"Don't give up, advocate for yourself": A pilot study examining healthcare experiences of people with Mayer Rokitansky Küster Hauser syndrome (MRKH).

IF 1.7 4区 医学 Q3 OBSTETRICS & GYNECOLOGY
Nisha Marshall, Zwetlana Rajesh, Kate Hunker, Jessica Merletti, Melody Garas, Ashley Clark, Sunni Anne Ball, M E Sophie Gibson, Caroline F Pukall
{"title":"\"Don't give up, advocate for yourself\": A pilot study examining healthcare experiences of people with Mayer Rokitansky Küster Hauser syndrome (MRKH).","authors":"Nisha Marshall, Zwetlana Rajesh, Kate Hunker, Jessica Merletti, Melody Garas, Ashley Clark, Sunni Anne Ball, M E Sophie Gibson, Caroline F Pukall","doi":"10.1016/j.jpag.2024.12.001","DOIUrl":null,"url":null,"abstract":"<p><strong>Study objective: </strong>Mayer Rokitansky Küster Hauser syndrome (MRKH) is characterized by the underdevelopment or absence of the uterus and upper vagina. Navigating healthcare interactions may present unique challenges for those with MRKH as there appears to be sparse clinical education and research available to healthcare providers. Additionally, limited research exists on the healthcare experiences of people with MRKH. This pilot study investigated the diagnostic journeys, post-diagnosis experiences, current healthcare interactions, and attitudes toward the healthcare system among individuals with MRKH.</p><p><strong>Methods: </strong>Participants with MRKH residing in the United States or Canada took part in semi-structured interviews on their MRKH-related healthcare experiences. Interview transcripts were thematically analyzed.</p><p><strong>Results: </strong>People with MRKH conveyed that: 1) MRKH was not well known by healthcare providers and they were seldom provided with information and resources about MRKH, 2) they often needed to advocate for themselves in the healthcare system to receive adequate care, 3) sensitivity, inclusion, and knowledge from healthcare providers was invaluable, and 4) healthcare-system level barriers prohibited access to adequate care.</p><p><strong>Conclusions: </strong>Information and resources for MRKH patients should be age appropriate, patient-centered, trauma informed, and locally based. Providers should have access to evidence-based information and resources about MRKH, which includes knowledge of local specialist physicians, mental health specialists, pelvic health physical therapists, and other allied health professionals. Providers should also limit assumptions and use sensitive and inclusive language when communicating with patients around MRKH diagnosis, education, and development of treatment plans. Lastly, strategies for mitigating healthcare barriers should consider those with MRKH.</p>","PeriodicalId":16708,"journal":{"name":"Journal of pediatric and adolescent gynecology","volume":" ","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2024-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of pediatric and adolescent gynecology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.jpag.2024.12.001","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Study objective: Mayer Rokitansky Küster Hauser syndrome (MRKH) is characterized by the underdevelopment or absence of the uterus and upper vagina. Navigating healthcare interactions may present unique challenges for those with MRKH as there appears to be sparse clinical education and research available to healthcare providers. Additionally, limited research exists on the healthcare experiences of people with MRKH. This pilot study investigated the diagnostic journeys, post-diagnosis experiences, current healthcare interactions, and attitudes toward the healthcare system among individuals with MRKH.

Methods: Participants with MRKH residing in the United States or Canada took part in semi-structured interviews on their MRKH-related healthcare experiences. Interview transcripts were thematically analyzed.

Results: People with MRKH conveyed that: 1) MRKH was not well known by healthcare providers and they were seldom provided with information and resources about MRKH, 2) they often needed to advocate for themselves in the healthcare system to receive adequate care, 3) sensitivity, inclusion, and knowledge from healthcare providers was invaluable, and 4) healthcare-system level barriers prohibited access to adequate care.

Conclusions: Information and resources for MRKH patients should be age appropriate, patient-centered, trauma informed, and locally based. Providers should have access to evidence-based information and resources about MRKH, which includes knowledge of local specialist physicians, mental health specialists, pelvic health physical therapists, and other allied health professionals. Providers should also limit assumptions and use sensitive and inclusive language when communicating with patients around MRKH diagnosis, education, and development of treatment plans. Lastly, strategies for mitigating healthcare barriers should consider those with MRKH.

“不要放弃,为自己辩护”:一项调查Mayer Rokitansky k斯特豪瑟综合征(MRKH)患者医疗保健经历的试点研究。
研究目的:Mayer Rokitansky k - ster - Hauser综合征(MRKH)以子宫和上阴道发育不全或缺失为特征。导航医疗互动可能会给那些MRKH患者带来独特的挑战,因为医疗保健提供者似乎缺乏临床教育和研究。此外,关于MRKH患者的医疗保健经历的研究有限。本初步研究调查了MRKH患者的诊断历程、诊断后经历、当前医疗互动以及对医疗系统的态度。方法:居住在美国或加拿大的MRKH患者参加了与MRKH相关的医疗经历的半结构化访谈。访谈记录按主题进行分析。结果:MRKH患者反映:1)MRKH不为医疗保健提供者所了解,他们很少获得MRKH的信息和资源;2)他们经常需要在医疗保健系统中为自己倡导以获得适当的护理;3)医疗保健提供者的敏感性、包容性和知识是无价的;4)医疗保健系统层面的障碍阻碍了他们获得适当的护理。结论:MRKH患者的信息和资源应与年龄相适应,以患者为中心,了解创伤,并以当地为基础。提供者应该能够获得关于MRKH的循证信息和资源,包括当地专科医生、心理健康专家、骨盆健康物理治疗师和其他联合卫生专业人员的知识。在与患者沟通MRKH诊断、教育和制定治疗计划时,提供者也应限制假设,并使用敏感和包容的语言。最后,减少保健障碍的战略应考虑到MRKH患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信