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Clinical risks and healthcare utilization of hematopoietic cell transplantation for sickle cell disease in the USA using merged databases

Advances in allogeneic hematopoietic cell transplantation for sickle cell disease have improved outcomes, but there is limited analysis of healthcare utilization in this setting. We hypothesized that, compared to late transplantation, early transplantation (at age <10 years) improves outcomes and...

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Autores principales: Arnold, Staci D., Brazauskas, Ruta, He, Naya, Li, Yimei, Aplenc, Richard, Jin, Zhezhen, Hall, Matt, Atsuta, Yoshiko, Dalal, Jignesh, Hahn, Theresa, Khera, Nandita, Bonfim, Carmem, Majhail, Navneet S., Diaz, Miguel Angel, Freytes, Cesar O., Wood, William A., Savani, Bipin N., Kamble, Rammurti T., Parsons, Susan, Ahmed, Ibrahim, Sullivan, Keith, Beattie, Sara, Dandoy, Christopher, Munker, Reinhold, Marino, Susana, Bitan, Menachem, Abdel-Azim, Hisham, Aljurf, Mahmoud, Olsson, Richard F., Joshi, Sarita, Buchbinder, Dave, Eckrich, Michael J., Hashmi, Shahrukh, Lazarus, Hillard, Marks, David I., Steinberg, Amir, Saad, Ayman, Gergis, Usama, Krishnamurti, Lakshmanan, Abraham, Allistair, Rangarajan, Hemalatha G., Walters, Mark, Lipscomb, Joseph, Saber, Wael, Satwani, Prakash
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ferrata Storti Foundation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664386/
https://www.ncbi.nlm.nih.gov/pubmed/28818869
http://dx.doi.org/10.3324/haematol.2017.169581
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author Arnold, Staci D.
Brazauskas, Ruta
He, Naya
Li, Yimei
Aplenc, Richard
Jin, Zhezhen
Hall, Matt
Atsuta, Yoshiko
Dalal, Jignesh
Hahn, Theresa
Khera, Nandita
Bonfim, Carmem
Majhail, Navneet S.
Diaz, Miguel Angel
Freytes, Cesar O.
Wood, William A.
Savani, Bipin N.
Kamble, Rammurti T.
Parsons, Susan
Ahmed, Ibrahim
Sullivan, Keith
Beattie, Sara
Dandoy, Christopher
Munker, Reinhold
Marino, Susana
Bitan, Menachem
Abdel-Azim, Hisham
Aljurf, Mahmoud
Olsson, Richard F.
Joshi, Sarita
Buchbinder, Dave
Eckrich, Michael J.
Hashmi, Shahrukh
Lazarus, Hillard
Marks, David I.
Steinberg, Amir
Saad, Ayman
Gergis, Usama
Krishnamurti, Lakshmanan
Abraham, Allistair
Rangarajan, Hemalatha G.
Walters, Mark
Lipscomb, Joseph
Saber, Wael
Satwani, Prakash
author_facet Arnold, Staci D.
Brazauskas, Ruta
He, Naya
Li, Yimei
Aplenc, Richard
Jin, Zhezhen
Hall, Matt
Atsuta, Yoshiko
Dalal, Jignesh
Hahn, Theresa
Khera, Nandita
Bonfim, Carmem
Majhail, Navneet S.
Diaz, Miguel Angel
Freytes, Cesar O.
Wood, William A.
Savani, Bipin N.
Kamble, Rammurti T.
Parsons, Susan
Ahmed, Ibrahim
Sullivan, Keith
Beattie, Sara
Dandoy, Christopher
Munker, Reinhold
Marino, Susana
Bitan, Menachem
Abdel-Azim, Hisham
Aljurf, Mahmoud
Olsson, Richard F.
Joshi, Sarita
Buchbinder, Dave
Eckrich, Michael J.
Hashmi, Shahrukh
Lazarus, Hillard
Marks, David I.
Steinberg, Amir
Saad, Ayman
Gergis, Usama
Krishnamurti, Lakshmanan
Abraham, Allistair
Rangarajan, Hemalatha G.
Walters, Mark
Lipscomb, Joseph
Saber, Wael
Satwani, Prakash
author_sort Arnold, Staci D.
collection PubMed
description Advances in allogeneic hematopoietic cell transplantation for sickle cell disease have improved outcomes, but there is limited analysis of healthcare utilization in this setting. We hypothesized that, compared to late transplantation, early transplantation (at age <10 years) improves outcomes and decreases healthcare utilization. We performed a retrospective study of children transplanted for sickle cell disease in the USA during 2000–2013 using two large databases. Univariate and Cox models were used to estimate associations of demographics, sickle cell disease severity, and transplant-related variables with mortality and chronic graft-versus-host disease, while Wilcoxon, Kruskal-Wallis, or linear trend tests were applied for the estimates of healthcare utilization. Among 161 patients with a 2-year overall survival rate of 90% (95% confidence interval [CI] 85–95%) mortality was significantly higher in those who underwent late transplantation versus early (hazard ratio (HR) 21, 95% CI 2.8–160.8, P=0.003) and unrelated compared to matched sibling donor transplantation (HR 5.9, 95% CI 1.7–20.2, P=0.005). Chronic graftversus host disease was significantly more frequent among those translanted late (HR 1.9, 95% CI 1.0–3.5, P=0.034) and those who received an unrelated graft (HR 2.5, 95% CI 1.2–5.4; P=0.017). Merged data for 176 patients showed that the median total adjusted transplant cost per patient was $467,747 (range: $344,029–$799,219). Healthcare utilization was lower among recipients of matched sibling donor grafts and those with low severity disease compared to those with other types of donor and disease severity types (P<0.001 and P=0.022, respectively); no association was demonstrated with late transplantation (P=0.775). Among patients with 2-year pre- and post-transplant data (n=41), early transplantation was associated with significant reductions in admissions (P<0.001), length of stay (P<0.001), and cost (P=0.008). Early transplant outcomes need to be studied prospectively in young children without severe disease and an available matched sibling to provide conclusive evidence for the superiority of this approach. Reduced post-transplant healthcare utilization inpatient care indicates that transplantation may provide a sustained decrease in healthcare costs over time.
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spelling pubmed-56643862017-11-07 Clinical risks and healthcare utilization of hematopoietic cell transplantation for sickle cell disease in the USA using merged databases Arnold, Staci D. Brazauskas, Ruta He, Naya Li, Yimei Aplenc, Richard Jin, Zhezhen Hall, Matt Atsuta, Yoshiko Dalal, Jignesh Hahn, Theresa Khera, Nandita Bonfim, Carmem Majhail, Navneet S. Diaz, Miguel Angel Freytes, Cesar O. Wood, William A. Savani, Bipin N. Kamble, Rammurti T. Parsons, Susan Ahmed, Ibrahim Sullivan, Keith Beattie, Sara Dandoy, Christopher Munker, Reinhold Marino, Susana Bitan, Menachem Abdel-Azim, Hisham Aljurf, Mahmoud Olsson, Richard F. Joshi, Sarita Buchbinder, Dave Eckrich, Michael J. Hashmi, Shahrukh Lazarus, Hillard Marks, David I. Steinberg, Amir Saad, Ayman Gergis, Usama Krishnamurti, Lakshmanan Abraham, Allistair Rangarajan, Hemalatha G. Walters, Mark Lipscomb, Joseph Saber, Wael Satwani, Prakash Haematologica Article Advances in allogeneic hematopoietic cell transplantation for sickle cell disease have improved outcomes, but there is limited analysis of healthcare utilization in this setting. We hypothesized that, compared to late transplantation, early transplantation (at age <10 years) improves outcomes and decreases healthcare utilization. We performed a retrospective study of children transplanted for sickle cell disease in the USA during 2000–2013 using two large databases. Univariate and Cox models were used to estimate associations of demographics, sickle cell disease severity, and transplant-related variables with mortality and chronic graft-versus-host disease, while Wilcoxon, Kruskal-Wallis, or linear trend tests were applied for the estimates of healthcare utilization. Among 161 patients with a 2-year overall survival rate of 90% (95% confidence interval [CI] 85–95%) mortality was significantly higher in those who underwent late transplantation versus early (hazard ratio (HR) 21, 95% CI 2.8–160.8, P=0.003) and unrelated compared to matched sibling donor transplantation (HR 5.9, 95% CI 1.7–20.2, P=0.005). Chronic graftversus host disease was significantly more frequent among those translanted late (HR 1.9, 95% CI 1.0–3.5, P=0.034) and those who received an unrelated graft (HR 2.5, 95% CI 1.2–5.4; P=0.017). Merged data for 176 patients showed that the median total adjusted transplant cost per patient was $467,747 (range: $344,029–$799,219). Healthcare utilization was lower among recipients of matched sibling donor grafts and those with low severity disease compared to those with other types of donor and disease severity types (P<0.001 and P=0.022, respectively); no association was demonstrated with late transplantation (P=0.775). Among patients with 2-year pre- and post-transplant data (n=41), early transplantation was associated with significant reductions in admissions (P<0.001), length of stay (P<0.001), and cost (P=0.008). Early transplant outcomes need to be studied prospectively in young children without severe disease and an available matched sibling to provide conclusive evidence for the superiority of this approach. Reduced post-transplant healthcare utilization inpatient care indicates that transplantation may provide a sustained decrease in healthcare costs over time. Ferrata Storti Foundation 2017-11 /pmc/articles/PMC5664386/ /pubmed/28818869 http://dx.doi.org/10.3324/haematol.2017.169581 Text en Copyright© Ferrata Storti Foundation Material published in Haematologica is covered by copyright. All rights are reserved to the Ferrata Storti Foundation. Use of published material is allowed under the following terms and conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode. Copies of published material are allowed for personal or internal use. Sharing published material for non-commercial purposes is subject to the following conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode, sect. 3. Reproducing and sharing published material for commercial purposes is not allowed without permission in writing from the publisher.
spellingShingle Article
Arnold, Staci D.
Brazauskas, Ruta
He, Naya
Li, Yimei
Aplenc, Richard
Jin, Zhezhen
Hall, Matt
Atsuta, Yoshiko
Dalal, Jignesh
Hahn, Theresa
Khera, Nandita
Bonfim, Carmem
Majhail, Navneet S.
Diaz, Miguel Angel
Freytes, Cesar O.
Wood, William A.
Savani, Bipin N.
Kamble, Rammurti T.
Parsons, Susan
Ahmed, Ibrahim
Sullivan, Keith
Beattie, Sara
Dandoy, Christopher
Munker, Reinhold
Marino, Susana
Bitan, Menachem
Abdel-Azim, Hisham
Aljurf, Mahmoud
Olsson, Richard F.
Joshi, Sarita
Buchbinder, Dave
Eckrich, Michael J.
Hashmi, Shahrukh
Lazarus, Hillard
Marks, David I.
Steinberg, Amir
Saad, Ayman
Gergis, Usama
Krishnamurti, Lakshmanan
Abraham, Allistair
Rangarajan, Hemalatha G.
Walters, Mark
Lipscomb, Joseph
Saber, Wael
Satwani, Prakash
Clinical risks and healthcare utilization of hematopoietic cell transplantation for sickle cell disease in the USA using merged databases
title Clinical risks and healthcare utilization of hematopoietic cell transplantation for sickle cell disease in the USA using merged databases
title_full Clinical risks and healthcare utilization of hematopoietic cell transplantation for sickle cell disease in the USA using merged databases
title_fullStr Clinical risks and healthcare utilization of hematopoietic cell transplantation for sickle cell disease in the USA using merged databases
title_full_unstemmed Clinical risks and healthcare utilization of hematopoietic cell transplantation for sickle cell disease in the USA using merged databases
title_short Clinical risks and healthcare utilization of hematopoietic cell transplantation for sickle cell disease in the USA using merged databases
title_sort clinical risks and healthcare utilization of hematopoietic cell transplantation for sickle cell disease in the usa using merged databases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664386/
https://www.ncbi.nlm.nih.gov/pubmed/28818869
http://dx.doi.org/10.3324/haematol.2017.169581
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