TY - JOUR
T1 - COVID-19 trajectories among 57 million adults in England
T2 - a cohort study using electronic health records
AU - Longitudinal Health and Wellbeing COVID-19 National Core Study and the CVD-COVID-UK/COVID-IMPACT Consortium
AU - Thygesen, Johan H.
AU - Tomlinson, Christopher
AU - Hollings, Sam
AU - Mizani, Mehrdad A.
AU - Handy, Alex
AU - Akbari, Ashley
AU - Banerjee, Amitava
AU - Cooper, Jennifer
AU - Lai, Alvina G.
AU - Li, Kezhi
AU - Mateen, Bilal A.
AU - Sattar, Naveed
AU - Sofat, Reecha
AU - Torralbo, Ana
AU - Wu, Honghan
AU - Wood, Angela
AU - Sterne, Jonathan A.C.
AU - Pagel, Christina
AU - Whiteley, William N.
AU - Sudlow, Cathie
AU - Hemingway, Harry
AU - Denaxas, Spiros
AU - Abbasizanjani, Hoda
AU - Ahmed, Nida
AU - Ahmed, Badar
AU - Akinoso-Imran, Abdul Qadr
AU - Allara, Elias
AU - Allery, Freya
AU - Angelantonio, Emanuele Di
AU - Ashworth, Mark
AU - Ayyar-Gupta, Vandana
AU - Babu-Narayan, Sonya
AU - Bacon, Seb
AU - Ball, Steve
AU - Banerjee, Ami
AU - Barber, Mark
AU - Barrett, Jessica
AU - Bennie, Marion
AU - Berry, Colin
AU - Beveridge, Jennifer
AU - Birney, Ewan
AU - Bojanić, Lana
AU - Bolton, Thomas
AU - Bone, Anna
AU - Boyle, Jon
AU - Braithwaite, Tasanee
AU - Bray, Ben
AU - Briffa, Norman
AU - Brind, David
AU - Toms, Renin
N1 - Publisher Copyright:
© 2022 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
PY - 2022/6/8
Y1 - 2022/6/8
N2 - Background: Updatable estimates of COVID-19 onset, progression, and trajectories underpin pandemic mitigation efforts. To identify and characterise disease trajectories, we aimed to define and validate ten COVID-19 phenotypes from nationwide linked electronic health records (EHR) using an extensible framework. Methods: In this cohort study, we used eight linked National Health Service (NHS) datasets for people in England alive on Jan 23, 2020. Data on COVID-19 testing, vaccination, primary and secondary care records, and death registrations were collected until Nov 30, 2021. We defined ten COVID-19 phenotypes reflecting clinically relevant stages of disease severity and encompassing five categories: positive SARS-CoV-2 test, primary care diagnosis, hospital admission, ventilation modality (four phenotypes), and death (three phenotypes). We constructed patient trajectories illustrating transition frequency and duration between phenotypes. Analyses were stratified by pandemic waves and vaccination status. Findings: Among 57 032 174 individuals included in the cohort, 13 990 423 COVID-19 events were identified in 7 244 925 individuals, equating to an infection rate of 12·7% during the study period. Of 7 244 925 individuals, 460 737 (6·4%) were admitted to hospital and 158 020 (2·2%) died. Of 460 737 individuals who were admitted to hospital, 48 847 (10·6%) were admitted to the intensive care unit (ICU), 69 090 (15·0%) received non-invasive ventilation, and 25 928 (5·6%) received invasive ventilation. Among 384 135 patients who were admitted to hospital but did not require ventilation, mortality was higher in wave 1 (23 485 [30·4%] of 77 202 patients) than wave 2 (44 220 [23·1%] of 191 528 patients), but remained unchanged for patients admitted to the ICU. Mortality was highest among patients who received ventilatory support outside of the ICU in wave 1 (2569 [50·7%] of 5063 patients). 15 486 (9·8%) of 158 020 COVID-19-related deaths occurred within 28 days of the first COVID-19 event without a COVID-19 diagnoses on the death certificate. 10 884 (6·9%) of 158 020 deaths were identified exclusively from mortality data with no previous COVID-19 phenotype recorded. We observed longer patient trajectories in wave 2 than wave 1. Interpretation: Our analyses illustrate the wide spectrum of disease trajectories as shown by differences in incidence, survival, and clinical pathways. We have provided a modular analytical framework that can be used to monitor the impact of the pandemic and generate evidence of clinical and policy relevance using multiple EHR sources. Funding: British Heart Foundation Data Science Centre, led by Health Data Research UK.
AB - Background: Updatable estimates of COVID-19 onset, progression, and trajectories underpin pandemic mitigation efforts. To identify and characterise disease trajectories, we aimed to define and validate ten COVID-19 phenotypes from nationwide linked electronic health records (EHR) using an extensible framework. Methods: In this cohort study, we used eight linked National Health Service (NHS) datasets for people in England alive on Jan 23, 2020. Data on COVID-19 testing, vaccination, primary and secondary care records, and death registrations were collected until Nov 30, 2021. We defined ten COVID-19 phenotypes reflecting clinically relevant stages of disease severity and encompassing five categories: positive SARS-CoV-2 test, primary care diagnosis, hospital admission, ventilation modality (four phenotypes), and death (three phenotypes). We constructed patient trajectories illustrating transition frequency and duration between phenotypes. Analyses were stratified by pandemic waves and vaccination status. Findings: Among 57 032 174 individuals included in the cohort, 13 990 423 COVID-19 events were identified in 7 244 925 individuals, equating to an infection rate of 12·7% during the study period. Of 7 244 925 individuals, 460 737 (6·4%) were admitted to hospital and 158 020 (2·2%) died. Of 460 737 individuals who were admitted to hospital, 48 847 (10·6%) were admitted to the intensive care unit (ICU), 69 090 (15·0%) received non-invasive ventilation, and 25 928 (5·6%) received invasive ventilation. Among 384 135 patients who were admitted to hospital but did not require ventilation, mortality was higher in wave 1 (23 485 [30·4%] of 77 202 patients) than wave 2 (44 220 [23·1%] of 191 528 patients), but remained unchanged for patients admitted to the ICU. Mortality was highest among patients who received ventilatory support outside of the ICU in wave 1 (2569 [50·7%] of 5063 patients). 15 486 (9·8%) of 158 020 COVID-19-related deaths occurred within 28 days of the first COVID-19 event without a COVID-19 diagnoses on the death certificate. 10 884 (6·9%) of 158 020 deaths were identified exclusively from mortality data with no previous COVID-19 phenotype recorded. We observed longer patient trajectories in wave 2 than wave 1. Interpretation: Our analyses illustrate the wide spectrum of disease trajectories as shown by differences in incidence, survival, and clinical pathways. We have provided a modular analytical framework that can be used to monitor the impact of the pandemic and generate evidence of clinical and policy relevance using multiple EHR sources. Funding: British Heart Foundation Data Science Centre, led by Health Data Research UK.
UR - http://www.scopus.com/inward/record.url?scp=85133102873&partnerID=8YFLogxK
U2 - 10.1016/S2589-7500(22)00091-7
DO - 10.1016/S2589-7500(22)00091-7
M3 - Article
C2 - 35690576
AN - SCOPUS:85133102873
SN - 2589-7500
VL - 4
SP - e542-e557
JO - The Lancet Digital Health
JF - The Lancet Digital Health
IS - 7
ER -