surgical management of ectopic pregnancy. 75 cases with EP, 52 were stable and eligible for medical treatment. 24 cases received MTX 50mg/m2, additional dose was given one week later if B-HCG did not decline by 15% between day 4 and 7, while 28 cases received MTX 50mg/m[2] on days 0 and 4, additional doses were given on day 7 and/or on day 11 if HCG levels did not decrease by 15% during the follow-up period. 23 cases underwent surgery. Hysterosalpingogram [HSG] was performed to assess future fertility of patients after receiving treatment for EP. Overall success rate for single-dose and double-dose protocol was 79% and 85.7% respectively. The difference in success rate between the two regimens was most evident at B-HCG concentrations between 2000-5000mIU/mL; 75% for the single dose regimen and 85.7% for the two-dose regimen which favor using the two-dose regimen in this category of patients. Treatment was well tolerated in both groups, most side effects were mild and transient. Regarding future fertility; tubal patency was 94.2% after medical treatment and 82.6% after salpingectomy. The 2-dose protocol is a hybrid between the two previously established protocols; the single dose and the multi-dose MTX. It may optimize the balance between convenience and efficacy. Single-dose regimen is most suitable for low B-HCG <2000mIU/mL mIU/mL, the 2-dose regimen is more suitable for higher B-HCG 2000-5000, while B-HCG >5000mIU/mL has a high failure rate with medical treatment. In a limted number of patients, no safety concerns were noted with either the single-dose or the 2-dose protocols. Medical treatment should be offered to stable patients whenever feasible because it preserves their future fertility meanwhile cost effective
Subject(s)
Humans , Female , Methotrexate , Safety , Fallopian Tube Patency Tests , Pregnancy , Chorionic Gonadotropin/blood , Methotrexate/administration & dosageABSTRACT
The purpose of this study is to compare the efficacy and safety of supra-cervical Foley Catheter and vaginal prostaglandin E[2] [PGE[2]] tablet and combination of supracervical Foley Catheter and PGE[2] tablet for cervical ripening and labor induction. 90 patients admitted for induction of labor with a Bishop score = 6 were randomized to receive a supracervical Foley catheter under traction [Foley group] or PGE[2] tablet vaginally [prostine group] or a combination of both [Foley + Prostine group]. Repeated insertion of prostine tablet after 8 hours was done if Bishop score was <7 in the last two groups. Oxytocin induction in the Foley group commenced once the catheter fell out spontaneously while in both the Prostine group and the Foley + Prostine group, after cervical ripening if regular uterine contractions were not achieved within 4 hours after the last PGE[2] tablet. No statistically significant differences were noted between groups in change in Bishop score, preinduction cervical ripening time and total induction time. Contractile abnormalities were more frequent in the Prostine group [20%] and the Foley + Prostine group [10%] than the Foley group [0%] [p=0.036]. There were no significant difference in mode of delivery or adverse neonatal outcomes. This study has shown that for preinduction cervical ripening, the Foley catheter is as effective as the PGE[2] tablet with added advantage of safety and more economic price, the addition of PGE[2] tablet to the Foley catheter did not provide additional efficacy, however better safety through decreased incidence of contractile abnormalities probably due to decreased dosage of prostine tablet