Reevaluating response and failure of medical treatment of endometriosis: a systematic review

被引:202
作者
Becker, Christian M. [1 ]
Gattrell, William T. [2 ,3 ,6 ]
Gude, Kerstin [4 ]
Singh, Sukhbir S. [5 ]
机构
[1] Univ Oxford, Endometriosis Care Ctr, Nuffield Dept Obstet & Gynaecol, Oxford, England
[2] Oxford Pharmagenesis, Res Evaluat Unit, Oxford, England
[3] Oxford Brookes Univ, Dept Mech Engn & Math Sci, Oxford, England
[4] Bayer, Med Affairs Womens Healthcare, Berlin, Germany
[5] Ottawa Hosp Res Inst, Dept Obstet & Gynaecol, Ottawa, ON, Canada
[6] Ipsen Biopharm, Abingdon, Oxon, England
关键词
Endometriosis; pain; medical therapy; systematic review; DEPOT MEDROXYPROGESTERONE ACETATE; ORAL GNRH ANTAGONIST; CHRONIC PELVIC PAIN; HORMONE AGONIST TREATMENT; PHENOTYPE DATA-COLLECTION; CROSS-SECTIONAL SURVEY; BONE-MINERAL DENSITY; ADD-BACK THERAPY; SYMPTOMATIC ENDOMETRIOSIS; LEUPROLIDE ACETATE;
D O I
10.1016/j.fertnstert.2017.05.004
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To assess patient response rates to medical therapies used to treat endometriosis-associated pain. Design: A systematic review with the use of Medline and Embase. Setting: Not applicable. Patient(s): Women receiving medical therapy to treat endometriosis. Interventions(s): None. Main Outcome Measure(s): The proportions of patients who: experienced no reduction in endometriosis-associated pain symptoms; had pain symptoms remaining at the end of the treatment period; had pain recurrence after treatment cessation; experienced an increase or no change in disease score during the study; were satisfied with treatment; and discontinued therapy owing to adverse events or lack of efficacy. The change in pain symptom severity experienced during and after treatment, as measured on the visual analog scale, was also assessed. Result(s): In total, 58 articles describing 125 treatment arms met the inclusion criteria. Data for the response of endometriosis-associated pain symptoms to treatment were presented in only 29 articles. The median proportions of women with no reduction in pain were 11%-19%; at the end of treatment, 5%-59% had pain remaining; and after follow-up, 17%-34% had experienced recurrence of pain symptoms after treatment cessation. After median study durations of 2-24 months, the median discontinuation rates due to adverse events or lack of efficacy were 5%-16%. Conclusion(s): Few studies of medical therapies for endometriosis report outcomes that are relevant to patients, and many women gain only limited or intermittent benefit from treatment. (C) 2017 John Radcliffe Hospital. Published by Elsevier Inc. on behalf of the American Society for Reproductive Medicine.
引用
收藏
页码:125 / 136
页数:12
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