Abstract

Comment Apparently two separate groups of Japanese researchers are simultaneously investigating the premedicating potential of oral clonidine, a centrally acting α-agonist. In awake adults, oral clonidine can cause bradycardia and hypotension and reduces the chronotropic response to intravenous atropine (Nishikawa et al.). In this investigation, high-dose (4 μg/kg) oral clonidine premedication in children, 10.8 ± 1.6 yr, also attenuated the increase in heart rate (HR) produced by intravenous atropine (10 μg/ kg) but did not cause significant changes in HR or blood pressure (BP) at the same or lower (2 M-g/kg) doses. No adverse effects of atropine were reported in this study, even though atropine doses as high as 30 μg/kg were required to increase HR 20 bpm in low-dose study patients, and atropine doses of 40 μg/kg were ineffective in 2 of 16 patients in the high-dose group. In addition, premedication with high-dose oral clonidine produced significandy higher (p <0.05, test statistic unreported) sedation scores than premedication with placebo or low-dose (2 μg/kg) oral clonidine. The authors concluded that effective (4 μg/kg) premedicating doses of oral clonidine can suppress the HR response to intravenous atropine in awake children; large doses (30–40+ μg/kg) of atropine may be required to increase HR 20 bpm in children

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