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本文引用的文献

1
Incidence and Severity of SARS-CoV-2 Infections in People With Primary Ciliary Dyskinesia.原发性纤毛运动障碍患者中严重急性呼吸综合征冠状病毒 2 感染的发生率和严重程度。
Int J Public Health. 2023 Aug 17;68:1605561. doi: 10.3389/ijph.2023.1605561. eCollection 2023.
2
The Impact on Parents of Diagnosing PCD in Young Children.幼儿被诊断为原发性纤毛运动障碍对父母的影响。
J Clin Med. 2022 Aug 16;11(16):4774. doi: 10.3390/jcm11164774.
3
The disease-specific clinical trial network for primary ciliary dyskinesia: PCD-CTN.原发性纤毛运动障碍疾病特异性临床试验网络:PCD-CTN
ERJ Open Res. 2022 Aug 15;8(3). doi: 10.1183/23120541.00139-2022. eCollection 2022 Jul.
4
Common needs in uncommon conditions: a qualitative study to explore the need for care in pediatric patients with rare diseases.常见条件下的罕见需求:一项定性研究,旨在探索罕见病儿科患者的护理需求。
Orphanet J Rare Dis. 2022 Apr 4;17(1):153. doi: 10.1186/s13023-022-02305-w.
5
COVID-19 Vaccinations: Perceptions and Behaviours in People with Primary Ciliary Dyskinesia.新冠病毒疫苗接种:原发性纤毛运动障碍患者的认知与行为
Vaccines (Basel). 2021 Dec 17;9(12):1496. doi: 10.3390/vaccines9121496.
6
Current and Future Treatments in Primary Ciliary Dyskinesia.原发性纤毛运动障碍的当前和未来治疗方法。
Int J Mol Sci. 2021 Sep 11;22(18):9834. doi: 10.3390/ijms22189834.
7
COVID-PCD: a participatory research study on the impact of COVID-19 in people with primary ciliary dyskinesia.新冠-原发性纤毛运动障碍研究:一项关于新冠病毒对原发性纤毛运动障碍患者影响的参与性研究。
ERJ Open Res. 2021 Mar 22;7(1). doi: 10.1183/23120541.00843-2020. eCollection 2021 Jan.
8
Understanding Primary Ciliary Dyskinesia and Other Ciliopathies.了解原发性纤毛运动障碍和其他纤毛病。
J Pediatr. 2021 Mar;230:15-22.e1. doi: 10.1016/j.jpeds.2020.11.040. Epub 2020 Nov 23.
9
Primary ciliary dyskinesia and psychological well-being in adolescence.原发性纤毛运动障碍与青少年心理健康。
PLoS One. 2020 Jan 23;15(1):e0227888. doi: 10.1371/journal.pone.0227888. eCollection 2020.
10
Autonomies in Interaction: Dimensions of Patient Autonomy and Non-adherence to Treatment.互动中的自主性:患者自主性的维度与治疗不依从性
Front Psychol. 2019 Aug 14;10:1857. doi: 10.3389/fpsyg.2019.01857. eCollection 2019.

“别让它阻碍你”——原发性纤毛运动障碍患者向成年期过渡的体验:诠释现象学分析。

'Don't let it hold you back' - The experience of transition to adulthood in young people with primary ciliary dyskinesia: An interpretative phenomenological analysis.

机构信息

Genetics & Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, UK.

Department of Psychological Sciences, Birkbeck University of London, London, UK.

出版信息

J Health Psychol. 2024 Aug;29(9):1029-1045. doi: 10.1177/13591053231223912. Epub 2024 Jan 28.

DOI:10.1177/13591053231223912
PMID:38282372
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11301960/
Abstract

Primary ciliary dyskinesia (PCD) is a rare, chronic genetic condition with variable features arising from motile cilia dysfunction, including recurrent respiratory infections, sinonasal disease, reduced hearing, infertility and situs inversus. The aim of the study was to understand the experiences of young people with PCD as they transition into adulthood and adult healthcare services. An interpretative phenomenological analytical method was applied. Semi-structured interviews were conducted with three participants aged 18-24 years. Four interconnected group experiential themes were identified: (1) reconceptualising a stigmatised identity, (2) sharing the journey to independence, (3) entering adulthood with newfound autonomy, (4) anticipating an uncertain future. Overall, we found that transition for young people with PCD presents as a complex period marked by identity-formation, creating systems of support and becoming an autonomous adult. Facilitation of personalised and integrated approaches to care should be prioritised. Our findings are important to help health professionals provide appropriate, anticipatory support.

摘要

原发性纤毛运动障碍(PCD)是一种罕见的慢性遗传疾病,其特征为纤毛运动功能障碍,包括反复呼吸道感染、鼻旁窦疾病、听力下降、不孕和内脏转位。本研究旨在了解年轻人在向成年和成人医疗保健服务过渡时的经历。采用解释性现象学分析方法。对 3 名 18-24 岁的参与者进行了半结构化访谈。确定了四个相互关联的组体验主题:(1)重新构想被污名化的身份,(2)共同踏上独立之路,(3)成年后获得新的自主权,(4)预期不确定的未来。总的来说,我们发现 PCD 患者的过渡是一个复杂的时期,其特点是身份形成、建立支持系统和成为自主的成年人。应优先考虑个性化和综合护理方法。我们的研究结果对于帮助卫生专业人员提供适当的、预期的支持非常重要。