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“感觉我的身体垮了”:探索长新冠患者的经历。

"I feel like my body is broken": exploring the experiences of people living with long COVID.

机构信息

School of Kinesiology, University of the Fraser Valley, Chilliwack, BC, Canada.

Faculty of Kinesiology, University of Calgary, Calgary, AB, Canada.

出版信息

Qual Life Res. 2022 Dec;31(12):3339-3354. doi: 10.1007/s11136-022-03176-1. Epub 2022 Jul 11.

Abstract

PURPOSE

Long COVID, an illness affecting a subset of individuals after COVID-19, is distressing, poorly understood, and reduces quality of life. The objective of this sub-study was to better understand and explore individuals' experiences with long COVID and commonly reported symptoms, using qualitative data collected from open-ended survey responses.

METHODS

Data were collected from adults living with long COVID who participated in a larger observational online survey. Participants had the option of answering seven open-ended items. Data from the open-ended items were analyzed following guidelines for reflective thematic analysis.

RESULTS

From 213 participants who were included in the online survey, 169 participants who primarily self-identified as women (88.2%), aged 40-49 (33.1%), who had been experiencing long COVID symptoms for ≥ 6 months (74%) provided open-ended responses. Four overlapping and interconnected themes were identified: (1) Long COVID symptoms are numerous and wearing, (2) The effects of long COVID are pervasive, (3) Physical activity is difficult and, in some cases, not possible, and (4) Asking for help when few are listening, and little is working.

CONCLUSION

Findings reaffirm prior research, highlighting the complex nature of long COVID. Further, results show the ways individuals affected by the illness are negatively impacted and have had to alter their daily activities. Participants recounted the challenges faced when advocating for themselves, adapting to new limitations, and navigating healthcare systems. The varied relapsing-remitting symptoms, unknown prognosis, and deep sense of loss over one's prior identity suggest interventions are needed to support this population.

摘要

目的

长新冠是一种在 COVID-19 后影响部分个体的疾病,其令人痛苦、了解甚少,并降低生活质量。本研究的目的是使用从开放式调查回复中收集的定性数据,更好地了解和探索个体的长新冠经历和常见报告症状。

方法

数据来自参与更大规模在线观察性研究的长新冠患者。参与者可选择回答七个开放式项目。根据反思性主题分析指南分析开放式项目的数据。

结果

在参与在线调查的 213 名患者中,169 名主要自我识别为女性(88.2%)、年龄在 40-49 岁(33.1%)、长新冠症状持续时间≥6 个月(74%)的患者提供了开放式回复。确定了四个重叠且相互关联的主题:(1)长新冠症状众多且令人疲惫,(2)长新冠的影响无处不在,(3)体力活动困难,在某些情况下无法进行,(4)寻求帮助时很少有人倾听,而且收效甚微。

结论

研究结果证实了先前的研究,强调了长新冠的复杂性质。此外,结果显示出受疾病影响的个体受到负面影响的方式,以及他们不得不改变日常生活的方式。参与者描述了为自己辩护、适应新限制和导航医疗保健系统时面临的挑战。各种反复发作的缓解症状、未知的预后以及对以前身份的深深失落感表明,需要干预措施来支持这一人群。

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The teachings of Long COVID.长期新冠的相关知识
Commun Med (Lond). 2021 Jul 12;1:15. doi: 10.1038/s43856-021-00016-0. eCollection 2021.

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