Reference Values for the Adolescent Post Version of the Postconcussion Symptom Inventory from the German General Population

Author:

Zeldovich Marina1,Krol Leonie2,Timmermann Dagmar3,Gioia Gerard4,Cunitz Katrin1,Buchheim Anna1,von Steinbuechel Nicole1

Affiliation:

1. University of Innsbruck

2. Philipps University of Marburg

3. University Medical Center Goettingen

4. Children's National Health System, George Washington University School of Medicine

Abstract

Abstract

Purpose The present study aims at providing reference values from the general pediatric population for the German version of the 21-item self-report post version of the Postconcussion Symptom Inventory for adolescents aged 13–17 years (PCSI-SR13) following pediatric traumatic brain injury (pTBI). Methods A total of N = 950 adolescents completed an adapted version of the PCSI-SR13. Prior to establishing reference values using percentiles, psychometric properties (i.e., reliability and factorial validity) and regression analyses were examined to identify factors contributing to PCSI-SR13 scores. In addition, construct assessment in the general population sample was compared to that in the pTBI sample (N = 234) using measurement invariance analyses and direct comparisons at the score levels. Results The results indicate good reliability (Cronbach’s α and McDonald’s ω of 0.97 each). The four-factor structure covering physical, emotional, cognitive, and fatigue symptom groups could be replicated with χ2(183) = 995.96, p < 0.001, χ2/df = 5.44, CFI = 0.99, TLI = 0.98, RMSEA[90% CI] = 0.068[0.064, 0.073], SRMR = 0.03. With minor restrictions, assessment of symptoms was comparable between the general population and the TBI samples. Participants in the pTBI sample reported a significantly higher symptom burden than those in the general population sample. Reference values were provided using the total sample without further stratification. Conclusions For the German post version of the PCSI-SR13, reference values are now available for direct score comparisons and for drawing conclusions about the clinical relevance of the reported symptoms, while considering the prevalence in a comparable general population without a history of pTBI. Trial registration The study is retrospectively registered in German Clinical Trials Register and in International Clinical Trials Registry Platform (ID DRKS00032854).

Publisher

Springer Science and Business Media LLC

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