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NEUROMUSCULAR
MONITORING
Dr. KAVITA KADYAN
What are we monitoring?
ā€¢ Monitor ā€“ skeletal muscle contraction in response to a stimulus.
ā€¢ Purpose ā€“ know the %age of Ach Nicotinic receptors blocked.
Use/objectives of NMM-
1. Onset of induction, dosage of nmbd for intubation
2. Determine level of block :
ā€¢ Tracheal intubation response
ā€¢ Surgical relaxation
ā€¢ Reversal of patient from ms relaxants.
Why need NMM ?
ADVERSE EFFECTS OF RESIDUAL NEUROMUSCULAR
BLOCKADE
Physiological
changes
Clinical
implications
https://resources.wfsahq.org/atotw/residual-neuromuscular-blockade-anaesthesia
Muscle Paralysed state Implication
Pharyngeal:
Tongue
Tongue fall Upper airway obstruction
ā€¢ (Desaturation,
ā€¢ Need of re-intubation)
Palatal ms Closure of oral airway ā€œ
Larynx:
Vocal cords No phonation Patient cant tell
Laryngeal muscles No abduction of vocal cords Difficulty in breathing
No adduction of vocal cords Risk of aspiration,
Inadequate cough
Chest & Diaphragm ā€¢ FRC, PEFR, VC ā†“
ā€¢ Impaired oxygenation-
ventilation
ā€¢ Impaired lung functions
ā€¢ Post op ventilator weaning
difficult,
ā€¢ Atelectasis ā†‘
ā€¢ Pneumoniaā†‘
ā€¢ Need of re-intubation
Rest of the body Weakness ā€¢ Functional capacity to work ā†“
Brain Hypoxic centre not activated ā€¢ ā†“sensitivity of chemoreceptors
to hypoxia
Conditions where NMM is ā€œessentialā€
1. Patient :
ā€¢ muscular disorder (myasthenia gravis, eaton lambert syndrome),
ā€¢ liver or renal dysfunction (pharmacokinetics change),
ā€¢ respiratory diseases, morbid obese
2. Surgery:
ā€¢ prolonged duration,
ā€¢ profound NM blockade (nmbd) ie neuro sx, ophthalmic sx, thoracic sx
3. Anesthesia:
ā€¢ prolonged infusions of nmbd ,
ā€¢ Reversal drugs may cause harm ( tachyyarythmias, cardiac failure)
Which muscles we monitor ?
ā€¢ Aim:
Procedure Paralysis required
Intubation time Laryngeal, diaphragm, abdominal ms
Surgical maintenance time Abdominal ms, peripheral muscles
Extubation time No muscle paralysis required
ā€¢ Q. Smooth, skeletal ???
ā€¢ Q. central or peripheral muscles?
ā€¢ Q. superficial or deep muscles?
Which muscles we monitor ?
Skeletal muscles.
Diaphragm, facial
muscles,
Thumb muscle,
Leg muscle
Peripheral
muscles(thumb,legs)
monitoring easy then
central muscles
(diaphragm, laryngeal
ms)
Can we measure central & deep muscles ?
Are all muscles equal in sensitivity to NMBD?
No ā€¼
Relative sensitivities of muscle groups to
muscle relaxants
Vocal cords: maximum resistant
Extra-ocular ms: least resistance
Differential
sensitivity of
muscle
groups to
NMBA
d/t variations in:
1. Ach-R density
2. Ach release
3. Ach esterase activity
4. Muscle fiber composition
5. Innervation ratio & no of NMJ
6. Blood flow
7. Muscle temparature
Relative sensitivities of muscle groups to
muscle relaxants
Vocal cords: maximum resistant
Extra-ocular ms: least resistance
Diaphragm & Laryngeal Ms:
ā€¢ More AchR,
ā€¢ More Ach ,
ā€¢ [hence most resistant to both
NMBA]
ā€¢ {1.4 to 2 times dose of muscle
relaxant as the adductor pollicis}
ā€¢ More blood supply
{faster onset & offset of paralysis}
L
A
S
T
F
I
R
S
T
ONSET
for nmbd
drugs
RECOVERY
for nmbd
drugs
F
I
R
S
T
L
A
S
T
closely reflect the extent of paralysis of D & L ms.
Pharyngeal & upper oesophageal muscles are most sensitive to NDMR, so they recover very late &
TOF ratio ā‰„ 0.9 @ adductor pollicis is required for extubation
Clinical signs of
neuromuscular
recovery
Clinical criteria of extubation?
Clinical criteria of extubation?
ā€¢ Eye opening
ā€¢ Tongue protrude
ā€¢ Head lift
ā€¢ Hand grip
ā€¢ Regular and adequate TV generate
But are these enough to prevent post operative
residual paralysis or recurarisation?
Things observed during NMM?
Ms. Contraction
after a
stimulus applied-
visual/tactile/
TOF %age
measure.
1.Count & %age
2.Fade
3.Potentiation
How to assess
muscle response?
Qualitative / subjective NMM
Muscle contraction is
subjectively assessed by
clinicians either
visually or tactically
Quantitative / objective NMM
Muscle response is objectively
measured with the help of
a sensor and displayed
on a screen
Fade ?
Fade = decrease in amplitude of muscle contraction in respective of
previous ms. contraction. i.e. T4/T1 or DBS2/DBS1 or ST1/ST control.
Or
Fade is progressive depression of height of subsequent response seen
with NDMR
No fade Fade is d/t blockade of
presynaptic AchR
which decrease Ach
release.
When we see fade ?
Fade can be seen at 2 times:
ā€¢ a) when we administer NMBD i.e. at ā€œINDUCTIONā€
ā€¢ B)when we see weaning off NMBD, i.e. As the neuromuscular block
begins to wear off, the muscle will begin to respond to a stimulus, but
the twitch will be less than full strength i.e. at ā€œEXTUBATIONā€
Induction extubation
Induction extubation
Ach Receptor occupancy and nmbd action ?
Mechanism of muscle contraction
Mechanism of muscle contraction
Brief mode of action of nondepolarizing
depolarizing drugs
Non- depolarizing
ATRACURIOUM & Ach compete,
More amount drug wins and attach to
receptor
Atracurium donā€™t open Na-K
NO AP
Depolarising /Sch/ non-
competitive
Phase I-
ā€¢ Sch bind to AchR,
ā€¢ Na-K open,
ā€¢ AP generation, fasiculation,
ā€¢ pseudocholinesterase takes time to act (blood),
ā€¢ Sch donā€™t dissociate from Ach R ,
ā€¢ hyperpolarisation
ā€¢ Flaccid paralysis,
ā€¢ Na-K closed
ā€¢ pseudoE destroys Sch
ā€¢ Receptor free from any drug
ā€¢ Ach act on Ach R
ā€¢ Normal muscle contract by opening Na-K
ā€¢ { thus no reversal needed}
ā€¢ Phase II=
ā€¢ Repeated Sch dosage
ā€¢ Sch never leaves this AchR { as Sch amount is more then Ach}
ā€¢ Repolarisation has occurred
ā€¢ AchR confrontational changes have occurred
ā€¢ Na-K donā€™t open
Brief mode of action of nondepolarizing
depolarizing drugs
ā€¢ Non- depolarising ā€¢ Depolarising /Sch/ non-
competitive
Principles of Peripheral Nerve stimulation
Supramaximal stimulation
ā€¢ Ohms law ļƒ  V = I Ɨ R
ā€¢ Current ( not voltage) is the determinant of
nerve stimulation
ā€¢ All or none phenomenon
ā€¢ Least amount of current required to begin
muscle contraction is called as threshold
current
ā€¢ Muscle response āˆ Force of contractionāˆ no.
of muscle fibres contracted āˆ Current
ā€¢ Current required to produce the contraction of
all muscle fibres is called as maximal current
Supramaximal
current = 2.5 to 3
times Threshold
current = 15 to 20%
higher than
maximal current
This ensures the stimulus to be truly
maximal throughout the whole period of
monitoring irrespective of potential
changes in skin resistance
intraoperatively
A 30 mA current will usually produce
supramaximal stimulation in most of the
patients when Ulnar n is stimulated
Higher current may be needed with
posterior tibial nerve stimulation, in
patients with increased skin resistance
such as diabetes, oedema
ā€¢ Frequency = no. of stimulus or electrical pulse per sec. (Hz)
ā€¢ Waveform must be rectangular and monophasic
ā€¢ The length of pulse should not exceed 0.2 to 0.3 ms
Safety range of
equipment
Neuromuscular block become
evident only after 70 to 80 % of
AchĀ® are occupied with nd-NMBD
For complete block 90 to 95% AchĀ®
has to be occupied
Currently available equipment
detect this 70 to 95% range of
receptor occupancy
i.e, during recovery from NMB, less
than 70 % of Ach_R occupancy is
not detectable by NMM
Calibration
To obtain accurate and
precise readings ,
equipment has to be
calibrated before use
ā€¢ is within measurement window of the device
ā€¢ & as close as possible to 100% control
response
Check whether
Muscle response to
supramaximal
stimulus
Types of electrodes
1. silver or silver chloride gel
based surface electrodes
2. Metal ball electrodes (with no
cable)
3. Needle electrodes (s/c tissue
parallel to nerve)
(Thick skin, oedema, cold skin)
Modes of NMM ?
SINGLE TWITCH STIMULATION
ā€¢ Single electrical stimuli at 1.0 Hz( 1
impulse in 1 sec) to 0.1 Hz(1 impulse
every 10 sec)
ā€¢ We compare the strength of muscle
contraction to the control value
before the administration of the
muscle relaxant.
ā€¢ The strength of response is expressed
as % of control (T1:Tc)
ā€¢ Progressive decrease in response height
with both dMR & ndmr
SINGLE TWITCH STIMULATION
ā€¢ The amplitude of muscle contraction decreases when about 75-
80% of the receptors are blocked, and
ā€¢ It disappears when 90-95% of the receptors are blocked,
ED-95 value
PTC
Double burst stimulation
1st
burst
2nd
burst
ā€¢ 2 short bursts of 50 Hz tetanic stimulation separated by 750 msec, with a 0.2 ms duration of each
square wave impulse in the burst
ā€¢ In DBS (3,3) modeļƒ  3 impulses in each burst
ā€¢ In DBS (3,2) modeļƒ 1st burst has 3 impulses & 2nd burst has 2 impulse
Fade in the response to second burst compared to that of first burst is the basis for evaluation
Double burst stimulation
Fade seen by D2 burst/D1 burst
Comparison with TOF ratio ?
ā€¢It approximates the TOFR when comparing the second to the
first response.
ā€¢It may increase sensitivity of qualitative assessments since
fade can be detected at a TOFR around 0.6 with this method.
ā€¢Manual tactile detection of DBS Fade is much better
appreciated then TOF fade.
Double burst stimulation
TRAIN OF FOUR
STIMULATION
One set of stimulus = Four single pulses of equal intensity at intervals of 0.5 s (2Hz) & each set of
stimuli is repeated every 10 to 20 sec.
Findings
1. TOF Count = no.of evident
responses after TOF
stimulation
2. TOF Ratio = amplitude of
fourth response / amp.of
first response
TOF RESPONSE
DEPOLARISING BLOCK/Sch phase I
ā€¢ No fade
ā€¢ CONSTANT but DIMINSHED
Non-depolarizing block/Atra/Roc OR
Sch phase II
ā€¢ Fade seen As block deepens , TOFR
decreases
TOF
TOF
T1 is last to go
T1 is 1st to appear
Application of TOF
TOF interpretation
Tetanic & Post Tetanic Count Stimulation
ā€¢ Tetanic stimulation: High frequency electrical stimuli of 50 to 100 hz given for 5 sec. Or 200 Hz
stimulation for 1 sec ( should not be repeated more often than every 6 min.)
ā€¢ PTC stimulation: Tetanic Stimulation ļƒ  after 3 sec.ļƒ  10-15 or 20 Single twitch stimuli @ 1 Hz
Tetanus fade
For muscle contraction, 2 things needed
1. Ach
2. free AchR at post synaptic membrane
Start of tetanic stimulation:
ļƒ˜ large amounts of acetylcholine are released from immediately available stores in
the presynaptic nerve terminal.
Continued tetanic stimulation: { stores become depleted : equilibrium achieved}
ļƒ˜ the rate of acetylcholine release decreases {mobilization} ā‰” synthesis
ļƒ˜ muscle response is maintained : acetylcholine released >the amount to evoke a
response.
Continued tetanic stimulation:
ļƒ˜ postsynaptic event: free AchR at post-synaptic membrane ā†“ {blocked by nmbd}
ļƒ˜ Presynaptic event: impaired mobilization of acetylcholine within the nerve
terminal
ļƒ˜ FADE seen: mainly a ā€œpresynaptic eventā€.
(Although the degree of fade depends primarily on the degree
of neuromuscular block, fade also depends on the frequency
(Hz), the length (seconds) of stimulation, and on how often
tetanic stimuli are applied)
Post Tetanic Count
Q. What are we counting ?
ā€¢ MUSCLE CONTRACTION Response to PTC stimulus.
Q. When to use ?
ā€¢ During deep block, when TOFC=0
Q. which surgeries should be monitored by PTC?
ā€¢ Surgery where movement is to be avoided, e.g. Ophthalmic surgery, neuro-surgery.
Q. when PTC=0, do we need to repeat the NMBD dose during maintenance?
ā€¢ No ā€¼ minimum PTC =1 needed to repeat the maintenance dosage.
Q. When we say that TOF twitch is imminent ( value of PTC)?
ā€¢ 8-9 counts of PTC, TOF of 1 will be in 10 mins.
Q. To avoid diaphragmatic movement during sx, PTC ?
ā€¢ ā‰¤3 PTC responses is recommended (neuromuscular block of the peripheral muscles must be deep
so that the PTC is 1-3 at the thumb).
Post Tetanic Count
facilitation or potentiation
ā€¢ As the deep block weakens, more and more
responses to post-tetanic twitch stimulation
appear.
Fade in the tetanic stimulus response is the
least sensitive subjective measure of
strength and is not reliably detected until the
TOFR falls below 0.4.
Post Tetanic Count
Q. After tetanic stimulation we observe any increase / decrease in the amplitude of
ms. contraction?
ā€¢ Post tetanic facilitation or potentiation is observed (INCREASE in ms. contraction)
ā€¢ Post Tetanic facilitation is the phenomenon of exaggerated response to
stimulation (which is seen max around 3 sec & last for 2 min) following a tetanic
stimulus.
ā€¢ It is d/t exxagarated release of Ach leading to high levels of Ach w.r.t receptor
blocking drugs at motor endplate
ā€¢ With dMR, response to TS will decrease in amplitude but sustained & no PTF
ā€¢ With NDMB, response to TS will decrease in amplitude ass. with fade + PTF
ā€¢ Note: Fade is due to Presynaptic Ach R block
Which mode when to
use?
ā€¢ INTUBATION
ā€¢ MAINTENANCE
ā€¢ RECOVERY
ā€¢ PACU
Which mode when to use?
Choice of Nerve-muscle unit ?
ā€¢ Q. Sensory or Motor or Mixed nerve ?
ā€¢ Q. Superficial or Deep nerves?
Choice of Nerve-muscle unit ?
ā€¢ Q. Central or peripheral muscles?
ā€¢ Q. Which among these muscles is the central acting muscle, which
corresponds to the onset of action of laryngeal ms. and diaphragm?
corrugator supercili
muscle
POLARITY ?
ā€¢ 1 negative(distal) and 1positive(proximal)electrode (colour coded, red & black)
Ulnar nerve
ā€¢ Most commonly used
ā€¢ Easily accessible if arm in outstretched & hand in
supine position
ā€¢ Lowest risk of direct muscle stimulation due to good
topographic separation
Posterior tibial nerve
ā€¢ Can be used when hands are inaccessible
Q.Flexor hallucis brevis is similar to what
muscle for nerve stimulation?
ā€¢ The onset & recovery of NMB at flexor hallucis brevis is
almost consistent with that of adductor pollicis muscle
1.Facial nerve (zygomatic br)-orbicularis oculi
2.Facial nerve (temporal br)-corrugator supercili muscle
ā€¢ High risk of direct muscle
stimulation due to close
proximity of nerve &
muscles
Facial nerve
Facial nerve
1. Which facial muscle behaves similarly to the
Adductor pollicis ms muscle for nerve
stimulation?
Ans. orbicularis oculi
2. What facial muscle is similar to the diaphragm
and laryngeal muscles?
Ans. corrugator supercili muscle
Assessment of response
How to assess
muscle response?
Qualitative / subjective NMM
Muscle contraction is
subjectively assessed by
clinicians either
visually or tactically
Quantitative / objective NMM
Muscle response is objectively
measured with the help of
a sensor and displayed
on a screen
Quantitative / objective NMM
Mechanomyography
ā€¢ measures the isometric contraction of a muscle
ā€¢ Preload of 200 to 300 g is applied to thumb
ā€¢ The arm and hand should be rigidly fixed, and care
should be taken to prevent overloading of the
transducer
ā€¢ A transducer converts Force of contraction generated at
adductor pollicis to electrical signal which is recorded,
amplified & displayed on screen
ā€¢ MMG is gold stantard of NMM
ā€¢ But not commercially available d/t bulky equipment &
used for research purpose only
Acceleromyography
ā€¢ Is based on Newtonā€™s 3rd law, F=ma
ā€¢ It measures isotonic acceleration of
stimulated muscle by using a piezoelectric
transducers
ā€¢ M/c commercially available monitor &
therefore become standard for qualitative
NMM today
Electromyography
ā€¢ Measures compound muscle action potential
generated by stimulation of a peripheral nerve
ā€¢ 3 electrodes
1. Active electrode (over muscle belly)
2. Reference electrode ( over tendon
insertion)
3. Ground electrode( between both) (neutral
site distant to the muscle)
Advantages over MMG:
ā€¢ The equipment is not as bulky and is easier to assemble.
ā€¢ The arm and hand do not need to be fixed as rigidly.
ā€¢ new sites for recording the EMG : the larynx and the diaphragm.
Disadvantages:
ā€¢ It is prone to interference: diathermy, Hand temperature, hand
movement, direct muscle stimulation.
Electromyography
Laryngeal EMG:
ā€¢ Laryngeal electrode attached to the
tracheal tube and placed between the
vocal cords.
ā€¢ Monitor: the onset of neuromuscular block
in the laryngeal muscles.
Electromyography (non-invasive)
Normal Šœ-wave from the diaphragm during stimulation of the phrenic
nerve in a child aged 12
Diaphragmatic EMG :
ā€¢ In paravertebral surface, the
recording electrodes are placed
on the right of vertebrae T12/L1
or L1/L2 for monitoring the
response of the right
diaphragmatic crux to
transcutaneous stimulation of the
right phrenic nerve at the neck
Electromyography (non-invasive)
Kinemyography
ā€¢ A bending sensor with a piezoelectric
core is placed b/w thumb & forefinger.
ā€¢ Muscle contraction causes bending of
sensor which is converted to electrical
signal by piezoelectric transducer.
PHONOMYOGRAPHY
ā€¢ PMG measures: low-frequency sounds of
muscle contraction with special microphones
following nerve stimulation.
Advantage:
ā€¢ adductor pollicis muscle, diaphragm, larynx,
and eye muscles.
ā€¢ In addition, the ease of application is
attractive.
Disadv.: PMG-based monitors are not currently
commercially available
CUFF PRESSURE MODALITY
ā€¢ Detects: changes in cuff pressure due to
muscle contraction.
Method:
ā€¢ Electrodes integrated into a BP cuff
stimulate the brachial plexus at the
humeral level.
ā€¢ The subsequent bulk contraction of the
upper arm generates pressure change in
the blood pressure cuff which is
analyzed and displayed at the monitor
COMPRESSOMYOGRAPHY
ā€¢ Measures: pressure changes in a
hand-held balloon.
ā€¢ Method: Following ulnar nerve
stimulation, the force of muscle
contraction of the hand muscles is
transmitted to a balloon secured in
the patientā€™s hand.
ā€¢
4 levels of NMB with NDMR are
1. Intense NMB
2. Deep NMB
3. Moderate NMB, also called
as surgical block, TOFC 1 or 2
is sufficient relaxation for
most surgical procedures
4. Recovery phase
Level of NMBD
DEEP AND INTENSE BLOCK disadvantage
1. Patient are completely paralyzed and cannot signal awareness with
voluntary or involuntary movements.
2. Another is that deep or intense block cannot readily be reversed by
neostigmine. Only sugammadex can reverse a deep or intense
neuromuscular block (if caused by rocuronium or vecuronium)
ASSESSMENT
ā€¢Tests including sustained head or leg lift, eye or mouth opening, and
hand grip can be performed at TOF ratios between 0.4-0.9.6
Qualitative Assessment of Strength: Clinical Tests
4. Recovery
from NMB
ā€¢ Return of the fourth response in the TOF marks the recovery
phase
ā€¢ TOFR is used to asses the extend of NMB recovery
ā€¢ TOFR ā‰¤ 0.4ļƒ  unable to lift head or arm, TV may be normal
but Inspiratory force & vital capacity is reduced
ā€¢ TOFR 0.5 to 0.6 ļƒ  most pts can lift head for 3 s, open eyes
widely, protrude tongue but vital capacity & Insp. force is still
reduced.
ā€¢ TOFR 0.7 to 0.75ļƒ  most pt can cough sufficiently, lift head for
5 s but hand grip strength is still low
ā€¢ TOFR ā‰„ 0.8ļƒ  VC & IF become normal, however, pt may still
have diplopia, blurred vision & facial weakness
ā€¢ To exclude clinically significant residual NMB with certainty
TOFR recorded with MMG or EMG must be ā‰„ 0.9 or with AMG
must be atleast 1.0
Unreliable signs
Reliable signs
ā€œSUSTAINEDā€
a) Head lift
b) Leg lift
c) Hand grip
ā‰„5 sec
Clinical signs of
neuromuscular
recovery
Clinical criteria of extubation?
Reversal- neostigmine or suggamadex?
Level of NMB with subsequent doses of NDMR is
monitored using PTC, TOFC & TOFR
Reversal with Neostigmine should not be attempted
until at least 2 responses to TOFC is present
For extubation, residual NMB has to be ruled out by
TOFR ā‰„ 0.9 with MMG/EMG or at least 1 with AMG
NEUROMUSCULAR MONITORING .pptx
NEUROMUSCULAR MONITORING .pptx
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NEUROMUSCULAR MONITORING .pptx

  • 2. What are we monitoring? ā€¢ Monitor ā€“ skeletal muscle contraction in response to a stimulus. ā€¢ Purpose ā€“ know the %age of Ach Nicotinic receptors blocked. Use/objectives of NMM- 1. Onset of induction, dosage of nmbd for intubation 2. Determine level of block : ā€¢ Tracheal intubation response ā€¢ Surgical relaxation ā€¢ Reversal of patient from ms relaxants.
  • 4. ADVERSE EFFECTS OF RESIDUAL NEUROMUSCULAR BLOCKADE Physiological changes Clinical implications https://resources.wfsahq.org/atotw/residual-neuromuscular-blockade-anaesthesia
  • 5. Muscle Paralysed state Implication Pharyngeal: Tongue Tongue fall Upper airway obstruction ā€¢ (Desaturation, ā€¢ Need of re-intubation) Palatal ms Closure of oral airway ā€œ Larynx: Vocal cords No phonation Patient cant tell Laryngeal muscles No abduction of vocal cords Difficulty in breathing No adduction of vocal cords Risk of aspiration, Inadequate cough Chest & Diaphragm ā€¢ FRC, PEFR, VC ā†“ ā€¢ Impaired oxygenation- ventilation ā€¢ Impaired lung functions ā€¢ Post op ventilator weaning difficult, ā€¢ Atelectasis ā†‘ ā€¢ Pneumoniaā†‘ ā€¢ Need of re-intubation Rest of the body Weakness ā€¢ Functional capacity to work ā†“ Brain Hypoxic centre not activated ā€¢ ā†“sensitivity of chemoreceptors to hypoxia
  • 6.
  • 7. Conditions where NMM is ā€œessentialā€ 1. Patient : ā€¢ muscular disorder (myasthenia gravis, eaton lambert syndrome), ā€¢ liver or renal dysfunction (pharmacokinetics change), ā€¢ respiratory diseases, morbid obese 2. Surgery: ā€¢ prolonged duration, ā€¢ profound NM blockade (nmbd) ie neuro sx, ophthalmic sx, thoracic sx 3. Anesthesia: ā€¢ prolonged infusions of nmbd , ā€¢ Reversal drugs may cause harm ( tachyyarythmias, cardiac failure)
  • 8. Which muscles we monitor ? ā€¢ Aim: Procedure Paralysis required Intubation time Laryngeal, diaphragm, abdominal ms Surgical maintenance time Abdominal ms, peripheral muscles Extubation time No muscle paralysis required
  • 9. ā€¢ Q. Smooth, skeletal ??? ā€¢ Q. central or peripheral muscles? ā€¢ Q. superficial or deep muscles? Which muscles we monitor ? Skeletal muscles. Diaphragm, facial muscles, Thumb muscle, Leg muscle Peripheral muscles(thumb,legs) monitoring easy then central muscles (diaphragm, laryngeal ms)
  • 10. Can we measure central & deep muscles ?
  • 11. Are all muscles equal in sensitivity to NMBD? No ā€¼
  • 12. Relative sensitivities of muscle groups to muscle relaxants Vocal cords: maximum resistant Extra-ocular ms: least resistance
  • 13. Differential sensitivity of muscle groups to NMBA d/t variations in: 1. Ach-R density 2. Ach release 3. Ach esterase activity 4. Muscle fiber composition 5. Innervation ratio & no of NMJ 6. Blood flow 7. Muscle temparature
  • 14. Relative sensitivities of muscle groups to muscle relaxants Vocal cords: maximum resistant Extra-ocular ms: least resistance Diaphragm & Laryngeal Ms: ā€¢ More AchR, ā€¢ More Ach , ā€¢ [hence most resistant to both NMBA] ā€¢ {1.4 to 2 times dose of muscle relaxant as the adductor pollicis} ā€¢ More blood supply {faster onset & offset of paralysis} L A S T F I R S T ONSET for nmbd drugs RECOVERY for nmbd drugs F I R S T L A S T closely reflect the extent of paralysis of D & L ms. Pharyngeal & upper oesophageal muscles are most sensitive to NDMR, so they recover very late & TOF ratio ā‰„ 0.9 @ adductor pollicis is required for extubation
  • 15.
  • 17. Clinical criteria of extubation? ā€¢ Eye opening ā€¢ Tongue protrude ā€¢ Head lift ā€¢ Hand grip ā€¢ Regular and adequate TV generate But are these enough to prevent post operative residual paralysis or recurarisation?
  • 18. Things observed during NMM? Ms. Contraction after a stimulus applied- visual/tactile/ TOF %age measure. 1.Count & %age 2.Fade 3.Potentiation
  • 19. How to assess muscle response? Qualitative / subjective NMM Muscle contraction is subjectively assessed by clinicians either visually or tactically Quantitative / objective NMM Muscle response is objectively measured with the help of a sensor and displayed on a screen
  • 20. Fade ? Fade = decrease in amplitude of muscle contraction in respective of previous ms. contraction. i.e. T4/T1 or DBS2/DBS1 or ST1/ST control. Or Fade is progressive depression of height of subsequent response seen with NDMR No fade Fade is d/t blockade of presynaptic AchR which decrease Ach release.
  • 21. When we see fade ? Fade can be seen at 2 times: ā€¢ a) when we administer NMBD i.e. at ā€œINDUCTIONā€ ā€¢ B)when we see weaning off NMBD, i.e. As the neuromuscular block begins to wear off, the muscle will begin to respond to a stimulus, but the twitch will be less than full strength i.e. at ā€œEXTUBATIONā€ Induction extubation Induction extubation
  • 22.
  • 23. Ach Receptor occupancy and nmbd action ?
  • 24. Mechanism of muscle contraction
  • 25. Mechanism of muscle contraction
  • 26. Brief mode of action of nondepolarizing depolarizing drugs Non- depolarizing ATRACURIOUM & Ach compete, More amount drug wins and attach to receptor Atracurium donā€™t open Na-K NO AP Depolarising /Sch/ non- competitive Phase I- ā€¢ Sch bind to AchR, ā€¢ Na-K open, ā€¢ AP generation, fasiculation, ā€¢ pseudocholinesterase takes time to act (blood), ā€¢ Sch donā€™t dissociate from Ach R , ā€¢ hyperpolarisation ā€¢ Flaccid paralysis, ā€¢ Na-K closed ā€¢ pseudoE destroys Sch ā€¢ Receptor free from any drug ā€¢ Ach act on Ach R ā€¢ Normal muscle contract by opening Na-K ā€¢ { thus no reversal needed} ā€¢ Phase II= ā€¢ Repeated Sch dosage ā€¢ Sch never leaves this AchR { as Sch amount is more then Ach} ā€¢ Repolarisation has occurred ā€¢ AchR confrontational changes have occurred ā€¢ Na-K donā€™t open
  • 27. Brief mode of action of nondepolarizing depolarizing drugs ā€¢ Non- depolarising ā€¢ Depolarising /Sch/ non- competitive
  • 28. Principles of Peripheral Nerve stimulation Supramaximal stimulation ā€¢ Ohms law ļƒ  V = I Ɨ R ā€¢ Current ( not voltage) is the determinant of nerve stimulation ā€¢ All or none phenomenon ā€¢ Least amount of current required to begin muscle contraction is called as threshold current ā€¢ Muscle response āˆ Force of contractionāˆ no. of muscle fibres contracted āˆ Current ā€¢ Current required to produce the contraction of all muscle fibres is called as maximal current
  • 29. Supramaximal current = 2.5 to 3 times Threshold current = 15 to 20% higher than maximal current This ensures the stimulus to be truly maximal throughout the whole period of monitoring irrespective of potential changes in skin resistance intraoperatively A 30 mA current will usually produce supramaximal stimulation in most of the patients when Ulnar n is stimulated Higher current may be needed with posterior tibial nerve stimulation, in patients with increased skin resistance such as diabetes, oedema
  • 30. ā€¢ Frequency = no. of stimulus or electrical pulse per sec. (Hz) ā€¢ Waveform must be rectangular and monophasic ā€¢ The length of pulse should not exceed 0.2 to 0.3 ms
  • 31. Safety range of equipment Neuromuscular block become evident only after 70 to 80 % of AchĀ® are occupied with nd-NMBD For complete block 90 to 95% AchĀ® has to be occupied Currently available equipment detect this 70 to 95% range of receptor occupancy i.e, during recovery from NMB, less than 70 % of Ach_R occupancy is not detectable by NMM
  • 32. Calibration To obtain accurate and precise readings , equipment has to be calibrated before use ā€¢ is within measurement window of the device ā€¢ & as close as possible to 100% control response Check whether Muscle response to supramaximal stimulus
  • 33. Types of electrodes 1. silver or silver chloride gel based surface electrodes 2. Metal ball electrodes (with no cable) 3. Needle electrodes (s/c tissue parallel to nerve) (Thick skin, oedema, cold skin)
  • 35. SINGLE TWITCH STIMULATION ā€¢ Single electrical stimuli at 1.0 Hz( 1 impulse in 1 sec) to 0.1 Hz(1 impulse every 10 sec) ā€¢ We compare the strength of muscle contraction to the control value before the administration of the muscle relaxant. ā€¢ The strength of response is expressed as % of control (T1:Tc) ā€¢ Progressive decrease in response height with both dMR & ndmr
  • 36. SINGLE TWITCH STIMULATION ā€¢ The amplitude of muscle contraction decreases when about 75- 80% of the receptors are blocked, and ā€¢ It disappears when 90-95% of the receptors are blocked,
  • 37.
  • 39.
  • 40. Double burst stimulation 1st burst 2nd burst ā€¢ 2 short bursts of 50 Hz tetanic stimulation separated by 750 msec, with a 0.2 ms duration of each square wave impulse in the burst ā€¢ In DBS (3,3) modeļƒ  3 impulses in each burst ā€¢ In DBS (3,2) modeļƒ 1st burst has 3 impulses & 2nd burst has 2 impulse Fade in the response to second burst compared to that of first burst is the basis for evaluation
  • 41. Double burst stimulation Fade seen by D2 burst/D1 burst Comparison with TOF ratio ? ā€¢It approximates the TOFR when comparing the second to the first response. ā€¢It may increase sensitivity of qualitative assessments since fade can be detected at a TOFR around 0.6 with this method. ā€¢Manual tactile detection of DBS Fade is much better appreciated then TOF fade.
  • 42.
  • 44. TRAIN OF FOUR STIMULATION One set of stimulus = Four single pulses of equal intensity at intervals of 0.5 s (2Hz) & each set of stimuli is repeated every 10 to 20 sec. Findings 1. TOF Count = no.of evident responses after TOF stimulation 2. TOF Ratio = amplitude of fourth response / amp.of first response
  • 45. TOF RESPONSE DEPOLARISING BLOCK/Sch phase I ā€¢ No fade ā€¢ CONSTANT but DIMINSHED Non-depolarizing block/Atra/Roc OR Sch phase II ā€¢ Fade seen As block deepens , TOFR decreases
  • 46. TOF
  • 47. TOF T1 is last to go T1 is 1st to appear Application of TOF
  • 49.
  • 50.
  • 51. Tetanic & Post Tetanic Count Stimulation ā€¢ Tetanic stimulation: High frequency electrical stimuli of 50 to 100 hz given for 5 sec. Or 200 Hz stimulation for 1 sec ( should not be repeated more often than every 6 min.) ā€¢ PTC stimulation: Tetanic Stimulation ļƒ  after 3 sec.ļƒ  10-15 or 20 Single twitch stimuli @ 1 Hz
  • 52. Tetanus fade For muscle contraction, 2 things needed 1. Ach 2. free AchR at post synaptic membrane Start of tetanic stimulation: ļƒ˜ large amounts of acetylcholine are released from immediately available stores in the presynaptic nerve terminal. Continued tetanic stimulation: { stores become depleted : equilibrium achieved} ļƒ˜ the rate of acetylcholine release decreases {mobilization} ā‰” synthesis ļƒ˜ muscle response is maintained : acetylcholine released >the amount to evoke a response. Continued tetanic stimulation: ļƒ˜ postsynaptic event: free AchR at post-synaptic membrane ā†“ {blocked by nmbd} ļƒ˜ Presynaptic event: impaired mobilization of acetylcholine within the nerve terminal ļƒ˜ FADE seen: mainly a ā€œpresynaptic eventā€. (Although the degree of fade depends primarily on the degree of neuromuscular block, fade also depends on the frequency (Hz), the length (seconds) of stimulation, and on how often tetanic stimuli are applied)
  • 53. Post Tetanic Count Q. What are we counting ? ā€¢ MUSCLE CONTRACTION Response to PTC stimulus. Q. When to use ? ā€¢ During deep block, when TOFC=0 Q. which surgeries should be monitored by PTC? ā€¢ Surgery where movement is to be avoided, e.g. Ophthalmic surgery, neuro-surgery. Q. when PTC=0, do we need to repeat the NMBD dose during maintenance? ā€¢ No ā€¼ minimum PTC =1 needed to repeat the maintenance dosage. Q. When we say that TOF twitch is imminent ( value of PTC)? ā€¢ 8-9 counts of PTC, TOF of 1 will be in 10 mins. Q. To avoid diaphragmatic movement during sx, PTC ? ā€¢ ā‰¤3 PTC responses is recommended (neuromuscular block of the peripheral muscles must be deep so that the PTC is 1-3 at the thumb).
  • 54. Post Tetanic Count facilitation or potentiation ā€¢ As the deep block weakens, more and more responses to post-tetanic twitch stimulation appear. Fade in the tetanic stimulus response is the least sensitive subjective measure of strength and is not reliably detected until the TOFR falls below 0.4.
  • 55. Post Tetanic Count Q. After tetanic stimulation we observe any increase / decrease in the amplitude of ms. contraction? ā€¢ Post tetanic facilitation or potentiation is observed (INCREASE in ms. contraction) ā€¢ Post Tetanic facilitation is the phenomenon of exaggerated response to stimulation (which is seen max around 3 sec & last for 2 min) following a tetanic stimulus. ā€¢ It is d/t exxagarated release of Ach leading to high levels of Ach w.r.t receptor blocking drugs at motor endplate ā€¢ With dMR, response to TS will decrease in amplitude but sustained & no PTF ā€¢ With NDMB, response to TS will decrease in amplitude ass. with fade + PTF ā€¢ Note: Fade is due to Presynaptic Ach R block
  • 56. Which mode when to use? ā€¢ INTUBATION ā€¢ MAINTENANCE ā€¢ RECOVERY ā€¢ PACU
  • 57. Which mode when to use?
  • 58. Choice of Nerve-muscle unit ? ā€¢ Q. Sensory or Motor or Mixed nerve ? ā€¢ Q. Superficial or Deep nerves?
  • 59. Choice of Nerve-muscle unit ? ā€¢ Q. Central or peripheral muscles? ā€¢ Q. Which among these muscles is the central acting muscle, which corresponds to the onset of action of laryngeal ms. and diaphragm? corrugator supercili muscle
  • 60. POLARITY ? ā€¢ 1 negative(distal) and 1positive(proximal)electrode (colour coded, red & black)
  • 61. Ulnar nerve ā€¢ Most commonly used ā€¢ Easily accessible if arm in outstretched & hand in supine position ā€¢ Lowest risk of direct muscle stimulation due to good topographic separation
  • 62. Posterior tibial nerve ā€¢ Can be used when hands are inaccessible Q.Flexor hallucis brevis is similar to what muscle for nerve stimulation? ā€¢ The onset & recovery of NMB at flexor hallucis brevis is almost consistent with that of adductor pollicis muscle
  • 63. 1.Facial nerve (zygomatic br)-orbicularis oculi 2.Facial nerve (temporal br)-corrugator supercili muscle ā€¢ High risk of direct muscle stimulation due to close proximity of nerve & muscles Facial nerve
  • 64. Facial nerve 1. Which facial muscle behaves similarly to the Adductor pollicis ms muscle for nerve stimulation? Ans. orbicularis oculi 2. What facial muscle is similar to the diaphragm and laryngeal muscles? Ans. corrugator supercili muscle
  • 66.
  • 67.
  • 68. How to assess muscle response? Qualitative / subjective NMM Muscle contraction is subjectively assessed by clinicians either visually or tactically Quantitative / objective NMM Muscle response is objectively measured with the help of a sensor and displayed on a screen
  • 70. Mechanomyography ā€¢ measures the isometric contraction of a muscle ā€¢ Preload of 200 to 300 g is applied to thumb ā€¢ The arm and hand should be rigidly fixed, and care should be taken to prevent overloading of the transducer ā€¢ A transducer converts Force of contraction generated at adductor pollicis to electrical signal which is recorded, amplified & displayed on screen ā€¢ MMG is gold stantard of NMM ā€¢ But not commercially available d/t bulky equipment & used for research purpose only
  • 71. Acceleromyography ā€¢ Is based on Newtonā€™s 3rd law, F=ma ā€¢ It measures isotonic acceleration of stimulated muscle by using a piezoelectric transducers ā€¢ M/c commercially available monitor & therefore become standard for qualitative NMM today
  • 72. Electromyography ā€¢ Measures compound muscle action potential generated by stimulation of a peripheral nerve ā€¢ 3 electrodes 1. Active electrode (over muscle belly) 2. Reference electrode ( over tendon insertion) 3. Ground electrode( between both) (neutral site distant to the muscle)
  • 73. Advantages over MMG: ā€¢ The equipment is not as bulky and is easier to assemble. ā€¢ The arm and hand do not need to be fixed as rigidly. ā€¢ new sites for recording the EMG : the larynx and the diaphragm. Disadvantages: ā€¢ It is prone to interference: diathermy, Hand temperature, hand movement, direct muscle stimulation. Electromyography
  • 74. Laryngeal EMG: ā€¢ Laryngeal electrode attached to the tracheal tube and placed between the vocal cords. ā€¢ Monitor: the onset of neuromuscular block in the laryngeal muscles. Electromyography (non-invasive)
  • 75. Normal Šœ-wave from the diaphragm during stimulation of the phrenic nerve in a child aged 12 Diaphragmatic EMG : ā€¢ In paravertebral surface, the recording electrodes are placed on the right of vertebrae T12/L1 or L1/L2 for monitoring the response of the right diaphragmatic crux to transcutaneous stimulation of the right phrenic nerve at the neck Electromyography (non-invasive)
  • 76. Kinemyography ā€¢ A bending sensor with a piezoelectric core is placed b/w thumb & forefinger. ā€¢ Muscle contraction causes bending of sensor which is converted to electrical signal by piezoelectric transducer.
  • 77. PHONOMYOGRAPHY ā€¢ PMG measures: low-frequency sounds of muscle contraction with special microphones following nerve stimulation. Advantage: ā€¢ adductor pollicis muscle, diaphragm, larynx, and eye muscles. ā€¢ In addition, the ease of application is attractive. Disadv.: PMG-based monitors are not currently commercially available
  • 78. CUFF PRESSURE MODALITY ā€¢ Detects: changes in cuff pressure due to muscle contraction. Method: ā€¢ Electrodes integrated into a BP cuff stimulate the brachial plexus at the humeral level. ā€¢ The subsequent bulk contraction of the upper arm generates pressure change in the blood pressure cuff which is analyzed and displayed at the monitor
  • 79. COMPRESSOMYOGRAPHY ā€¢ Measures: pressure changes in a hand-held balloon. ā€¢ Method: Following ulnar nerve stimulation, the force of muscle contraction of the hand muscles is transmitted to a balloon secured in the patientā€™s hand.
  • 80. ā€¢ 4 levels of NMB with NDMR are 1. Intense NMB 2. Deep NMB 3. Moderate NMB, also called as surgical block, TOFC 1 or 2 is sufficient relaxation for most surgical procedures 4. Recovery phase
  • 82.
  • 83. DEEP AND INTENSE BLOCK disadvantage 1. Patient are completely paralyzed and cannot signal awareness with voluntary or involuntary movements. 2. Another is that deep or intense block cannot readily be reversed by neostigmine. Only sugammadex can reverse a deep or intense neuromuscular block (if caused by rocuronium or vecuronium)
  • 85. ā€¢Tests including sustained head or leg lift, eye or mouth opening, and hand grip can be performed at TOF ratios between 0.4-0.9.6 Qualitative Assessment of Strength: Clinical Tests
  • 86. 4. Recovery from NMB ā€¢ Return of the fourth response in the TOF marks the recovery phase ā€¢ TOFR is used to asses the extend of NMB recovery ā€¢ TOFR ā‰¤ 0.4ļƒ  unable to lift head or arm, TV may be normal but Inspiratory force & vital capacity is reduced ā€¢ TOFR 0.5 to 0.6 ļƒ  most pts can lift head for 3 s, open eyes widely, protrude tongue but vital capacity & Insp. force is still reduced. ā€¢ TOFR 0.7 to 0.75ļƒ  most pt can cough sufficiently, lift head for 5 s but hand grip strength is still low ā€¢ TOFR ā‰„ 0.8ļƒ  VC & IF become normal, however, pt may still have diplopia, blurred vision & facial weakness ā€¢ To exclude clinically significant residual NMB with certainty TOFR recorded with MMG or EMG must be ā‰„ 0.9 or with AMG must be atleast 1.0
  • 87.
  • 89. Reliable signs ā€œSUSTAINEDā€ a) Head lift b) Leg lift c) Hand grip ā‰„5 sec
  • 92. Level of NMB with subsequent doses of NDMR is monitored using PTC, TOFC & TOFR Reversal with Neostigmine should not be attempted until at least 2 responses to TOFC is present For extubation, residual NMB has to be ruled out by TOFR ā‰„ 0.9 with MMG/EMG or at least 1 with AMG