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Volume 1, Issue 7, Pages 604-611 (July 2009)


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Spatiotemporal and Kinematic Effect of Peroneal Nerve Stimulation Versus an Ankle-Foot Orthosis in Patients With Multiple Sclerosis: A Case Series

A portion of this material was presented in poster format at the Neural Interfaces Workshop, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, August 21 to 23, 2006.

Lynne R. Sheffler, MDaCorresponding Author Informationemail address, Stephanie Nogan Bailey, BSEb, John Chae, MDc

Received 17 November 2008; accepted 8 April 2009.

Objective

To compare the effect of a surface peroneal nerve stimulator (PNS) versus an ankle-foot orthosis (AFO) on spatiotemporal and kinematic parameters of gait in patients with multiple sclerosis.

Design

This was a case series design.

Participants

Four subjects with multiple sclerosis and dorsiflexion weakness.

Intervention

Quantitative gait analysis with the use of (1) no device, (2) AFO, and (3) PNS as a single point-in-time assessment.

Outcome Measures

Included walking speed, stride length, cadence, and double support time; kinematic parameters included peak pelvic obliquity during swing, peak contralateral hip abduction during stance, peak knee flexion and hip flexion during swing, ankle dorsiflexion at initial contact, and peak ankle internal rotation during swing.

Results

One-way analysis of variance was used to compare intrasubject performance under the 3 device conditions. The PNS significantly increased ankle dorsiflexion angle at initial contact, as compared with both no device and the AFO, in 3 of the 4 subjects. However, other spatiotemporal and kinematic gait parameters were more variably affected by the device conditions.

Conclusions

With the exception of ankle dorsiflexion angle at initial contact, PNS and AFO have a variable effect on spatiotemporal and kinematic gait parameters in individual subjects with multiple sclerosis. Further studies are indicated to determine the clinical significance of intrasubject differences between device conditions.

a Departments of Physical Medicine and Rehabilitation, Cleveland Functional Electrical Stimulation Center; and Department of Physical Medicine and Rehabilitation, MetroHealth Medical Center, 2500 MetroHealth Drive S1-107A, Cleveland, OH 44109

b Departments of Physical Medicine and Rehabilitation, Cleveland Functional Electrical Stimulation Center; and Department of Research, Louis Stokes Veterans Affairs Medical Center, Cleveland, OH

c Departments of Physical Medicine and Rehabilitation, Cleveland Functional Electrical Stimulation Center; Department of Physical Medicine and Rehabilitation, MetroHealth Medical Center; and Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH§

Corresponding Author InformationAddress correspondence to: L.R.S.

 Disclosure Key can be found on the Table of Contents and at www.pmrjournal.org

 Disclosure: 8A, supported by the Neurostimulation and Neuromodulation Partnership, Ohio Board of Regents, BRTT03-005.

 Disclosure: nothing to disclose

§ Disclosure: 8B, BRTT State of Ohio grant

PII: S1934-1482(09)00394-3

doi:10.1016/j.pmrj.2009.04.002


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