BACKGROUND:Endometriosis is a common gynaecological condition that frequently presents with the symptom of pain. The precise pathogenesis (mode of development) of endometriosis is unclear but it is evident that endometriosis arises by the dissemination of endometrium to ectopic sites and the subsequent establishment of deposits of ectopic endometrium. The observation that endometriosis is rarely seen in the hypo-oestrogenic (low levels of oestrogen) post-menopausal woman led to the concept of medical treatment by induction of a pseudo-menopause using Gonadotrophin Releasing Hormone Analogues (GnRHas). When administered in a non-pulsatile manner (the pituitary is normally stimulated by pulses of natural GnRH and all analogues act on the pituitary at a constant level) their use results in down regulation (switching off) of the pituitary and a hypogonadotrophic hypogonadal state (low levels of female hormones due to non stimulation of the ovary). OBJECTIVES:To determine the effectiveness of Gonadotrophin Releasing Hormone analogues (GnRHas) in the treatment of the painful symptoms of endometriosis by comparing them with no treatment, placebo, other recognised medical treatments, and surgical interventions. SEARCH STRATEGY:The search strategy of the Menstrual Disorders and Subfertility review group (please see Review Group details) was used to identify all randomised trials of the use of GnRHas for the treatment of the painful symptoms of endometriosis. SELECTION CRITERIA:Trials were included if they were randomised, and considered the effectiveness of GnRHas in the treatment of the painful symptoms of endometriosis. DATA COLLECTION AND ANALYSIS:Twenty-six studies had data appropriate for inclusion in the review. The largest group (15 studies) compared GnRHas with danazol. There are five studies comparing GnRHas with GnRHas plus add-back therapy, three comparing GnRHa with GnRHa in a different form or dose, one compares them with gestrinone, one with the combined oral contraceptive pill, and one with placebo. Data was extracted independently by two reviewers. The authors of eleven studies have been contacted to clarify missing or unclear data. Only four have replied to date. Data on relief of pain, change in revised American Fertility Society (rAFS) scores, and side effects was collected. MAIN RESULTS:No difference was found between GnRHas and any of the other active comparators with respect to pain relief or reduction in endometriotic deposits. The side effect profiles of the different treatments were different, with danazol and gestrinone having more androgenic side effects, while GnRHas tend to produce more hypo-oestrogenic symptoms. AUTHORS' CONCLUSIONS:There is little or no difference in the effectiveness of GnRHas in comparison with other medical treatments for endometriosis. GnRHas do appear to be an effective treatment. Differences that do exist relate to side effect profiles. Side effects of GnRHas can be ameliorated by the addition of addback therapy.

译文

背景:子宫内膜异位症是一种常见的妇科疾病,常伴有疼痛症状。子宫内膜异位症的确切发病机理(发展模式)尚不清楚,但很明显子宫内膜异位症是由子宫内膜散布到异位部位并随后建立异位子宫内膜而引起的。在绝经后的低雌激素(低水平的雌激素)中很少见到子宫内膜异位症的观察导致了通过使用促性腺激素释放激素类似物(GnRHas)诱导假绝经来进行医学治疗的概念。当以非搏动方式给药时(通常由天然GnRH的脉冲刺激垂体,并且所有类似物均以恒定水平作用于垂体),其使用会导致垂体下调(关闭)和性腺功能减退性腺功能减退状态(由于不刺激卵巢而导致女性荷尔蒙水平低)。
目的:通过比较未经治疗,安慰剂,其他公认的药物治疗和外科手术干预措施,确定促性腺激素释放激素类似物(GnRHas)在治疗子宫内膜异位症疼痛症状中的有效性。
搜索策略:月经障碍和亚生育力审查组(请参阅审查组详细信息)的搜索策略用于确定所有使用GnRHas治疗子宫内膜异位症痛苦症状的随机试验。
选择标准:如果试验是随机的,则包括在内,并考虑了GnRHas在治疗子宫内膜异位症的痛苦症状中的有效性。
数据收集与分析:26项研究具有适合纳入评价的数据。最大的一组(15个研究)比较了GnRHas和达那唑。有五项研究比较了GnRHas与GnRHas加上加用疗法,三项研究比较了GnRHa与GnRHa在不同形式或剂量下的关系,一项与孕酮进行比较,一项与口服避孕药联合使用,一项与安慰剂进行比较。数据由两名审阅者独立提取。已与11项研究的作者联系,以澄清缺失或不清楚的数据。迄今为止,只有四个答复。收集有关疼痛缓解,美国生育协会(rAFS)评分修改的数据以及副作用的数据。
主要结果:在疼痛缓解或子宫内膜异位症沉积减少方面,GnRHas与任何其他活性比较剂之间均未发现差异。不同疗法的副作用不同,但达那唑和孕酮具有更多的雄激素副作用,而GnRHas倾向于产生更多的低雌激素症状。
作者的结论:与其他治疗子宫内膜异位症的药物相比,GnRHas的疗效几乎没有差异。 GnRHas似乎确实是一种有效的治疗方法。确实存在差异与副作用情况有关。 GnRHas的副作用可以通过添加回加疗法来改善。

+1
+2
100研值 100研值 ¥99课程
检索文献一次
下载文献一次

去下载>

成功解锁2个技能,为你点赞

《SCI写作十大必备语法》
解决你的SCI语法难题!

技能熟练度+1

视频课《玩转文献检索》
让你成为检索达人!

恭喜完成新手挑战

手机微信扫一扫,添加好友领取

免费领《Endnote文献管理工具+教程》

微信扫码, 免费领取

手机登录

获取验证码
登录