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. 2025 Dec 19;9(4):BJGPO.2024.0140.
doi: 10.3399/BJGPO.2024.0140. Print 2025 Dec.

Patient characteristics associated with clinically coded long COVID: an OpenSAFELY study using electronic health records

Affiliations

Patient characteristics associated with clinically coded long COVID: an OpenSAFELY study using electronic health records

Yinghui Wei et al. BJGP Open. .

Abstract

Background: Clinically coded long COVID cases in electronic health records (EHRs) are incomplete, despite reports of rising cases of long COVID.

Aim: To determine patient characteristics associated with clinically coded long COVID.

Design & setting: With the approval of NHS England, we conducted a cohort study using EHRs within the OpenSAFELY-TPP platform in England, to study patient characteristics associated with clinically coded long COVID from 29 January 2020 to 31 March 2022.

Method: We summarised the distribution of characteristics for people with clinically coded long COVID. We estimated age-sex adjusted hazard ratios (aHRs) and fully aHRs for coded long COVID. Patient characteristics included demographic factors, and health behavioural and clinical factors.

Results: Among 17 986 419 adults, 36 886 (0.21%) were clinically coded with long COVID. Patient characteristics associated with coded long COVID included female sex, younger age (aged <60 years), obesity, living in less deprived areas, ever smoking, greater consultation frequency, and history of diagnosed asthma, mental health conditions, pre-pandemic post-viral fatigue, or psoriasis. These associations were attenuated following two doses of COVID-19 vaccines compared with before vaccination. Differences in the predictors of coded long COVID between the pre-vaccination and post-vaccination cohorts may reflect the different patient characteristics in these two cohorts rather than the vaccination status. Incidence of coded long COVID was higher in those with hospitalised COVID-19 than with those with non-hospitalised COVID-19.

Conclusion: We identified variation in coded long COVID by patient characteristic. Results should be interpreted with caution as long COVID was likely under-recorded in EHRs.

Keywords: COVID-19; Long COVID; SARS-CoV-2; post-acute COVID-19 syndrome.

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Conflict of interest statement

Over the past five years BG has received research funding from the Laura and John Arnold Foundation, the NHS National Institute for Health Research (NIHR), the NIHR School of Primary Care Research, the NIHR Oxford Biomedical Research Centre, the Mohn-Westlake Foundation, NIHR Applied Research Collaboration Oxford and Thames Valley, the Wellcome Trust, the Good Thinking Foundation, Health Data Research UK (HDRUK), the Health Foundation, and the World Health Organization; he also receives personal income from speaking and writing for lay audiences on the misuse of science

Figures

Figure 1.
Figure 1.. Primary and post-COVID diagnosis cohorts: age-and-sex adjusted and fully adjusted hazard ratios of coded long COVID for demographic variables. BMI = body mass index. IMD = Index of Multiple Deprivation
Figure 2.
Figure 2.. Pre-vaccination and post-vaccination cohorts: age-and-sex adjusted and fully adjusted hazard ratios of coded long COVID for demographic variables. BMI = body mass index. IMD = Index of Multiple Deprivation
Figure 3.
Figure 3.. Primary and post-COVID diagnosis cohorts: age-and-sex adjusted and fully adjusted hazard ratios of coded long COVID for health behavioural and clinical variables. SLE = systemic lupus erythematosus
Figure 4.
Figure 4.. Pre-vaccination and post-vaccination cohorts: age-and-sex adjusted and fully adjusted hazard ratios of coded long COVID for health behavioural and clinical variables. SLE = systemic lupus erythematosus

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