4.7 Article

Quantification of the risk of liver injury associated with flucloxacillin: a UK population-based cohort study

Journal

JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
Volume 72, Issue 9, Pages 2636-2646

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jac/dkx183

Keywords

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Funding

  1. Innovative Medicine Initiative Joint Undertaking [115004]
  2. European Union
  3. European Federation of Pharmaceutical Industries and Associations (EFPIA)
  4. PROTECT
  5. Wellcome Trust
  6. Royal Society
  7. National Institute of Health Research Collaboration for Leadership in Applied Health Research and Care [BZR00180/P2-503/BZ35.17]
  8. Wellcome Trust Senior Clinical Fellowship [WT 098504/Z/12/Z]
  9. MRC Population Health Scientist Fellowship [MR/M014649/1]
  10. GlaxoSmithKline
  11. MRC [G0802403, MR/M014649/1] Funding Source: UKRI
  12. Medical Research Council [G0802403] Funding Source: researchfish

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Background: Flucloxacillin is an established cause of liver injury. Despite this, there are a lack of published data on both the strength of association after adjusting for potential confounders, and the absolute incidence among different subgroups of patients. Objectives: To assess the relative and absolute risks of liver injury following exposure to flucloxacillin and identify subgroups at potentially increased risk. Methods: A cohort study between 1 January 2000 and 1 January 2012 using the UK Clinical Practice Research Datalink, including 1046699 people with a first prescription for flucloxacillin (861962) or oxytetracycline (184737). Absolute risks of experiencing both symptom-defined (jaundice) and laboratory-confirmed liver injury within 1-45 and 46-90 days of antibiotic initiation were estimated. Multivariable logistic regression was used to estimate 1-45 day relative effects. Results: There were 183 symptom-defined cases (160 prescribed flucloxacillin) and 108 laboratory-confirmed cases (102 flucloxacillin). The 1-45 day adjusted risk ratio for laboratory-confirmed injury was 5.22 (95% CI 1.64-16.62) comparing flucloxacillin with oxytetracycline use. The 1-45 day risk of laboratoryconfirmed liver injury was 8.47 per 100000 people prescribed flucloxacillin (95% CI 6.64-10.65). People who received consecutive flucloxacillin prescriptions had a 1-45 day risk of jaundice of 39.00 per 100000 (95% CI 26.85-54.77), while those aged >70 receiving consecutive prescriptions had a risk of 110.57 per 100000 (95% CI 70.86-164.48). Conclusions: The short-term risk of laboratory-confirmed liver injury was.5-fold higher after a flucloxacillin prescription than an oxytetracycline prescription. The risk of flucloxacillin-induced liver injury is particularly high within those aged.70 and those who receive multiple flucloxacillin prescriptions. The stratified risk estimates from this study could help guide clinical care.

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