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dc.contributor.authorSimpson, Colin R.
dc.contributor.authorKerr, Steven
dc.contributor.authorKatikireddi, Srinivasa Vittal
dc.contributor.authorMcCowan, Colin
dc.contributor.authorRitchie, Lewis D.
dc.contributor.authorPan, Jiafeng
dc.contributor.authorStock, Sarah J.
dc.contributor.authorRudan, Igor
dc.contributor.authorTsang, Ruby S. M.
dc.contributor.authorde Lusignan, Simon
dc.contributor.authorHobbs, F. D. Richard
dc.contributor.authorAkbari, Ashley
dc.contributor.authorLyons, Ronan A.
dc.contributor.authorRobertson, Chris
dc.contributor.authorSheikh, Aziz
dc.date.accessioned2022-08-16T14:30:02Z
dc.date.available2022-08-16T14:30:02Z
dc.date.issued2022-08-15
dc.identifier280730399
dc.identifierd89e350a-3c0c-426d-8155-bc034ee860f9
dc.identifier85135990893
dc.identifier000840984400015
dc.identifier.citationSimpson , C R , Kerr , S , Katikireddi , S V , McCowan , C , Ritchie , L D , Pan , J , Stock , S J , Rudan , I , Tsang , R S M , de Lusignan , S , Hobbs , F D R , Akbari , A , Lyons , R A , Robertson , C & Sheikh , A 2022 , ' Second-dose ChAdOx1 and BNT162b2 COVID-19 vaccines and thrombocytopenic, thromboembolic and hemorrhagic events in Scotland ' , Nature Communications , vol. 13 , 4800 . https://doi.org/10.1038/s41467-022-32264-6en
dc.identifier.issn2041-1723
dc.identifier.otherRIS: urn:391EFD9B032B41CD1066DD204A6CB771
dc.identifier.otherRIS: urn:391EFD9B032B41CD1066DD204A6CB771
dc.identifier.otherRIS: Simpson2022
dc.identifier.otherORCID: /0000-0002-9466-833X/work/117567679
dc.identifier.urihttps://hdl.handle.net/10023/25855
dc.descriptionEAVE II is funded by the Medical Research Council (MR/R008345/1) with the support of BREATHE - The Health Data Research Hub for Respiratory Health [MC_PC_19004], which is funded through the UK Research and Innovation Industrial Strategy Challenge Fund and delivered through Health Data Research UK. This research is part of the Data and Connectivity National Core Study, led by Health Data Research UK in partnership with the Office for National Statistics and funded by UK Research and Innovation (grant ref MC_PC_20058). Additional support has been provided through Public Health Scotland and Scottish Government DG Health and Social Care. FDRH acknowledges part support as Director of the NIHR Applied Research Collaboration (ARC) Oxford Thames Valley, and Theme Lead of the NIHR OUH BRC.en
dc.description.abstractWe investigated thrombocytopenic, thromboembolic and hemorrhagic events following a second dose of ChAdOx1 and BNT162b2 using a self-controlled case series analysis. We used a national prospective cohort with 2.0 million(m) adults vaccinated with two doses of ChAdOx or 1.6 m with BNT162b2. The incidence rate ratio (IRR) for idiopathic thrombocytopenic purpura (ITP) 14–20 days post-ChAdOx1 second dose was 2.14, 95% confidence interval (CI) 0.90–5.08. The incidence of ITP post-second dose ChAdOx1 was 0.59 (0.37–0.89) per 100,000 doses. No evidence of an increased risk of CVST was found for the 0–27 day risk period (IRR 0.83, 95% CI 0.16 to 4.26). However, few (≤5) events arose within this risk period. It is perhaps noteworthy that these events all clustered in the 7–13 day period (IRR 4.06, 95% CI 0.94 to 17.51). No other associations were found for second dose ChAdOx1, or any association for second dose BNT162b2 vaccination. Second dose ChAdOx1 vaccination was associated with increased borderline risks of ITP and CVST events. However, these events were rare thus providing reassurance about the safety of these vaccines. Further analyses including more cases are required to determine more precisely the risk profile for ITP and CVST after a second dose of ChAdOx1 vaccine.
dc.format.extent7
dc.format.extent771891
dc.language.isoeng
dc.relation.ispartofNature Communicationsen
dc.subjectRA0421 Public health. Hygiene. Preventive Medicineen
dc.subjectQR180 Immunologyen
dc.subject3rd-DASen
dc.subjectSDG 3 - Good Health and Well-beingen
dc.subjectMCCen
dc.subject.lccRA0421en
dc.subject.lccQR180en
dc.titleSecond-dose ChAdOx1 and BNT162b2 COVID-19 vaccines and thrombocytopenic, thromboembolic and hemorrhagic events in Scotlanden
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.contributor.institutionUniversity of St Andrews. Sir James Mackenzie Institute for Early Diagnosisen
dc.contributor.institutionUniversity of St Andrews. Population and Behavioural Science Divisionen
dc.identifier.doi10.1038/s41467-022-32264-6
dc.description.statusPeer revieweden


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