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Safety and outcome of treatment of latent tuberculosis infection in liver transplant recipients

Authors
Lee, Yun WooChung, HyeminKim, Sung-HanSung, HeungsupHa, Su-MinJwa, Eun-KyoungJung, Dong-HwanMoon, Deok-BogLee, Sung-GyuLee, Sang-Oh
Issue Date
Jun-2024
Publisher
SPRINGER HEIDELBERG
Keywords
Tuberculosis; Latent tuberculosis infection; Liver transplantation; Interferon-gamma-releasing assay; Isoniazid
Citation
INFECTION, v.52, no.3, pp 1055 - 1061
Pages
7
Journal Title
INFECTION
Volume
52
Number
3
Start Page
1055
End Page
1061
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/73530
DOI
10.1007/s15010-023-02161-1
ISSN
0300-8126
1439-0973
Abstract
Purpose Liver transplant (LT) recipients have an increased risk of tuberculosis (TB), which is associated with higher mortality rates. This retrospective cohort study assessed the outcome and tolerability of screening and treatment of latent tuberculosis infection (LTBI) in LT recipients. Methods Between March 2020 and February 2022, all adult LT candidates at our institution were screened for LTBI. The candidates who tested positive for interferon-gamma-releasing assay or met epidemiological or clinical-radiological criteria for LTBI were treated and monitored. Results Among the 857 LT recipients, 199 (23.2%) were diagnosed with LTBI, of which 171 (85.9%) initiated LTBI treatment. The median duration of follow-up was 677 days. Adequate LTBI treatment occurred in 141/171 (82.5%) patients and was discontinued prematurely in 30/171 (17.5%) patients. The most common reason for discontinuation was liver enzyme elevation (11/30, 36.7%), although only five discontinued treatment due to suspicion of isoniazid-associated hepatotoxicity. None of the LTBI-treated patients developed active TB during the follow-up period, while 3.6% (1/28) of untreated LTBI patients and 0.6% (4/658) of patients without LTBI developed TB. Conclusion These findings demonstrate that LTBI screening and treatment is a safe and effective strategy to prevent TB in LT recipients. However, monitoring for adverse events and liver enzyme elevation is recommended.
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의과대학 (의학부(임상-광명))
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