Lived experience of patients with Long COVID: a qualitative study in the UK 2023 Thomas et al

Discussion in 'Long Covid research' started by Andy, Apr 27, 2023.

  1. Andy

    Andy Committee Member

    Messages:
    22,407
    Location:
    Hampshire, UK
    Background
    Long COVID is a rapidly evolving global health crisis requiring interdisciplinary support strategies that incorporate the lived experience of patients. Currently, there is a paucity of research documenting the day-to-day experiences of patients living with Long COVID.

    Objective
    To explore the lived experience of Long COVID patients.

    Study design
    Longitudinal, observation study.

    Setting
    An inductive, data-driven, qualitative approach was used to evaluate hand-written diaries obtained from individuals who had been referred to a Derbyshire Long COVID clinic.

    Participants
    12 participants (11 females, age 49±10 years, 11 Caucasians) were recruited. Participants were included if they had a previous confirmed or suspected COVID-19 infection with ongoing recovery, >18 years old, understood the study requirements and provided informed consent.

    Method
    Participants were directed to complete self-report diaries over 16 weeks. Responses were transcribed verbatim and analysed using thematic analysis.

    Results
    Three key themes were highlighted: (1) understanding who helps patients manage symptoms, (2) daily activities and the impact on quality of life and health status and (3) the effect of turbulent and episodic symptom profiles on personal identity and recovery.

    Conclusions
    The novel challenges presented by Long COVID are complex with varying inter-related factors that are broadly impacting functional status and quality of life. Support mechanisms must incorporate the lived experiences and foster true collaborations between health professionals, patients and researchers to improve patient outcomes.

    Open access, https://bmjopen.bmj.com/content/13/4/e068481.full
     
    Peter Trewhitt, ahimsa, Wonko and 2 others like this.
  2. Andy

    Andy Committee Member

    Messages:
    22,407
    Location:
    Hampshire, UK
    The sole mention of ME/CFS.

    "For example, meaning development, art therapies and journaling advanced by the four-phase model30 are proposed to be especially useful in grief management for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome patients who suffer from similar, but not identical, broad, long-term symptoms such as tiredness, sleep disturbances and brain fog. Further research is needed to deepen the understanding and integration between physical, mental and emotional support mechanisms."
     
  3. Hutan

    Hutan Moderator Staff Member

    Messages:
    27,999
    Location:
    Aotearoa New Zealand
    Rapid responses to the paper are possible, if anyone has the energy and inclination to quote some of the papers that have found significant numbers of Long covid people meet ME/CFS criteria.

    We have a tag "lc=me/cfs" that can be put on papers that assess LC patients against ME/CFS criteria, so if you see any such papers, please do add the tag. It feels like an issue where a good quote could come in handy for advocacy.
     

Share This Page