PHYSIOLOGICAL BENEFITS OF ELECTRICALLY-ASSISTED AMBULATION
IN PERSONS WITH SPINAL CORD INJURIES
Patrick L. Jacobs
Department of Neurological Surgery, and the
University
of
1600
Northwest 10th Avenue, R-48;
ABSTRACT
Clinical
investigation of Functional Electrical Stimulation (FES) in persons with spinal
cord injury (SCI) has generally concentrated on hardware and control system
issues in the attempt to increase functional outcome. Previous studies have reported deficits in
Survivors
of SCI are known to experience significant negative physiological outcomes and
higher rates of secondary disability than non-disabled peers. Exercise
opportunities following SCI are often limited to activities using intact
musculature above the lesion. Electrically stimulated cycle ergometry
is an example of
INTRODUCTION
Survivors of spinal cord injury (SCI) are faced with challenges in virtually every daily activity. Limitations in voluntary motor control and bowel/bladder control are the most obvious. However, essentially every physical system displays a level of dysfunction following interruption of normal neurological innervation. Muscle atrophy is apparent in the paralyzed limbs within weeks following traumatic SCI. Similar atrophy develops within the vascular system and results in diminished circulation throughout the affected limbs. Persons with SCI exhibit significantly slower rates of lower extremity peripheral healing and dramatically higher rates of skin ulcers. Osteoporosis is a consequence of complete SCI and results in relatively higher rates of fractures.1,2 The lifestyle of persons with SCI tends to be sedentary with a number of increased health risk factors including decreased cardiovascular fitness,3 unfavorable blood lipid profiles,4,5 increased rate of diabetes,6 and increased incidence of hypertension.7,8
It has been well established within the general population that exercise activity provides physiological benefits in deconditioned persons. Beneficial exercise activities in persons with SCI are generally limited to activities utilizing the muscles spared above the point of injury. Upper extremity exercise capacity is limited by relatively smaller size, greater peripheral resistance, and less mechanical efficiency (in comparison to leg exercise). Decreased venous return from the paralyzed limbs has been associated with decreased stroke volume and compensatory increases of heart rate at subpeak levels of arm exercise.9,10 Persons with SCI paraplegia also reach lower levels of peak power output and peak oxygen uptake (VO2peak) than matched cohorts without disability. A notable incidence of shoulder and elbow injuries (60-70%) has been reported recently in the general SCI population with even higher injury rates in the wheelchair athletic population.11,12 While regular wheelchair and arm ergometry exercise training has been demonstrated to provide training adaptations, these benefits are generally limited to the peripheral systems above the point of injury. Thus, neither the central cardiovascular, nor the peripheral systems below the injury site, are significantly affected by this type of training.
Systems
of functional electrical stimulation (
METHODS AND RESULTS
Thirty
persons with complete SCI paraplegia, injury levels ranging from T4
to T11, participated in a series of research studies over a five
year period. Testing and training procedures were explained to the subjects and
written informed consents were obtained in accordance with The University of
Miami Human Subjects Medical Sciences Subcommittee. Electrically-assisted knee extension
strengthening exercises were performed until each subject was able to stand for
three minutes. The
Exercise
Performance: The distance and time
of each walking bout was recorded and walking pace was calculated.14
Daily and weekly values of average and peak ambulation
distance, time, and pace were also calculated.
All subjects displayed a regular increase of time, distance, and pace of
Energy
Cost/Efficiency: Following the
training period, subjects participated in a peak electrically assisted
ambulation test. Subjects walked along a 10 m walkway with incrementally increased
pace from minimal to peak velocity. Metabolic activity was continually assessed
via open circuit spirometry and heart rate was
measured with direct palpation. Energy cost and energy efficiency of
Arm
Ergometry Stress Testing: A peak incremental arm ergometry
test was performed by all subjects.15 Power output was increased 10
watts per three minute work stage to the point of volitional exhaustion.
Metabolic activity was continually assessed via open circuit spirometry and heart rate was measured with a 12 lead EKG.
Pre- and post-training cardiopulmonary responses were compared a peak exertion
and at matched subpeak levels of power output. Following the 12 week
Lower Extremity Muscular Mass: Anthropometric measure were taken at seven sites including midthigh and calf as well as respective skinfold measures. Thigh cross sectional area (CSA) was calculated.14 Total volumes of each measure was calculated mathematically. Anthropometric testing revealed significant increases in thigh girth (mean=2.6cm) and calf girth (mean=1.4cm). The increased girth was calculated (with skinfolds) to relate increases in thigh CSA ranging from 20 to 25% in most subjects. A subsequent study used sequential MR images to assess thigh total CSA, muscle mass CSA of each compartment, and adipose CSA. These studies confirmed these estimates and documented increases up to 48% in the anterior thigh compartments.
Lower Extremity Circulation: Doppler ultrasound technology was used to the end diastolic CSA of the common femoral artery.16 These CSAs were taken at rest and at regular intervals following five minutes of thigh occlusion. Significant increases in CSA of the common femoral artery (25%) and arterial inflow volume (56%) were noted following training. Similar increases were documented in the pulse volume and arterial inflow volume responses to occlusion at matched time intervals.
Bone Density: Bone mineral density at the femoral head, neck, and Ward=s triangle were measured using dual-photon densitometry prior to and following the FES training.17 There were no significant effects of training noted in bone mineral density following 12 weeks of FES ambulation training.
Psychological: Two measures were used to assess possible psychological effects of participation in a FES walking program.18 The Physical Self subscale (PSS) of the Tennessee Self-Concept Scale and the Beck Depression Inventory (BDI) were utilized prior to and after the 12 week training program. Following training, significant increases were reported in the PSS and the scores on the BDI were reported to indicate significant improvements in that domain.
CONCLUSION
Generally,
the use of
REFERENCES
1) Ragnarsson KT, Sell GH. Lower extremity fractures after spinal cord injury: A retrospective study. Arch Phys Med Rehabil. 1981;62:418-423.
2)
3) Noreau AU, Shepard RJ. Spinal cord injury, exercise, and the quality of life. Sports Med. 1995;20:226-250.
4) Dearwater SR, LaPorte RE, Robertson RJ. Activity in the spinal cord injured athlete: an epidemiologic analysis of metabolic parameters. Med Sci Exerc Sport. 1986;18:541-544.
5) Bauman WA, Spunger AM. Coronary artery disease: Metabolic risk factors and latent disease in individuals with paraplegia. Mt Sinai J Med. 1992;59:163-168.
6) Duckworth WS, Solomon SS, Jallepalli P, et al. Glucose tolerance to insulin resistance in patients with spinal cord injuries. 1980;29:906-910.
7) Imai K, Kadowaki T, Aizawa Y, Fukutomi K. Morbidity rates of complications in persons with spinal cord injury secondary to site of injury and with special reference to hypertension. Paraplegia. 1994;324:246-252.
8) Yeukutiel M, Brooks ME, Ohry A, Yarom J, Carel R. The prevalence of hypertension, ischaemic heart disease and diabetes in traumatic spinal cord injured patinets amputees. Paraplegia. 1992;30:381-388.
9) Debruin Mi, Binkhorst RA. Cardiac output of paraplegics during exercise. Int J Sports Med. 1984;5:175-176.
10) VanLoan M, McCluer S, Loftin JM, Boileau RA. Comparisons of physiological responses to maximal arm exercise among able-bodied, paraplegics, and quadriplegics. Paraplegia. 1987;25:397-405.
11) Curtis
KA,
12) Goldstein B, Young J, Escobedo EM. Rotator cuff repairs in individuals with paraplegia. Am J Phys Med rehabil. 1997;76:316-322.
13) Graupe D, Kahn KH. Functional electrical stimulation for ambulation for paraplegics. Malabar, FL. Krieger; 1994.
14) Klose KJ, Jacobs PL, Broton JG, et al. Evaluation of a training program for persons with SCI paraplegia using the Parastep-1 ambulation system: Ambulation performance and anthropometric measures. Arch Phys Med Rehabil. 1997;78:789-793.
15) Jacobs PL, Nash, MS, Klose KJ, et al. Evaluation of a training program for persons with SCI paraplegia using the Parastep-1 ambulation system: Effects on physiological responses to peak arm ergometry. Arch Phys Med Rehabil. 1997;78:794-798.
16) Nash MS, Jacobs PL, Montalvo BM, et al. Evaluation of a training program for persons with SCI paraplegia using the Parastep-1 ambulation system: Lower extremity blood flow and hyperremic responses to occlusion are augted by ambulation training. Arch Phys Med Rehabil. 1997;78:808-14.
17) Needham-Shropshire BM, Broton JG, Klose KJ, et al. Evaluation of a training program for persons with SCI paraplegia using the Parastep-1 ambulation system: Lack of effect on bone density. Arch Phys Med Rehabil. 1997;78:799-803.
18) Guest, RS, Klose KJ, Needham-Shropshire BM, Jacobs PL. Evaluation of a training program for persons with SCI paraplegia using the Parastep-1 ambulation system: Effect on physical self-concept and depression. Arch Phys Med Rehabil. 1997;78:804-807.