Effect of tetanic stimulation prior to the train-of-four monitoring on the time to muscle response stabilisation in patients aged 60 to 80 years: a randomised controlled trial

Author:

Ribeiro Angela Henrique Silva1,Verçosa Nubia2,Filho Paulo A Germano1,Braga Estêvão Luiz C1,Micuci Angelo Jorge3,Cavalcanti Ismar L1

Affiliation:

1. Universidade Federal Fluminense (UFF)

2. Universidade Federal do Rio de Janeiro (UFRJ)

3. Hospital Federal de Bonsucesso

Abstract

Abstract Purpose To determine the effect of tetanic stimulation in patients aged 60 to 80 years on the time to achieve stabilisation of the T1 height. Methods This multicentre, randomised, open-label and controlled trial was conducted in two tertiary public hospitals in Brazil from December 2019 to February 2022. Seventy patients aged 60 to 80 years undergoing elective surgery under general anaesthesia were randomly allocated to receive tetanic stimulation to achieve T1 height stabilisation on train-of-four monitoring or not. We evaluated the effect of tetanic stimulation in patients aged 60–80 years on the time to achieve stabilisation of the T1 height, time to the onset of action of the neuromuscular blocking agent, and neuromuscular block recovery times after a single dose of rocuronium 0.6 mg.kg− 1. Results There was no statistically significant difference between the two groups in the time to T1 height stabilisation (control: 5.8 [2.0-10.5] min; tetanic: 4.3 [2.0–8.0] min; p = 0.42), onset time of the neuromuscular blocking agent (control: 2.2 [± 1.0] min; tetanic: 1.9 [± 0.7] min; p = 0.295), or neuromuscular block recovery times to normalised TOF values of 0.7 (control: 91.7 [± 27.5] min; tetanic: 106.1 [± 37.2] min; p = 0.126), 0.8 (control: 97.8 [± 28.9] min; tetanic: 114.3 [± 40.1] min; p = 0.101), 0.9 (control: 106.9 [± 30.6] min; tetanic: 126.5 [± 44.0] min; p = 0.074), or 1.0 (control: 123 [± 43.5] min; tetanic: 134.1 [± 44.5] min; p = 0.425). Conclusion The recommendation to use tetanic stimulation to shorten the time to T1 height stabilisation in neuromuscular monitoring does not apply to patients older than 60 years. Trial registration : The study was registered on the Brazilian Clinical Trials Registry (ReBEC) platform (number RBR-35msdt).

Publisher

Research Square Platform LLC

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