Illness presentation and quality of life in myalgic encephalomyelitis/chronic fatigue syndrome and post COVID-19 condition: a pilot Australian cross-sectional study.

IF 3.3 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Breanna Weigel, Natalie Eaton-Fitch, Kiran Thapaliya, Sonya Marshall-Gradisnik
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引用次数: 0

Abstract

Purpose: Post COVID-19 Condition (PCC), being persistent COVID-19 symptoms, is reminiscent of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)-a chronic multi-systemic illness characterised by neurocognitive, autonomic, endocrinological and immunological disturbances. This novel cross-sectional investigation aims to: (1) compare symptoms among people with ME/CFS (pwME/CFS) and people with PCC (pwPCC) to inform developing PCC diagnostic criteria; and (2) compare health outcomes between patients and people without acute or chronic illness (controls) to highlight the illness burdens of ME/CFS and PCC.

Methods: Sociodemographic and health outcome data were collected from n = 61 pwME/CFS, n = 31 pwPCC and n = 54 controls via validated, self-administered questionnaires, including the 36-Item Short-Form Health Survey version 2 (SF-36v2) and World Health Organization Disability Assessment Schedule version 2.0 (WHODAS 2.0). PwME/CFS and pwPCC also provided self-reported severity and frequency of symptoms derived from the Canadian and International Consensus Criteria for ME/CFS and the World Health Organization case definition for PCC.

Results: Both illness cohorts similarly experienced key ME/CFS symptoms. Few differences in symptoms were observed, with memory disturbances, muscle weakness, lymphadenopathy and nausea more prevalent, light-headedness more severe, unrefreshed sleep more frequent, and heart palpitations less frequent among pwME/CFS (all p < 0.05). The ME/CFS and PCC participants' SF-36v2 or WHODAS 2.0 scores were comparable (all p > 0.05); however, both cohorts returned significantly lower scores in all SF-36v2 and WHODAS 2.0 domains when compared with controls (all p < 0.001).

Conclusion: This Australian-first investigation demonstrates the congruent and debilitating nature of ME/CFS and PCC, thereby emphasising the need for multidisciplinary care to maximise patient health outcomes.

Abstract Image

肌痛性脑脊髓炎/慢性疲劳综合征和 COVID-19 后病情的疾病表现和生活质量:一项澳大利亚试点横断面研究。
目的:COVID-19 后症状(PCC)是一种持续性 COVID-19 症状,让人联想到肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)--一种以神经认知、自主神经、内分泌和免疫学紊乱为特征的多系统慢性疾病。这项新颖的横断面调查旨在:(1) 比较 ME/CFS 患者(pwME/CFS)和 PCC 患者(pwPCC)的症状,为制定 PCC 诊断标准提供依据;(2) 比较患者和无急性或慢性疾病者(对照组)的健康结果,以突出 ME/CFS 和 PCC 的疾病负担:通过有效的自填式问卷,包括36项短式健康调查2版(SF-36v2)和世界卫生组织残疾评估表2.0版(WHODAS 2.0),收集了n = 61名ME/CFS患者、n = 31名PCC患者和n = 54名对照者的社会人口学和健康结果数据。ME/CFS患者和PCC患者还提供了根据加拿大和国际ME/CFS共识标准以及世界卫生组织PCC病例定义得出的症状严重程度和频率的自我报告:结果:两组患病者的主要 ME/CFS 症状相似。观察到的症状差异很小,其中记忆障碍、肌肉无力、淋巴腺肿大和恶心在男性和女性 ME/CFS 患者中更为普遍,头重脚轻更为严重,睡眠不安稳更为常见,心悸更为少见(所有 p 均为 0.05);然而,与对照组相比,两组患者在所有 SF-36v2 和 WHODAS 2.0 领域的得分都明显较低(所有 p 均为 0.05):这项澳大利亚首次开展的调查表明,ME/CFS 和 PCC 具有共同性和削弱性,因此强调需要进行多学科护理,以最大限度地改善患者的健康状况。
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来源期刊
Quality of Life Research
Quality of Life Research 医学-公共卫生、环境卫生与职业卫生
CiteScore
6.50
自引率
8.60%
发文量
224
审稿时长
3-8 weeks
期刊介绍: Quality of Life Research is an international, multidisciplinary journal devoted to the rapid communication of original research, theoretical articles and methodological reports related to the field of quality of life, in all the health sciences. The journal also offers editorials, literature, book and software reviews, correspondence and abstracts of conferences. Quality of life has become a prominent issue in biometry, philosophy, social science, clinical medicine, health services and outcomes research. The journal''s scope reflects the wide application of quality of life assessment and research in the biological and social sciences. All original work is subject to peer review for originality, scientific quality and relevance to a broad readership. This is an official journal of the International Society of Quality of Life Research.
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