BackgroundThe diagnosis of latent tuberculosis infection (LTBI) in liver transplantation candidates (LTC) is not well defined. Objective To evaluate the usefulness of the QuantiFERON-TB Gold In-Tube (QFT-GIT) compared with the tuberculin skin test (TST) for the diagnosis of LTBI and its risk factors in LTC.
Patients and methodsPatients were assessed for LTBI by TST using a purified protein derivative (PPD) or with QFT-GIT. LTBI was defined as either a positive TST or a positive QFT-GIT test.
ResultsOf the 97 patients who underwent TST, 19 (19.59%) had a positive result. With the QFT-GIT test, 25 patients (25.77%) had a positive result and seven (7.22%) had an indeterminate result. The clinical risk factors for TB infection were identified in only two of the 19 TST-positive patients (10.5%) but were detected in six (24%) of QFT-GITpositive patients and none of the QFT-GIT-indeterminate patients. The QFT-GIT test showed a sensitivity of 89%, a specificity of 89%, an accuracy of 89%, positive and negative predictive values of 68 and 97%, respectively. Out of the 10 patients with discordant results between both the tests, two patients had a positive TST but negative QFT-GIT, and no clinical risk factors for LTBI were found. Eight patients had a negative TST but positive QFT-GIT; of these, the clinical risk factors for LTBI were observed in two patients (25%).
ConclusionThis study showed that the QFT-GIT test might be more useful for the diagnosis of LTBI than TST among LTC on the basis of the frequency of clinical risk factors.
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