| Literature DB >> 31452317 |
Laneshia Karee Tague1, Davide Scozzi2, Michael Wallendorf3, Brian F Gage4, Alexander S Krupnick5, Daniel Kreisel2, Derek Byers1, Ramsey R Hachem1, Andrew E Gelman2,6.
Abstract
Although neutropenia is a common complication after lung transplant, its relationship with recipient outcomes remains understudied. We evaluated a retrospective cohort of 228 adult lung transplant recipients between 2008 and 2013 to assess the association of neutropenia and granulocyte colony-stimulating factor (GCSF) treatment with outcomes. Neutropenia was categorized as mild (absolute neutrophil count 1000-1499), moderate (500-999), or severe (<500) and as a time-varying continuous variable. Associations with survival, acute rejection, and chronic lung allograft dysfunction (CLAD) were assessed with the use of Cox proportional hazards regression. GCSF therapy impact on survival, CLAD, and acute rejection development was analyzed by propensity score matching. Of 228 patients, 101 (42.1%) developed neutropenia. Recipients with severe neutropenia had higher mortality rates than those of recipients with no (adjusted hazard ratio [aHR] 2.97, 95% confidence interval [CI] 1.05-8.41, P = .040), mild (aHR 14.508, 95% CI 1.58-13.34, P = .018), or moderate (aHR 3.27, 95% CI 0.89-12.01, P = .074) neutropenia. Surprisingly, GCSF treatment was associated with a higher risk for CLAD in mildly neutropenic patients (aHR 3.49, 95% CI 0.93-13.04, P = .063), although it did decrease death risk in severely neutropenic patients (aHR 0.24, 95% CI 0.07-0.88, P = .031). Taken together, our data point to an important relationship between neutropenia severity and GCSF treatment in lung transplant outcomes.Entities:
Keywords: clinical decision-making; clinical research/practice; complication: infectious; innate immunity; lung transplantation/pulmonology; patient survival; rejection
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Year: 2019 PMID: 31452317 PMCID: PMC6940547 DOI: 10.1111/ajt.15581
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086