“…Rocuronium is not dependent on renal blood flow for its major route of excretion, but is taken up by the liver and excreted into the bile in high concentrations [9]. Although hepatic uptake and biliary elimination are thought to be the main routes of elimination for rocuronium, it seems that renal failure can have a marked effect on rocuronium pharmacokinetics and pharmacodynamics, although not consistently so [16][17][18]. In patients with no or minimum renal function, the clinical duration and recovery time of rocuronium 0.6 mg/kg increased significantly [16][17][18].…”
Sugammadex rapidly and effectively reversed rocuronium-induced neuromuscular block in anesthetized cats, even when both renal pedicles were ligated and renal elimination of the drugs was no longer possible.
“…Rocuronium is not dependent on renal blood flow for its major route of excretion, but is taken up by the liver and excreted into the bile in high concentrations [9]. Although hepatic uptake and biliary elimination are thought to be the main routes of elimination for rocuronium, it seems that renal failure can have a marked effect on rocuronium pharmacokinetics and pharmacodynamics, although not consistently so [16][17][18]. In patients with no or minimum renal function, the clinical duration and recovery time of rocuronium 0.6 mg/kg increased significantly [16][17][18].…”
Sugammadex rapidly and effectively reversed rocuronium-induced neuromuscular block in anesthetized cats, even when both renal pedicles were ligated and renal elimination of the drugs was no longer possible.
“…Sugammadex has been used also in patients with end-stage renal failure (114). Even though elimination kinetics of rocuronium is known to be prolonged in renal failure (115), the study could not find any difference of reversal characteristics between the patients with end-stage renal failure and those with normal renal function (114). When sugammadex 2 mgAEkg )1 was administered at the reappearance of the second twitch response, it took 2.0 ± 0.7 and 1.7 ± 0.6 min, respectively, to attain a TOF ratio of 0.90.…”
Even though neuromuscular blocking agents are an essential part of balanced anesthesia and the risks of residual paralysis are well documented, many anesthetists seldomly monitor neuromuscular block. Classical reversal agent neostigmine is unable to antagonise a deep neuromuscular block and is rather slow to antagonise even a moderate block. These caveats may have introduced a practice to use muscle relaxants mainly for an endotracheal intubation. This review presents current views on the effects of muscle relaxants and their reversal agents in pediatric patients. This may help clinicians to reconsider the value of muscle relaxants during anesthesia in children.
“…We estimated a 10 min sd for time to reappearance of T4 based on two previous studies. 1,13 We considered a difference in time to reappearance of T4 of 10 min between the IBW and CBW40% groups to be clinically relevant. We calculated that a sample size of 17 patients in each group would allow us to detect this difference, with 5% Type 1 error risk, 80% power, and 10% dropout.…”
Section: Danish Medicines Agency and The Local Ethicsmentioning
In obese patients undergoing gastric banding or gastric bypass, rocuronium dosed according to IBW provided a shorter duration of action without a significantly prolonged onset time or compromised conditions for tracheal intubation.
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