ABBREVIATIONS
DBSDeep brain stimulation HMD Hyperkinetic movement disorders ICC Intraclass correlation coefficient QFM Quality Function Measure AIM To examine intra-and interrater reliability/agreement, and time taken to score, when the Quality Function Measure (QFM) is applied to children with hyperkinetic movement disorders (HMD; e.g. dystonia, chorea, athetosis, tremor, and myoclonus).METHOD Fifteen ambulant children with HMD participated (eight males, seven females; mean age 13y 7mo, SD 3y 7mo). Three trained raters (two physiotherapists, one occupational therapist) independently scored the QFM using videos of each child performing Gross Motor Function Measure (GMFM) Stand and Walk/Run/Jump dimensions. Reliability was evaluated using intraclass correlation coefficient (ICC) model 2.1, Standard Error of Measurement (SEM), and Bland-Altman methods.RESULTS Rater reliability was excellent for all five QFM attributes: intrarater ICCs ≥0.98 (95% confidence interval [CI] 0.83-1.00), and interrater ICCs ≥0.96 (95% CI 0.91-1.00). SEM varied from 2.07% to 4.72% points for intra-and interrater scores across QFM attributes. BlandAltman tests demonstrated close agreement between ratings, with absolute mean differences varying from 0.34% to 3.23% (intrarater) to 1.67% to 3.82% (interrater). Median scoring duration time was 83 minutes (range 56-144min, SD 16.02).INTERPRETATION Low measurement error attributable to rater effects suggests the QFM has potential as an evaluative measure in research studies involving children with HMD, though its lengthy scoring requirements are an important consideration for clinical practice. Evaluation of test-retest reliability and responsiveness is required.Hyperkinetic movement disorders (HMD) are associated with excessive involuntary movements including dystonia, chorea, athetosis, tremor, and myoclonus. 1 Such disorders are seen frequently in children with neurological conditions, being associated with dyskinetic/dystonic cerebral palsy (CP) and numerous other congenital, acquired, and neurodegenerative conditions.2 In addition to involuntary movements, paediatric movement disorders are often accompanied by multiple concomitant impairments, such as weakness and spasticity, which also contribute to disability.
1Although diverse in aetiology and clinical presentation, the different movement disorders hold in common a disturbance of central motor control that manifests in alterations of posture and movement.2 Along with restricted motor function, children may exhibit impairments in the quality of motor performance including disordered force and spatiotemporal characteristics, 3 excess movement variability, 4 postural instability, and malalignment. 5 Even in mild to moderate forms, children may have difficulty adapting their postural activity and/or motor behaviour to specific conditions or tasks.6 While the impact of these motor (and other non-motor) impairments on activity and participation has not been fully explored, children and families report diverse concerns including pain, compromi...