• Aran Singanayagam, Saranya Sridhar, Jaideep Dhariwal, Dalia Abdel-Aziz, Kerry Munro, David W Connell, Peter M George, Philip L Molyneaux, Graham S Cooke, Andrew K Burroughs, Ajit Lalvani, Melissa Wickremas... more inghe, and Onn Min Kon. less
• Department of Respiratory Medicine, St. Mary's Hospital, Imperial College Healthcare NHS Trust, London, UK.
• Am. J. Respir. Crit. Care Med.. 2012 Mar 15;185(6):653-9.

RationaleThe optimum strategy for monitoring liver function during antituberculous therapy is unclear.ObjectivesTo assess the value of the American Thoracic Society risk-factor approach for predicting drug-induced liver injury and to compare with a uniform policy of liver function testing in all patients at 2 weeks.MethodsWe conducted an observational study of adult patients undergoing therapy for active tuberculosis at a tertiary center. All patients had alanine transferase measurement at baseline and 2 weeks following commencement of therapy. Sensitivity, specificity, and positive and negative predictive values were used to assess strategies.Measurements And Main ResultsThere were 288 patients included, and 21 (7.3%) developed drug-induced liver injury (57.1% "early" at 2 wk and 42.9% "late," after 2 wk). There were increased rates of individuals with HIV infection in the early drug-induced liver injury group compared with no drug-induced liver injury and late drug-induced liver injury groups (33% vs. 7.1% vs. 0%; P = 0.004). The American Thoracic Society algorithm had a sensitivity and specificity of 66.7 and 65.6%, respectively, for prediction of early and 22.2% and 63.7% for late drug-induced liver injury. The uniform monitoring policy had poor sensitivity but better specificity (22.2 and 82.1%) for prediction of late drug-induced liver injury.ConclusionsIn our urban, ethnically diverse population, a risk-factor approach is neither sensitive nor specific for prediction of drug-induced liver injury. A uniform policy of liver function testing at 2 weeks is useful for prompt identification of a subgroup who develop early drug-induced liver injury and may offer better specificity in ruling out late drug-induced liver injury.

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