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Association of COVID-19 With Major Arterial and Venous Thrombotic Diseases: A Population-Wide Cohort Study of 48 Million Adults in England and Wales.
Knight, Rochelle; Walker, Venexia; Ip, Samantha; Cooper, Jennifer A; Bolton, Thomas; Keene, Spencer; Denholm, Rachel; Akbari, Ashley; Abbasizanjani, Hoda; Torabi, Fatemeh; Omigie, Efosa; Hollings, Sam; North, Teri-Louise; Toms, Renin; Jiang, Xiyun; Angelantonio, Emanuele Di; Denaxas, Spiros; Thygesen, Johan H; Tomlinson, Christopher; Bray, Ben; Smith, Craig J; Barber, Mark; Khunti, Kamlesh; Davey Smith, George; Chaturvedi, Nishi; Sudlow, Cathie; Whiteley, William N; Wood, Angela M; Sterne, Jonathan A C.
  • Knight R; Department of Population Health Sciences, Bristol Medical School, University of Bristol, UK (R.K., V.W., J.A.C., R.D., T.-L.N., R.T., G.D.S., J.A.C.S.).
  • Walker V; NIHR Bristol Biomedical Research Centre, UK (R.K., J.A.C., R.D., J.A.C.S.).
  • Ip S; NIHR Applied Research Collaboration West, Bristol, UK (R.K.).
  • Cooper JA; MRC Integrative Epidemiology Unit, Bristol, UK (R.K., V.W., G.D.S.).
  • Bolton T; Department of Population Health Sciences, Bristol Medical School, University of Bristol, UK (R.K., V.W., J.A.C., R.D., T.-L.N., R.T., G.D.S., J.A.C.S.).
  • Keene S; MRC Integrative Epidemiology Unit, Bristol, UK (R.K., V.W., G.D.S.).
  • Denholm R; British Heart Foundation Cardiovascular Epidemiology Unit (S.I., T.B., S.K., X.J., E.D.A., A.M.W.), University of Cambridge, UK.
  • Akbari A; Centre for Cancer Genetic Epidemiology (S.I.), University of Cambridge, UK.
  • Abbasizanjani H; Department of Population Health Sciences, Bristol Medical School, University of Bristol, UK (R.K., V.W., J.A.C., R.D., T.-L.N., R.T., G.D.S., J.A.C.S.).
  • Torabi F; NIHR Bristol Biomedical Research Centre, UK (R.K., J.A.C., R.D., J.A.C.S.).
  • Omigie E; British Heart Foundation Cardiovascular Epidemiology Unit (S.I., T.B., S.K., X.J., E.D.A., A.M.W.), University of Cambridge, UK.
  • Hollings S; Department of Public Health and Primary Care, NIHR Blood and Transplant Research Unit in Donor Health and Genomics (T.B., S.K., E.D.A., A.M.W.), University of Cambridge, UK.
  • North TL; British Heart Foundation Data Science Centre (T.B., C.S.), London.
  • Toms R; British Heart Foundation Cardiovascular Epidemiology Unit (S.I., T.B., S.K., X.J., E.D.A., A.M.W.), University of Cambridge, UK.
  • Jiang X; Department of Public Health and Primary Care, NIHR Blood and Transplant Research Unit in Donor Health and Genomics (T.B., S.K., E.D.A., A.M.W.), University of Cambridge, UK.
  • Angelantonio ED; Department of Population Health Sciences, Bristol Medical School, University of Bristol, UK (R.K., V.W., J.A.C., R.D., T.-L.N., R.T., G.D.S., J.A.C.S.).
  • Denaxas S; NIHR Bristol Biomedical Research Centre, UK (R.K., J.A.C., R.D., J.A.C.S.).
  • Thygesen JH; Health Data Research UK South-West, Bristol (R.D., J.A.C.S.).
  • Tomlinson C; Population Data Science, Swansea University Medical School, Swansea University, Wales, UK (A.A., H.A., F.T.).
  • Bray B; Population Data Science, Swansea University Medical School, Swansea University, Wales, UK (A.A., H.A., F.T.).
  • Smith CJ; Population Data Science, Swansea University Medical School, Swansea University, Wales, UK (A.A., H.A., F.T.).
  • Barber M; National Health Service Digital, Leeds, UK (E.O., S.H.).
  • Khunti K; National Health Service Digital, Leeds, UK (E.O., S.H.).
  • Davey Smith G; Department of Population Health Sciences, Bristol Medical School, University of Bristol, UK (R.K., V.W., J.A.C., R.D., T.-L.N., R.T., G.D.S., J.A.C.S.).
  • Chaturvedi N; Department of Population Health Sciences, Bristol Medical School, University of Bristol, UK (R.K., V.W., J.A.C., R.D., T.-L.N., R.T., G.D.S., J.A.C.S.).
  • Sudlow C; School of Health Sciences, Cardiff Metropolitan University, UK (R.T.).
  • Whiteley WN; British Heart Foundation Cardiovascular Epidemiology Unit (S.I., T.B., S.K., X.J., E.D.A., A.M.W.), University of Cambridge, UK.
  • Wood AM; British Heart Foundation Cardiovascular Epidemiology Unit (S.I., T.B., S.K., X.J., E.D.A., A.M.W.), University of Cambridge, UK.
  • Sterne JAC; Department of Public Health and Primary Care, NIHR Blood and Transplant Research Unit in Donor Health and Genomics (T.B., S.K., E.D.A., A.M.W.), University of Cambridge, UK.
Circulation ; 146(12): 892-906, 2022 Sep 20.
Статья в английский | MEDLINE | ID: covidwho-2089002
ABSTRACT

BACKGROUND:

Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) induces a prothrombotic state, but long-term effects of COVID-19 on incidence of vascular diseases are unclear.

METHODS:

We studied vascular diseases after COVID-19 diagnosis in population-wide anonymized linked English and Welsh electronic health records from January 1 to December 7, 2020. We estimated adjusted hazard ratios comparing the incidence of arterial thromboses and venous thromboembolic events (VTEs) after diagnosis of COVID-19 with the incidence in people without a COVID-19 diagnosis. We conducted subgroup analyses by COVID-19 severity, demographic characteristics, and previous history.

RESULTS:

Among 48 million adults, 125 985 were hospitalized and 1 319 789 were not hospitalized within 28 days of COVID-19 diagnosis. In England, there were 260 279 first arterial thromboses and 59 421 first VTEs during 41.6 million person-years of follow-up. Adjusted hazard ratios for first arterial thrombosis after COVID-19 diagnosis compared with no COVID-19 diagnosis declined from 21.7 (95% CI, 21.0-22.4) in week 1 after COVID-19 diagnosis to 1.34 (95% CI, 1.21-1.48) during weeks 27 to 49. Adjusted hazard ratios for first VTE after COVID-19 diagnosis declined from 33.2 (95% CI, 31.3-35.2) in week 1 to 1.80 (95% CI, 1.50-2.17) during weeks 27 to 49. Adjusted hazard ratios were higher, for longer after diagnosis, after hospitalized versus nonhospitalized COVID-19, among Black or Asian versus White people, and among people without versus with a previous event. The estimated whole-population increases in risk of arterial thromboses and VTEs 49 weeks after COVID-19 diagnosis were 0.5% and 0.25%, respectively, corresponding to 7200 and 3500 additional events, respectively, after 1.4 million COVID-19 diagnoses.

CONCLUSIONS:

High relative incidence of vascular events soon after COVID-19 diagnosis declines more rapidly for arterial thromboses than VTEs. However, incidence remains elevated up to 49 weeks after COVID-19 diagnosis. These results support policies to prevent severe COVID-19 by means of COVID-19 vaccines, early review after discharge, risk factor control, and use of secondary preventive agents in high-risk patients.
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Полный текст: Имеется в наличии Коллекция: Международные базы данных база данных: MEDLINE Основная тема: Thrombosis / Vascular Diseases / Venous Thrombosis / Venous Thromboembolism / COVID-19 Тип исследования: Когортное исследование / Наблюдательное исследование / Прогностическое исследование Темы: Длинный Ковид / Вакцина Пределы темы: Взрослые / Люди Страна как тема: Европа Язык: английский Журнал: Circulation Год: 2022 Тип: Статья

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Полный текст: Имеется в наличии Коллекция: Международные базы данных база данных: MEDLINE Основная тема: Thrombosis / Vascular Diseases / Venous Thrombosis / Venous Thromboembolism / COVID-19 Тип исследования: Когортное исследование / Наблюдательное исследование / Прогностическое исследование Темы: Длинный Ковид / Вакцина Пределы темы: Взрослые / Люди Страна как тема: Европа Язык: английский Журнал: Circulation Год: 2022 Тип: Статья