Abstract:The differences in acceleration possibly account for the different muscle responses, which may suggest acceleration, rather than velocity-dependency of the stretch reflex. Future prototypes of instrumented spasticity assessments should standardize movement profiles, preferably by developing profiles that mimic functional tasks such as walking.
“…Instrumented spasticity assessment was carried out using a motor‐driven footplate (MOOG, Nieuw‐Vennep, The Netherlands) . The patient was seated in an adjustable chair with the right foot fixed onto a custom designed adjustable footplate (Figure C).…”
Section: Investigationsmentioning
confidence: 99%
“…Instrumented spasticity assessment was carried out using a motor-driven footplate (MOOG, Nieuw-Vennep, The Netherlands). 11,18 The patient was seated in an adjustable chair with the right foot fixed onto a custom designed adjustable footplate 15,19 ( Figure 1C). This footplate allowed adjustments targeted to fix the talocalcaneal joint during foot plate rotations (for details see Huijing et al 15 ) The motor-driven footplate applied two slow (15°/s) and two fast (150°/s) speed controlled dorsiflexion movements over the patient's maximum ankle ROM (determined manually).…”
Comprehensive instrumented muscle and joint assessments should be considered when prescribing Botulinum NeuroToxin‐A (BoNT‐A) treatment in spastic paresis. In a child with spastic paresis, comprehensive evaluation following treatment with BoNT‐A, serial casting, and physiotherapy showed that short‐term improvements in gait occurred without changes in muscle morphology. Rather, foot flexibility increased.
“…Instrumented spasticity assessment was carried out using a motor‐driven footplate (MOOG, Nieuw‐Vennep, The Netherlands) . The patient was seated in an adjustable chair with the right foot fixed onto a custom designed adjustable footplate (Figure C).…”
Section: Investigationsmentioning
confidence: 99%
“…Instrumented spasticity assessment was carried out using a motor-driven footplate (MOOG, Nieuw-Vennep, The Netherlands). 11,18 The patient was seated in an adjustable chair with the right foot fixed onto a custom designed adjustable footplate 15,19 ( Figure 1C). This footplate allowed adjustments targeted to fix the talocalcaneal joint during foot plate rotations (for details see Huijing et al 15 ) The motor-driven footplate applied two slow (15°/s) and two fast (150°/s) speed controlled dorsiflexion movements over the patient's maximum ankle ROM (determined manually).…”
Comprehensive instrumented muscle and joint assessments should be considered when prescribing Botulinum NeuroToxin‐A (BoNT‐A) treatment in spastic paresis. In a child with spastic paresis, comprehensive evaluation following treatment with BoNT‐A, serial casting, and physiotherapy showed that short‐term improvements in gait occurred without changes in muscle morphology. Rather, foot flexibility increased.
“…This type of musculoskeletal modeling combined with spasticity measurement may allow for individually tailored spasticity treatments. Further, investigation of fast and slow passive rotations imposed during manual and motorized assessments may yield greater insights into the development of movement profiles to better mimic spasticity imposed during functional tasks such as walking (Sloot et al, 2016). …”
Section: Neuromuscular Deficits Of Cerebral Palsymentioning
Cerebral palsy (CP) is the most common movement disorder in children. A diagnosis of CP is often made based on abnormal muscle tone or posture, a delay in reaching motor milestones, or the presence of gait abnormalities in young children. Neuroimaging of high-risk neonates and of children diagnosed with CP have identified patterns of neurologic injury associated with CP, however, the neural underpinnings of common gait abnormalities remain largely uncharacterized. Here, we review the nature of the brain injury in CP, as well as the neuromuscular deficits and subsequent gait abnormalities common among children with CP. We first discuss brain injury in terms of mechanism, pattern, and time of injury during the prenatal, perinatal, or postnatal period in preterm and term-born children. Second, we outline neuromuscular deficits of CP with a focus on spastic CP, characterized by muscle weakness, shortened muscle-tendon unit, spasticity, and impaired selective motor control, on both a microscopic and functional level. Third, we examine the influence of neuromuscular deficits on gait abnormalities in CP, while considering emerging information on neural correlates of gait abnormalities and the implications for strategic treatment. This review of the neural basis of gait abnormalities in CP discusses what is known about links between the location and extent of brain injury and the type and severity of CP, in relation to the associated neuromuscular deficits, and subsequent gait abnormalities. Targeted treatment opportunities are identified that may improve functional outcomes for children with CP. By providing this context on the neural basis of gait abnormalities in CP, we hope to highlight areas of further research that can reduce the long-term, debilitating effects of CP.
“…Sloot 18 reported a battery of manual instrumentation-based tests, including measurements of joint velocity, imposed force, and muscle activity, used to objectively measure spasticity in CP. 18 The authors of that study verified that the measurements matched the subjects' gait profiles. Furthermore, Russian investigators have reported the use of an ultrasonographic technique to objectively evaluate the degree of muscle degeneration related to spasticity.…”
Section: Which Was Developed Bymentioning
confidence: 62%
“…It is also invasive and may be resisted by some children. Sloot reported a battery of manual instrumentation‐based tests, including measurements of joint velocity, imposed force, and muscle activity, used to objectively measure spasticity in CP . The authors of that study verified that the measurements matched the subjects’ gait profiles.…”
Pediatric movement disorders (PMDs) are common and have recently received increasing attention. As these disorders have special clinical features, the selection of appropriate behavioral assessment tools that can clearly distinguish movement disorders from other diseases (eg, epilepsy and neuromuscular disorders) is crucial for achieving an accurate diagnosis and treatment. However, few studies have focused on behavioral assessments in children. The present report attempts to provide a critical review of the available subjective and objective assessment tests for common PMDs. We believe that the principles of objectification, multi-purpose use, and simplification are also applicable to the selection and development of satisfactory pediatric behavioral assessment tools. We expect that the development of wearable sensors, virtual reality, and augmented reality will lead to the establishment of more reliable and simple tests. In addition, more rigorous randomized controlled trials that have been specifically designed to evaluate behavioral testing in children are also expected in the future.
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