Respiratory drive (i.e., the output of respiratory centers to respiratory muscles) is challenging to evaluate due to the obtrusive, often impractical nature of evaluative methods such as functional magnetic resonance imaging (fMRI). Moreover, the small size of the respiratory centers located in the brain stem is difficult to localize and is sensitive to alterations by physiologic noise1,2. Measurements of respiratory drive are important because of their association with important clinical outcomes such as dyspnea, an indication of respiratory distress. Electromyography (EMG) is a surrogate of respiratory drive to the respiratory muscles3. Respiratory muscle EMG allows the determination of muscle activity and its intensity by way of the root mean square (RMS) of the EMG signal. Additionally, the timing of muscle activation can be assessed by identifying the onset and offset of their activity (EMG, onset and EMG, offset, respectively)1,2,3,4,5,6,7,8,9,10,11.
The magnitude of the EMG signal refers to the electrical potential generated by muscle cells when they contract, indicating their level of muscle activation12. The magnitude of the EMG signal can vary depending on factors such as the intensity of muscle contraction, the number of motor units recruited, the electrode placement, the movement of muscle and subcutaneous tissues, and the specific characteristics of the muscle being measured12.
The timing of the EMG signal refers to when the electrical activity occurs relative to a specific event or action (e.g., relative to inspiratory flow for breathing)13. The onset timing indicates when muscle activation begins, while the offset timing indicates when muscle activity decreases, ceases, or is in the relaxation phase13. Timing among the activation of several respiratory muscles will facilitate an understanding of coordination and control mechanisms during breathing. Assessing the consistency or variability of timing patterns over time or in individuals can help identify physiologic and pathophysiologic motor control strategies associated with acute or chronic ventilatory failure.
Both the magnitude and timing of the respiratory muscle EMG have been associated with important clinical outcomes12,13,14. The diaphragm generates the majority of ventilation at rest15. When the respiratory demand increases, such as during exercise or increased inspiratory loading associated with lung diseases (e.g., chronic obstructive pulmonary disease, interstitial lung disease, or acute respiratory distress syndrome), extradiaphragmatic respiratory muscles boost ventilation, which can augment or offset diaphragm contractile requirements15. Thus, in addition to the increasing magnitude of diaphragm EMG, the magnitude of extradiaphragmatic muscle EMG will also increase.
Activation of extradiaphragmatic respiratory muscles can protect the diaphragm from developing fatigue16. However, early activation (onset) and prolonged activation have been associated with acute and chronic ventilatory failure14,17,18. The objective here is to describe a protocol to acquire and analyze both the timing and magnitude of respiratory muscle EMG signals in both healthy adults and patients with suspected or confirmed respiratory pathophysiology. This protocol includes previously validated steps from data acquisition to quantify the timing and magnitude of EMG activity13,19.