What is the intubating dose of Rocuronium (rocuronium)?

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Last updated: April 8, 2025View editorial policy

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From the Guidelines

The intubating dose of rocuronium for rapid sequence intubation (RSI) is 0.9 to 1.2 mg/kg intravenously, as recommended by recent guidelines. This dose is supported by the most recent and highest quality study, which found that rocuronium at a dose of 0.9 to 1.2 mg/kg provides excellent intubating conditions [ 1 ]. For patients with significant cardiovascular disease, renal impairment, or hepatic dysfunction, consider using the lower end of the dosing range.

Key Points to Consider

  • The choice of rocuronium as a muscle relaxant for RSI is based on its rapid onset of action and its suitability for patients with contraindications to succinylcholine [ 1 ].
  • The availability of sugammadex to reverse rocuronium rapidly may have encouraged the use of rocuronium in some settings when a selective relaxant binding agent (SRBA) is available [ 1 ].
  • Rocuronium's duration of action is approximately 30-40 minutes at the 0.6 mg/kg dose and 60-70 minutes at higher doses.
  • The medication works by competitively binding to nicotinic acetylcholine receptors at the neuromuscular junction, preventing acetylcholine from binding and thus blocking muscle contraction.

Important Considerations

  • Unlike succinylcholine, rocuronium doesn't cause hyperkalemia or malignant hyperthermia, making it suitable for patients with contraindications to succinylcholine.
  • Recent guidelines from the European Society of Anaesthesiology and Intensive Care make a strong recommendation, based on a moderate level of evidence, for the use of a fast-acting muscle relaxant such as succinylcholine 1–2 mg kg-1 or rocuronium 0.9 to 1.2 mg kg-1 for RSII [ 1 ].

From the FDA Drug Label

2.2 Dose for Tracheal Intubation The recommended initial dose of rocuronium bromide injection, regardless of anesthetic technique, is 0.6 mg/kg. Neuromuscular block sufficient for intubation (80% block or greater) is attained in a median (range) time of 1 (0.4 to 6) minute(s) and most patients have intubation completed within 2 minutes.

The intubating dose of rocuronium is 0.6 mg/kg. This dose may provide 31 (15 to 85) minutes of clinical relaxation under opioid/nitrous oxide/oxygen anesthesia. A lower dose of 0.45 mg/kg may also be used, providing 22 (12 to 31) minutes of clinical relaxation under opioid/nitrous oxide/oxygen anesthesia. For rapid sequence intubation, a dose of 0.6 to 1.2 mg/kg can be administered. 2

From the Research

Intubating Dose of Rocuronium

The intubating dose of rocuronium is a topic of interest in the field of anesthesia. According to the studies, the recommended dose of rocuronium for rapid sequence intubation is:

  • 0.6 mg/kg, as mentioned in the study by 3
  • 0.6 mg/kg, as mentioned in the study by 4
  • 1.0 mg/kg, as mentioned in the study by 5
  • 1.2 mg/kg, as mentioned in the study by 6

Comparison with Succinylcholine

Rocuronium is often compared to succinylcholine, another muscle relaxant commonly used for rapid sequence intubation. The studies suggest that:

  • Succinylcholine creates superior intubation conditions to rocuronium, as mentioned in the study by 6 and 7
  • Rocuronium may be associated with fewer adverse effects, as mentioned in the study by 3
  • The optimal dose of rocuronium for emergency airway management is not clear, as mentioned in the study by 5

Key Findings

Some key findings from the studies include:

  • The rate of excellent intubating conditions was 46% with MgSO4-rocuronium and 45% with saline-succinylcholine, as mentioned in the study by 3
  • The incidence of oxygen desaturations did not differ between succinylcholine and rocuronium, as mentioned in the study by 4
  • Rocuronium dosed ≥1.4 mg/kg was associated with higher first-attempt success when using direct laryngoscopy, as mentioned in the study by 5

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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