Changes in executive function in pediatric brain tumor survivors

Objective Pediatric oncology survivors are at risk for executive function (EF) and working memory (WM) deficits, which can be measured via performance‐based measures or rating scales. Previous studies have shown these measurement methods to be weakly correlated. This study aimed to describe parent‐r...

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Bibliographic Details
Published inPediatric blood & cancer Vol. 69; no. 4; pp. e29483 - n/a
Main Authors Peterson, Rachel K., Jacobson, Lisa A.
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.04.2022
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Summary:Objective Pediatric oncology survivors are at risk for executive function (EF) and working memory (WM) deficits, which can be measured via performance‐based measures or rating scales. Previous studies have shown these measurement methods to be weakly correlated. This study aimed to describe parent‐rated EF and performance‐based WM (PBWM) in pediatric brain tumor (BT) survivors, examine change in EF and PBWM across time, and investigate the relationship between parent‐rated WM and PBWM. Method The sample included 56 patients diagnosed with a BT in childhood (Mage = 6.94 years; SD = 4.05) seen twice for clinical neuropsychological evaluation. PBWM was examined via the auditory WM scale from a Wechsler intelligence measure or Differential Ability Scales‐II. Parents completed the Behavior Rating Inventory of Executive Function (BRIEF)/BRIEF‐P/BRIEF‐2 as a measure of global EF (Global Executive Composite [GEC]), metacognitive skills (Metacognitive Index/Cognitive Regulation Index [MI/CRI]), behavioral regulation (Behavior Regulation Index [BRI]), and emotional regulation (Emotion Regulation Index [ERI]). Results GEC, MI/CRI, and ERI at Time 1 were significantly above the mean (p < .01); BRI and PBWM did not differ from the normative mean. All measures were significantly higher than the normative mean at Time 2 (p < .05). PBWM was both clinically and statistically elevated (p < .001). There was a significant change across time in PBWM (p < .05), but not GEC, MI/CRI, ERI, or BRI. PBWM was weakly correlated with the BRIEF WM subscale at Time 1 and Time 2 (all p > .05). Conclusions Multiple measures of EF should be considered when providing diagnoses and recommendations for pediatric BT survivors. Furthermore, given declines across time, findings document need for continued monitoring and reassessment of survivors as they get further out from treatment.
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ISSN:1545-5009
1545-5017
DOI:10.1002/pbc.29483