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. 2024 Sep;33(9):2489-2507.
doi: 10.1007/s11136-024-03710-3. Epub 2024 Jul 3.

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

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

Breanna Weigel et al. Qual Life Res. 2024 Sep.

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.

Keywords: Long COVID; Myalgic encephalomyelitis/chronic fatigue syndrome; Post COVID-19 condition; Post-Acute sequelae of COVID-19; Quality of life.

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Conflict of interest statement

The authors have no financial or non-financial competing interests relevant to the present manuscript to disclose.

Figures

Fig. 1
Fig. 1
Severity and frequency for symptoms returning significance between the two illness cohorts. Figure generated with GraphPad. PwME/CFS people with myalgic encephalomyelitis/chronic fatigue syndrome, PwPCC People with Post COVID-19 Condition. Symptom severity and frequency data is provided for participants experiencing the symptom in question within the month prior to completing the questionnaire and attributing the symptom in question to their chronic multi-systemic illness. *p < 0·05

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