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Hospital survival following pediatric HSCT: changes in complications, ICU therapies and outcomes over 10 years

INTRODUCTION: Hematopoietic stem cell transplantation (HSCT) is an increasingly utilized therapy for malignant and non-malignant pediatric diseases. HSCT complications, including infection, organ dysfunction, and graft-versus-host-disease (GVHD) often require intensive care unit (ICU) therapies and...

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Autores principales: Olson, Taylor L., Pollack, Murray M., Dávila Saldaña, Blachy J., Patel, Anita K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601648/
https://www.ncbi.nlm.nih.gov/pubmed/37900687
http://dx.doi.org/10.3389/fped.2023.1247792
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author Olson, Taylor L.
Pollack, Murray M.
Dávila Saldaña, Blachy J.
Patel, Anita K.
author_facet Olson, Taylor L.
Pollack, Murray M.
Dávila Saldaña, Blachy J.
Patel, Anita K.
author_sort Olson, Taylor L.
collection PubMed
description INTRODUCTION: Hematopoietic stem cell transplantation (HSCT) is an increasingly utilized therapy for malignant and non-malignant pediatric diseases. HSCT complications, including infection, organ dysfunction, and graft-versus-host-disease (GVHD) often require intensive care unit (ICU) therapies and are associated with mortality. Our aims were to identify the HSCT characteristics, complications and ICU therapies associated with (1) survival, and (2) survival changes over a ten-year period in a national dataset. METHODS: A national sample from the Health Facts (Cerner Corporation, Kansas City, MO) database from 2009 to 2018 was utilized. Inclusion criteria were age 30 days to <22 years and HSCT procedure code. For patients with >1 HSCT, the first was analyzed. Data included demographics, hospital length of stay (LOS), hospital outcome, transplant type and indication. HSCT complications included GVHD and infections. ICU therapies were positive pressure ventilation (PPV), vasoactive infusion, and dialysis. Primary outcome was survival to discharge. Statistical methods included bivariate analyses and multivariate logistic regression. RESULTS: 473 patients underwent HSCT with 93% survival. 62% were allogeneic (89% survival) and 38% were autologous (98% survival). GVHD occurred in 33% of allogeneic HSCT. Infections occurred in 26% of all HSCT. ICU therapies included PPV (11% of patients), vasoactive (25%), and dialysis (3%). Decreased survival was associated with allogeneic HSCT (p < 0.01), GVHD (p = 0.02), infection (p < 0.01), and ICU therapies (p < 0.01). Survival improved from 89% (2009–2013) to 96% (2014–2018) (p < 0.01). Allogeneic survival improved (82%–94%, p < 0.01) while autologous survival was unchanged. Survival improvement over time was associated with decreasing infections (33%–21%, p < 0.01) and increasing vasoactive infusions (20%–28%, p = 0.05). On multivariate analysis, later time period was associated with improved survival (p < 0.01, adjusted OR 4.28). DISCUSSION: Hospital survival for HSCT improved from 89% to 96% from 2009 to 2018. Factors associated with mortality included allogeneic HSCT, GVHD, infections and ICU therapies. Improving survival coincided with decreasing infections and increasing vasoactive use.
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spelling pubmed-106016482023-10-27 Hospital survival following pediatric HSCT: changes in complications, ICU therapies and outcomes over 10 years Olson, Taylor L. Pollack, Murray M. Dávila Saldaña, Blachy J. Patel, Anita K. Front Pediatr Pediatrics INTRODUCTION: Hematopoietic stem cell transplantation (HSCT) is an increasingly utilized therapy for malignant and non-malignant pediatric diseases. HSCT complications, including infection, organ dysfunction, and graft-versus-host-disease (GVHD) often require intensive care unit (ICU) therapies and are associated with mortality. Our aims were to identify the HSCT characteristics, complications and ICU therapies associated with (1) survival, and (2) survival changes over a ten-year period in a national dataset. METHODS: A national sample from the Health Facts (Cerner Corporation, Kansas City, MO) database from 2009 to 2018 was utilized. Inclusion criteria were age 30 days to <22 years and HSCT procedure code. For patients with >1 HSCT, the first was analyzed. Data included demographics, hospital length of stay (LOS), hospital outcome, transplant type and indication. HSCT complications included GVHD and infections. ICU therapies were positive pressure ventilation (PPV), vasoactive infusion, and dialysis. Primary outcome was survival to discharge. Statistical methods included bivariate analyses and multivariate logistic regression. RESULTS: 473 patients underwent HSCT with 93% survival. 62% were allogeneic (89% survival) and 38% were autologous (98% survival). GVHD occurred in 33% of allogeneic HSCT. Infections occurred in 26% of all HSCT. ICU therapies included PPV (11% of patients), vasoactive (25%), and dialysis (3%). Decreased survival was associated with allogeneic HSCT (p < 0.01), GVHD (p = 0.02), infection (p < 0.01), and ICU therapies (p < 0.01). Survival improved from 89% (2009–2013) to 96% (2014–2018) (p < 0.01). Allogeneic survival improved (82%–94%, p < 0.01) while autologous survival was unchanged. Survival improvement over time was associated with decreasing infections (33%–21%, p < 0.01) and increasing vasoactive infusions (20%–28%, p = 0.05). On multivariate analysis, later time period was associated with improved survival (p < 0.01, adjusted OR 4.28). DISCUSSION: Hospital survival for HSCT improved from 89% to 96% from 2009 to 2018. Factors associated with mortality included allogeneic HSCT, GVHD, infections and ICU therapies. Improving survival coincided with decreasing infections and increasing vasoactive use. Frontiers Media S.A. 2023-10-12 /pmc/articles/PMC10601648/ /pubmed/37900687 http://dx.doi.org/10.3389/fped.2023.1247792 Text en © 2023 Olson, Pollack, Dávila Saldaña and Patel. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Olson, Taylor L.
Pollack, Murray M.
Dávila Saldaña, Blachy J.
Patel, Anita K.
Hospital survival following pediatric HSCT: changes in complications, ICU therapies and outcomes over 10 years
title Hospital survival following pediatric HSCT: changes in complications, ICU therapies and outcomes over 10 years
title_full Hospital survival following pediatric HSCT: changes in complications, ICU therapies and outcomes over 10 years
title_fullStr Hospital survival following pediatric HSCT: changes in complications, ICU therapies and outcomes over 10 years
title_full_unstemmed Hospital survival following pediatric HSCT: changes in complications, ICU therapies and outcomes over 10 years
title_short Hospital survival following pediatric HSCT: changes in complications, ICU therapies and outcomes over 10 years
title_sort hospital survival following pediatric hsct: changes in complications, icu therapies and outcomes over 10 years
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601648/
https://www.ncbi.nlm.nih.gov/pubmed/37900687
http://dx.doi.org/10.3389/fped.2023.1247792
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