4.6 Article

IVIg-exposure and thromboembolic event risk: findings from the UK Biobank

Journal

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
Volume 93, Issue 8, Pages 876-885

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/jnnp-2022-328881

Keywords

CARDIOLOGY; IMMUNOLOGY; NEUROPATHY; PHARMACOLOGY

Funding

  1. Bethlehem Griffiths Research Foundation [BGRF1810-1]
  2. Australian Government Research Training Program (RTP) Scholarship
  3. National Institute for Health Research University College London Hospitals Biomedical Research
  4. National Health and Medical Research Council (NHMRC) Early Career Fellowship [APP1161499]

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This study aimed to calculate the risk of arterial and venous thromboembolic events (TEEs) associated with exposure to intravenous immunoglobulin (IVIG). The study found that IVIG exposure was independently associated with increased risk of TEEs in individuals with prior history of an event. However, IVIG exposure did not increase the risk of TEEs in individuals with no previous history.
Background Arterial and venous thromboembolic events (TEEs) have been associated with intravenous Ig use, but the risk has been poorly quantified. We aimed to calculate the risk of TEEs associated with exposure to intravenous Ig. Methods We included participants from UK Biobank recruited over 3 years, data extracted September 2020. The study endpoints were incidence of myocardial infarction, other acute ischaemic heart disease, stroke, pulmonary embolism and other venous embolism and thrombosis. Predictors included known TEE risk factors: age, sex, hypertension, smoking status, type 2 diabetes mellitus, hypercholesterolaemia, cancer and past history of TEE. Intravenous Ig and six other predictors were added in the sensitivity analysis. Information from participants was collected prospectively, while data from linked resources, including death, cancer, hospital admissions and primary care records were collected retrospectively and prospectively. Findings 14 794 of 502 492 individuals had an incident TEE during the study period. The rate of incident events was threefold higher in those with prior history of TEE (8 .7%) than those without previous history of TEE (3.0%). In the prior TEE category, intravenous Ig exposure was independently associated with increased risk of incident TEE (OR=3.69 (95% CI 1.15 to 11.92), p=0.03) on multivariate analysis. The number needed to harm by exposure to intravenous Ig in those with a history of TEE was 5.8 (95% CI 2.3 to 88.3). Intravenous Ig exposure did not increase risk of TEE in those with no previous history of TEE. Interpretation Intravenous Ig is associated with increased risk of further TEE in individuals with prior history of an event with one further TEE for every six people exposed. In practice, this will influence how clinicians consent for and manage overall TEE risk on intravenous Ig exposure.

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