Construct validity of the definition of primary graft dysfunction after lung transplantation JOURNAL OF HEART AND LUNG TRANSPLANTATION Christie, J. D., Bellamy, S., Ware, L. B., Lederer, D., Hadjiliadis, D., Lee, J., Robinson, N., Localio, A. R., Wille, K., Lama, V., Palmer, S., Orens, J., Weinacker, A., Crespo, M., Demissie, E., Kimmel, S. E., Kawut, S. M. 2010; 29 (11): 1231-1239

Abstract

This study tested the discriminant validity of International Society for Heart and Lung Transplantation (ISHLT) primary graft dysfunction (PGD) grades with lung injury biomarker profiles and survival.The study samples consisted of a multicenter prospective cohort study for the biomarker analysis and a cohort study of 450 patients for the mortality analyses. PGD was defined according to ISHLT consensus at 24, 48, and 72 hours after transplantation. We compared the changes in plasma markers of acute lung injury between PGD grades using longitudinal data models. To test predictive validity, we compared differences in the 30-day mortality and long-term survival according to PGD grade.PGD Grade 3 demonstrated greater differences between plasma intercellular adhesion molecule 1 (ICAM-1), protein C, and plasminogen activator inhibitor type 1 (PAI-1) levels than did PGD Grades 0 to 2 at 24, 48, and 72 hours after lung transplantation (p < 0.05 for each). Grade 3 had the highest 30-day (test for trend p < 0.001) and overall mortality (log rank p < 0.001), with PGD Grades 1 and 2 demonstrating intermediate risks of mortality. The ability to discriminate both 30-day and overall mortality improved as the time of grading moved away from the time of transplantation (test for trend p < 0.001).The ISHLT grading system has good discriminant validity, based on plasma markers of lung injury and mortality. Grade 3 PGD was associated with the most severely altered plasma biomarker profile and the worst outcomes, regardless of the time point of grading. PGD grade at 48 and 72 hours discriminated mortality better than PGD grade at 24 hours.

View details for DOI 10.1016/j.healun.2010.05.013

View details for Web of Science ID 000284030700005

View details for PubMedID 20655249

View details for PubMedCentralID PMC2963709