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Unraveling Dexamethasone-Induced Neurobehavioral and Sleep Problems in Children With ALL: Which Determinants Are Important?

PURPOSE: Dexamethasone, the preferred corticosteroid in most treatment protocols for pediatric acute lymphoblastic leukemia (ALL), can induce undesirable side effects. Neurobehavioral and sleep problems are frequently reported, but the interpatient variability is high. We therefore aimed to identify...

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Autores principales: van Hulst, Annelienke M., Grootenhuis, Martha A., Verwaaijen, Emma J., van Litsenburg, Raphaële R.L., Li, Letao, van Zelst, Bertrand D., Broer, Linda, Pluijm, Saskia M.F., Pieters, Rob, Fiocco, Marta, van den Akker, Erica L.T., van den Heuvel-Eibrink, Marry M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10309531/
https://www.ncbi.nlm.nih.gov/pubmed/37343203
http://dx.doi.org/10.1200/PO.22.00678
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author van Hulst, Annelienke M.
Grootenhuis, Martha A.
Verwaaijen, Emma J.
van Litsenburg, Raphaële R.L.
Li, Letao
van Zelst, Bertrand D.
Broer, Linda
Pluijm, Saskia M.F.
Pieters, Rob
Fiocco, Marta
van den Akker, Erica L.T.
van den Heuvel-Eibrink, Marry M.
author_facet van Hulst, Annelienke M.
Grootenhuis, Martha A.
Verwaaijen, Emma J.
van Litsenburg, Raphaële R.L.
Li, Letao
van Zelst, Bertrand D.
Broer, Linda
Pluijm, Saskia M.F.
Pieters, Rob
Fiocco, Marta
van den Akker, Erica L.T.
van den Heuvel-Eibrink, Marry M.
author_sort van Hulst, Annelienke M.
collection PubMed
description PURPOSE: Dexamethasone, the preferred corticosteroid in most treatment protocols for pediatric acute lymphoblastic leukemia (ALL), can induce undesirable side effects. Neurobehavioral and sleep problems are frequently reported, but the interpatient variability is high. We therefore aimed to identify determinants for parent-reported dexamethasone-induced neurobehavioral and sleep problems in pediatric ALL. METHODS: Our prospective study included patients with medium-risk ALL and their parents during maintenance treatment. Patients were assessed before and after one 5-day dexamethasone course. Primary end points were parent-reported dexamethasone-induced neurobehavioral and sleep problems, measured with the Strengths and Difficulties Questionnaire and Sleep Disturbance Scale for Children, respectively. Analyzed determinants included patient and parent demographics, disease and treatment characteristics, parenting stress (Parenting Stress Index and Distress Thermometer for Parents), dexamethasone pharmacokinetics, and genetic variation (candidate single-nucleotide polymorphisms rs41423247 and rs4918). Statistically significant determinants identified in univariable logistic regression analyses were incorporated in a multivariable model. RESULTS: We included 105 patients: median age was 5.4 years (range, 3.0-18.8) and 61% were boys. Clinically relevant dexamethasone-induced neurobehavioral and sleep problems were reported by parents in 70 (67%) and 61 (59%) patients, respectively. In our multivariable regression models, we identified parenting stress as a significant determinant for parent-reported neurobehavioral (odds ratio [OR], 1.16; 95% CI, 1.07 to 1.26) and sleep problems (OR, 1.06; 95% CI, 1.02 to 1.10). Furthermore, parents who experienced more stress before start of a dexamethasone course reported more sleep problems in their child (OR, 1.16; 95% CI, 1.02 to 1.32). CONCLUSION: We identified parenting stress, and not dexamethasone pharmacokinetics, genetic variation, patient/parent demographics, or disease/treatment characteristics, as a significant determinant for parent-reported dexamethasone-induced neurobehavioral and sleep problems. Parenting stress may be a modifiable target to reduce these problems.
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spelling pubmed-103095312023-06-30 Unraveling Dexamethasone-Induced Neurobehavioral and Sleep Problems in Children With ALL: Which Determinants Are Important? van Hulst, Annelienke M. Grootenhuis, Martha A. Verwaaijen, Emma J. van Litsenburg, Raphaële R.L. Li, Letao van Zelst, Bertrand D. Broer, Linda Pluijm, Saskia M.F. Pieters, Rob Fiocco, Marta van den Akker, Erica L.T. van den Heuvel-Eibrink, Marry M. JCO Precis Oncol ORIGINAL REPORTS PURPOSE: Dexamethasone, the preferred corticosteroid in most treatment protocols for pediatric acute lymphoblastic leukemia (ALL), can induce undesirable side effects. Neurobehavioral and sleep problems are frequently reported, but the interpatient variability is high. We therefore aimed to identify determinants for parent-reported dexamethasone-induced neurobehavioral and sleep problems in pediatric ALL. METHODS: Our prospective study included patients with medium-risk ALL and their parents during maintenance treatment. Patients were assessed before and after one 5-day dexamethasone course. Primary end points were parent-reported dexamethasone-induced neurobehavioral and sleep problems, measured with the Strengths and Difficulties Questionnaire and Sleep Disturbance Scale for Children, respectively. Analyzed determinants included patient and parent demographics, disease and treatment characteristics, parenting stress (Parenting Stress Index and Distress Thermometer for Parents), dexamethasone pharmacokinetics, and genetic variation (candidate single-nucleotide polymorphisms rs41423247 and rs4918). Statistically significant determinants identified in univariable logistic regression analyses were incorporated in a multivariable model. RESULTS: We included 105 patients: median age was 5.4 years (range, 3.0-18.8) and 61% were boys. Clinically relevant dexamethasone-induced neurobehavioral and sleep problems were reported by parents in 70 (67%) and 61 (59%) patients, respectively. In our multivariable regression models, we identified parenting stress as a significant determinant for parent-reported neurobehavioral (odds ratio [OR], 1.16; 95% CI, 1.07 to 1.26) and sleep problems (OR, 1.06; 95% CI, 1.02 to 1.10). Furthermore, parents who experienced more stress before start of a dexamethasone course reported more sleep problems in their child (OR, 1.16; 95% CI, 1.02 to 1.32). CONCLUSION: We identified parenting stress, and not dexamethasone pharmacokinetics, genetic variation, patient/parent demographics, or disease/treatment characteristics, as a significant determinant for parent-reported dexamethasone-induced neurobehavioral and sleep problems. Parenting stress may be a modifiable target to reduce these problems. Wolters Kluwer Health 2023-06-21 /pmc/articles/PMC10309531/ /pubmed/37343203 http://dx.doi.org/10.1200/PO.22.00678 Text en © 2023 by American Society of Clinical Oncology https://creativecommons.org/licenses/by-nc-nd/4.0/Creative Commons Attribution Non-Commercial No Derivatives 4.0 License: http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle ORIGINAL REPORTS
van Hulst, Annelienke M.
Grootenhuis, Martha A.
Verwaaijen, Emma J.
van Litsenburg, Raphaële R.L.
Li, Letao
van Zelst, Bertrand D.
Broer, Linda
Pluijm, Saskia M.F.
Pieters, Rob
Fiocco, Marta
van den Akker, Erica L.T.
van den Heuvel-Eibrink, Marry M.
Unraveling Dexamethasone-Induced Neurobehavioral and Sleep Problems in Children With ALL: Which Determinants Are Important?
title Unraveling Dexamethasone-Induced Neurobehavioral and Sleep Problems in Children With ALL: Which Determinants Are Important?
title_full Unraveling Dexamethasone-Induced Neurobehavioral and Sleep Problems in Children With ALL: Which Determinants Are Important?
title_fullStr Unraveling Dexamethasone-Induced Neurobehavioral and Sleep Problems in Children With ALL: Which Determinants Are Important?
title_full_unstemmed Unraveling Dexamethasone-Induced Neurobehavioral and Sleep Problems in Children With ALL: Which Determinants Are Important?
title_short Unraveling Dexamethasone-Induced Neurobehavioral and Sleep Problems in Children With ALL: Which Determinants Are Important?
title_sort unraveling dexamethasone-induced neurobehavioral and sleep problems in children with all: which determinants are important?
topic ORIGINAL REPORTS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10309531/
https://www.ncbi.nlm.nih.gov/pubmed/37343203
http://dx.doi.org/10.1200/PO.22.00678
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