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Low cyclosporine concentrations in children and time to acute graft versus host disease

BACKGROUND: Achievement of target blood concentrations of cyclosporine (CsA) early after transplantation is known to be highly effective for reducing the incidence of acute graft versus host disease (aGVHD). However, no research has been conducted for predicting aGVHD occurrence with low CsA concent...

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Autores principales: Chung, Eun Kyung, Yee, Jeong, Kim, Jae Youn, Gwak, Hye Sun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7212619/
https://www.ncbi.nlm.nih.gov/pubmed/32393210
http://dx.doi.org/10.1186/s12887-020-02125-6
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author Chung, Eun Kyung
Yee, Jeong
Kim, Jae Youn
Gwak, Hye Sun
author_facet Chung, Eun Kyung
Yee, Jeong
Kim, Jae Youn
Gwak, Hye Sun
author_sort Chung, Eun Kyung
collection PubMed
description BACKGROUND: Achievement of target blood concentrations of cyclosporine (CsA) early after transplantation is known to be highly effective for reducing the incidence of acute graft versus host disease (aGVHD). However, no research has been conducted for predicting aGVHD occurrence with low CsA concentrations at different time periods. The objective of this study was to investigate the risk of aGVHD according to low CsA concentrations at lag days in children with allogenic hematopoietic stem cell transplantation (HSCT). METHODS: The records of 61 consecutive children who underwent allogeneic HSCT and received CsA as prophylaxis against aGVHD between May 2012 and March 2015 were retrospectively evaluated. The main outcome was any association between low CsA concentrations at lag days and aGVHD occurrence, which was examined for the first month after transplantation. Mean CsA concentrations at three lag periods were calculated: lag days 0–6, 7–13, and 14–20 before aGVHD occurrence. RESULTS: Patients whose mean CsA concentrations at lag days 0–6 did not reach the initial target concentration had 11.0-fold (95% confidence interval [CI]: 2.3–51.9) greater incidence of aGVHD. In addition, the AORs of low CsA concentrations at lag days 7–13 and 14–20 for developing aGVHD were 108.2 (95% CI: 7.7–1515.5) and 12.1 (95% CI: 1.1–138.1), respectively. CONCLUSIONS: After low CsA concentrations are detected, careful attention needs to be paid to prevent aGVHD.
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spelling pubmed-72126192020-05-18 Low cyclosporine concentrations in children and time to acute graft versus host disease Chung, Eun Kyung Yee, Jeong Kim, Jae Youn Gwak, Hye Sun BMC Pediatr Research Article BACKGROUND: Achievement of target blood concentrations of cyclosporine (CsA) early after transplantation is known to be highly effective for reducing the incidence of acute graft versus host disease (aGVHD). However, no research has been conducted for predicting aGVHD occurrence with low CsA concentrations at different time periods. The objective of this study was to investigate the risk of aGVHD according to low CsA concentrations at lag days in children with allogenic hematopoietic stem cell transplantation (HSCT). METHODS: The records of 61 consecutive children who underwent allogeneic HSCT and received CsA as prophylaxis against aGVHD between May 2012 and March 2015 were retrospectively evaluated. The main outcome was any association between low CsA concentrations at lag days and aGVHD occurrence, which was examined for the first month after transplantation. Mean CsA concentrations at three lag periods were calculated: lag days 0–6, 7–13, and 14–20 before aGVHD occurrence. RESULTS: Patients whose mean CsA concentrations at lag days 0–6 did not reach the initial target concentration had 11.0-fold (95% confidence interval [CI]: 2.3–51.9) greater incidence of aGVHD. In addition, the AORs of low CsA concentrations at lag days 7–13 and 14–20 for developing aGVHD were 108.2 (95% CI: 7.7–1515.5) and 12.1 (95% CI: 1.1–138.1), respectively. CONCLUSIONS: After low CsA concentrations are detected, careful attention needs to be paid to prevent aGVHD. BioMed Central 2020-05-11 /pmc/articles/PMC7212619/ /pubmed/32393210 http://dx.doi.org/10.1186/s12887-020-02125-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Chung, Eun Kyung
Yee, Jeong
Kim, Jae Youn
Gwak, Hye Sun
Low cyclosporine concentrations in children and time to acute graft versus host disease
title Low cyclosporine concentrations in children and time to acute graft versus host disease
title_full Low cyclosporine concentrations in children and time to acute graft versus host disease
title_fullStr Low cyclosporine concentrations in children and time to acute graft versus host disease
title_full_unstemmed Low cyclosporine concentrations in children and time to acute graft versus host disease
title_short Low cyclosporine concentrations in children and time to acute graft versus host disease
title_sort low cyclosporine concentrations in children and time to acute graft versus host disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7212619/
https://www.ncbi.nlm.nih.gov/pubmed/32393210
http://dx.doi.org/10.1186/s12887-020-02125-6
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