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A Child as a Donor for Hematopoietic Stem Cell Transplantation: Bioethical Justification—A Case Study on Sickle Cell Disease

Hematopoietic stem cell transplantation (HSCT) is an important treatment option for children with severe and refractory sickle cell disease (SCD) with debilitating clinical complications. HSCT with cells from the bone marrow of a HLA-identical sibling used in SCD has a low mortality risk, high cure...

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Autores principales: Pereira, Andrea Z., Hellman, Ricardo, Hamerschlak, Nelson, Kondo, Andrea, de Souza, Polianna Mara Rodrigues, Pedreira, Wilson Leite, Mantovani, Luiz Fernando Alves Lima, Troster, Eduardo Juan, Grunspun, Henrique, Bueno, Marco Aurélio Scarpinella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343239/
https://www.ncbi.nlm.nih.gov/pubmed/28326208
http://dx.doi.org/10.1155/2017/8394732
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author Pereira, Andrea Z.
Hellman, Ricardo
Hamerschlak, Nelson
Kondo, Andrea
de Souza, Polianna Mara Rodrigues
Pedreira, Wilson Leite
Mantovani, Luiz Fernando Alves Lima
Troster, Eduardo Juan
Grunspun, Henrique
Bueno, Marco Aurélio Scarpinella
author_facet Pereira, Andrea Z.
Hellman, Ricardo
Hamerschlak, Nelson
Kondo, Andrea
de Souza, Polianna Mara Rodrigues
Pedreira, Wilson Leite
Mantovani, Luiz Fernando Alves Lima
Troster, Eduardo Juan
Grunspun, Henrique
Bueno, Marco Aurélio Scarpinella
author_sort Pereira, Andrea Z.
collection PubMed
description Hematopoietic stem cell transplantation (HSCT) is an important treatment option for children with severe and refractory sickle cell disease (SCD) with debilitating clinical complications. HSCT with cells from the bone marrow of a HLA-identical sibling used in SCD has a low mortality risk, high cure rate, and high event-free survival rate after a median follow-up of 5-6 years. However, matched donors are found in only about 20% of the patients. A boy aged 8 years with SCD had a sister, <2 years old, a fully compatible donor. The boy met all eligibility criteria to undergo HSCT, and he was suffering from cognitive and neurologic impairment due to ischemic events. A Bioethical Committee jointly discussed the ethical issues on this case after a pediatric evaluation released the very young sister for donation. The justification was that the sister would benefit from the donation too because of the greater likelihood of survival and cure and less suffering of her brother. The parents were informed about the risks and benefits for both children, and the family was psychologically evaluated. After their consent, HSCT was performed and the patient is cured from SCD. The complication for the donor was the need for blood transfusion.
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spelling pubmed-53432392017-03-21 A Child as a Donor for Hematopoietic Stem Cell Transplantation: Bioethical Justification—A Case Study on Sickle Cell Disease Pereira, Andrea Z. Hellman, Ricardo Hamerschlak, Nelson Kondo, Andrea de Souza, Polianna Mara Rodrigues Pedreira, Wilson Leite Mantovani, Luiz Fernando Alves Lima Troster, Eduardo Juan Grunspun, Henrique Bueno, Marco Aurélio Scarpinella Case Rep Hematol Case Report Hematopoietic stem cell transplantation (HSCT) is an important treatment option for children with severe and refractory sickle cell disease (SCD) with debilitating clinical complications. HSCT with cells from the bone marrow of a HLA-identical sibling used in SCD has a low mortality risk, high cure rate, and high event-free survival rate after a median follow-up of 5-6 years. However, matched donors are found in only about 20% of the patients. A boy aged 8 years with SCD had a sister, <2 years old, a fully compatible donor. The boy met all eligibility criteria to undergo HSCT, and he was suffering from cognitive and neurologic impairment due to ischemic events. A Bioethical Committee jointly discussed the ethical issues on this case after a pediatric evaluation released the very young sister for donation. The justification was that the sister would benefit from the donation too because of the greater likelihood of survival and cure and less suffering of her brother. The parents were informed about the risks and benefits for both children, and the family was psychologically evaluated. After their consent, HSCT was performed and the patient is cured from SCD. The complication for the donor was the need for blood transfusion. Hindawi Publishing Corporation 2017 2017-02-23 /pmc/articles/PMC5343239/ /pubmed/28326208 http://dx.doi.org/10.1155/2017/8394732 Text en Copyright © 2017 Andrea Z. Pereira et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Pereira, Andrea Z.
Hellman, Ricardo
Hamerschlak, Nelson
Kondo, Andrea
de Souza, Polianna Mara Rodrigues
Pedreira, Wilson Leite
Mantovani, Luiz Fernando Alves Lima
Troster, Eduardo Juan
Grunspun, Henrique
Bueno, Marco Aurélio Scarpinella
A Child as a Donor for Hematopoietic Stem Cell Transplantation: Bioethical Justification—A Case Study on Sickle Cell Disease
title A Child as a Donor for Hematopoietic Stem Cell Transplantation: Bioethical Justification—A Case Study on Sickle Cell Disease
title_full A Child as a Donor for Hematopoietic Stem Cell Transplantation: Bioethical Justification—A Case Study on Sickle Cell Disease
title_fullStr A Child as a Donor for Hematopoietic Stem Cell Transplantation: Bioethical Justification—A Case Study on Sickle Cell Disease
title_full_unstemmed A Child as a Donor for Hematopoietic Stem Cell Transplantation: Bioethical Justification—A Case Study on Sickle Cell Disease
title_short A Child as a Donor for Hematopoietic Stem Cell Transplantation: Bioethical Justification—A Case Study on Sickle Cell Disease
title_sort child as a donor for hematopoietic stem cell transplantation: bioethical justification—a case study on sickle cell disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343239/
https://www.ncbi.nlm.nih.gov/pubmed/28326208
http://dx.doi.org/10.1155/2017/8394732
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