Systematic fungal biomarker or polymerase chain reaction testing in lung transplant recipients: Retrospective analysis to optimize their use

Author:

Boutin Catherine‐Audrey12,Ison Michael G3

Affiliation:

1. Department of Medicine Divisions of Infectious Diseases and Organ Transplantation Northwestern University Feinberg School of Medicine Chicago Illinois USA

2. Department of Medicine Division of Infectious Disease University of Montreal Hospital Center Montreal Canada

3. Respiratory Diseases Branch Division of Microbiology and Infectious Diseases NIAID, NIH Rockville Maryland USA

Abstract

AbstractBackgroundAmong lung transplant recipients, serial bronchoscopies are performed frequently. Often, serial galactomannan (GM), 1,3‐β‐d‐glucan (BDG), and Pneumocystis jirovecii (PJ) testing is performed with these broncho‐alveolar lavages (BALs) as standard of care with limited data to support their routine use.MethodsAfter Institutional Review Board approval, we retrospectively collected all blood and BAL GM, BDG, and PJ test results from January 2015 to July 20, 2022. Primary data collection from the Northwestern Medicine EDW was supplemented by manual chart review.ResultsDuring the study period, 236 lung transplant recipients were cared for by our center. Of these patients, 217 (91.9%) had 1418 GM tests performed; 61 (4.3%) were positive (index ≥1). Fungal cultures were requested for most BAL‐GM (90.7%). Out of duplicates in same BAL, results discrepancy was minimal (3.4%). 172 (72.9%) had BDG tests were performed; 25.6% were positive. Thirteen patients had multiple BDG during one hospitalization (mean 2.3 tests); none of the negative test repeated became positive. Eleven negative BDG were seen in patients with invasive aspergillosis (IA). Note that, 577 PJ testing were performed (direct fluorescent antibody [n = 494] or polymerase chain reaction [PCR] [n = 80], or both [n = 3]) in 174 different patients. None were positive.ConclusionDespite supplemental GM, BDG, and Pneumocystis jirovecii pneumonia PCR being performed routinely on lung transplant recipients undergoing BAL at our center, the data suggests a more tailored approach may be appropriate. There is no role for routine serial testing with these assays during a single hospitalization. BDG confers no added‐value over GM with cultures for IA diagnosis. image

Publisher

Wiley

Subject

Infectious Diseases,Transplantation

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