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一种基于循证医学的子宫内膜异位症相关性慢性盆腔疼痛治疗方法:安慰剂对照研究

An evidence-based medicine approach to the treatment of endometriosis-associated chronic pelvic pain: placebo-controlled studies.

作者信息

Howard F M

机构信息

Department of Obstetrics and Gynecology, University of Rochester Medical Center, 601 Elmwood Avenue, Box 668, Rochester, NY 14642, USA.

出版信息

J Am Assoc Gynecol Laparosc. 2000 Nov;7(4):477-88. doi: 10.1016/s1074-3804(05)60360-x.

Abstract

OBJECTIVE

Use an evidence-based medicine (EBM) approach to evaluate the evidence regarding efficacy of treatment of endometriosis-associated chronic pelvic pain (CPP) in placebo-controlled randomized clinical trials (RCT).

DESIGN

Review of six randomized, controlled trials (Canadian Task Force classification I).

SETTING

University of Rochester School of Medicine and Dentistry. Patients. Three hundred eighty-one women with endometriosis enrolled in placebo-controlled randomized clinical trials. Intervention. A MEDLINE search of published medical articles from January 1976, to January 1998.

MEASUREMENTS AND MAIN RESULTS

Six placebo-controlled randomized clinical trials were found that addressed the treatment of pelvic pain associated with endometriosis and met validity criteria; one was a study of surgical treatment, two of medical therapies, and three of combined surgical and medical treatments. They clearly show that laparoscopic surgery and medical treatment with medroxyprogesterone acetate, danazol, or nafarelin are more effective than placebo. Evidence for efficacy of leuprolide acetate is weaker. At 6 months, absolute decreases in pain scores are quite similar with surgical or medical treatment. Medical therapy after surgical treatment significantly reduced pain, but six months after it was stopped there was no difference between women treated and not treated postoperatively.

CONCLUSIONS

Although either surgical or medical treatment of endometriosis in women with CPP is clearly indicated, pain relief of 6 or more months' duration can be expected in only 40 to 70% of women with endometriosis-associated CPP.

摘要

目的

采用循证医学方法,在安慰剂对照随机临床试验(RCT)中评估子宫内膜异位症相关性慢性盆腔痛(CPP)治疗效果的证据。

设计

六项随机对照试验的综述(加拿大工作组分类I)。

地点

罗切斯特大学医学与牙科学院。患者:381名患有子宫内膜异位症的女性参与了安慰剂对照随机临床试验。干预措施:对1976年1月至1998年1月发表的医学文章进行MEDLINE检索。

测量指标及主要结果

发现六项安慰剂对照随机临床试验涉及子宫内膜异位症相关盆腔痛的治疗且符合有效性标准;一项是手术治疗研究,两项是药物治疗研究,三项是手术与药物联合治疗研究。这些研究清楚地表明,腹腔镜手术以及用醋酸甲羟孕酮、达那唑或那法瑞林进行药物治疗比安慰剂更有效。醋酸亮丙瑞林疗效的证据较弱。在6个月时,手术或药物治疗后疼痛评分的绝对降低幅度相当相似。手术治疗后的药物治疗显著减轻了疼痛,但停药6个月后,接受治疗和未接受治疗的女性之间没有差异。

结论

虽然对于患有CPP的女性,子宫内膜异位症的手术或药物治疗均明确适用,但只有40%至70%患有子宫内膜异位症相关性CPP的女性有望获得持续6个月或更长时间的疼痛缓解。

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