This unit covers Descriptions of most commonly employed biofeedback modalities: Respiration, EKG and heart rate (III-A) and Structure and function of the autonomic nervous system (V-A).
Students completing this unit will be able to discuss:
An incentive inspirometer consists of a calibrated cylinder with a piston
that moves upward as the patient inhales and indicates the volume of air
inhaled in a single breath (the incentive). Peper and colleagues pioneered
the use of incentive inspirometer feedback to train asthma patients to
effortlessly increase inhalation volume. This strategy can also be used
with hyperventilation syndrome and chronic obstructive pulmonary disease
patients.
Strain gauge biofeedback uses a flexible sensor band that is placed around
the chest, abdomen, or both. The strain gauge method can provide feedback
about the relative expansion/contraction of the chest and abdomen, detect
reverse breathing, and measure respiration rate. Below is a
BioGraph ® Infiniti display of chest and abdominal strain gauge movement.
Note the slow rhythmic abdominal breathing pattern.
Timmons (1994) showed that strain
gauge biofeedback is superior to visual observation.
Strain gauge biofeedback has two limitations: measurements are in relative
units and breathing mechanics can look correct while end-tidal CO2 and RSA
are reduced due to excessive effort, and while heart rate changes are out
of phase from breathing (Shaffer, Bergman, & Dougherty, 1998).
Surface EMG (SEMG) biofeedback for accessory breathing muscles and facial muscles
has been used to treat asthma patients. Peper and Tibbetts (1992)
demonstrated that SEMG accessory muscle/incentive inspirometer biofeedback
for asthma patients increased inhalation volumes and reduced asthma
symptoms, medication use, emergency room visits, and breathless episodes.
An SEMG placement to monitor accessory muscles (trapezius and scalene)
is shown below.
The BioGraph ® Infiniti screen below provides strain gauge
and SEMG biofeedback to teach rhythmic breathing while maintaining
relaxed accessory muscles.
Capnometric biofeedback provides the patient with continuous information
about end-tidal CO2. The goal of training is to normalize end-tidal CO2 to
about 5% (36 torr).
Fried (1990) reported successful treatment of patients
diagnosed with hyperventilation syndrome with capnometric biofeedback.
Heart rate variability (HRV) is measured by detecting the
interbeat
interval between successive R-waves using either EKG sensors
on the wrists or torso, or a PPG sensor on a finger or earlobe.
The SDNN is the standard deviation of the N-to-N interval. The N-to-N interval is the normalized interbeat interval. The SDNN measures how these intervals vary over time and is expressed in milliseconds (ms).
The SDNN is more accurate when calculated over 24 hours than during the shorter periods monitored during biofeedback sessions. This measure is a frequently-used medical index of heart rate
variability that is used to estimate cardiac risk (Shaffer & Moss, 2006). Below is a BioGraph ® Infiniti SDNN display.
The pNN50 is the percentage of adjacent N-to-N intervals that differ from each other by more than 50 milliseconds. This may be a more reliable index than the SDNN for the brief samples used in biofeedback. At least a 2-min sample is required to calculate an accurate pNN50.
HR Max – HR Min is the difference between the highest heart rate and the lowest heart rate within each cardiac cycle, measured in beats per minute.
Following normal skin preparation for SEMG,
active EKG electrodes (which can be identical to SEMG
electrodes) should
be placed on the wrist over the radial artery on the left and right
hands. The reference electrode can be placed over the dorsal aspect
of the wrist on the right hand. This placement, described by Papillo and
Shapiro (1990), is an excellent way to detect the EKG signal since this
wrist-to-wrist configuration creates a large-surface area antenna.
A photoplethysmographic (PPG) sensor provides an alternative method of calculating heart rate (beats per minute) by measuring the interbeat interval (time period between successive heartbeats). Divide the time interval between peaks by 60 s to calculate heart rate (Peper, Harvey, Lin, Tylova, & Moss, 2007).
Caption: Heart rate is derived from measures of blood volume pulse by measuring the interbeat interval and then transforming this information into beats per minute. For example, the interbeat interval of 0.80 seconds is equal to a heart rate of 75 beats per minute, whereas the interbeat interval of 0.93 seconds is equal to a heart rate of 64.5.
Portable HRV systems utilizing a PPG sensor, like the emWave by the Institute of HeartMath and the StressEraser by Helicor Inc. have been developed.
A breathing harness can be placed snuggly over the
chest and abdomen (navel).
Shaffer and Moss (2006) describe
HRV training: "Therapists use either the
electrocardiogram (EKG) or photoplethysmograph (PPG) to monitor the
frequency bands that comprise heart rate variability. They also use a
respiratory strain gauge to measure abdominal or chest expansion and
contraction during each respiratory cycle and respiration rate. Relaxed
breathing produces a biofeedback display showing a smooth sinusoidal
line, depicting exhalation and inhalation, and a parallel smooth
sinusoidal line showing heart rate variation. Anxious thoughts, on the
other hand, produce a jagged irregular respiration signal and a jagged
irregular variation in heart rate. Producing this coherence––or
smoothly organized and regular variation––of the respiratory and heart
rate displays is also a training goal for biofeedback."
The BioTrace+ / NeXus-10 display below shows patients how heart
rate changes during inspiration and expiration. In healthy patients, it
should increase during inspiration and decrease during expiration. In
patients who hyperventilate or show a thoracic breathing pattern, there
may be minimal heart rate variability and the heart rate trace may be
out-of-phase with the abdominal strain gauge trace.
Heart rate variability is produced by the interaction of multiple
regulatory mechanisms that operate on different time scales (Moss,
2004). Spectral analysis separates
heart rate variability into its component rhythms that operate within
different frequency bands. The Task Force of
the European Society of Cardiology and the North American Society of
Pacing and Electrophysiology (1996) has divided heart rate
oscillations into the following bands:
The ultra low frequency (ULF) band (below
0.0033 Hz) represents very slow-acting biological processes
and is too gradual to train using conventional biofeedback.
The very low frequency (VLF) band (0.005-0.05
Hz) may represent sympathetic activation.
Worry and rumination increase the power of this waveform.
The low frequency (LF) band (0.05-0.15 Hz) may represent the influence of both the parasympathetic and sympathetic branches and blood pressure regulation via baroreceptors or blood pressure receptors (Lehrer, 2007). Meditation and slow breathing, like the
“tanden breathing” practiced by Rinzai Zen monks, increase the power of
this waveform.
The high frequency (HF) or respiratory band
(0.15-.40 Hz) represents the inhibition and activation of the
vagus nerves by breathing at normal rates (Moss, 2004).
In HRV training, the clinician teaches clients to gradually slow
respiration to their personal resonant frequency, from 4.5-7.5 breaths per
minute, to increase the amplitude around .1 Hz. This maximizes HRV
because it combines the influence of baroreceptors and the
parasympathetic system.
The BioGraph Infiniti display below is
designed to increase the percentage of power in the low frequency
band.
Now that you have completed this module, describe the method you use to
monitor client breathing and the types of measurements you record. If
you use a strain gauge to measure breathing, where do you place the
strain gauge and why? What precautions do you take when attaching the
strain gauge to female clients?
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