Safety and Efficacy of Oral Triclofos in the Evaluation of Young and Uncooperative Children in Pediatric Ophthalmology Clinic
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چکیده
Subjects and Methods: This interventional prospective cohort study included children between 1 and 16 years of age. Children without an acute medical condition and normal cardio respiratory status, uncooperative for the relevant ocular examination were administered oral triclofos at a dose of 75mg/kg. The pulse oximetry, onset and duration of sedation, post sedation neurobehaviour and cognition were recorded.
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