Background & objectives: Tuberculosis (TB) is a common infection in patients on haemodialysis. There is a definite role of treatment of latent TB (LTB) in these patients. However, diagnosis of LTB in these patients by tuberculin skin test (TST) is unreliable. There is suggestion that interferon gamma release assay (IGRA) will be more reliable test for diagnosis of LTB in this setting. Thus, we evaluated value of IGRA and TST for the diagnosis of LTB in patients on dialysis in an Indian setting. Methods: Patients with end stage kidney disease on dialysis were included. Patients with active TB were excluded. Each patient was subjected to TST (induration of >= 10 mm was taken as positive) and QuantiFERON TB Gold In-Tube test (QFT-GIT) for diagnosis of LTB. Results: A total of 185 patients were included; 129 (69.7%) were males and mean age was 36.7 +/- 12.3 yr. Past history of TB was present in 18 (9.7%) patients. One hundred and thirty four (72.4%) patients had scar of BCG vaccination. QFT-GIT test was positive in 66 (36%), TST in 32 (17%) and both in 13 (7%) patients. Of the 66 patients positive with QFT-GIT, only 13 (19.6%) were positive for TST. Of the 32 patients positive with TST, only 13 (40.6%) were positive with QFT-GIT; 100 (54%) patients were negative for both the tests. Overall, 85 (45.9%) patients were positive for either of the two tests. Poor agreement was shown between the two methods. On logistic regression analysis, odds of QFT-GIT to be positive in patients with BCG vaccination was 1.23 and with history of TB 0.99, both being insignificant. odds of tuberculin skin test to be positive in patients with BCG vaccination was 1.04 and with history of TB 0.99, both again being insignificant. Interpretation & conclusions: Our findings showed that more number of patients (36%) on haemodialysis were positive for QuantiFERON Gold In-Tube test as compared to TST (17%). There was poor agreement between the two tests. no significant effect of BCG vaccination and history of TB in past was observed on both tests.
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Univ Paris 05, Hop Necker Enfants Malades, AP HP,Inst Imagine,Sorbonne Paris Cite, Serv Malad Infect & Trop,Ctr Infectiol Necker Pas, F-75006 Paris, FranceUniv Paris 05, Hop Necker Enfants Malades, AP HP,Inst Imagine,Sorbonne Paris Cite, Serv Malad Infect & Trop,Ctr Infectiol Necker Pas, F-75006 Paris, France
Henry, B.
Bourgarit, A.
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Univ Paris 13, Hop Jean Verdier, AP HP, HUPSSD,SmBH,Serv Med Interne, F-93140 Bondy, France
INSERM, UMR CRI 1149, F-75013 Paris, FranceUniv Paris 05, Hop Necker Enfants Malades, AP HP,Inst Imagine,Sorbonne Paris Cite, Serv Malad Infect & Trop,Ctr Infectiol Necker Pas, F-75006 Paris, France
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Gachon Univ Med & Sci, Dept Internal Med, Inchon 405760, South Korea
Seoul Natl Univ, Coll Med, Transplantat Res Inst, Seoul, South KoreaGachon Univ Med & Sci, Dept Internal Med, Inchon 405760, South Korea
Chung, W. K.
Zheng, Z. L.
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Gachon Univ Med & Sci, Dept Internal Med, Inchon 405760, South KoreaGachon Univ Med & Sci, Dept Internal Med, Inchon 405760, South Korea
Zheng, Z. L.
Sung, J. Y.
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Gachon Univ Med & Sci, Dept Internal Med, Inchon 405760, South KoreaGachon Univ Med & Sci, Dept Internal Med, Inchon 405760, South Korea
Sung, J. Y.
Kim, S.
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Gachon Univ Med & Sci, Dept Internal Med, Inchon 405760, South KoreaGachon Univ Med & Sci, Dept Internal Med, Inchon 405760, South Korea
Kim, S.
Lee, H. H.
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Gachon Univ Med & Sci, Dept Internal Med, Inchon 405760, South KoreaGachon Univ Med & Sci, Dept Internal Med, Inchon 405760, South Korea
Lee, H. H.
Choi, S. J.
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Gachon Univ Med & Sci, Dept Radiol, Inchon 405760, South KoreaGachon Univ Med & Sci, Dept Internal Med, Inchon 405760, South Korea
Choi, S. J.
Yang, J.
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Gachon Univ Med & Sci, Dept Internal Med, Inchon 405760, South Korea
Seoul Natl Univ, Coll Med, Transplantat Res Inst, Seoul, South Korea
Canc Res Inst, Seoul, South KoreaGachon Univ Med & Sci, Dept Internal Med, Inchon 405760, South Korea