Rates of medical or surgical treatment for women with heavy menstrual bleeding: the ECLIPSE trial 10-year observational follow-up study.

IF 3.5 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Health technology assessment Pub Date : 2023-10-01 DOI:10.3310/JHSW0174
Joe Kai, Brittany Dutton, Yana Vinogradova, Nicholas Hilken, Janesh Gupta, Jane Daniels
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Abstract

Background: Heavy menstrual bleeding is a common problem that can significantly affect women's lives until menopause. There is a lack of evidence on longer-term outcomes after seeking health care and treatment for heavy menstrual bleeding.

Objectives: To assess the continuation rates of medical treatments and the rates of ablative and surgical interventions among women who had participated in the ECLIPSE trial (ISRCTN86566246) 10 years after initial management for heavy menstrual bleeding in primary care. To explore experiences of heavy menstrual bleeding and influences on treatment for women.

Design: This was a prospective observational cohort study, with a parallel qualitative study.

Setting: Primary care.

Participants: A total of 206 women with heavy menstrual bleeding who had participated in the ECLIPSE trial consented to providing outcome data via a questionnaire approximately 10 years after original randomisation. Their mean age at follow-up was 54 years (standard deviation 5 years). A purposeful sample of 36 women also participated in semistructured qualitative interviews.

Interventions: The ECLIPSE trial randomised participants to either the levonorgestrel-releasing intrauterine system (52 mg) or the usual medical treatment (oral tranexamic acid, mefenamic acid, combined oestrogen-progestogen or progesterone alone, chosen as clinically appropriate by general practitioners and women). Women could subsequently swap or cease their allocated treatment.

Main outcome measures: The main outcome measures were rates of ablative and surgical treatments; the rate of continuation of medical treatments; and quality of life using the Short Form questionnaire-36 items and EuroQol-5 Dimensions; women's experiences of heavy menstrual bleeding; and the influences on their decisions around treatment.

Results: Over the 10-year follow-up period, 60 out of 206 (29%) women had received a surgical intervention [hysterectomy, n = 34 (17%); endometrial ablation, n = 26 (13%)]. Between 5 and 10 years post trial intervention, 89 women (43%) had ceased all medical treatments and 88 (43%) were using the levonorgestrel-releasing intrauterine system alone or in combination with other oral treatments. More women in the usual medical treatment group had also used the levonorgestrel-releasing intrauterine system than women in the levonorgestrel-releasing intrauterine system group. Fifty-six women (28%) used the levonorgestrel-releasing intrauterine system at 10 years. There was no statistically significant difference in generic quality-of-life scores between the two original trial groups, although small improvements in the majority of domains were seen in both groups across time. Women reported wide-ranging impacts on their quality of life and normalisation of their heavy menstrual bleeding experience as a result of the taboo around menstruation. Women's treatment decisions and experiences were influenced by the perceived quality of health-care interactions with clinicians and their climacteric status.

Limitations: Fewer than half of the original 571 participants participated; however, the cohort was clinically and demographically representative of the original trial population.

Conclusions: Medical treatments for women with heavy menstrual bleeding can be initiated in primary care, with low rates of surgical intervention and improvement in quality of life observed 10 years later. Clinicians should be aware of the considerable challenges that women with heavy menstrual bleeding experience at presentation and subsequently over time, and the importance and value to women of patient-centred communication in this context.

Future work: Any further evaluation of treatments for heavy menstrual bleeding should include long-term evaluation of outcomes and adherence.

Trial registration: The original ECLIPSE trial was registered as ISRCTN86566246.

Funding: This project was funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 27, No. 17. See the NIHR Journals Library website for further project information.

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女性月经大出血的内科或外科治疗率:ECLIPSE试验10年观察性随访研究。
背景:月经大出血是一个常见的问题,会严重影响女性的生活,直到更年期。对于月经大出血寻求医疗保健和治疗后的长期结果,缺乏证据。目的:评估参与ECLIPSE试验(ISRCTN86566246)的女性在初级保健中首次治疗月经大出血10年后的药物治疗持续率以及消融和手术干预率。探讨女性月经大出血的经验及对治疗的影响。设计:这是一项前瞻性观察性队列研究,同时进行了一项定性研究。设置:初级保健。参与者:共有206名月经大出血的女性参与了ECLIPSE试验,她们同意在最初的随机分组后约10年通过问卷提供结果数据。随访时的平均年龄为54岁(标准差为5岁)。有目的的36名女性样本也参加了半结构的定性访谈。干预措施:ECLIPSE试验将参与者随机分配到左炔诺孕酮释放宫内系统(52 mg)或常规药物治疗(口服氨甲环酸、甲非那米酸、联合雌激素-孕激素或单独的孕激素,由全科医生和妇女根据临床情况选择)。妇女随后可以交换或停止分配的治疗。主要疗效指标:主要疗效指标为消融率和手术治疗率;继续接受治疗的比率;使用简短问卷-36项和EuroQol-5维度的生活质量;妇女月经大出血的经历;以及对他们治疗决策的影响。结果:在10年的随访期内,206名女性中有60名(29%)接受了手术干预[子宫切除术 = 34例(17%);子宫内膜切除术,n = 26(13%)]。在试验干预后5至10年内,89名女性(43%)停止了所有药物治疗,88名(43%)单独或与其他口服治疗联合使用左炔诺孕酮释放宫内系统。常规药物治疗组中也使用左炔诺孕酮释放宫内系统的女性比左炔诺孕释放宫内系统组中的女性多。56名妇女(28%)在10岁时使用左炔诺孕酮释放宫内节育器。两个原始试验组之间的一般生活质量评分没有统计学上的显著差异,尽管随着时间的推移,两组在大多数领域都有小幅改善。女性报告称,由于月经禁忌,她们的生活质量和月经大出血经历的正常化受到了广泛影响。妇女的治疗决策和经历受到与临床医生的医疗保健互动质量及其更年期状况的影响。局限性:在最初的571名参与者中,只有不到一半的人参加;然而,该队列在临床和人口学上代表了原始试验人群。结论:女性月经大出血的医疗治疗可以在初级保健中开始,手术干预率低,10年后观察到生活质量的改善。临床医生应该意识到,月经大出血的女性在就诊时以及随后的一段时间内所经历的巨大挑战,以及在这种情况下以患者为中心的沟通对女性的重要性和价值。未来的工作:对月经大出血治疗的任何进一步评估都应包括对结果和依从性的长期评估。试验注册:最初的ECLIPSE试验注册为ISRCTN86566246。资助:该项目由美国国立卫生与保健研究所(NIHR)健康技术评估计划资助,并将在《健康技术评估》上全文发表;第27卷第17期。有关更多项目信息,请访问NIHR期刊图书馆网站。
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来源期刊
Health technology assessment
Health technology assessment 医学-卫生保健
CiteScore
6.90
自引率
0.00%
发文量
94
审稿时长
>12 weeks
期刊介绍: Health Technology Assessment (HTA) publishes research information on the effectiveness, costs and broader impact of health technologies for those who use, manage and provide care in the NHS.
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