2000
DOI: 10.1034/j.1399-6576.2000.441002.x
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Pharmacokinetic studies of neuromuscular blocking agents: Good Clinical Research Practice (GCRP)

Abstract: In September 1997, an international consensus conference on standardization of studies of neuromuscular blocking agents was held in Copenhagen, Denmark. Based on the conference, a set of guidelines for good clinical research practice (GCRP) in pharmacokinetic studies of neuromuscular blocking agents is presented. Guidelines include: design of the study; relevant patient groups to investigate; test drug administration, sampling and analysis; pharmacokinetic analysis; pharmacokinetic/pharmacodynamic modeling; po… Show more

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Cited by 46 publications
(26 citation statements)
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References 79 publications
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“…Neuromuscular transmission monitoring complied with GCRP (good clinical research practice) 6,7 , using TOF-Watch ® SX (Organon) NMT monitor. After induction, but before administration of the neuromuscular blocking drug, the TOF-Watch ® SX NMT monitor was calibrated using its automatic start-up-procedure, and we then applied 0.1 Hz single twitch stimulation.…”
Section: Neuromuscular Monitoringmentioning
confidence: 99%
“…Neuromuscular transmission monitoring complied with GCRP (good clinical research practice) 6,7 , using TOF-Watch ® SX (Organon) NMT monitor. After induction, but before administration of the neuromuscular blocking drug, the TOF-Watch ® SX NMT monitor was calibrated using its automatic start-up-procedure, and we then applied 0.1 Hz single twitch stimulation.…”
Section: Neuromuscular Monitoringmentioning
confidence: 99%
“…Neuromuscular transmission monitoring complied with GCRP (good clinical research practice) 7,8 , using the NMT module of Datex-Ohmeda S/5™ Anaesthesia Monitor. Both oesophageal and skin temperature were Cisatracurium vs. rocuronium: a prospective, comparative, randomized study in adult patients under total intravenous anaesthesia continuously recorded.…”
Section: Neuromuscular Block and Monitoringmentioning
confidence: 99%
“…The evaluation included: 1) cisatracurium onset time (time interval [sec] between starting cisatracurium injection and obtaining ≥ 95% reduction in the amplitude response of adductor pollicis muscle); 2) clinical condition of tracheal intubation according to the scores proposed by Viby-Mogensen et al 2 , considering the following variables: diffi cult laryngoscopy (degree), vocal cords position, and reaction to tracheal tube insertion (Table 1) -intubation was considered acceptable when all variables were considered excellent or good and unacceptable when at least one variable was considered poor; 3 ) hemodynamic parameters (mean arterial pressure [MAP] and heart rate [HR]), measured immediately before anesthesia induction (T0), after anesthesia induction, before laryngoscopy and tracheal intubation (M1), and 1 minute after intubation (M2).…”
Section: Methodsmentioning
confidence: 99%
“…This time interval can be infl uenced by factors, such as hypnotics and those associated with neuromuscular block monitoring (e.g., time to muscle stabilization, control, and frequency of stimulation used) [1][2][3][4][5] . Among drugs used in anesthesia, some hypnotics have certain peculiarities and different mechanisms, with may interfere with muscle relaxation induced by nondepolarizing neuromuscular blockers (NDNMB) 5,[6][7][8] .…”
Section: Introductionmentioning
confidence: 99%