{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,22]],"date-time":"2026-09-22T11:15:23Z","timestamp":1790075723283,"version":"4.0.1"},"reference-count":31,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2016,3,9]],"date-time":"2016-03-09T00:00:00Z","timestamp":1457481600000},"content-version":"vor","delay-in-days":8,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Internal Medicine Journal"],"published-print":{"date-parts":[[2016,3]]},"abstract":"<jats:sec><jats:title>Background<\/jats:title><jats:p>One of the cornerstones of Australia's public health programmes to eliminate tuberculosis (TB) is the identification and treatment of latent tuberculosis infection (LTBI).<\/jats:p><\/jats:sec><jats:sec><jats:title>Aims<\/jats:title><jats:p>The main aim of this study is to determine the demographics, compliance, completion rates and adverse events of patients on preventive therapy (<jats:styled-content style=\"fixed-case\">PT<\/jats:styled-content>) for <jats:styled-content style=\"fixed-case\">LTBI<\/jats:styled-content> at our institution. The secondary aim is to determine the rates of isoniazid (<jats:styled-content style=\"fixed-case\">INH<\/jats:styled-content>) hepatotoxicity and identify any contributory factors.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>The method used was an audit using medical records of 100 consecutive patients (2010\u20132014) treated with <jats:styled-content style=\"fixed-case\">PT<\/jats:styled-content> for <jats:styled-content style=\"fixed-case\">LTBI<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Seventy\u2010two patients with confirmed <jats:styled-content style=\"fixed-case\">LTBI<\/jats:styled-content> started 9 months of <jats:styled-content style=\"fixed-case\">INH<\/jats:styled-content> and 22 started 4 months of rifampicin (<jats:styled-content style=\"fixed-case\">RIF<\/jats:styled-content>). The median age was 30 years. Half the patients were born in high TB\u2010prevalence countries. Fifty\u2010six per cent were contacts of index cases with confirmed TB, and 26% were pre\u2010immunosuppression. Seventy\u2010seven per cent completed <jats:styled-content style=\"fixed-case\">PT<\/jats:styled-content> with adequate compliance. Thirty\u2010three per cent on <jats:styled-content style=\"fixed-case\">INH<\/jats:styled-content> and 23% on <jats:styled-content style=\"fixed-case\">RIF<\/jats:styled-content> experienced some liver function test (<jats:styled-content style=\"fixed-case\">LFT<\/jats:styled-content>) abnormality while on treatment. <jats:styled-content style=\"fixed-case\">INH<\/jats:styled-content> was ceased in 3% due to asymptomatic hepatic dysfunction (transaminases &gt;5x upper limit of normal). No patients had permanent liver damage. Significant risk factors for liver dysfunction during <jats:styled-content style=\"fixed-case\">PT<\/jats:styled-content> were risk factors for liver disease (<jats:inline-graphic xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"graphic\/imj12979-math-0001.png\" xlink:title=\"urn:x-wiley:14440903:media:imj12979:imj12979-math-0001\"\/> = 8.7; <jats:italic>P<\/jats:italic> = 0.03) or abnormal pre\u2010therapy <jats:styled-content style=\"fixed-case\">LFT<\/jats:styled-content> (<jats:inline-graphic xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"graphic\/imj12979-math-0002.png\" xlink:title=\"urn:x-wiley:14440903:media:imj12979:imj12979-math-0002\"\/> = 22.4; <jats:italic>P<\/jats:italic> &lt; 0.001). No patients developed active <jats:styled-content style=\"fixed-case\">TB<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>The completion rate of 77% and rate of <jats:styled-content style=\"fixed-case\">INH<\/jats:styled-content>\u2010induced hepatic dysfunction of 3% is comparable with the literature. We found no age association with the risk of <jats:styled-content style=\"fixed-case\">INH<\/jats:styled-content>\u2010induced hepatic dysfunction; however, there was a significant and linear association with the degree of liver function abnormality during <jats:styled-content style=\"fixed-case\">INH<\/jats:styled-content> therapy and the presence of abnormal baseline LFT. Routine <jats:styled-content style=\"fixed-case\">LFT<\/jats:styled-content> monitoring allowed early cessation of <jats:styled-content style=\"fixed-case\">INH<\/jats:styled-content> in those with significant but asymptomatic hepatitis who did not meet criteria for <jats:styled-content style=\"fixed-case\">ATS<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">CDC LFT<\/jats:styled-content> monitoring.<\/jats:p><\/jats:sec>","DOI":"10.1111\/imj.12979","type":"journal-article","created":{"date-parts":[[2015,12,9]],"date-time":"2015-12-09T16:46:05Z","timestamp":1449679565000},"page":"281-287","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":23,"title":["Baseline abnormal liver function tests are more important than age in the development of isoniazid\u2010induced hepatoxicity for patients receiving preventive therapy for latent tuberculosis infection"],"prefix":"10.1111","volume":"46","author":[{"given":"E. L.","family":"Gray","sequence":"first","affiliation":[{"name":"Department of Respiratory Medicine Prince of Wales Hospital  Sydney New South Wales Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H. 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