Train of Four Monitoring for Cisatracurium (Nimbex)
Quantitative neuromuscular monitoring is essential when administering cisatracurium (Nimbex), with a target train-of-four (TOF) ratio >0.9 before extubation to prevent residual neuromuscular blockade and associated complications. 1
Recommended Monitoring Protocol for Cisatracurium
- Quantitative neuromuscular monitoring should be applied before administration of cisatracurium and used throughout all phases of anesthesia 1
- The ulnar nerve is the most reliable site for monitoring, with the adductor pollicis muscle providing the most accurate assessment 1
- Monitor should be activated after induction of general anesthesia but before administration of cisatracurium 1
- When using cisatracurium in the ICU, train-of-four monitoring should be performed at least every 4 hours 2
- Additional doses of cisatracurium should not be given before there is a definite response to nerve stimulation 3
Interpretation of TOF Monitoring
- With increasing depth of neuromuscular blockade, twitches decrease in force with the fourth twitch (T4) lost first, followed by T3, T2, and finally T1 1
- Absence of tactile or visible TOF fade using a peripheral nerve stimulator only indicates TOF ratio recovery to 0.4 or greater 1
- The "monitoring gap" between 0.4 and 0.9 can only be assessed using quantitative monitoring 1
- Clinical tests of recovery (sustained head-lift, hand grip, tongue depressor tests) are inadequate with sensitivities of only 10-30% 1
Reversal of Cisatracurium
- Adequacy of recovery (TOF ratio >0.9) must be demonstrated and documented before patient awakening and extubation 1
- When using neostigmine for reversal:
- If using sugammadex (for rocuronium, not cisatracurium):
Common Pitfalls and Considerations
- Residual neuromuscular blockade (TOF ratio <0.9) occurs in approximately 40% of patients receiving cisatracurium when not properly monitored 6
- Consequences of inadequate recovery include:
- Many factors can affect the duration of cisatracurium's action:
- Alternative monitoring sites (facial or tibial nerve) may be used if the hand is inaccessible, but facial nerve monitoring increases the risk of residual paralysis five-fold 1
Special Considerations
- Patients with renal dysfunction may have approximately 1 minute slower onset time 3
- Patients with end-stage liver disease may have approximately 1 minute faster onset time 3
- Patients with hemiparesis or paraparesis may demonstrate resistance to cisatracurium in affected limbs; monitoring should be performed on a non-paretic limb 3
- For ICU patients receiving prolonged cisatracurium infusions, continuous monitoring is essential with additional doses administered only after definite response to nerve stimulation 3