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Long COVID in healthcare workers: longitudinal mixed-methods study. | LitMetric

AI Article Synopsis

  • Healthcare workers (HCWs) are experiencing higher rates of long COVID (LC) and its impact on their lives is still uncertain, affecting their health and work productivity.
  • This study aimed to explore the lived experiences of HCWs suffering from LC, focusing on their health-related quality of life, healthcare usage, work, personal life, and finances.
  • Findings showed that many HCWs faced ongoing complex symptoms, worked reduced hours, and expressed fears about future reinfection, job stability, and financial security, with limited healthcare support.

Article Abstract

Background: Healthcare workers (HCWs) report higher rates of long coronavirus disease (COVID) (LC) than other occupational groups. It is still unclear whether LC is a lifelong condition. Workforce shortfalls are apparent due to sick leave, reduced hours and lower productivity.

Aims: To investigate the lived experience of LC on a range of HCWs, including impact on health-related quality-of-life (HRQL), use of health services, working and personal lives and household finances.

Methods: Longitudinal mixed methods with online surveys and qualitative interviews 6-months apart. HCWs including healthcare professionals, ancillary and administration staff who self-report LC were recruited through social media and National Health Service channels. Interviewees were purposively sampled from survey responses.

Results: The first survey was completed by 471 HCWs (S1) and 302 (64%) the follow-up (S2). A total of 50 HCWs were interviewed initially and 44 at second interview. All participants experienced various relapsing, remitting, changing and prolonged LC symptoms (mean 7.1 [SD 4.8] at S2) and a third reported day-to-day activities 'limited a lot'. Most participants were working in a reduced capacity: reduced hours, different role or location. Healthcare was limited, and often unsatisfactory. Participants feared reinfection, their future, ability to work and financial security (59% (n = 174) at S2). They experienced stigma, distress, grief for their former self and some felt unsupported, however, as awareness of LC grew some experienced improved understanding and support.

Conclusions: Most participants continued working, managing complex and dynamic symptoms effecting their everyday life and ability to work. Most did not report significant improvements over time and feared for their future and financial security.

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Source
http://dx.doi.org/10.1093/occmed/kqae113DOI Listing

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