Speakers - 2025

Rozita Khodashahi

  • Designation: Transplant Research Center, Clinical Research Institute, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Country: Iran
  • Title: Latent Tuberculosis Management in Liver Transplant Recipients: Insights from a Retrospective Analysis

Biography

My name is Rozita Khodashahi, and I am an infectious disease specialist and associate professor at Mashhad University of Medical Sciences. I also serve as the Research Deputy at the Transplant Hospital and General Imam Reza Hospital, as well as the Head of the Clinical Research and Development Unit at Imam Reza Hospital, Faculty of Medicine, Mashhad University of Medical Sciences. I have published 56 articles in my field. My professional areas of expertise include immunocompromised patients, solid organ transplantation (SOT), bone marrow transplantation (BMT), all types of transplant patients, hematologic malignancies, and cancers.

Abstract

Objective: This retrospective cross-sectional study aimed to investigate latent tuberculosis infection (LTBI) management in liver transplant recipients, assessing the impact of isoniazid prophylaxis and patient outcomes.
Methods: Data from liver transplant recipients (2013-2021) at Montaseriyeh Hospital, Mashhad, were analyzed. Inclusion criteria comprised patients with a positive tuberculin skin test (PPD) or interferon-gamma release assay (IGRA) in either the donor or recipient (n = 30). Demographic, clinical, and laboratory information, including the duration of isoniazid use, liver enzyme levels, and patient outcomes, was collected. Statistical analyses included descriptive statistics, non-parametric tests, and logistic regression.
Results: Thirty liver transplant recipients received isoniazid prophylaxis (up to 9 months). Isoniazid usage duration and liver enzyme level distribution were non-normal. The distribution of isoniazid use duration and liver enzyme levels did not follow a normal distribution. No significant increase was found in liver enzyme levels (serum glutamic oxaloacetic transaminase (SGOT) and serum glutamate pyruvate transaminase (SGPT)) across different intervals. When examining each variable separately, higher SGOT and SGPT levels at the end of the first month after isoniazid consumption were significantly associated with increased mortality risk. The duration of isoniazid use and liver enzyme levels in subsequent months did not exhibit a significant relationship with patient survival.
Conclusions: Managing LTBI in liver transplant recipients presents challenges in isoniazid prophylaxis and predicting outcomes. Elevated SGOT and SGPT levels at the end of the first month after isoniazid consumption were associated with increased mortality risk. Further research is required for optimizing LTBI management in this patient population.
Keywords: Isoniazid, Alanine Transaminase, Tuberculin, Glutamates, Infection
 

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