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本文引用的文献

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Navigating liminal spaces together: a qualitative metasynthesis of youth and parent experiences of healthcare transition.共同跨越临界空间:对青少年及其父母医疗保健过渡经历的质性元综合研究
J Transit Med. 2023 Jul 26;5(1):20220004. doi: 10.1515/jtm-2022-0004. eCollection 2023 Jan.
2
Bridging research and policy: The Disability and health journal and the Final Rule of Section 504 of the rehabilitation act of 1973.架起研究与政策之间的桥梁:《残疾与健康期刊》与1973年《康复法案》第504条最终规则
Disabil Health J. 2024 Jul;17(3):101644. doi: 10.1016/j.dhjo.2024.101644. Epub 2024 May 31.
3
Shared Decision Making in Perinatal Care.围产期护理中的共同决策
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4
The Power of Language in Hospital Care for Pregnant and Birthing People: A Vision for Change.语言在孕产妇医院护理中的力量:变革愿景。
Obstet Gynecol. 2023 Oct 1;142(4):795-803. doi: 10.1097/AOG.0000000000005333. Epub 2023 Sep 7.
5
Centering disability visibility in reproductive health care: Dismantling barriers to achieve reproductive equity.将残疾可见性纳入生殖健康护理的中心位置:消除障碍,实现生殖公平。
Womens Health (Lond). 2023 Jan-Dec;19:17455057231197166. doi: 10.1177/17455057231197166.
6
Maternal Health Experiences of Black Deaf and Hard of Hearing Women in the United States.美国黑聋哑女性的孕产妇健康体验。
Womens Health Issues. 2023 Nov-Dec;33(6):610-617. doi: 10.1016/j.whi.2023.07.005. Epub 2023 Aug 28.
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The rise of checklists and the fall of reflexivity in qualitative research.定性研究中清单的兴起与反思性的衰落。
Nurs Health Sci. 2023 Sep;25(3):267-270. doi: 10.1111/nhs.13046. Epub 2023 Aug 22.
8
Supporting disabled parents and their families: perspectives and recommendations from parents, attorneys, and child welfare professionals.支持残疾父母及其家庭:来自父母、律师和儿童福利专业人员的观点与建议。
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9
Prenatal Care Experiences of Childbearing People With Disabilities in Ontario, Canada.加拿大安大略省残疾生育者的产前保健体验。
J Obstet Gynecol Neonatal Nurs. 2023 May;52(3):235-247. doi: 10.1016/j.jogn.2023.02.001. Epub 2023 Mar 17.
10
Unmet needs, limited access: A qualitative study of postpartum health care experiences of people with disabilities.未满足的需求,有限的渠道:一项关于残疾人士产后健康护理体验的定性研究。
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对残疾人士围产期医疗保健经历的定性元分析。

A qualitative meta-synthesis of the perinatal healthcare experiences of people with disability.

作者信息

Harkins Sarah E, Hahn Alexandria L, Didier Meghan, Walsh Caroline, Barcelona Veronica, Melton Katherine, George Maureen

机构信息

Columbia University School of Nursing, New York, NY, United States.

Columbia University School of Nursing, New York, NY, United States.

出版信息

Disabil Health J. 2025 Jul;18(3):101828. doi: 10.1016/j.dhjo.2025.101828. Epub 2025 Mar 27.

DOI:10.1016/j.dhjo.2025.101828
PMID:40175223
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12145249/
Abstract

BACKGROUND

Significant perinatal health disparities exist between people with and without disability in the United States and Canada. However, less is known about the perinatal healthcare experiences of people with different types of disability in those countries. Understanding this experience is crucial for developing tailored interventions to improve perinatal health outcomes.

OBJECTIVE

To synthesize qualitative studies describing the perinatal healthcare experiences of people with physical, sensory, or cognitive disability in the United States and Canada.

METHODS

We conducted a qualitative meta-synthesis following Sandelowski and Barroso's methods. Four databases and forward and backward citation searching were used to identify relevant studies in March 2024. Studies were appraised based on their reporting of Guba's essential criteria for trustworthy qualitative research. We coded qualitative findings and synthesized results into themes and subthemes. GRADE-CERQual was used to rate the level of confidence in each subtheme.

RESULTS

Twenty-one studies describing the perinatal healthcare experiences of 225 people with disability were the basis of this synthesis. Three themes emerged: (1) Pervasive Ableism, (2) An Uninformed and Unaccommodating Experience, and (3) Resilience in the Face of Ableism.

CONCLUSIONS

People with different types of disability shared similar perinatal healthcare experiences, including facing stigma, encountering clinicians with limited knowledge of disability and pregnancy, and demonstrating resilience through self-advocacy and support networks. Accessibility barriers and a lack of disability competency among clinicians were specific to each disability type. Future research should prioritize the development of interventions that promote perinatal health equity for people with disability.

摘要

背景

在美国和加拿大,残疾人和非残疾人之间存在显著的围产期健康差异。然而,对于这些国家中不同类型残疾人的围产期医疗保健经历,人们了解得较少。了解这种经历对于制定针对性的干预措施以改善围产期健康结果至关重要。

目的

综合定性研究,描述美国和加拿大身体、感官或认知残疾者的围产期医疗保健经历。

方法

我们按照桑德洛维茨和巴罗斯的方法进行了定性元综合分析。2024年3月,使用四个数据库以及向前和向后的引文检索来识别相关研究。根据古巴关于可信定性研究的基本标准的报告对研究进行评估。我们对定性研究结果进行编码,并将结果综合为主题和子主题。使用GRADE-CERQual对每个子主题的信心水平进行评级。

结果

21项描述225名残疾人围产期医疗保健经历的研究是本综合分析的基础。出现了三个主题:(1)普遍存在的能力主义,(2)信息不足和缺乏适应性的经历,(3)面对能力主义时的复原力。

结论

不同类型的残疾人有着相似的围产期医疗保健经历,包括面临耻辱感、遇到对残疾和怀孕知识有限的临床医生,以及通过自我倡导和支持网络展现出复原力。无障碍障碍和临床医生缺乏残疾方面的能力因残疾类型而异。未来的研究应优先开发促进残疾人士围产期健康公平的干预措施。