AI Article Synopsis

  • Poor agreement among lung transplant pathologists in assessing rejection has been noted, making inter-rater reliability crucial for effective patient care and clinical trial inclusion criteria.
  • A survey and diagnostic sessions with nine pathologists from eight centers evaluated their practices and scoring of high-risk histopathologic findings related to chronic lung allograft dysfunction (CLAD).
  • The results showed good inter-rater reliability for identifying high-risk findings after these alignment sessions, indicating that collaborative discussions improved consensus among pathologists.

Article Abstract

Background: Poor agreement among lung transplant (LTx) pathologists has been reported in the assessment of rejection. In addition to acute rejection (AR) and lymphocytic bronchiolitis (LB), acute lung injury (ALI) and organizing pneumonia (OP) were recently identified as histopathologic risk factors for chronic lung allograft dysfunction (CLAD). Therefore, maximizing inter-rater reliability (IRR) for identifying these histopathologic risk factors is important to guide individual patient care and to support incorporating them in inclusion criteria for clinical trials in lung transplantation.

Methods: Nine pathologists across 8 North American LTx centers were surveyed for practices in the assessment of LTx transbronchial biopsies. We conducted 7 diagnostic alignment sessions with pathologists discussing histomorphologic features of CLAD high-risk histopathology. Then, each pathologist blindly scored 75 digitized slides. Fleiss' kappa, accounting for agreement across numerous observers, was used to determine IRR across all raters for the presence of any high-risk finding and each individual entity.

Results: IRR (95% confidence intervals) and % agreement for any high-risk finding (AR, LB, ALI, and/or OP) and each individual finding is as follows: Any Finding, k = 0.578 (0.487, 0.668), 78.9%; AR, k = 0.582 (0.481, 0.651), 79.1%; LB, k = 0.683 (0.585, 0.764), 83.5%; ALI, k = 0.418 (0.312, 0.494), 70.9%; and OP, k = 0.621 (0.560, 0.714), 81.0%.

Conclusions: After prestudy diagnostic alignment sessions, a multicenter group of LTx pathologists seeking to identify histopathology high-risk for CLAD achieved good IRR.

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Source
http://dx.doi.org/10.1016/j.healun.2024.10.007DOI Listing

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