首页> 外文期刊>BJOG: an international journal of obstetrics and gynaecology >First trimester threatened miscarriage treatment with human chorionic gonadotrophins: a randomised controlled trial.
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First trimester threatened miscarriage treatment with human chorionic gonadotrophins: a randomised controlled trial.

机译:早孕期威胁用人绒毛膜促性腺激素进行流产:一项随机对照试验。

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Objective To determine whether administration of exogenous human chorionic gonadotrophin (hCG) treatment improve the pregnancy outcome in first trimester threatened miscarriages. Design A prospective, double blind, randomised, placebo-controlled trial. Setting The Early Pregnancy Assessment Unit, Royal Bolton Hospital, Bolton, United Kingdom. Population One hundred and eighty-three women with vaginal bleeding and a viable fetus seen on ultrasound scan (USS) in the first 12 weeks of pregnancy. Methods The patients were randomised to receive either hCG or placebo treatment until 14 weeks of gestation. Main outcome measures The primary objective of the trial was to determine the miscarriage rate in the hCG arm compared from the placebo arm. Results Of the 183 cases, 87 were randomised to treatment with hCG while 96 were randomised to receive a placebo. Forty-seven (25%) did not comply with the study protocol. The mean [SD] gestational age at presentation was 7 [1.33] weeks. The mean [SD] age of women in study was 27 [5] years in the placebo and 28 [5] in the hCG group. The mean body mass index (kg/m(2)) was 25 [5] in the study. The number of patients actively bleeding per vaginum at presentation was 85 (93%) in placebo group and 79 (96%) in the hCG group. The median number of hCG or placebo injections for both groups was 7. Ten women (11%) in the placebo group proceeded to have a complete miscarriage, as did 10 women (12%) in the hCG group, relative risk (RR) [95% confidence interval (CI)] of 1.1 (0.63-1.6). Conclusion Our study showed no evidence of a difference in the outcome of threatened miscarriages when treated with hCG in the first trimester, this may be because our study sample size was small and follow up was suboptimal. A large, randomised, multicentre trial is still needed to establish the usefulness of hCG treatment in cases of threatened miscarriage.
机译:目的确定外源性人绒毛膜促性腺激素(hCG)治疗是否可改善早孕先兆流产的妊娠结局。设计前瞻性,双盲,随机,安慰剂对照试验。英国博尔顿皇家博尔顿医院设置早期妊娠评估小组。人口怀孕头12周内有183例阴道流血和可存活胎儿的妇女在超声扫描(USS)上看到。方法将患者随机分组接受hCG或安慰剂治疗,直至妊娠14周。主要结局指标该试验的主要目的是确定与安慰剂组相比,hCG组的流产率。结果183例患者中,有87例被随机分配接受hCG治疗,而96例被随机接受安慰剂治疗。 47(25%)不符合研究方案。出现时的平均[SD]胎龄为7 [1.33]周。研究中女性的平均[SD]年龄在安慰剂组为27 [5]岁,在hCG组为28 [5]。在这项研究中,平均体重指数(kg / m(2))为25 [5]。安慰剂组每例出现主动阴道出血的患者人数为85(93%),hCG组为79(96%)。两组的hCG或安慰剂注射的中位数为7。安慰剂组中有10名妇女(11%)进行了完全流产,hCG组中有10名妇女(12%)发生了完全流产,相对危险度[RR] [ 95(95%置信区间(CI)]为1.1(0.63-1.6)。结论我们的研究没有证据表明在妊娠早期使用hCG治疗时,先兆流产的结果没有差异,这可能是因为我们的研究样本量较小且随访欠佳。仍需要进行大规模,多中心的随机试验来确定在有先兆流产的情况下hCG治疗的有效性。

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