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207. Burden of Post-Transplant Neutropenia and Leukopenia among Kidney Transplant Recipients: A Multi-Institutional Real-World Observational Study

BACKGROUND: Kidney transplant recipients (KTRs) are commonly prescribed valganciclovir/ganciclovir (V/G) prophylactically to prevent cytomegalovirus (CMV) infection; however, prolonged exposure to these medications is associated with an increased risk of post-transplant neutropenia (PTN) and leukope...

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Autores principales: Raval, Amit D, Turzhitsky, Vladimir, Fazio-Eynullayeva, Elnara, Jin, Harry, Merchant, Sanjay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751561/
http://dx.doi.org/10.1093/ofid/ofac492.284
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author Raval, Amit D
Turzhitsky, Vladimir
Fazio-Eynullayeva, Elnara
Jin, Harry
Merchant, Sanjay
author_facet Raval, Amit D
Turzhitsky, Vladimir
Fazio-Eynullayeva, Elnara
Jin, Harry
Merchant, Sanjay
author_sort Raval, Amit D
collection PubMed
description BACKGROUND: Kidney transplant recipients (KTRs) are commonly prescribed valganciclovir/ganciclovir (V/G) prophylactically to prevent cytomegalovirus (CMV) infection; however, prolonged exposure to these medications is associated with an increased risk of post-transplant neutropenia (PTN) and leukopenia (PTL). Real-world evidence characterizing the incidence of PTN and PTL and their associated consequences on a national level are limited. METHODS: This retrospective cohort study utilized the TriNetX Dataworks – USA Network, a global federated network of de-identified electronic health record (EHR) data for 82.5 million patients across 49 US healthcare organizations. Adult KTRs who were treated with V/G between January 1, 2012 and September 30, 2020, were included in this analysis. PTN was defined as absolute neutrophil count< 1500/μL and PTL was defined as white blood cell count< 3,500/μL. We estimated the proportion of PTN and PTL among KTRs and examined differences in granulocyte colony-stimulating factor (G-CSF) use and clinical outcomes between KTRs with and without PTN or PTL in the 1-year following KT. RESULTS: Overall, 8,791 patients included in the analyses had a mean age of 52.8 years, 40.7% were females, 41.6% White and 32.6% Black. 3,383 patients (38.5%) developed PTN and 6,127 patients (69.7%) developed PTL based on the laboratory definitions. The incidence rates of PTN and PTL were 15.5/100 person-days and 53.4/100 person-days, respectively. There were no significant differences between comparison groups with respect to demographic characteristics at baseline. KTRs with PTN had higher G-CSF use compared to those without PTNs (38.9% vs.3.61%). Similarly, those with PTLs had higher G-CSF use compared to those without (22.8% vs. 4.2%). Both PTN and PTL were also associated with increased risk of CMV infection, graft rejection, and loss (Table 1, all p< 0.001). [Figure: see text] CONCLUSION: The results of this large EHR study demonstrate that a sizeable proportion of V/G treated KTRs develop PTN and/or PTL, both of which are associated with increased medication use and suboptimal health outcomes. These findings underscore the importance of taking steps to mitigate the risk of neutropenia and leukopenia where possible to help improve outcomes in KTRs. DISCLOSURES: Amit D. Raval, PhD, Merck and Co., Inc.: Employee of Merck|Merck and Co., Inc.: Stocks/Bonds Vladimir Turzhitsky, PhD, Merck & Co., Inc.,: Employee|Merck & Co., Inc.,: Stocks/Bonds Sanjay Merchant, PhD, Merck & Co., Inc.: Stocks/Bonds.
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spelling pubmed-97515612022-12-16 207. Burden of Post-Transplant Neutropenia and Leukopenia among Kidney Transplant Recipients: A Multi-Institutional Real-World Observational Study Raval, Amit D Turzhitsky, Vladimir Fazio-Eynullayeva, Elnara Jin, Harry Merchant, Sanjay Open Forum Infect Dis Abstracts BACKGROUND: Kidney transplant recipients (KTRs) are commonly prescribed valganciclovir/ganciclovir (V/G) prophylactically to prevent cytomegalovirus (CMV) infection; however, prolonged exposure to these medications is associated with an increased risk of post-transplant neutropenia (PTN) and leukopenia (PTL). Real-world evidence characterizing the incidence of PTN and PTL and their associated consequences on a national level are limited. METHODS: This retrospective cohort study utilized the TriNetX Dataworks – USA Network, a global federated network of de-identified electronic health record (EHR) data for 82.5 million patients across 49 US healthcare organizations. Adult KTRs who were treated with V/G between January 1, 2012 and September 30, 2020, were included in this analysis. PTN was defined as absolute neutrophil count< 1500/μL and PTL was defined as white blood cell count< 3,500/μL. We estimated the proportion of PTN and PTL among KTRs and examined differences in granulocyte colony-stimulating factor (G-CSF) use and clinical outcomes between KTRs with and without PTN or PTL in the 1-year following KT. RESULTS: Overall, 8,791 patients included in the analyses had a mean age of 52.8 years, 40.7% were females, 41.6% White and 32.6% Black. 3,383 patients (38.5%) developed PTN and 6,127 patients (69.7%) developed PTL based on the laboratory definitions. The incidence rates of PTN and PTL were 15.5/100 person-days and 53.4/100 person-days, respectively. There were no significant differences between comparison groups with respect to demographic characteristics at baseline. KTRs with PTN had higher G-CSF use compared to those without PTNs (38.9% vs.3.61%). Similarly, those with PTLs had higher G-CSF use compared to those without (22.8% vs. 4.2%). Both PTN and PTL were also associated with increased risk of CMV infection, graft rejection, and loss (Table 1, all p< 0.001). [Figure: see text] CONCLUSION: The results of this large EHR study demonstrate that a sizeable proportion of V/G treated KTRs develop PTN and/or PTL, both of which are associated with increased medication use and suboptimal health outcomes. These findings underscore the importance of taking steps to mitigate the risk of neutropenia and leukopenia where possible to help improve outcomes in KTRs. DISCLOSURES: Amit D. Raval, PhD, Merck and Co., Inc.: Employee of Merck|Merck and Co., Inc.: Stocks/Bonds Vladimir Turzhitsky, PhD, Merck & Co., Inc.,: Employee|Merck & Co., Inc.,: Stocks/Bonds Sanjay Merchant, PhD, Merck & Co., Inc.: Stocks/Bonds. Oxford University Press 2022-12-15 /pmc/articles/PMC9751561/ http://dx.doi.org/10.1093/ofid/ofac492.284 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstracts
Raval, Amit D
Turzhitsky, Vladimir
Fazio-Eynullayeva, Elnara
Jin, Harry
Merchant, Sanjay
207. Burden of Post-Transplant Neutropenia and Leukopenia among Kidney Transplant Recipients: A Multi-Institutional Real-World Observational Study
title 207. Burden of Post-Transplant Neutropenia and Leukopenia among Kidney Transplant Recipients: A Multi-Institutional Real-World Observational Study
title_full 207. Burden of Post-Transplant Neutropenia and Leukopenia among Kidney Transplant Recipients: A Multi-Institutional Real-World Observational Study
title_fullStr 207. Burden of Post-Transplant Neutropenia and Leukopenia among Kidney Transplant Recipients: A Multi-Institutional Real-World Observational Study
title_full_unstemmed 207. Burden of Post-Transplant Neutropenia and Leukopenia among Kidney Transplant Recipients: A Multi-Institutional Real-World Observational Study
title_short 207. Burden of Post-Transplant Neutropenia and Leukopenia among Kidney Transplant Recipients: A Multi-Institutional Real-World Observational Study
title_sort 207. burden of post-transplant neutropenia and leukopenia among kidney transplant recipients: a multi-institutional real-world observational study
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751561/
http://dx.doi.org/10.1093/ofid/ofac492.284
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