Levonorgestrel Intrauterine System versus Medical Therapy for Menorrhagia

被引:107
|
作者
Gupta, Janesh
Kai, Joe [3 ,4 ]
Middleton, Lee [2 ]
Pattison, Helen [5 ]
Gray, Richard [6 ]
Daniels, Jane [1 ,2 ]
机构
[1] Univ Birmingham, Clin Trials Unit, ECLIPSE Trial Off, Sch Clin & Expt Med, Birmingham B15 2TT, W Midlands, England
[2] Univ Birmingham, Birmingham Clin Trials Unit, Birmingham B15 2TT, W Midlands, England
[3] Univ Nottingham, Div Primary Care, Nottingham NG7 2RD, England
[4] Univ Nottingham, Natl Inst Hlth Res, Sch Primary Care Res, Nottingham NG7 2RD, England
[5] Aston Univ, Sch Hlth & Life Sci, Birmingham B4 7ET, W Midlands, England
[6] Univ Oxford, Clin Trial Serv Unit, Oxford, England
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2013年 / 368卷 / 02期
关键词
QUALITY-OF-LIFE; THERMAL BALLOON ABLATION; ENDOMETRIAL ABLATION; MENSTRUAL PROBLEMS; COST-EFFECTIVENESS; HYSTERECTOMY; WOMEN; PATIENT; MIRENA; TRIAL;
D O I
10.1056/NEJMoa1204724
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Menorrhagia is a common problem, yet evidence to inform decisions about therapy is limited. In a pragmatic, multicenter, randomized trial, we compared the levonorgestrel-releasing intrauterine system (levonorgestrel-IUS) with usual medical treatment in women with menorrhagia who presented to their primary care providers. METHODS We randomly assigned 571 women with menorrhagia to treatment with levonorgestrel-IUS or usual medical treatment (tranexamic acid, mefenamic acid, combined estrogen-progestogen, or progesterone alone). The primary outcome was the patient-reported score on the Menorrhagia Multi-Attribute Scale (MMAS) (ranging from 0 to 100, with lower scores indicating greater severity), assessed over a 2-year period. Secondary outcomes included general quality-of-life and sexual-activity scores and surgical intervention. RESULTS MMAS scores improved from baseline to 6 months in both the levonorgestrel-IUS group and the usual-treatment group (mean increase, 32.7 and 21.4 points, respectively; P<0.001 for both comparisons). The improvements were maintained over a 2-year period but were significantly greater in the levonorgestrel-IUS group than in the usual-treatment group (mean between-group difference, 13.4 points; 95% confidence interval, 9.9 to 16.9; P<0.001). Improvements in all MMAS domains (practical difficulties, social life, family life, work and daily routine, psychological well-being, and physical health) were significantly greater in the levonorgestrel-IUS group than in the usual-treatment group, and this was also true for seven of the eight quality-of-life domains. At 2 years, more of the women were still using the levonorgestrel-IUS than were undergoing the usual medical treatment (64% vs. 38%, P<0.001). There were no significant between-group differences in the rates of surgical intervention or sexual-activity scores. There were no significant differences in serious adverse events between groups. CONCLUSIONS In women with menorrhagia who presented to primary care providers, the levonorgestrel-IUS was more effective than usual medical treatment in reducing the effect of heavy menstrual bleeding on quality of life. (Funded by the National Institute of Health Research Health Technology Assessment Programme; ECLIPSE Controlled-Trials.com number, ISRCTN86566246.)
引用
收藏
页码:128 / 137
页数:10
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