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The risk of acute liver injury among users of antibiotic medications: a comparison of case-only studies.
Brauer, Ruth; Ruigómez, Ana; Klungel, Olaf; Reynolds, Robert; Feudjo Tepie, Maurille; Smeeth, Liam; Douglas, Ian.
Affiliation
  • Brauer R; Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Ruigómez A; Fundación Centro Español de Investigación Farmacoepidemiológica, (CEIFE), Madrid, Spain.
  • Klungel O; Faculty of Science, Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht University, Utrecht, The Netherlands.
  • Reynolds R; Epidemiology, Pfizer Research and Development, New York, USA.
  • Feudjo Tepie M; Amgen NV, London, United Kingdom.
  • Smeeth L; Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Douglas I; Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Pharmacoepidemiol Drug Saf ; 25 Suppl 1: 39-46, 2016 Mar.
Article in En | MEDLINE | ID: mdl-26248609
ABSTRACT

PURPOSE:

The aims of this study were two-fold (i) to investigate the effect of exposure to antibiotic agents on the risk of acute liver injury using a self-controlled case series and case-crossover study and (ii) to compare the results between the case-only studies.

METHODS:

For the self-controlled case series study relative incidence ratios (IRR) were calculated by dividing the rate of acute liver injury experienced during patients' periods of exposure to antibiotics to patients' rate of events during non-exposed time using conditional Poisson regression. For the case-crossover analysis we calculated Odds Ratios (OR) using conditional logistic regression by comparing exposure during 14- and 30-day risk windows with exposure during control moments.

RESULTS:

Using the self-controlled case series approach, the IRR was highest during the first 7 days after receipt of a prescription (10.01, 95% CI 6.59-15.18). Omitting post-exposure washout periods lowered the IRR to 7.2. The highest estimate in the case-crossover analysis was found when two 30-day control periods 1 year prior to the 30-day ALI risk period were retained in the

analysis:

OR = 6.5 (95% CI, 3.95-10.71). The lowest estimate was found when exposure in the 14-day risk period was compared to exposure in four consecutive 14-day control periods immediately prior to the risk period (OR = 3.05, 95% CI, 2.06-4.53).

CONCLUSION:

An increased relative risk of acute liver injury was consistently observed using both self-controlled case series and case-crossover designs. Case-only designs can be used as a viable alternative study design to study the risk of acute liver injury, albeit with some limitations.
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Full text: 1 Database: MEDLINE Main subject: Chemical and Drug Induced Liver Injury / Anti-Bacterial Agents Type of study: Clinical_trials / Etiology_studies / Observational_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Year: 2016 Type: Article

Full text: 1 Database: MEDLINE Main subject: Chemical and Drug Induced Liver Injury / Anti-Bacterial Agents Type of study: Clinical_trials / Etiology_studies / Observational_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Year: 2016 Type: Article