Depth of anaesthesia and neurophysiological monitoring

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Chapter 17 Depth of anaesthesia and neurophysiological monitoring

Neurological function may be monitored for many reasons in anaesthesia and intensive care. Nerve stimulation can help with pharmacological neuromuscular blockade, anatomical localization during peripheral nerve blockade and confirmation of the integrity of neural pathways during spinal surgery. Analysis of cortical electrical activity is the underlying principle of most devices which purport to reflect anaesthetic depth. Finally, some monitors are available which may reduce the risk of cerebral ischaemia and neurological deficit in particular surgical circumstances where oxygen delivery to the brain may be compromised.

Nerve stimulators

Nerve stimulators are designed to administer electrical stimuli to peripheral nerves. The responses may be assessed in different ways. The strength of an electrical stimulus applied to a nerve is defined by its charge (coulombs, Q). This is equivalent to the product of the current passed (amperes, A) and the duration (seconds, s) of that pulse of current.

Most nerve stimulators employ constant current circuitry, in which the difference between the current set by the user and the actual current delivered is detected and the applied voltage is automatically adjusted to minimize any disparity. This situation may arise when a dried-out skin electrode causes high impedance and consequently a low initial current flow.

Assessment of neuromuscular blockade

During assessment of neuromuscular blockade a supramaximal stimulus (i.e. one in which all axons in the nerve are made to discharge) is administered to a motor nerve through a pair of ordinary adhesive silver/silver chloride electrodes, applied to the overlying skin. Typically, the stimulus pulse duration might be 0.2 ms, the current 60 mA and the resulting charge, 12 µC. With pulses shorter than 0.2 ms, the amplitude required to generate a supramaximal stimulus may exceed the capacity of the stimulator, while pulses longer than 0.3 ms run the risk of repetitive nerve or muscle stimulation. Higher charges than are classically used may be required to guarantee supramaximal stimulation in nerves with prolonged conduction times (e.g. in diabetic neuropathy).1 The charge required to deliver a supramaximal stimulus is less when the negative electrode is placed distally.2

Basic hand-held devices provide a stimulus with a fixed current and pulse width and permit a limited range of stimulation patterns (Fig. 17.1). Other models have liquid crystal screens and user-variable current, enabling both neuromuscular monitoring and nerve localization.

The motor response evoked by peripheral nerve stimulation may be measured in different ways, but is typically evaluated visually. Usually, contraction of adductor pollicis is observed following ulnar nerve stimulation at the wrist. The facial nerve in the cheek is also used, but direct muscle stimulation may contribute to the resulting contraction. More advanced devices attempt to quantify the (force of) muscular contraction elicited by peripheral nerve stimulation.

Currently available monitors allowing objective assessment of the motor response to neural stimulation use accelerometric or kinemyographic technology.

Piezoelectric methods (‘Kinemyography’)

When compressed or distorted, piezoelectric materials produce a charge proportional to the degree of alteration in shape. The M-NMT module for the S/5 anaesthesia monitor (GE Healthcare) uses a piezoelectric sensor incorporated into a clip placed on the patient’s thumb and index finger (Fig. 17.3). Thumb movement on stimulation is converted to an electrical signal and displayed graphically as a proportion of the maximal response. Monitoring, therefore, needs to be started before neuromuscular blockade but after anaesthetic induction. The module initially determines the current required for a supramaximal stimulus and sets a reference response level. By using different patient interface attachments the module can also be used for electromyographic recording or for nerve localization.

Nerve stimulators for regional anaesthesia

Despite the growing use of ultrasound (see Chapter 13), there remains a need for peripheral nerve stimulators designed specifically for localization of nerves during regional anaesthesia (see Fig. 13.7). A positive surface electrode is applied to the skin and the negative electrode cable is plugged into a unipolar stimulating needle.

User-adjustable constant current is necessary and the ability to adjust stimulus frequency and duration is desirable. Usually an initial current of 1–2 mA (compare with currents needed for transcuteaneous stimulation of ∼60 mA) with a frequency of 2 Hz is appropriate as the needle is advanced toward the nerve. Lower frequencies increase the risk of going past the nerve, but may be desirable to reduce discomfort secondary to movement in injured patients.

Once contractions of the relevant muscle are seen, the current can be reduced. The stimulator-delivered charge required to generate a nerve impulse is proportional to the square of the distance from needle tip to nerve (by Coulomb’s law). Advantage can be taken of this phenomenon during neuraxial blockade in children, where a nerve stimulator attached to an insulated epidural needle may help determine whether the tip is epidural or intrathecal.8 For peripheral nerve blocks, traditional teaching is that injection of local anaesthetic is likely to be effective at the point where a response is still seen at a stimulating current of ≤0.3 mA.9 Recent work, however, suggests a similar probability of successful nerve block in paediatric patients whether the stimulation threshold is below or above 0.5 mA.10

Stimulus duration is adjustable on many devices. This should generally be set at less than 300 µs to avoid repetitive stimulation, though up to 1.0 ms may be required in neuropathic nerves, even with high currents.11 Because chronaxie (the minimum stimulus duration required to elicit a response) is longer in sensory than in motor nerves, pulses longer than 0.15 ms are selected when attempting to locate a purely sensory nerve by inducing paraesthesia.

The accuracy with which peripheral nerve stimulators deliver the selected current tends to deteriorate as the current decreases. Manufacturers often quote accuracy of typically 1–5%, for a current setting of 1 mA. Amplitudes used for peripheral nerve localization, however, are less than 0.5 mA, where variability may be more than 80%.12 A stimulator which delivers less than the set current may increase the risk of nerve damage during peripheral nerve block – with one that delivers more, a failed block may be more likely.

Nerve blocks carry a small risk of intraneural local anaesthetic injection with concomitant damage. Some nerve stimulators currently under evaluation calculate the electrical impedance (EI) of the circuit through the patient. This might be used to reduce the risk of intraneural injection, EI being higher when the stimulating needle is intraneural.13 The exact mechanism for this finding is yet to be elucidated and is controversial.14

Transient pacemaker inhibition by peripheral nerve stimulators has been reported,15 as has interference with the display of pacemaker impulses on the ECG monitor.16

Assessment of neural integrity

Spinal cord/nerve roots

Somatosensory evoked potentials

The incidence of neurological damage, secondary to traction and ischaemia of the spinal cord during scoliosis correction is approximately 0.5%. This may be reduced by monitoring somatosensory evoked potentials (SSEP).18 The monitors are complex and require an experienced neurophysiologist. Typically a pair of stimulating electrodes is placed over each posterior tibial nerve at the ankles for lumbar surgery, or over the median nerves for cervical surgery. Stimuli are administered at about 30 mA and 5 Hz. Recording electrodes may be applied at various points adjacent to the ascending tracts and proximal to the site of surgery. Usually two or more scalp electrodes are used (e.g. one frontal and one cervical), together with a reference and a ground electrode. The recorded responses are passed through a digital signal converter and a band-pass filter (20–1000 Hz). An average response is calculated from as many as 200 individual sweeps and the result displayed on the monitor screen. The period of interest is the first 100 ms after the stimulus, during which a characteristic W-shaped potential is seen in recordings from cortical electrodes (Fig. 17.4). Response latency also depends on the distance between the point of stimulation and the recording electrode.

image

Figure 17.4 Somatosensory evoked response. The stimulating electrode is over the median nerve. Recording electrodes are over A. the somatosensory cortex and B. the seventh vertebra. The sequential peaks and troughs in the evoked response are named according to their latency (ms) and direction. Particular periods of the response correspond to specific neuro-anatomical regions as shown.

(Thornton C, Sharpe RM (1998) Evoked responses in anaesthesia. British Journal of Anaesthesia 81: 771–781, © The Board of Management and Trustees of the British Journal of Anaesthesia. Reproduced by permission of Oxford University Press/British Journal of Anaesthesia.)

A baseline SSEP is recorded before induction of anaesthesia. If subsequent intraoperative spinal manipulation completely prevents conduction of the ascending impulse, the SSEP disappears altogether. When conduction is merely impaired, an increase in SSEP latency and a decrease in amplitude are observed. A 50% increase in latency compared to baseline would be regarded as a critical change and the operator would inform the surgeon accordingly. Surgical disruption apart, a number of factors affect SSEPs, including volatile anaesthetic agents, nitrous oxide, hypothermia, hypoxia and hypotension.

Monitoring ‘depth of anaesthesia’

For decades, anaesthetists have sought a monitor which might reflect the conscious level of patients undergoing general anaesthesia. A number of different variables, which may relate to consciousness, can be derived from the electrical activity of the cerebral cortex. Ideally, in variables of this sort, the range of values seen in the conscious state should not overlap with that seen in the unconscious state (i.e. a cut-off value would exist which is 100% sensitive and specific for consciousness). Furthermore, ideally any cut-off value should not be affected by patient physiology or the choice of anaesthetic agent.21

At present, the variables derived by available monitors do not meet these ideals. Current monitors generally work on one of two principles:

EEG

General principles, signal processing and artefact rejection

The EEG represents current flow in the cortical extracellular fluid, which is the result of post-synaptic potentials in cortical neurons. It is acquired through scalp electrodes. In anaesthetic monitors, between one and four electrodes are usually used, together with a reference electrode. Impedance should be kept to a minimum (i.e. less than 5 kΩ). EEG voltage is measured as the potential difference between two electrodes.

The complex waveform of the EEG comprises many individual sine waves, whose frequencies lie from zero to approximately 50 Hz (Fig. 17.5). Classically these are grouped into frequency bands (Table 17.1). For the purposes of analysis, the EEG is split into epochs of 1–4 s.

Table 17.1 Electroencephalographic frequency bands

BAND NAME APPROXIMATE FREQUENCY RANGE (Hz)
Alpha 8–13
Beta 13–30
Theta 4–8
Delta <4

In order to allow processing, the EEG is converted from a smooth continuous analogue signal into a digital one. The fidelity of this conversion depends on the degree of resolution for both voltage and time. The greater the number of bits used, the smaller the change in voltage that can be translated from analogue to digital. EEG monitors usually use 12–16 bits of resolution. The frequency at which the analogue signal is sampled is also important. Too slow a sampling frequency fails to take account of the fastest sine waves and results in ‘aliasing’, where the digital signal incorrectly identifies a low-frequency waveform (Fig. 17.6). EEG monitors usually sample at frequencies above 250 Hz. Signal processing then enables rejection of artefact due to the electrocardiogram, ocular movement or mains interference.

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