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Original Article
Procalcitonin elevation in febrile recipients during pre-transplant conditioning with anti-thymocyte globulin
Takahiro Shima1,2, Mariko Minami1, Taro Tochigi1, Yu Kochi1, Fumiaki Jinnouchi1, Takuji Yamauchi1, Yasuo Mori1, Goichi Yoshimoto1, Shinichi Mizuno2, Toshihiro Miyamoto1, Koji Kato1, Koichi Akashi1,3

1Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medicine, Fukuoka, Japan

2Center for Advanced Medical Innovation, Kyushu University Hospital, Fukuoka, Japan

3Center for Cellular and Molecular Medicine, Kyushu University Hospital, Fukuoka, Japan

Keywords
Procalcitonin, Febrile, ATG
Submitted:November 6, 2023
Accepted:February 1, 2024
Published online:April 26, 2024

Abstract

Infection is a major contributor to non-relapse mortality in allogeneic hematopoietic stem cell transplantation (allo-HSCT). Detecting infectious diseases in febrile patients during pretransplant conditioning is crucial for subsequent transplant success. Procalcitonin (PCT) is an auxiliary diagnostic marker of severe bacterial infections and has been proposed as a useful predictor of infection in patients undergoing allo-HSCT. Pre-transplant use of anti-thymocyte globulin (ATG) can cause side effects, such as fever and hypotension, which must be distinguished from infectious diseases. Although ATG administration may increase PCT levels, data on PCT levels in febrile patients after ATG administration are limited. Furthermore, no studies have compared PCT levels during allo-HSCT conditioning using ATG or non-ATG regimens. To investigate whether ATG increases PCT levels during febrile episodes in pre-transplant conditioning and whether PCT could be used to discriminate infections during this period, we analyzed 17 ATG and 59 non-ATG patients with fever and who underwent PCT level measurements during pre-transplant conditioning. Our findings revealed that ATG administration was the only significant factor that increased PCT positivity during fever (p = 0.01). In contrast, infectious diseases did not affect PCT positivity in the ATG group (p = 0.24). Furthermore, bloodstream infection was a significant risk factor for PCT positivity in patients who received non-ATG regimens (p < 0.01). Incorporating PCT levels into the diagnostic workup for infectious diseases requires careful consideration, particularly for patients receiving ATG regimens.

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Online ISSN:2432-7026