Harper K, Proctor M, Hughes E
c/o Cochrane Menstrual Disorders and Subfertility Group, Dept of Obstetrics and Gynaecology, University of Auckland, National Women's Hospital, Claude Rd, Epsom, Auckland, NEW ZEALAND, 1003.
Cochrane Database Syst Rev. 2003(3):CD000099. doi: 10.1002/14651858.CD000099.
In an effort to improve outcomes of in vitro fertilisation (IVF) cycles the use of growth hormone (GH) has been considered. Most studies investigate the role of GH in normally ovulating infertile women but there is also an interest in the effect of GH on women who respond poorly to ovulation induction and IVF.
To assess the effectiveness of GH or growth hormone releasing (GRF) adjuvant therapy, primarily in terms of improving livebirth rate, for women undergoing ovulation induction prior to IVF in (a) patients with no previous history of poor response and (b) patients with a history of poor response.
We searched the Cochrane Menstrual Disorders and Subfertility Group's trials register (24 March 2003), the Cochrane Central Register of Controlled Trials (Cochrane Library Issue 1, 2003), MEDLINE (1966 to Feb 2003), EMBASE (1988 to Feb 2003) and Biological Abstracts (1969 to Feb 2003). Reference lists of articles were also searched.
All randomised controlled trials were included if they addressed the research question and provided outcome data for intervention and control subjects.
Assessment of trial quality and extraction of relevant data was performed independently by two reviewers. Validity was assessed in terms of method of randomisation, completeness of follow-up and co-intervention.
Nine studies (401 couples) were included. Three trials concerned patients with no history of poor response to IVF (91 women) and six investigated previous poor responders (302 women). There was no evidence that routine use of GH affected the outcome of livebirth (3 RCTs; OR 1.17, 95% CI 0.38 to 3.59). In women who had previously responded poorly to IVF there was no significant differences in livebirth when combining trials of GH and GRF (4 RCTs; OR 2.42, 95% CI 0.94 to 6.23). However when trials using GH were analysed separately there was an increase in livebirths (3 RCTs; OR 4.37, 95% CI 1.06 to 18.01). There was no significant differences in any adverse events, but these were poorly and inconsistently reported.
REVIEWER'S CONCLUSIONS: Although the use of GH in previous poor responders has been found to show a significant improvement in livebirth rate, this result was only just significant. Also, this data is from just three small trials. Therefore, before recommending GH in IVF further research is necessary to fully define its role. Meanwhile GH should only be considered in the context of a clinical trial.
为了改善体外受精(IVF)周期的结局,人们考虑使用生长激素(GH)。大多数研究调查了生长激素在正常排卵的不孕妇女中的作用,但人们也对生长激素对排卵诱导和体外受精反应不良的妇女的影响感兴趣。
评估生长激素或生长激素释放因子(GRF)辅助治疗的有效性,主要从提高活产率方面评估,用于在体外受精前进行排卵诱导的妇女,包括(a)既往无反应不良史的患者和(b)有反应不良史的患者。
我们检索了Cochrane月经紊乱与不育症小组的试验注册库(2003年3月24日)、Cochrane对照试验中央注册库(Cochrane图书馆2003年第1期)、MEDLINE(1966年至2003年2月)、EMBASE(1988年至2003年2月)和生物学文摘(1969年至2003年2月)。还检索了文章的参考文献列表。
如果所有随机对照试验涉及研究问题并提供干预组和对照组的结局数据,则纳入。
由两名评价员独立进行试验质量评估和相关数据提取。根据随机化方法、随访完整性和联合干预情况评估有效性。
纳入9项研究(401对夫妇)。3项试验涉及既往对体外受精无反应不良史的患者(91名女性),6项试验调查既往反应不良者(302名女性)。没有证据表明常规使用生长激素会影响活产结局(3项随机对照试验;比值比1.17,95%可信区间0.38至3.59)。在既往对体外受精反应不良的女性中,联合生长激素和生长激素释放因子的试验中活产率无显著差异(4项随机对照试验;比值比2.42,95%可信区间0.94至6.23)。然而,当单独分析使用生长激素的试验时,活产率有所增加(3项随机对照试验;比值比4.37,95%可信区间1.06至18.01)。任何不良事件均无显著差异,但报告情况不佳且不一致。
尽管已发现对既往反应不良者使用生长激素可使活产率显著提高,但这一结果仅具有边缘显著性。此外,这些数据仅来自3项小型试验。因此,在推荐生长激素用于体外受精之前,有必要进行进一步研究以充分明确其作用。同时,生长激素仅应在临床试验的背景下考虑使用。