Metadata

Name CCU002_02 Thrombophilia
Type Disease or Syndrome
Group Disease or Syndrome
Data Sources




Clinical Terminologies SNOMED-CT
ICD-10
Codelists covid_impact_ccu00202_thrombophilia_England_SNOMEDCT.csv covid_impact_ccu00202_thrombophilia_England_ICD10.csv
Valid Event Data Range 08/12/2020 - 18/03/2021
Sex Female
Male
Authors CVD-COVID-UK consortium, William N Whiteley, Samantha Ip, Jennifer A Cooper, Thomas Bolton, Spencer Keene, Venexia Walker, Rachel Denholm, Ashley Akbari, Efosa Omigie, Sam Hollings, Emanuele Di Angelantonio, Spiros Denaxas, Angela Wood, Jonathan A C Sterne, Cathie Sudlow
Agreement Date 23 Aug 2021
Version (UUID) Revision 1 (COVID-IMPACT)

Phenotypes

Code type is set to 1 for incident events, and 0 for prevalent events.

England primary care EHR: Thrombophilia diagnosis

terminology code term code_type
SNOMEDCT 441945008 Thrombophilia due to trauma 1.0
SNOMEDCT 442121006 Thrombophilia due to vascular anomaly 1.0
SNOMEDCT 439125003 Thrombophilia due to acquired protein S deficiency 1.0
SNOMEDCT 439698008 Primary thrombophilia 1.0
SNOMEDCT 234467004 Thrombophilia 1.0
SNOMEDCT 439126002 Thrombophilia due to acquired antithrombin III deficiency 1.0
SNOMEDCT 439002002 Thrombophilia due to acquired protein C deficiency 1.0
SNOMEDCT 442197003 Thrombophilia caused by drug therapy 1.0
SNOMEDCT 441697004 Thrombophilia associated with pregnancy 1.0
SNOMEDCT 442760001 Thrombophilia caused by antineoplastic agent therapy 1.0
SNOMEDCT 441882000 History of thrombophilia 1.0
SNOMEDCT 439001009 Acquired thrombophilia 1.0
SNOMEDCT 442078001 Thrombophilia due to malignant neoplasm 1.0
SNOMEDCT 441946009 Thrombophilia due to myeloproliferative disorder 1.0
SNOMEDCT 441079006 Thrombophilia due to antiphospholipid antibody 1.0
SNOMEDCT 441762006 Thrombophilia due to immobilisation 1.0
SNOMEDCT 442654007 Thrombophilia caused by hormone therapy 1.0
SNOMEDCT 442363001 Thrombophilia caused by vascular device 1.0
SNOMEDCT 439698008 Hereditary thrombophilia 1.0
SNOMEDCT 783250007 Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency 1.0
SNOMEDCT 441990004 Thrombophilia due to paroxysmal nocturnal haemoglobinuria 1.0

England hospitalization EHR: Thrombophilia diagnosis

terminology code term code_type
ICD10 D68.5 Primary thrombophilia 1.0
ICD10 D68.6 Other thrombophilia 1.0

Publication

Association of COVID-19 vaccines ChAdOx1 and BNT162b2 with major venous, arterial, and thrombocytopenic events: whole population cohort study in 46 million adults in England

CVD-COVID-UK consortium, William N Whiteley, Samantha Ip, Jennifer A Cooper, Thomas Bolton, Spencer Keene, Venexia Walker, Rachel Denholm, Ashley Akbari, Efosa Omigie, Sam Hollings, Emanuele Di Angelantonio, Spiros Denaxas, Angela Wood, Jonathan A C Sterne, Cathie Sudlow

medRxiv 2021.08.18.21262222; doi: https://doi.org/10.1101/2021.08.18.21262222