The pharmacokinetics of rocuronium bromide in pediatric patients (n=146) aged 0 - 17 years was analyzed by population analysis of the pooled pharmacokinetic datasets from two clinical trials in which anesthesia was induced with sevoflurane and maintained with isoflurane/nitrous oxide. All pharmacokinetic parameters were found to be linearly proportional to body weight, demonstrated by similar CL. The Vd and T1/2 decreased with age (years). The pharmacokinetic parameters of the characteristic pediatric patient within each age group are summarized in table 1 (SmpC Esmeron; Wierda 1997; Vuksanaj 1995).
Table 1. Estimated PK parameters (mean) of rocuronium bromide in characteristic pediatric patients during sevoflurane and nitrous oxide (induction) and isoflurane/ nitrous oxide (maintenance anesthesia) (SmpC Esmeron; Wierda 1997; Vuksanaj 1995).
| Cl (l/kg/hour) | Vd (l/kg) | t½ (hours) | |
|---|---|---|---|
| 0-27 days | 0.31 | 0.42 | 1.1 |
| 1-2 months | 0.3 | 0.31 | 0.9 |
| 3-23 months | 0.33 | 0.23 | 0.8 |
| 2-11 yrs | 0.35 | 0.18 | 0.7 |
| 12-17 yrs | 0.29 | 0.18 | 0.8 |
The mean time before onset of action is slightly shorter in infants, toddlers, and children than in neonates, adolescents, and adults. A good intubation condition is independent of the onset time, which varies based on dose and patient-related factors. The duration of action and time to recovery are usually shorter in children than in infants and adults. In neonates and infants, the duration of action of the single intubation dose will be longer than in older childre
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| Neuromuscular blockade |
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GFR ≥10 ml/min/1.73m2: In renal impairment, the duration of action is prolonged. For emergency induction, an initial dose of 0.6 mg/kg and a maintenance dose of 0.075-0.1 mg/kg is recommended, regardless of the method of anesthesia. When administered as a continuous infusion, the recommended maintenance dose is 0.3-0.4 mg/kg per hour (KNMP-IM).
GFR <10 ml/min/1.73m2: a general recommendation cannot be given.
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The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Tachycardia in 1,4% of patients [SmPC]
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The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
No information available on specific contra indications in children.
The complete list of all warnings and precautions can be found in the national Summary of Product Characteristics (SmPC) – click here
Monitor neuromuscular function. The duration of action for muscle relaxants is so variable that relaxation measurement should be considered before extubation and antagonized if necessary.
In children with obesity, ideal-body weight or adjust body weight in calculating the dose of rocuronium is recommended instead of use of total body weight (Ross 2015; NHS 2021).
Cross hypersensitivity - including from other groups - is possible. This may be based on the excipients but also on the active ingredient. Advice is to consult a pediatric allergist in case of a suspected allergic reaction to a muscle relaxant and to also test for safety of alternative muscle relaxants.
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| Choline derivatives | ||
|---|---|---|
| M03AB01 | ||
| Other quaternary ammonium compounds | ||
|---|---|---|
| M03AC04 | ||
| M03AC11 | ||
| M03AC10 | ||
| M03AC01 | ||
| M03AC03 | ||
| Other muscle relaxants, peripherally acting agents | ||
|---|---|---|
| M03AX01 | ||
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