Dynamic Knee-Ankle-Foot-Orthosis (KAFO) with power assist/ressist motion
©STUDIO CATERIN
Dynamic Knee-Ankle-Foot-Orthosis (KAFO) with power assist/ressist motion
©STUDIO CATERIN
Dynamic Knee-Ankle-Foot-Orthosis (KAFO) with power assist/ressist motion
©STUDIO CATERIN
©STUDIO CATERIN

Detailed description

This proprietary technology has been developed through a Cooperative Research and Development Afreement with the National Institutes of Health (NIH, Bethesda, USA).

The SpryStep® Agilik™ KAFO is intended for patients with lower extremity weakness resulting in gait pathology such as, but not limited to crouch gait from a diagnosis of cerebral pals y, muscular dystrophy, spina bifida, incomplete spinal cord
injury or stroke hemiparesis. It is intended for patients aged 5 years and above, who can understand and follow simple directions based on a parental report and physician observations during recent history and physical examination, and able
to walk at least 3m (10 feet) without stopping with or without a walking aid. It is the responsibility of the therapist/clinician to determine if the patient is physically and cognitively able to use and understand the product.

As it is a smart system, there is a real-time gait phase detection which drives the assistance. Thuasne® trains a member of the patient's clinical team (normally either their orthotist or physical therapist) to tune the SpryStep® Agilik™ KAFO using this app. 

A test-unit is available for patient assessments and demonstrations. Super lightweight, the Test Drive comes with multiple sizes of thigh cuffs and footplates to fit a range of 127-185cm (4'2'' to 6'1'') tall (arrangements can be made for shorter or taller ranges). 

With test drive and definitive SpryStep® Agilik™ KAFO it can be seen the following potential patient improvements:
- on gait biomechanics: increased step length1, improved knee extension during stance and swing gait phases2, improved knee flexion during swing phase.
- on ambulation abilities: increased walking distance and speed1-6, improved functional mobility, reduced energy costs5, aid with balance and coordination6, may reduce the need for wheelcair use 
- on long-term patient implications: may reduce fatigue6 and joint deterioration7, may reduce progression of muscle contractures8, may increase patient time in physical therapy. 

Contact a Thuasne - SpryStep® Agilik™ KAFO specialist
Order form available here

1. Hachisuka, K. et al. 2007 ‘Oxygen consumption, oxygen cost and physiological cost index in polio survivors: A comparison of walking without orthosis, with an ordinary or a carbon fibre reinforced plastic knee ankle-foot orthosis’, Journal of Rehabilitation Medicine, 39(8), pp. 646 650. doi : 10.2340/16501977 0105..
2. Zachary F. Lerner et al. ,A lower-extremity exoskeleton improves knee extension in children with crouch gait from cerebral palsy.Sci. Transl. Med.9,eaam9145(2017).DOI:10.1126/scitranslmed.aam9145.
3. IEEE Transactions on Neural Systems and Rehabilitation Engineering, vol. 31, pp. 3265-3274, 2023, doi: 10.1109/TNSRE.2023.3303777..
4. Steinfeldt F, Seifert W, Gunther KP. ‘Modern carbon Fibre orthoses in the management of polio patients a critical evaluation of the functional aspects.’ Z Orthop Ihre Grenzgeb 2003; 141:357 361.
5. Brehm, M. A. et al. 2007 ‘Effect of carbon composite knee ankle-foot orthoses on walking efÏciency and gait in former polio patients’, Journal of Rehabilitation Medicine, 39(8), pp. 651 657.
6. Arazpour M, Moradi A, Samadian M, et al. The influence of a powered knee–ankle–foot orthosis on walking in poliomyelitis subjects: A pilot study. Prosthetics and Orthotics International. 2015;40(3):377-383. doi:10.1177/0309364615592703.
7. Steele, K. M., DeMers, M. S., Schwartz, M. H., & Delp, S. L. (2012). Compressive tibiofemoral force during crouch gait. Gait & posture, 35(4), 556-560.
8. Miccinilli, S.; Santacaterina, F.; Della Rocca, R.; Sterzi, S.; Bressi, F.; Bravi, M. Efficacy of Lower Limb Orthoses in the Rehabilitation of Children Affected by Cerebral Palsy: A Systematic Review. Children 2024, 11, 212. https://doi.org/10.3390/children11020212.

Patient profile

  • NeurologicalNeurological

Specifications

  • The product is intended for patients with lower extremity weakness resulting in gait pathology such as, but not limited to crouch gait from a diagnosis of cerebral palsy, muscular dystrophy, spina bifida, or incomplete spinal cord injury or post stroke hemiparesis.

  • Do not use the product if the diagnosis has not been confirmed.
    Do not apply the product in direct contact with broken skin.
    Do not use in the event of known allergy to any of the components.
    Do not use for patients weighing < 20 kg / 44 lbs and > 135 kg / 300 lbs.
    Open ulcers of the foot, ankle or lower leg.
    Severe loss of sensation in the lower limb.
    Running/jumping/high impact activities on lower limb.
    Orthoprosthesis.
    Moderate to severe foot deformities (including fixed ankle varus or valgus conditions).
    Flexion contracture of more than 20° in the knee and/or hip joint.
    Unability to initiate swing phase.
    Children below the age of 5 years.
    Moderate to severe spasticity of the foot and ankle (as determined by the clinician).

  • Rigid components: carbon fibre - glass fibre - high density polyethylene - ethylene propylene diene monomer - stainless steel.
    Textile components: polyamide - elastane - polyurethane - ethylene vinyl acetate.

Instructions for use

The version of the manual available online is the current version.
Depending on the date of manufacture and place of purchase of the product, this original version of the manual may differ from the version physically present with the product.

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