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BronchoscopyNebulized Lidocaine Administered to Infants and Children Undergoing Flexible Bronchoscopy
Section snippets
Study Participants
Twenty infants and children were enrolled in the study. Approval for the study was obtained from the Institutional Review Board, and informed consent was obtained from the subjects’ parents. Patients were eligible if they were undergoing FOB for diagnostic or therapeutic purposes. Exclusion criteria included patients with known hepatic or cardiac disease and intubated patients. The patients were randomized into two groups: group 1 subjects received a low dose of 4 mg/kg of 2% lidocaine and
Results
The patients in both groups were similar in indications for FOB and underlying pathologic conditions. Three of the 10 patients in each group had BAL. No subject had transbronchial biopsy. Demographics for the two study groups are illustrated in Table 1. The low-dose group was older. The groups received nearly identical sedative doses (Table 1). Nine of ten patients in the low-dose group and all ten patients in the high-dose group received meperidol. Eight of the ten patients in the low-dose
Discussion
There is no recommended dosage of lidocaine given by the nebulized route for infants or children. We chose doses of 8 and 4 mg/kg because the standard adult nebulized dose of 4 mL of 4% lidocaine1 would approximate 4 mg/kg and the maximum pediatric squirted dose was suggested to be 8.5 mg/kg.2
Nebulized 2% lidocaine at doses of 8 and 4 mg/kg was shown to be extremely safe in infants and children, with all levels obtained well below the toxic range. Total doses of up to 19.6 mg/kg still did not
Conclusion
Lidocaine is a good local anesthetic, but at toxic levels it can cause seizures, cardiac arrhythmias, cardiac arrest, coma, parasthesia, and death.3 Therefore administration in an efficacious manner with low serum concentrations is beneficial. Although the sample size in this study was small, up to 8 mg/kg nebulized lidocaine administered by face mask was safe, was well-tolerated, and provided adequate topical anesthesia for half the patients.
ACKNOWLEDGMENTS
Dr. I. Argani provided laboratory assistance with the lidocaine levels and Ms. Jane Uman performed statistical analysis.
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