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Evaluation of the safety and efficacy of low-dose rasburicase in critically ill children with haematological malignancies

Background The recommended dose of rasburicase is quite expensive, thus limiting its use. Whether a lower dose of rasburicase would be equally effective for critically ill children, who often have more complicated situations and a higher risk of hospital death, is still unknown. Objective To explore...

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Autores principales: Pei, Yuxin, Li, Yu, Liang, Yujian, Xu, Lingling, Huang, Xueqiong, Li, Yijuan, Tang, Wen, Jiang, Xiaoyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603475/
https://www.ncbi.nlm.nih.gov/pubmed/32974856
http://dx.doi.org/10.1007/s11096-020-01144-8
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author Pei, Yuxin
Li, Yu
Liang, Yujian
Xu, Lingling
Huang, Xueqiong
Li, Yijuan
Tang, Wen
Jiang, Xiaoyun
author_facet Pei, Yuxin
Li, Yu
Liang, Yujian
Xu, Lingling
Huang, Xueqiong
Li, Yijuan
Tang, Wen
Jiang, Xiaoyun
author_sort Pei, Yuxin
collection PubMed
description Background The recommended dose of rasburicase is quite expensive, thus limiting its use. Whether a lower dose of rasburicase would be equally effective for critically ill children, who often have more complicated situations and a higher risk of hospital death, is still unknown. Objective To explore the safety and efficacy of low-dose rasburicase in critically ill children with haematological malignancies who are at high risk of tumour lysis syndrome. Setting A single-centre retrospective cohort study. Method Children with haematological malignancies who had a history of rasburicase exposure during an intensive care unit stay were enrolled. Patients were divided into two groups according to the initial dosage of rasburicase: the standard-dose group (> 0.1 mg/kg/day) and the low-dose group (≤ 0.1 mg/kg/day). The adverse events and short-term prognosis of the two groups were compared. Results Thirty-seven children were selected, 22 in the standard-dose group and 15 in the low-dose group. The most common tumour type was Burkitt’s lymphoma (81%), followed by acute lymphoblastic leukaemia (11%). All patients were at high risk of tumour lysis syndrome, and 73% of them had 3 or more tumour lysis syndrome risk factors. The uric acid levels of 90% of patients with hyperuricaemia returned to the normal range within 12 h (100% in the standard-dose group and 75% in the low-dose group, P = 0.083). Eighty-four percent of patients presented serious complications, including tumour lysis syndrome (73%), acute kidney injury (59%), renal replacement treatment (24%), respiratory failure (24%), disseminated intravascular coagulation (16%) and heart failure (11%). There was no significant difference in the incidence of serious complications between the two groups. The overall 7-day and 28-day survival rates after intensive care unit admission were 86% and 84%, respectively. The average length of stay in the intensive care unit was 9.92 ± 5.13 days. Neither the short-term mortality nor the length of stay in the intensive care unit were significantly different between the two groups. Conclusion Low-dose rasburicase is effective and may be an acceptable choice for critically ill children with haematological malignancies.
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spelling pubmed-76034752020-11-10 Evaluation of the safety and efficacy of low-dose rasburicase in critically ill children with haematological malignancies Pei, Yuxin Li, Yu Liang, Yujian Xu, Lingling Huang, Xueqiong Li, Yijuan Tang, Wen Jiang, Xiaoyun Int J Clin Pharm Research Article Background The recommended dose of rasburicase is quite expensive, thus limiting its use. Whether a lower dose of rasburicase would be equally effective for critically ill children, who often have more complicated situations and a higher risk of hospital death, is still unknown. Objective To explore the safety and efficacy of low-dose rasburicase in critically ill children with haematological malignancies who are at high risk of tumour lysis syndrome. Setting A single-centre retrospective cohort study. Method Children with haematological malignancies who had a history of rasburicase exposure during an intensive care unit stay were enrolled. Patients were divided into two groups according to the initial dosage of rasburicase: the standard-dose group (> 0.1 mg/kg/day) and the low-dose group (≤ 0.1 mg/kg/day). The adverse events and short-term prognosis of the two groups were compared. Results Thirty-seven children were selected, 22 in the standard-dose group and 15 in the low-dose group. The most common tumour type was Burkitt’s lymphoma (81%), followed by acute lymphoblastic leukaemia (11%). All patients were at high risk of tumour lysis syndrome, and 73% of them had 3 or more tumour lysis syndrome risk factors. The uric acid levels of 90% of patients with hyperuricaemia returned to the normal range within 12 h (100% in the standard-dose group and 75% in the low-dose group, P = 0.083). Eighty-four percent of patients presented serious complications, including tumour lysis syndrome (73%), acute kidney injury (59%), renal replacement treatment (24%), respiratory failure (24%), disseminated intravascular coagulation (16%) and heart failure (11%). There was no significant difference in the incidence of serious complications between the two groups. The overall 7-day and 28-day survival rates after intensive care unit admission were 86% and 84%, respectively. The average length of stay in the intensive care unit was 9.92 ± 5.13 days. Neither the short-term mortality nor the length of stay in the intensive care unit were significantly different between the two groups. Conclusion Low-dose rasburicase is effective and may be an acceptable choice for critically ill children with haematological malignancies. Springer International Publishing 2020-09-24 2020 /pmc/articles/PMC7603475/ /pubmed/32974856 http://dx.doi.org/10.1007/s11096-020-01144-8 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/.
spellingShingle Research Article
Pei, Yuxin
Li, Yu
Liang, Yujian
Xu, Lingling
Huang, Xueqiong
Li, Yijuan
Tang, Wen
Jiang, Xiaoyun
Evaluation of the safety and efficacy of low-dose rasburicase in critically ill children with haematological malignancies
title Evaluation of the safety and efficacy of low-dose rasburicase in critically ill children with haematological malignancies
title_full Evaluation of the safety and efficacy of low-dose rasburicase in critically ill children with haematological malignancies
title_fullStr Evaluation of the safety and efficacy of low-dose rasburicase in critically ill children with haematological malignancies
title_full_unstemmed Evaluation of the safety and efficacy of low-dose rasburicase in critically ill children with haematological malignancies
title_short Evaluation of the safety and efficacy of low-dose rasburicase in critically ill children with haematological malignancies
title_sort evaluation of the safety and efficacy of low-dose rasburicase in critically ill children with haematological malignancies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603475/
https://www.ncbi.nlm.nih.gov/pubmed/32974856
http://dx.doi.org/10.1007/s11096-020-01144-8
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