Systematic review: ibuprofen-induced liver injury.
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Abstract
Background: Nonsteroidal anti-inflammatory drugs (NSAIDs) are a leading cause of
drug-induced liver injury (DILI) across the world. Ibuprofen is one of the most commonly
used and safest NSAIDs, nevertheless reports on ibuprofen-induced hepatotoxicity are
available.
Aim: To analyse previously published information on ibuprofen-induced liver injury for
a better characterisation of its phenotypic expression.
Method: A systematic search was performed and information on ibuprofen-induced liver
injury included in case series and case reports, in terms of demographic, clinical,
biochemical and outcome data, was analysed.
Results: Twenty-two idiosyncratic ibuprofen hepatotoxicity cases were identified in the
literature, suggesting a very low prevalence of this type of DILI. These patients had a
mean age of 31 years and 55% were females. Mean cumulative dose of ibuprofen and
time to onset were 30 g and 12 days, respectively. Hepatocellular injury was the most
frequently involved liver injury pattern. Six cases developed vanishing bile duct
syndrome. Full recovery occurred in 11 patients after a mean time of 14 weeks, whereas
five cases evolved to acute liver failure leading to death/liver transplantation.
Conclusions: When assessing potential hepatotoxicity cases, physicians should keep in
mind that ibuprofen has been associated with hepatotoxicity in the literature. Ibuprofenassociated DILI presents commonly as hepatocellular damage after a short latency period.
Published reports on ibuprofen hepatotoxicity leading to liver failure resulting in liver
transplantation or death are available. However, due to the apparent low absolute risk of
ibuprofen-induced liver complications, ibuprofen can be regarded as an efficacious and
safe NSAID.
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https://openpolicyfinder.jisc.ac.uk/id/publication/81
Bibliographic citation
Miguel E Zoubek, María Isabel Lucena, Raúl J Andrade, Camilla Stephens. Systematic review: ibuprofen-induced liver injury. Aliment Pharmacol Ther 2020 Mar;51(6):603-611
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