Introduction: The appropriate duration of therapy for uncomplicated gram-negative bloodstream infection (GN-BSI) in liver transplant (LTx) recipients remains unknown. This study aims to explore the effectiveness of a short-course antimicrobial therapy.
Methods: This retrospective study was performed in a single LTx center in Japan. All LTx recipients with GN-BSI receiving 6-16 days of therapy with adequate source control between 2010 and 2022 were included. We collected data on demographics, underlying medical conditions, clinical manifestations, laboratory and microbiology data, ID consultation, oral switch therapy, and subsequent clinical course through chart review. We compared the 30-day composite outcome comprising mortality and recurrence of BSI or local infection between patients receiving a short-course (6-10 days) therapy and those receiving a long-course (11-16 days) therapy.
Results: Of 91 study participants, 27 (29.7%) and 64 (70.3%) received short-course and long-course antimicrobial therapy, respectively. Cholangitis was the most common source of BSI (57/91 [62.6%]). Overall, the primary composite outcome occurred in 18 patients (19.8%), most of which was the recurrence of local infection (n = 14). The primary composite outcome was numerically compatible between these groups (5/27 [18.5%] vs. 13/64 [20.3%]; p = 0.84).
Conclusions: A short-course therapy may be an effective option in selected LTx recipients with uncomplicated GN-BSI. Whether a short-course oral switch therapy is a viable option or not warrants further research.
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http://dx.doi.org/10.1111/tid.14434 | DOI Listing |
Transpl Infect Dis
December 2024
Department of Infectious Diseases, The University of Tokyo Hospital, Tokyo, Japan.
Introduction: The appropriate duration of therapy for uncomplicated gram-negative bloodstream infection (GN-BSI) in liver transplant (LTx) recipients remains unknown. This study aims to explore the effectiveness of a short-course antimicrobial therapy.
Methods: This retrospective study was performed in a single LTx center in Japan.
Eur J Cardiothorac Surg
December 2024
Department of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.
Objectives: In patients with interstitial lung disease (ILD), the diaphragm typically rises as the lungs chronically shrink. However, the grade of restriction differs in each patient. It is currently unknown, how disparities between actual and predicted recipient total lung capacity (TLC), impact changes in lung function parameters and long-term outcomes following lung transplantation (LTx).
View Article and Find Full Text PDFGen Thorac Cardiovasc Surg
December 2024
Department of Thoracic Surgery, Kyoto University, 54 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan.
Objectives: Generally, HLA matching between donors and recipients is not performed in lung transplantation (LTx). Therefore, whether HLA mismatch between donors and recipients (D/R mismatch) influences postoperative outcomes after LTx remains uncertain. In this study, we investigated the influence of D/R mismatch on postoperative outcomes after cadaveric LTx (CLT).
View Article and Find Full Text PDFCell Mol Life Sci
December 2024
Laboratory of Molecular Immunology, Rega Institute, Department of Microbiology, Immunology and Transplantation, KU Leuven, Rega - Herestraat 49, box 1042, Leuven, 3000, Belgium.
Elevated neutrophil counts in broncho-alveolar lavage (BAL) fluids of lung transplant (LTx) patients with chronic lung allograft dysfunction (CLAD) are associated with disease pathology. However, phenotypical characteristics of these cells remained largely unknown. Moreover, despite enhanced levels of the most potent human neutrophil-attracting chemokine CXCL8 in BAL fluid, no discrimination had been made between natural NH-terminally truncated CXCL8 proteoforms, which exhibit up to 30-fold differences in biological activity.
View Article and Find Full Text PDFbioRxiv
November 2024
Department of Surgery, Washington University School of Medicine, St. Louis, MO, USA.
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