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Adverse events and development of tuberculosis after 4 months of rifampicin prophylaxis in a tuberculosis outbreak

Authors
Lee S.H.Yim J.-J.Kim H.J.Shim T.S.Seo H.S.Cho Y.S.Lee H.-K.Lee Y.M.Lee E.J.Lew W.J.
Issue Date
2012
Keywords
Antibiotic prophylaxis; drug toxicity; multidrug-resistant tuberculosis; rifampicin; tuberculosis
Citation
Epidemiology and Infection, v.140, no.6, pp 1028 - 1035
Pages
8
Indexed
SCI
SCIE
SCOPUS
Journal Title
Epidemiology and Infection
Volume
140
Number
6
Start Page
1028
End Page
1035
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/12779
DOI
10.1017/S0950268811001476
ISSN
0950-2688
1469-4409
Abstract
We screened tuberculosis (TB) contacts as an outbreak investigation with tuberculin skin test (TST) and interferon-gamma release assay (IGRA). We evaluated adverse events and TB incidence in all persons screened after rifampicin (RFP) prophylaxis, and specifically assessed the new TB cases in relation to initial TST and IGRA results. The 180 contacts were divided into four groups: TST+/IGRA+ (n=101), TST+/IGRA- (n=22), TST-/IGRA+ (n=16), and TST-/IGRA- (n=41). RFP treatment (4 months) was prescribed only to the TST+/IGRA+ group. Of 87 contacts who initiated prophylaxis, adverse events occurred in 21 contacts (24·1%) including hepatotoxicity (11·5%), flu-like syndrome (5·7%), and thrombocytopenia (3·4%). TB developed in two TST+/IGRA+ subjects after completion of prophylaxis, including one multidrug-resistant (MDR)-TB case during 21·8 months of follow-up. Adverse events were frequent, and development of TB including MDR-TB occurred after RFP prophylaxis. © 2011 Cambridge University Press.
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Lee, Seung Heon
Ansan Hospital (Department of Pulmonary, Allergy, and Critical Care Medicine, Ansan Hospital)
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