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成人和家长的生活体验:患有食管闭锁和气管食管瘘的患儿向成人保健的过渡。

The lived experience of adults and parents: Transitioning from paediatric to adult health care with oesophageal atresia and tracheo-oesophageal fistula.

机构信息

Department of Clinical Psychology, University of Bath, Bath, UK.

出版信息

J Clin Nurs. 2023 Apr;32(7-8):1433-1442. doi: 10.1111/jocn.16333. Epub 2022 Apr 22.

Abstract

AIM AND OBJECTIVE

To explore the experience of healthcare transition from paediatric to adult health care for adults born with oesophageal atresia and tracheo-oesophageal fistula (OA/TOF) and parents.

BACKGROUND

OA/TOF is a rare and chronic health condition that can require lifelong medical follow-up and management. There is evidence to suggest that transitioning from paediatric to adult health care can be problematic for people with rare and chronic conditions, including OA/TOF. The previous literature suggests that the experience of transitioning with a rare condition is more complex than transitioning with a common chronic condition.

DESIGN

The current study was a qualitative, cross-sectional, survey-based study.

METHODS

Data were collected through an online survey. Parents of children born with OA/TOF (n = 23) and adults born with OA/TOF (n = 16) were recruited through a UK-based OA/TOF patient charity. Data from six open-ended questions were analysed using a hybrid approach combining elements of inductive and deductive thematic analyses. Throughout the research process, the SRQR were followed.

RESULTS

Five themes were constructed during the analysis, reflecting the experience of parents and adults transitioning from paediatric to adult health care: thrown into the unknown; a cultural shift; stepping back and stepping up; 'no transition as such'; and living with uncertainty.

CONCLUSIONS

The findings suggested that a formalised, managed healthcare transition is not commonly experienced by people born with OA/TOF and parents.

RELEVANCE TO CLINICAL PRACTICE

We recommend a formalised healthcare transition process in OA/TOF, including preparation for transition and having a named key worker to manage the multidisciplinary transition process. The results also highlighted the need for adults born with OA/TOF to have access to a specialist health service with knowledge and understanding of issues related to OA/TOF.

摘要

目的和目标

探索患有食管闭锁和气管食管瘘(OA/TOF)的成年人及其父母从儿科医疗过渡到成人保健的体验。

背景

OA/TOF 是一种罕见的慢性健康状况,可能需要终身医疗随访和管理。有证据表明,对于患有罕见和慢性疾病的人来说,从儿科医疗过渡到成人保健可能会有问题,包括 OA/TOF。先前的文献表明,患有罕见疾病的过渡体验比患有常见慢性疾病的过渡体验更为复杂。

设计

本研究是一项定性、横断面、基于调查的研究。

方法

通过在线调查收集数据。通过英国的一家 OA/TOF 患者慈善机构招募了患有 OA/TOF 的儿童的父母(n=23)和患有 OA/TOF 的成年人(n=16)。使用归纳和演绎主题分析相结合的混合方法分析了六个开放式问题的数据。在整个研究过程中,都遵循了 SRQR 原则。

结果

在分析过程中构建了五个主题,反映了父母和成年人从儿科医疗过渡到成人保健的体验:陷入未知;文化转变;退后一步,向前迈进;“没有真正的过渡”;和生活在不确定之中。

结论

研究结果表明,患有 OA/TOF 的人及其父母通常没有经历过正式的、有管理的医疗过渡。

临床相关性

我们建议在 OA/TOF 中采用正式的医疗过渡流程,包括过渡准备和指定一名关键工作人员来管理多学科过渡过程。研究结果还强调了患有 OA/TOF 的成年人需要获得具有相关 OA/TOF 知识和理解的专门医疗服务。

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