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Prescription Psychoactive Medication Use in Adolescent Survivors of Childhood Cancer and Association With Adult Functional Outcomes

BACKGROUND: This study estimates the prevalence and identifies predictors of psychoactive medication use in adolescent survivors of childhood cancer (aged 12-18 years) and its associations with functional outcomes at young adulthood (aged 18-28 years). METHODS: This retrospective cohort study includ...

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Autores principales: Cheung, Yin Ting, Liu, Wei, Brinkman, Tara M, Srivastava, Deokumar, Leisenring, Wendy M, Howell, Rebecca M, Ullrich, Nicole J, Lommel, Karen M, Brouwers, Pim, Gibson, Todd M, Robison, Leslie L, Armstrong, Gregory T, Krull, Kevin R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583158/
https://www.ncbi.nlm.nih.gov/pubmed/33134833
http://dx.doi.org/10.1093/jncics/pkaa057
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author Cheung, Yin Ting
Liu, Wei
Brinkman, Tara M
Srivastava, Deokumar
Leisenring, Wendy M
Howell, Rebecca M
Ullrich, Nicole J
Lommel, Karen M
Brouwers, Pim
Gibson, Todd M
Robison, Leslie L
Armstrong, Gregory T
Krull, Kevin R
author_facet Cheung, Yin Ting
Liu, Wei
Brinkman, Tara M
Srivastava, Deokumar
Leisenring, Wendy M
Howell, Rebecca M
Ullrich, Nicole J
Lommel, Karen M
Brouwers, Pim
Gibson, Todd M
Robison, Leslie L
Armstrong, Gregory T
Krull, Kevin R
author_sort Cheung, Yin Ting
collection PubMed
description BACKGROUND: This study estimates the prevalence and identifies predictors of psychoactive medication use in adolescent survivors of childhood cancer (aged 12-18 years) and its associations with functional outcomes at young adulthood (aged 18-28 years). METHODS: This retrospective cohort study includes 5665 adolescent survivors of childhood cancer at no less than 5 years postdiagnosis (53.8% male, median age = 15 years, interquartile range [IQR] = 13-16 years) and 921 adolescent sibling controls. Parent-reported psychoactive medication use during adolescence was collected at baseline. After a median of 8 years, functional outcomes and social attainment were self-reported during adulthood (n = 3114, median age = 22 years, IQR = 20-24 years). Multivariable log-binomial models evaluated associations among risk factors, medication use, and adult outcomes. RESULTS: Higher prevalence of psychoactive medication use was reported in survivors compared with siblings (18.3% vs 6.6%; 2-sided P < .001), with trends for increasing antidepressant and stimulant use in recent treatment eras. After adjusting for cancer treatment and baseline cognitive problems, psychoactive medication use during adolescence was associated with impaired task efficiency (relative risk [RR] = 1.20, 95% confidence interval [CI] = 1.01 to 1.43) and memory (RR = 1.27, 95% CI = 1.05 to 1.52) during adulthood. Survivors who reported continued use of medications from adolescence to adulthood demonstrated poorer emotional regulation (RR = 1.68, 95% CI = 1.24 to 2.27) and organization (RR = 1.82, 95% CI = 1.28 to 2.59) compared with nonusers. Adolescent opioid use was associated with somatization symptoms (RR = 1.72, 95% CI = 1.09 to 2.73) during adulthood, after adjusting for cancer treatment and baseline behavioral problems. They were also more likely to not complete college (RR = 1.21, 95% CI = 1.04 to 1.41) or work full-time (RR = 1.60, 95% CI = 1.23 to 2.08) compared with nonusers. CONCLUSION: Use of psychoactive medication is more prevalent among adolescent survivors compared with siblings and does not normalize adult outcomes, as evidenced by poorer functional outcomes during young adulthood.
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spelling pubmed-75831582020-10-29 Prescription Psychoactive Medication Use in Adolescent Survivors of Childhood Cancer and Association With Adult Functional Outcomes Cheung, Yin Ting Liu, Wei Brinkman, Tara M Srivastava, Deokumar Leisenring, Wendy M Howell, Rebecca M Ullrich, Nicole J Lommel, Karen M Brouwers, Pim Gibson, Todd M Robison, Leslie L Armstrong, Gregory T Krull, Kevin R JNCI Cancer Spectr Article BACKGROUND: This study estimates the prevalence and identifies predictors of psychoactive medication use in adolescent survivors of childhood cancer (aged 12-18 years) and its associations with functional outcomes at young adulthood (aged 18-28 years). METHODS: This retrospective cohort study includes 5665 adolescent survivors of childhood cancer at no less than 5 years postdiagnosis (53.8% male, median age = 15 years, interquartile range [IQR] = 13-16 years) and 921 adolescent sibling controls. Parent-reported psychoactive medication use during adolescence was collected at baseline. After a median of 8 years, functional outcomes and social attainment were self-reported during adulthood (n = 3114, median age = 22 years, IQR = 20-24 years). Multivariable log-binomial models evaluated associations among risk factors, medication use, and adult outcomes. RESULTS: Higher prevalence of psychoactive medication use was reported in survivors compared with siblings (18.3% vs 6.6%; 2-sided P < .001), with trends for increasing antidepressant and stimulant use in recent treatment eras. After adjusting for cancer treatment and baseline cognitive problems, psychoactive medication use during adolescence was associated with impaired task efficiency (relative risk [RR] = 1.20, 95% confidence interval [CI] = 1.01 to 1.43) and memory (RR = 1.27, 95% CI = 1.05 to 1.52) during adulthood. Survivors who reported continued use of medications from adolescence to adulthood demonstrated poorer emotional regulation (RR = 1.68, 95% CI = 1.24 to 2.27) and organization (RR = 1.82, 95% CI = 1.28 to 2.59) compared with nonusers. Adolescent opioid use was associated with somatization symptoms (RR = 1.72, 95% CI = 1.09 to 2.73) during adulthood, after adjusting for cancer treatment and baseline behavioral problems. They were also more likely to not complete college (RR = 1.21, 95% CI = 1.04 to 1.41) or work full-time (RR = 1.60, 95% CI = 1.23 to 2.08) compared with nonusers. CONCLUSION: Use of psychoactive medication is more prevalent among adolescent survivors compared with siblings and does not normalize adult outcomes, as evidenced by poorer functional outcomes during young adulthood. Oxford University Press 2020-06-29 /pmc/articles/PMC7583158/ /pubmed/33134833 http://dx.doi.org/10.1093/jncics/pkaa057 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Article
Cheung, Yin Ting
Liu, Wei
Brinkman, Tara M
Srivastava, Deokumar
Leisenring, Wendy M
Howell, Rebecca M
Ullrich, Nicole J
Lommel, Karen M
Brouwers, Pim
Gibson, Todd M
Robison, Leslie L
Armstrong, Gregory T
Krull, Kevin R
Prescription Psychoactive Medication Use in Adolescent Survivors of Childhood Cancer and Association With Adult Functional Outcomes
title Prescription Psychoactive Medication Use in Adolescent Survivors of Childhood Cancer and Association With Adult Functional Outcomes
title_full Prescription Psychoactive Medication Use in Adolescent Survivors of Childhood Cancer and Association With Adult Functional Outcomes
title_fullStr Prescription Psychoactive Medication Use in Adolescent Survivors of Childhood Cancer and Association With Adult Functional Outcomes
title_full_unstemmed Prescription Psychoactive Medication Use in Adolescent Survivors of Childhood Cancer and Association With Adult Functional Outcomes
title_short Prescription Psychoactive Medication Use in Adolescent Survivors of Childhood Cancer and Association With Adult Functional Outcomes
title_sort prescription psychoactive medication use in adolescent survivors of childhood cancer and association with adult functional outcomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583158/
https://www.ncbi.nlm.nih.gov/pubmed/33134833
http://dx.doi.org/10.1093/jncics/pkaa057
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