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In This Article

  • Summary
  • Abstract
  • Protocol
  • Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

The purpose of this publication is to present our original work on a multi-muscle surface electromyographic approach to quantitatively characterize respiratory muscle activation patterns in individuals with chronic spinal cord injury using vector-based analysis.

Abstract

During breathing, activation of respiratory muscles is coordinated by integrated input from the brain, brainstem, and spinal cord. When this coordination is disrupted by spinal cord injury (SCI), control of respiratory muscles innervated below the injury level is compromised1,2 leading to respiratory muscle dysfunction and pulmonary complications. These conditions are among the leading causes of death in patients with SCI3. Standard pulmonary function tests that assess respiratory motor function include spirometrical and maximum airway pressure outcomes: Forced Vital Capacity (FVC), Forced Expiratory Volume in one second (FEV1), Maximal Inspiratory Pressure (PImax) and Maximal Expiratory Pressure (PEmax)4,5. These values provide indirect measurements of respiratory muscle performance6. In clinical practice and research, a surface electromyography (sEMG) recorded from respiratory muscles can be used to assess respiratory motor function and help to diagnose neuromuscular pathology. However, variability in the sEMG amplitude inhibits efforts to develop objective and direct measures of respiratory motor function6. Based on a multi-muscle sEMG approach to characterize motor control of limb muscles7, known as the voluntary response index (VRI)8, we developed an analytical tool to characterize respiratory motor control directly from sEMG data recorded from multiple respiratory muscles during the voluntary respiratory tasks. We have termed this the Respiratory Motor Control Assessment (RMCA)9. This vector analysis method quantifies the amount and distribution of activity across muscles and presents it in the form of an index that relates the degree to which sEMG output within a test-subject resembles that from a group of healthy (non-injured) controls. The resulting index value has been shown to have high face validity, sensitivity and specificity9-11. We showed previously9 that the RMCA outcomes significantly correlate with levels of SCI and pulmonary function measures. We are presenting here the method to quantitatively compare post-spinal cord injury respiratory multi-muscle activation patterns to those of healthy individuals.

Protocol

1. Settings

  1. Surface electrode heads were placed over the muscle bellies of left (L) and right (R) respiratory muscles: sternocleidomastoid (SC), scalene (S), upper trapezius on midclavicular line (UT), clavicular portion of pectoralis on midclavicular line (P), diaphragm on parasternal line (D), intercostal at 6th intercostal space on anterior axillary line (IC), rectus abdominus at umbilical level (RA), obliquus abdominis on midaxillary line (O), lower trapezius paraspinally at midscapular level (LT), and paraspinal paraspinally on iliac intercrestal line (PS)6. The ground electrodes were placed over the acromion processes. A Motion Lab System Back Pack Unit, with attached electrodes, was connected to a Motion Lab EMG Desk Top Unit and Powerlab System (Figure 1).
  2. T-piece Monitoring Circuit to record the airway pressure was assembled as shown in Figure 2 and connected to the Low Pressure Transducer (MP45) using air tube.
  3. MP45 was connected to CD15 and Powerlab System (Figure 1 and Table 1).

2. RMCA Protocol

  1. The respiratory motor tasks consisted of Maximum Inspiratory Pressure Task (MIPT) and Maximum Expiratory Pressure Task (MEPT). To perform MIPT or MEPT, subjects were asked to produce maximum inspiratory effort from residual volume or expiratory efforts from total lung capacity for 5 sec using a T-piece Monitoring Circuit (Figures 1 and 2). Each maneuver was cued by an audible 5-sec long tone and repeated 3x. At least 1 min of rest was allowed between each effort.
  2. EMG input was amplified with a gain of 2,000; filtered at 30-1,000 Hz and sampled at 2,000 Hz. Airway pressure input was calibrated at 100 cm of water and sampled at 2,000 Hz. The EMG and airway pressure inputs were converted by the Powerlab acquisition system using 16-bit full scale ADC resolution. Airway pressure, sEMG and marker signals were recorded simultaneously9.

3. Data Analysis

  1. Multi-muscle activity distribution analysis windows of 5 sec each for MIPT or MEPT were determined from the event marker and airway pressure recorded with the cuing tone that signaled the subject when to begin and end the task (Figure 3). The sEMG activity for each muscle was calculated using a root mean square (RMS) algorithm6,12 (Figure 4). Three repeated trials for each task were averaged13 for each muscle (channel).
  2. The multi-muscle activation patterns were evaluated based on a vector analysis method known as the Voluntary Response Index (VRI)8 (Figures 4-6) using custom-made Matlab software (MathWorks). For each maneuver, the VRI calculation produces two values, a Magnitude and a Similarity Index (SI) (Figures 5-6). The Magnitude parameter, the amount of combined sEMG activity for all muscles within the specific time window, was calculated as a length of the Response Vector (RV) for specific task (Figure 7). The Similarity Index (SI) provides a value that expresses how similar the RV of SCI subject is to the Prototype Response Vector (PRV) obtained from healthy subjects during the same task. The SI value was computed for each task as a cosine of the angle between the SCI subject RV and PRV. The SI value ranges between 0 and 1.0 where value of 1.0 represents the best match for compared vectors9 (Figure 8) .

Results

Figure 3 represents the electromyogram and airway pressure (on top) simultaneously recorded during MEPT from a non-injured (left) and SCI (right) individuals. Note decreased airway pressure and absence of sEMG activity in expiratory muscles in an SCI subject when compared to a non-injured individual (marked with gray ellipses). Note also that start of the task, as marked on the bottom, is associated with increased sEMG activity and raising airway pressure.

Figure 4

Discussion

Standard clinical tests to evaluate respiratory motor function after SCI and other disorders include the pulmonary function tests and the American Spinal Injury Association Impairment Scale (AIS) evaluation14,15. However, these tools are not designed for quantitative evaluation of the trunk and respiratory motor control. In our previously published work9, we have shown that the RMCA is a valid method to quantitatively evaluate the respiratory motor function affected by SCI. We have demonstrated that...

Disclosures

No conflict of interest to declare.

Acknowledgements

This work was supported by Christopher and Dana Reeve Foundation (Grant CDRF OA2-0802-2), Kentucky Spinal Cord and Head Injury Research Trust (Grant 9-10A - KSCHIRT), Craig H. Neilsen Foundation (Grant 1000056824 - HN000PCG) and National Institutes of Health: National Heart Lung and Blood Institute (Grant 1R01HL103750-01A1).

Materials

NameCompanyCatalog NumberComments
PowerLab System 16/35ADInstrumentsPL3516Number of units depends on number of channels recorded
EMG System MA 300Motion Lab SystemsMA300-XVINumber of units depends on number of channels recorded
Low Pressure Transducer MP45ValidyneMP45-40-871
Basic Carrier Demodulator CD15ValidyneCD15-A-2-A-1
Air Pressure ManometerBoehringer4103Needed for MP45 calibration
Event MarkerHand held switch that when pressed gives a DC voltage and sound output (including 5-sec long mark)
Alcohol WipesHenry Schein1173771Needed for electrodes placement
Electrode GelLectron II36-3000-25Needed for electrodes placement
TagadermHenry Schein7779152Needed for electrodes placement
Noseclip Henry Schein1089460
T-piece Ventilator Monitoring Circuit with One-way Valves Alleglance (Airlife)1504
Air Tube UnoMedical400E
Table 1. List of specific equipment and supplies used for the Respiratory Motor Control Assessment.

References

  1. Schilero, G. J., Spungen, A. M., Bauman, W. A., Radulovic, M., Lesser, M. Pulmonary function and spinal cord injury. Respir. Physiol. Neurobiol. 166, 129-141 (2009).
  2. Winslow, C., Rozovsky, J. Effect of spinal cord injury on the respiratory system. Am. J. Phys. Med. Rehabil. 82, 803-814 (2003).
  3. Garshick, E., et al. A prospective assessment of mortality in chronic spinal cord injury. Spinal Cord. 43, 408-416 (2005).
  4. Jain, N. B., Brown, R., Tun, C. G., Gagnon, D., Garshick, E. Determinants of forced expiratory volume in 1 second (FEV1), forced vital capacity (FVC), and FEV1/FVC in chronic spinal cord injury. Arch. Phys. Med. Rehabil. 87, 1327-1333 (2006).
  5. Stolzmann, K. L., Gagnon, D. R., Brown, R., Tun, C. G., Garshick, E. Longitudinal change in FEV1 and FVC in chronic spinal cord injury. Am. J. Respir. Crit. Care Med. 177, 781-786 (2008).
  6. . American Thoracic Society/European Respiratory Society. ATS/ERS Statement on respiratory muscle testing. Am. J. Respir. Crit. Care Med. 166, 518-624 (2002).
  7. Sherwood, A. M., McKay, W. B., Dimitrijevic, M. R. Motor control after spinal cord injury: assessment using surface EMG. Muscle Nerve. 19, 966-979 (1996).
  8. Lee, D. C., et al. Toward an objective interpretation of surface EMG patterns: a voluntary response index (VRI). J. Electromyogr. Kinesiol. 14, 379-388 (2004).
  9. Ovechkin, A., Vitaz, T., de Paleville, D. T., Aslan, S., McKay, W. Evaluation of respiratory muscle activation in individuals with chronic spinal cord injury. Respir. Physiol. Neurobiol. 173, 171-178 (2010).
  10. Lim, H. K., Sherwood, A. M. Reliability of surface electromyographic measurements from subjects with spinal cord injury during voluntary motor tasks. J. Rehabil. Res. Dev. 42, 413-422 (2005).
  11. Lim, H. K., et al. Neurophysiological assessment of lower-limb voluntary control in incomplete spinal cord injury. Spinal Cord. 43, 283-290 (2005).
  12. Sherwood, A. M., Graves, D. E., Priebe, M. M. Altered motor control and spasticity after spinal cord injury: subjective and objective. 37, 41-52 (2000).
  13. McKay, W. B., Lim, H. K., Priebe, M. M., Stokic, D. S., Sherwood, A. M. Clinical neurophysiological assessment of residual motor control in post-spinal cord injury paralysis. Neurorehabil. Neural Repair. 18, 144-153 (2004).
  14. Marino, R. J., et al. International standards for neurological classification of spinal cord injury. J. Spinal. Cord. Med. 26, S50-S56 (2003).
  15. American Spinal Injury Association and International Spinal Cord Society. . International Standards for Neurological Classification of Spinal Cord Injury. , (2006).

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Keywords Respiratory Muscle ActivationRespiratory Motor Control Assessment RMCAChronic Spinal Cord InjuryPulmonary FunctionSurface Electromyography sEMGVoluntary Response Index VRIMulti muscle SEMG ApproachRespiratory Motor FunctionNeuromuscular Pathology

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