How Accelerography Works in Neuromuscular Blockade Assessment
Accelerography (acceleromyography) measures neuromuscular blockade by detecting the acceleration of muscle movement in response to peripheral nerve stimulation using a piezoelectric transducer attached to the thumb or other muscle, converting mechanical acceleration into an electrical signal that quantifies the degree of neuromuscular block. 1, 2
Technical Mechanism
Core Technology
- A piezoelectric ceramic wafer with electrodes on each side is attached to the thumb (typically over the adductor pollicis muscle) 2
- When the ulnar nerve is electrically stimulated, the resulting muscle contraction causes thumb movement 2
- The acceleration of this movement generates a voltage difference between the two electrodes on the transducer 2
- This voltage is measured and registered in a computing unit that calculates the train-of-four (TOF) ratio 2
Key Advantage Over Other Methods
- Accelerography does not require preload tension on the muscle, only that the muscle can move freely 2
- This makes setup significantly faster than mechanomyography—reliable evaluation can be achieved in less than 2 minutes in clinical practice 2
Clinical Application and Monitoring Protocol
Essential Requirements
- Quantitative neuromuscular monitoring with acceleromyography is essential when administering neuromuscular blocking agents, and should be used throughout all phases of anesthesia 1
- The monitor must be activated after induction of general anesthesia but before neuromuscular blockade 1
- The ulnar nerve with thumb adduction (adductor pollicis) is the most reliable monitoring site 1
Train-of-Four Interpretation
- Four electrical stimuli are delivered in rapid succession 1
- With increasing neuromuscular blockade depth, twitches decrease progressively: T4 is lost first, then T3, T2, and finally T1 3
- The critical "monitoring gap" exists between TOF ratio 0.4 and 0.9—absence of visible fade only indicates recovery to 0.4 or greater, not adequate recovery 1
- A TOF ratio >0.9 must be documented before extubation to prevent residual paralysis complications 1
Important Limitations and Pitfalls
Accuracy Concerns
- Acceleromyography can underestimate block depth during onset (maximal at ~50% twitch depression) and overestimate block during recovery 4
- When one device reads TOF 0.7, acceleromyography readings can vary between 0.4 and 1.0 4
- Acceleromyography is more susceptible to drift than mechanomyography 4
- Different acceleromyography devices are not interchangeable—clinical decisions for deep neuromuscular blockade should be made cautiously due to significant variability between devices 5
Patient and Technical Factors Affecting Accuracy
- If thumb movement is impeded (hand inaccessible during surgery), readings become unreliable with acceleromyography devices 1
- Patient factors that influence results include: monitoring site location, patient temperature, diaphoresis, peripheral edema, and skin resistance 1
- In neonates and small infants, automatic baseline calibration may fail—manual gain adjustment is often required to achieve 100% baseline twitch height 6
- Hypothermia can cause inadequate response despite apparent adequate TOF readings 1
Site-Specific Variations
- Facial nerve monitoring increases the risk of residual paralysis five-fold compared to ulnar nerve monitoring—revert to ulnar nerve at surgery end 1
- Response differs between adductor pollicis, orbicularis oculi, and respiratory muscles (chest wall/diaphragm) due to varying nicotinic receptor density 1
- Accelerographic monitoring over vastus medialis shows faster onset and higher TOF ratios than thumb monitoring 7
Clinical Integration
Comprehensive Assessment Required
- Acceleromyography must be incorporated into a more comprehensive patient assessment that includes clinical evaluation—TOF monitoring alone should not determine adequacy of reversal 1, 8
- Clinical tests (sustained head-lift, hand grip, tongue depressor) have sensitivities of only 10-30% and cannot exclude residual blockade 1
- Continue monitoring for adequacy of reversal for a period ensuring full recovery based on patient condition and pharmacokinetics of both the neuromuscular blocking agent and reversal agent used 8