TY - CHAP M1 - Book, Section TI - Chapter 34. Monitoring and Managing Neuromuscular Blockade A1 - Pino, Richard M. A1 - Ali, Hassan H. A2 - Longnecker, David E. A2 - Brown, David L. A2 - Newman, Mark F. A2 - Zapol, Warren M. Y1 - 2012 N1 - T2 - Anesthesiology, 2e AB - Muscle response to stimulation can be measured by mechanomyography, electromyography, acceleromyography, and direct palpation.Commonly used patterns of stimulation are a single twitch, train of four, double burst, tetanic, and posttetanic count.Succinylcholine, a depolarizing neuromuscular blocking drug (NMBD), is metabolized by plasma cholinesterase. Atypical pseudocholinesterases cannot metabolize pseudocholinesterase at a normal rate, and prolonged neuromuscular blockade may result.Immobility, prolonged use of NMBDs, and upper and lower motor neuron disease may cause a proliferation of extrajunctional receptors. These receptors affect severe hyperkalemia when stimulated with succinylcholine.Nondepolarizing NMBDs are benzylisoquinoline (mivacurium, atracurium, cisatracurium) and steroidal molecules (vecuronium, rocuronium, pancuronium).The degradation of atracurium, cisatracurium, and mivacurium is independent of organ-specific elimination.Pancuronium and vecuronium are metabolized in the liver to derivatives that are cleared by the kidney and that exhibit neuromuscular blocking activities. These derivatives accumulate with prolonged administration and renal insufficiency.Reversal agents increase the concentration of acetylcholine in the junctional clefts to compete with the NMBDs to restore muscle activity.Clinical criteria, in addition to evoked responses, should be used to assess the recovery of neuromuscular blockade.Residual neuromuscular blockade is a persistent and common clinical problem. SN - PB - The McGraw-Hill Companies CY - New York, NY Y2 - 2024/04/16 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=56631928 ER -