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Dose-dependent effect of esketamine on preventing rocuronium-induced limb withdrawal in preschool children
Jie Wang1, Zhiguo Zhou1, Wen-Lu Ma1
1Department of Surgical Anesthesia, Hangzhou Children's Hospital, China.
Insights
Pre-anesthesia esketamine effectively reduces rocuronium-induced limb withdrawal reactions in preschool children. A 0.1 mg/kg dose of esketamine significantly lowered reaction incidence and severity during anesthesia induction.
Area of Science:
- Anesthesiology
- Pediatric Pharmacology
- Pain Management
Background:
- Rocuronium injection commonly causes limb withdrawal reactions in preschool children during anesthesia induction.
- These reactions can lead to adverse effects, necessitating mitigation strategies.
- The optimal dose of esketamine for preventing these reactions is not well-established.
Purpose of the Study:
- To evaluate the efficacy of different prophylactic esketamine doses in mitigating rocuronium-induced limb withdrawal reactions.
- To compare the incidence and severity of limb withdrawal reactions across varying esketamine dosages.
- To assess the impact of esketamine on hemodynamic parameters during anesthesia induction.
Main Methods:
- Ninety preschool children (2-6 years, ASA I-II) undergoing elective surgery were randomized into three groups: control (saline), esketamine 0.1 mg/kg, and esketamine 0.2 mg/kg.
- Esketamine or saline was administered intravenously 30 seconds prior to rocuronium injection.
- Mean arterial pressure (MAP) and heart rate (HR) were monitored, along with the incidence and severity of limb withdrawal reactions.
Main Results:
- The incidence of limb withdrawal reactions was significantly lower in the esketamine groups (16.67% for 0.1 mg/kg, 13.33% for 0.2 mg/kg) compared to the control group (43.33%).
- Both incidence and severity of limb withdrawal reactions showed statistically significant differences among the three groups.
- Hemodynamic parameters (MAP and HR) showed varied changes, with significant increases noted in the control group post-rocuronium and in the 0.2 mg/kg esketamine group at specific time points.
Conclusions:
- Prophylactic intravenous administration of 0.1 mg/kg esketamine is effective in reducing limb withdrawal reactions caused by rocuronium injection in preschool children.
- The 0.1 mg/kg dose of esketamine appears to be an optimal choice for mitigating these reactions.
- Further research may explore the 0.2 mg/kg dose's specific hemodynamic effects and long-term implications.
Background:
Rocuronium injection often causes limb withdrawal reactions in preschool children during anesthesia induction, which can lead to adverse effects. Esketamine has been reported to reduce such reactions, but the optimal dose remains unclear.
Objectives:
To observe the effect of different doses of esketamine administered in advance on limb withdrawal reactions caused by rocuronium in preschool children.
Material And Methods:
From January to December 2024, children aged 2-6 years (American Society of Anesthesiologists Physical Status Classification System (ASA) I-II) undergoing elective surgery with general anesthesia induction using rocuronium at Hangzhou Children's Hospital were enrolled, regardless of gender (90 cases in total). Patients were divided using a random number table into 3 groups: a control group (group C), an esketamine 0.1 mg/kg group (group K1), and an esketamine 0.2 mg/kg group (group K2). Each group received either saline (group C), 0.1 mg/kg esketamine (group K1), or 0.2 mg/kg esketamine (group K2), with 30 cases in each group. Thirty seconds later, all patients were administered rocuronium intravenously. Mean arterial pressure (MAP) and heart rate (HR) were recorded at 4 time points: before anesthesia induction (T0), before test drug injection (T1), before rocuronium injection (T2), and after rocuronium injection (T3). The incidence and severity of limb withdrawal reactions after rocuronium injection and adverse reactions were recorded.
Results:
Compared with T0, MAP and HR significantly decreased in all 3 groups before test drug injection (T1) (p < 0.05). After rocuronium injection (T3), MAP and HR significantly increased in group C (p < 0.05). Heart rate significantly increased at T2 and T3 in group K2 (p < 0.05). The incidence of limb withdrawal reactions was 43.33% in group C, 16.67% in group K1, and 13.33% in group K2, with statistically significant differences among the groups. The severity of limb withdrawal reactions also differed significantly among the 3 groups.
Conclusions:
Prophylactic intravenous injection of 0.1 mg/kg esketamine effectively reduces the limb withdrawal reaction caused by rocuronium injection.
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