Experiences of Pelvic and Generalized Persistent Pain Syndromes in MRKH: A Scoping Review

IF 1.7 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Journal of pediatric and adolescent gynecology Pub Date : 2024-07-20 DOI:10.1016/j.jpag.2024.07.002
R.U. Gaikaiwari MBBS (Hons) , C. Prinsloo MBBS (Hons) , S.R. Grover MBBS, FRANZCOG, MD, FFPMANZCA , I. Wright MBBS, DCH, MRCP(UK)Paeds, FRACP , N. Drever MBBS, BMedSci, FRANZCOG
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Abstract

Study Objective

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by the congenital absence of the uterus and vagina, sometimes with associated extragenital anomalies. Currently, there is limited literature on pelvic pain and comorbid pain syndromes in people with MRKH. The aims of this scoping review were to summarize existing literature on pelvic and generalized persistent pain syndromes associated with MRKH and to identify knowledge gaps for further research into this field.

Methods

This scoping review followed the Joanna Briggs Institute framework. The population of interest was patients with a diagnosis of MRKH. MEDLINE, CINAHL, Scopus, Cochrane, Embase, and Emcare databases were searched. Articles that did not meet the inclusion criteria or critical appraisal standards were excluded. The resultant articles were reviewed by 2 independent researchers, and a third was used in cases of disagreement. A descriptive analytical method was used for data analysis.

Results

We screened 3348 articles for eligibility. Of these, 39 articles, which described 1353 cases of MRKH, met the criteria. Four studies described baseline pelvic pain in MRKH, 19 described acute presentations, and 13 described postintervention pain levels.

Conclusion

Despite the paucity of research, this review found that cyclic pelvic pain was mostly present in women with uterine remnants, whereas pelvic pain in those without remnants was poorly understood. There were no studies exploring generalized persistent pain syndromes in MRKH. Further cross-sectional studies are needed to elucidate the prevalence and levels of pain syndromes in MRKH.

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MRKH 骨盆和全身持续性疼痛综合征的经验:范围综述。
研究目的Mayer-Rokitansky-Küster-Hauser综合征(MRKH)的特征是先天性无子宫和阴道,有时伴有生殖器外畸形。目前,有关 MRKH 患者盆腔疼痛和合并疼痛综合征的文献十分有限。本范围综述旨在总结与MRKH相关的盆腔和全身持续性疼痛综合征的现有文献,并找出该领域进一步研究的知识缺口:本范围界定综述遵循乔安娜-布里格斯研究所(Joanna Briggs Institute)的框架。研究对象为确诊为 MRKH 的患者。检索了 MEDLINE、CINAHL、Scopus、Cochrane、Embase 和 Emcare 数据库。排除了不符合纳入标准或关键评估标准的文章。由此产生的文章由两名独立的研究人员进行审查,在出现分歧时再由第三名研究人员进行审查。数据分析采用描述性分析方法:我们筛选了3348篇文章进行资格审查,39篇文章符合标准,其中描述了1353例MRKH病例。4 项研究描述了 MRKH 骨盆疼痛的基线,19 项研究描述了急性表现,13 项研究描述了干预后的疼痛水平:尽管研究较少,但本综述发现,周期性盆腔疼痛主要出现在有子宫残留的妇女身上,而对无子宫残留妇女的盆腔疼痛则知之甚少。没有研究探讨 MRKH 中的全身持续性疼痛综合征。需要进一步开展横断面研究,以阐明MRKH中疼痛综合征的患病率和程度。
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来源期刊
CiteScore
3.90
自引率
11.10%
发文量
251
审稿时长
57 days
期刊介绍: Journal of Pediatric and Adolescent Gynecology includes all aspects of clinical and basic science research in pediatric and adolescent gynecology. The Journal draws on expertise from a variety of disciplines including pediatrics, obstetrics and gynecology, reproduction and gynecology, reproductive and pediatric endocrinology, genetics, and molecular biology. The Journal of Pediatric and Adolescent Gynecology features original studies, review articles, book and literature reviews, letters to the editor, and communications in brief. It is an essential resource for the libraries of OB/GYN specialists, as well as pediatricians and primary care physicians.
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