German general practitioners' experiences of managing post-COVID-19 syndrome: A qualitative interview study.
COVID-19
Primary health care
pandemics
post-acute COVID-19 syndrome
qualitative research
Journal
The European journal of general practice
ISSN: 1751-1402
Titre abrégé: Eur J Gen Pract
Pays: England
ID NLM: 9513566
Informations de publication
Date de publication:
Dec 2024
Dec 2024
Historique:
medline:
22
10
2024
pubmed:
21
10
2024
entrez:
21
10
2024
Statut:
ppublish
Résumé
The management of the long-term sequelae of coronavirus disease 2019 (COVID-19) infection, known as post-COVID-19 syndrome (PCS), continues to challenge the medical community, largely owing to a significant gap in the understanding of its aetiology, diagnosis and effective treatment. To examine general practitioners' (GPs) experiences of caring for patients with PCS and to identify unmet care needs and opportunities for improvement. This study follows a qualitative design, using in-depth semi-structured telephone interviews with GPs ( Interviews were audio-recorded, transcribed verbatim and analysed using qualitative content analysis. GPs reported that they were often the first point of contact for patients with persistent symptoms following SARS-CoV-2 infection, with symptoms typically resolving within weeks. While ongoing symptomatic COVID-19 is perceived to be more common, the relevance of PCS to GP practices is considerable given its severe impact on patients' functioning, social participation and the substantial time required for patient care. GPs coordinate diagnosis and treatment but face challenges because of the unclear definition of PCS and difficulties in attributing symptoms, resulting in a cautious approach to ICD-10 coding. Interviewees highlight lengthy diagnostic pathways and barriers to accessing specialist care. The findings confirm the high functional limitations and psychosocial burden of PCS on patients, and the central role of GPs in their care. The study suggests a need for further research and health policy measures to support GPs in navigating diagnostic uncertainty, interprofessional communication and the limited evidence on effective treatments. Limited evidence on causes and treatment of PCS challenges GPs.The findings illustrate symptom-driven approaches adopted by GPs to diagnose and manage PCS and highlight the role of psychosocial support.Efforts should focus on supporting GPs in their central role in the management of PCS to handle diagnostic uncertainty, improving interprofessional communication and addressing barriers to accessing specialist care.
Sections du résumé
BACKGROUND
UNASSIGNED
The management of the long-term sequelae of coronavirus disease 2019 (COVID-19) infection, known as post-COVID-19 syndrome (PCS), continues to challenge the medical community, largely owing to a significant gap in the understanding of its aetiology, diagnosis and effective treatment.
AIM
UNASSIGNED
To examine general practitioners' (GPs) experiences of caring for patients with PCS and to identify unmet care needs and opportunities for improvement.
DESIGN AND SETTING
UNASSIGNED
This study follows a qualitative design, using in-depth semi-structured telephone interviews with GPs (
METHOD
UNASSIGNED
Interviews were audio-recorded, transcribed verbatim and analysed using qualitative content analysis.
RESULTS
UNASSIGNED
GPs reported that they were often the first point of contact for patients with persistent symptoms following SARS-CoV-2 infection, with symptoms typically resolving within weeks. While ongoing symptomatic COVID-19 is perceived to be more common, the relevance of PCS to GP practices is considerable given its severe impact on patients' functioning, social participation and the substantial time required for patient care. GPs coordinate diagnosis and treatment but face challenges because of the unclear definition of PCS and difficulties in attributing symptoms, resulting in a cautious approach to ICD-10 coding. Interviewees highlight lengthy diagnostic pathways and barriers to accessing specialist care.
CONCLUSION
UNASSIGNED
The findings confirm the high functional limitations and psychosocial burden of PCS on patients, and the central role of GPs in their care. The study suggests a need for further research and health policy measures to support GPs in navigating diagnostic uncertainty, interprofessional communication and the limited evidence on effective treatments.
Limited evidence on causes and treatment of PCS challenges GPs.The findings illustrate symptom-driven approaches adopted by GPs to diagnose and manage PCS and highlight the role of psychosocial support.Efforts should focus on supporting GPs in their central role in the management of PCS to handle diagnostic uncertainty, improving interprofessional communication and addressing barriers to accessing specialist care.
Autres résumés
Type: plain-language-summary
(eng)
Limited evidence on causes and treatment of PCS challenges GPs.The findings illustrate symptom-driven approaches adopted by GPs to diagnose and manage PCS and highlight the role of psychosocial support.Efforts should focus on supporting GPs in their central role in the management of PCS to handle diagnostic uncertainty, improving interprofessional communication and addressing barriers to accessing specialist care.
Identifiants
pubmed: 39432372
doi: 10.1080/13814788.2024.2413095
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM