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Psychometric evaluation of the pediatric and parent-proxy Patient-Reported Outcomes Measurement Information System and the Neurology and Traumatic Brain Injury Quality of Life measurement item banks in pediatric traumatic brain injury

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Abstract

Purpose

The primary objective is to provide evidence of convergent and discriminant validity for the pediatric and parent-proxy versions of the Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety, Depression, Anger, Peer Relations, Mobility, Pain Interference, and Fatigue item banks, the Neurology Quality of Life measurement system (Neuro-QOL) Cognition-General Concerns and Stigma item banks, and the Traumatic Brain Injury Quality of Life (TBI-QOL) Executive Function and Headache item banks in a pediatric traumatic brain injury (TBI) sample.

Methods

Participants were 134 parent–child (ages 8–18 years) days. Children all sustained TBI and the dyads completed outcome ratings 6 months after injury at one of six medical centers across the United States. Ratings included PROMIS, Neuro-QOL, and TBI-QOL item banks, as well as the Pediatric Quality of Life inventory (PedsQL), the Health Behavior Inventory (HBI), and the Strengths and Difficulties Questionnaire (SDQ) as legacy criterion measures against which these item banks were validated.

Results

The PROMIS, Neuro-QOL, and TBI-QOL item banks demonstrated good convergent validity, as evidenced by moderate to strong correlations with comparable scales on the legacy measures. PROMIS, Neuro-QOL, and TBI-QOL item banks showed weaker correlations with ratings of unrelated constructs on legacy measures, providing evidence of discriminant validity.

Conclusion

Our results indicate that the constructs measured by the PROMIS, Neuro-QOL, and TBI-QOL item banks are valid in our pediatric TBI sample and that it is appropriate to use these standardized scores for our primary study analyses.

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Abbreviations

CAT:

Computer Adaptive Test

CDC:

Centers for Disease Control and Prevention

GCS:

Glasgow Coma Scale

HRQOL:

Health-related quality of life

IRB:

Institutional Review Board

IRT:

Item response theory

NEURO-QOL:

Neurology Quality of Life (measurement system)

PedsQL:

Pediatric Quality of Life (outcome measure)

PRO:

Patient-reported outcomes

PROMIS:

Patient-Reported Outcomes Measurement Information System

SF:

Short form

TBI:

Traumatic brain injury

TBI-QOL:

Traumatic Brain Injury Quality of Life

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Acknowledgements

This project was funded by the United States Centers for Disease Control and Prevention, Grant Number U01CE002196. The authors would like to thank Marni Levy and Natalie Jenkins for their dedicated efforts in acquiring the data described in this manuscript.

Author contributions

All the authors contributed significantly to the design, analysis, and writing of this manuscript. The contents represent the original work and have not been published elsewhere.

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Correspondence to Hilary Bertisch.

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Conflict of interest

This study was funded by the Centers for Disease Control and Prevention (Grant Number U01CE002196). The authors have no financial disclosures related to this project. Dr. David Tulsky serves on the board of the PROMIS Health Organization but does not receive compensation or royalties related to this role. No commercial party having a direct financial interest in the results of the research supporting this article has or will confer a benefit upon the authors or upon any organization with which the authors are associated.

Ethical approval

Institutional Review Board (IRB) approval was attained at each of the local recruitment sites [University of Washington (Harborview Medical Center/Seattle Children’s Hospital), Nationwide Children’s Hospital, The Children’s Hospital of Philadelphia, University of Pittsburgh Medical Center’s Children’s Hospital of Pittsburgh, Children’s Healthcare of Atlanta, and Texas Children’s Hospital] and at NYU School of Medicine prior to study initiation. Parental consent and child assent (for those who were younger than age 18 at recruitment) were attained from all individual participants included at each local recruitment site prior to enrollment. Children who turned 18 during the course of this study provided informed consent as adults prior to further participation in study procedures.

Research involving human and animal rights

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Informed consent/assent was obtained from all individuals included in the study.

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Bertisch, H., Rivara, F.P., Kisala, P.A. et al. Psychometric evaluation of the pediatric and parent-proxy Patient-Reported Outcomes Measurement Information System and the Neurology and Traumatic Brain Injury Quality of Life measurement item banks in pediatric traumatic brain injury. Qual Life Res 26, 1887–1899 (2017). https://doi.org/10.1007/s11136-017-1524-6

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  • DOI: https://doi.org/10.1007/s11136-017-1524-6

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