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Research Project
Leaders for Tevhnical Industries - LTI - Deep neuromuscular blckade monitoring: closed-loop monitor system for deep neuromuscular blockade during surgery
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TOF-Watch NMB monitoring misleading display output during moderate neuromuscular blockade
Publication . Couto, Mafalda; Nunes, Catarina S.; Amorim, Pedro; Mendes, Joaquim
In general anesthesia, Neuromuscular Blockade (NMB) agents are
administered to ensure intubation quality and complete immobilization. Monitoring NMB, based on the evoked response evaluation after a peripheral nerve
stimulation, is essential to provide insight on medication dosing and suitable
approaches for NMB reversal. Professionals often rely on the data displayed on
the monitor screen after TOF stimuli, assuming measurements present the
expected fade and a TOF-ratio > 90% is enough to rule out residual paralysis.
This can be inaccurate and mislead the clinician to extubate before adequate
NMB curarization. Data from 31 patients that underwent general anesthesia
were retrospectively analyzed. All patients received a standard dose of rocuronium (0.6 mg/kg) for intubation, during maintenance additional rocuronium
boluses were administered if solicited. NMB monitoring was done continuously
applying TOF stimuli at the adductor pollicis with TOF-Watch SX®. Two types
of monitoring display errors were studied: (1) valid TOF value without fade
effect (invalid T1 > T2 > T3 > T4); (2) in the 30 min before extubation a valid
TOF-ratio value > 90% (without error type 1) with T1 < 70%. Results show a
mean (SD) of type 1 error on 42.0 (17.5)% of valid TOF measurements, type 2
error in 63 (45)%. Only 9 patients (29%) presented a TOF with no errors before
extubation. These results may increase the distrust in the NMB monitoring
devices, however its use should not be rejected when NMB agents are administered. Careful evaluation of the NMB is recommended and additional efforts
should be placed in the accuracy of monitors data display to avoid errors.
Comparison of two pharmacokinetic–pharmacodynamic models of rocuronium bromide during profound neuromuscular block: analysis of estimated and measured post-tetanic count effect
Publication . Couto, Mafalda; Vide, Sérgio; Marco-Ariño, Nicolás; Troconiz, Iñaki F.; Esteves, Simão; Nunes, Catarina S.; Amorim, Pedro; Mendes, Joaquim
Background: Profound neuromuscular block (NMB) is important in surgeries where complete immobility is considered essential to improve tracheal intubation and surgical conditions. Rocuronium bromide is a commonly used NMB agent.
This work describes a noninvasive approach for estimation of post-tetanic count (PTC) based on two pharmacokinetic (PK) models, the Saldien and the De Haes models. The aim was to investigate the rocuronium bromide PKepharmacodynamic (PD) relationship in estimating the PTC effect during profound NMB.
Methods: In this prospective, non-randomised, observational study, an induction bolus of rocuronium bromide was administered followed by continuous infusion for maintenance of a PTC of 1-2. measured every 3 min. Measurements were analysed as discrete categorical data and by applying the nonlinear mixed-effect modelling approach. Performance of the selected models was evaluated through simulation model-based diagnostics, further assessing the precision of the parameter estimates and the performance of the models at the individual level.
Results: Data from 30 adult patients undergoing elective abdominal or neurosurgical procedures were included. Posttetanic count response profiles during rocuronium bromide infusion were successfully characterised using the population PD analysis. The models showed a good performance for all PTC categories, albeit with a moderate over-prediction of PTC >6.
Conclusions: Our findings indicate that using plasma concentrations of rocuronium bromide estimated with either of the two models, combined with a PD model, provides equal model performance when predicting PTC. These promising results may provide an important advance in guiding rocuronium bromide administration when profound NMB in routine clinical practice is desired.
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Funding agency
Fundação para a Ciência e a Tecnologia
Funding programme
POR_NORTE
Funding Award Number
PD/BD/114378/2016