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Rapid Sequence Induction With a Standard Intubation Dose of Rocuronium After Magnesium Pretreatment Compared With Succinylcholine: A Randomized Clinical Trial

Succinylcholine remains the muscle relaxant of choice for rapid sequence induction (RSI) but has many adverse effects. High-dose rocuronium bromide may be an alternative to succinylcholine for RSI but recovery times are nearly doubled compared with a standard intubating dose of rocuronium. Magnesium...

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Detalles Bibliográficos
Autores principales: Czarnetzki, Christoph, Albrecht, Eric, Masouyé, Philippe, Baeriswyl, Moira, Poncet, Antoine, Robin, Matthias, Kern, Christian, Tramèr, Martin R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkin 2020
Materias:
48
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8568325/
https://www.ncbi.nlm.nih.gov/pubmed/33337797
http://dx.doi.org/10.1213/ANE.0000000000005324
Descripción
Sumario:Succinylcholine remains the muscle relaxant of choice for rapid sequence induction (RSI) but has many adverse effects. High-dose rocuronium bromide may be an alternative to succinylcholine for RSI but recovery times are nearly doubled compared with a standard intubating dose of rocuronium. Magnesium sulfate significantly shortens the onset time of a standard intubating dose of rocuronium. We set out to investigate whether intravenous (IV) pretreatment with MgSO(4) followed by a standard intubating dose of rocuronium achieved superior intubation conditions compared with succinylcholine. METHODS: Adults were randomized to receive a 15-minute IV infusion of MgSO(4) (60 mg·kg(–1)) immediately before RSI with propofol 2 mg·kg(–1), sufentanil 0.2 μg·kg(–)(1) and rocuronium 0.6 mg·kg(–1), or a matching 15-minute IV infusion of saline immediately before an identical RSI, but with succinylcholine 1 mg·kg(–1). Primary end point was the rate of excellent intubating conditions 60 seconds after administration of the neuromuscular blocking agent and compared between groups using multivariable log-binomial regression model. Secondary end points were blood pressure and heart rate before induction, before and after intubation, and adverse events up to 24 hours postoperatively. RESULTS: Among 280 randomized patients, intubating conditions could be analyzed in 259 (133 MgSO(4)-rocuronium and 126 saline-succinylcholine). The rate of excellent intubating conditions was 46% with MgSO(4)-rocuronium and 45% with saline-succinylcholine. The analysis adjusted for gender and center showed no superiority of MgSO(4)-rocuronium compared with saline-succinylcholine (relative risk [RR] 1.06, 95% confidence interval [CI], 0.81-1.39, P = .659). The rate of excellent intubating conditions was higher in women (54% [70 of 130]) compared with men (37% [48 of 129]; adjusted RR 1.42, 95% CI, 1.07-1.91, P = .017). No significant difference between groups was observed for systolic and diastolic blood pressures. Mean heart rate was significantly higher in the MgSO(4)-rocuronium group. The percentage of patients with at least 1 adverse event was lower with MgSO(4)-rocuronium (11%) compared with saline-succinylcholine (28%) (RR 0.38, 95% CI, 0.22-0.66, P < .001). With saline-succinylcholine, adverse events consisted mainly of postoperative muscle pain (n = 26 [19%]) and signs of histamine release (n = 13 [9%]). With MgSO(4)-rocuronium, few patients had pain on injection, nausea and vomiting, or skin rash during the MgSO(4)-infusion (n = 5 [4%]). CONCLUSIONS: IV pretreatment with MgSO(4) followed by a standard intubating dose of rocuronium did not provide superior intubation conditions to succinylcholine but had fewer adverse effects.