Sleep Measure Validation in a Pediatric Neurocritical Care Acquired Brain Injury Population.


Journal

Neurocritical care
ISSN: 1556-0961
Titre abrégé: Neurocrit Care
Pays: United States
ID NLM: 101156086

Informations de publication

Date de publication:
08 2020
Historique:
pubmed: 5 12 2019
medline: 17 8 2021
entrez: 5 12 2019
Statut: ppublish

Résumé

Lingering morbidities including physical, cognitive, emotional, and psychosocial sequelae, termed the Post-Intensive Care Syndrome, persist years after pediatric neurocritical care (PNCC) hospitalization. Sleep disturbances impact other Post-Intensive Care Syndrome domains and are under-evaluated to date due to a lack of appropriate measurement tools. The present study evaluated the validity of the Sleep Disturbance Scale for Children (SDSC) to address the growing need for assessing sleep problems after PNCC. We conducted a prospective observational study of youth aged 3-17 years with acquired brain injury (N = 69) receiving care through longitudinal PNCC programs at two tertiary academic medical centers. Parents completed the SDSC and provided proxy reports of internalizing symptoms, health-related quality of life (HRQOL), fatigue, pain behavior, and cognitive function within 3 months of hospital discharge. Evidence for the validity of the SDSC was established by utilizing the full sample for psychosocial measure comparisons and by comparing SDSC outcomes by severity (Low Risk, Mild-Moderate Risk, and High Risk defined by reported standardized T-scores). Internal consistency of the SDSC was good (α = .81). Within the full sample, increased sleep disturbances on the SDSC were significantly correlated with Post-Intensive Care Syndrome measures, including worse physical (r = .65), psychological (r = .62), and cognitive (r = - .74) sequelae. Youth in the High Risk group evidenced greater dysfunction in mental acuity, pain behavior, internalizing symptoms, and social engagement. Findings revealed both statistically and clinically significant impacts of sleep disturbances as measured by the SDSC on HRQOL. The SDSC is a valid and reliable measure for assessing sleep disturbances in children after PNCC. Results support the use of the SDSC to measure sleep disturbances after PNCC. Targeted interventions for sleep disturbances may be key to overall patient recovery.

Sections du résumé

BACKGROUND/OBJECTIVE
Lingering morbidities including physical, cognitive, emotional, and psychosocial sequelae, termed the Post-Intensive Care Syndrome, persist years after pediatric neurocritical care (PNCC) hospitalization. Sleep disturbances impact other Post-Intensive Care Syndrome domains and are under-evaluated to date due to a lack of appropriate measurement tools. The present study evaluated the validity of the Sleep Disturbance Scale for Children (SDSC) to address the growing need for assessing sleep problems after PNCC.
METHODS
We conducted a prospective observational study of youth aged 3-17 years with acquired brain injury (N = 69) receiving care through longitudinal PNCC programs at two tertiary academic medical centers. Parents completed the SDSC and provided proxy reports of internalizing symptoms, health-related quality of life (HRQOL), fatigue, pain behavior, and cognitive function within 3 months of hospital discharge. Evidence for the validity of the SDSC was established by utilizing the full sample for psychosocial measure comparisons and by comparing SDSC outcomes by severity (Low Risk, Mild-Moderate Risk, and High Risk defined by reported standardized T-scores).
RESULTS
Internal consistency of the SDSC was good (α = .81). Within the full sample, increased sleep disturbances on the SDSC were significantly correlated with Post-Intensive Care Syndrome measures, including worse physical (r = .65), psychological (r = .62), and cognitive (r = - .74) sequelae. Youth in the High Risk group evidenced greater dysfunction in mental acuity, pain behavior, internalizing symptoms, and social engagement. Findings revealed both statistically and clinically significant impacts of sleep disturbances as measured by the SDSC on HRQOL.
CONCLUSIONS
The SDSC is a valid and reliable measure for assessing sleep disturbances in children after PNCC. Results support the use of the SDSC to measure sleep disturbances after PNCC. Targeted interventions for sleep disturbances may be key to overall patient recovery.

Identifiants

pubmed: 31797275
doi: 10.1007/s12028-019-00883-5
pii: 10.1007/s12028-019-00883-5
pmc: PMC7266703
mid: NIHMS1545017
doi:

Types de publication

Journal Article Observational Study Research Support, N.I.H., Extramural Research Support, U.S. Gov't, P.H.S. Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

196-206

Subventions

Organisme : NINDS NIH HHS
ID : K23 NS099472
Pays : United States
Organisme : NHLBI NIH HHS
ID : K12 HL133115
Pays : United States
Organisme : AHRQ HHS
ID : K12 HS022981
Pays : United States

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Auteurs

Katrina M Poppert Cordts (KM)

Department of Psychiatry, University of Nebraska Medical Center, Omaha, NE, USA.
Division of Pediatric Psychology, Department of Pediatrics, Institute on Development and Disability, Oregon Health and Science University and Doernbecher Children's Hospital, Portland, OR, USA.

Trevor A Hall (TA)

Division of Pediatric Psychology, Department of Pediatrics, Institute on Development and Disability, Oregon Health and Science University and Doernbecher Children's Hospital, Portland, OR, USA.
Pediatric Critical Care and Neurotrauma Recovery Program, Oregon Health and Science University, 3181 SW Sam Jackson Park Rd, Portland, OR, 97239, USA.

Mary E Hartman (ME)

Division of Pediatric Critical Care, Department of Pediatrics, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO, USA.

Madison Luther (M)

Pediatric Critical Care and Neurotrauma Recovery Program, Oregon Health and Science University, 3181 SW Sam Jackson Park Rd, Portland, OR, 97239, USA.

Amanda Wagner (A)

Division of Pediatric Psychology, Department of Pediatrics, Institute on Development and Disability, Oregon Health and Science University and Doernbecher Children's Hospital, Portland, OR, USA.

Juan Piantino (J)

Division of Pediatric Neurology, Department of Pediatrics, Oregon Health and Science University and Doernbecher Children's Hospital, Portland, OR, USA.

Kristin P Guilliams (KP)

Division of Pediatric Critical Care, Department of Pediatrics, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO, USA.
Division of Pediatric and Developmental Neurology, Department of Neurology, Washington University School of Medicine, St Louis Children's Hospital, St. Louis, MO, USA.

Rejean M Guerriero (RM)

Division of Pediatric and Developmental Neurology, Department of Neurology, Washington University School of Medicine, St Louis Children's Hospital, St. Louis, MO, USA.

Jalane Jara (J)

Pediatric Critical Care and Neurotrauma Recovery Program, Oregon Health and Science University, 3181 SW Sam Jackson Park Rd, Portland, OR, 97239, USA.

Cydni N Williams (CN)

Pediatric Critical Care and Neurotrauma Recovery Program, Oregon Health and Science University, 3181 SW Sam Jackson Park Rd, Portland, OR, 97239, USA. willicyd@ohsu.edu.
Division of Pediatric Critical Care, Department of Pediatrics, Oregon Health and Science University and Doernbecher Children's Hospital, Portland, OR, USA. willicyd@ohsu.edu.

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