Intranasal dexmedetomidine vs oral triclofos sodium for sedation of children with autism undergoing electroencephalograms

被引:4
|
作者
Kaplan, Eytan [1 ,2 ,4 ]
Shifeldrim, Adi [2 ]
Kraus, Dror [3 ,4 ]
Weissbach, Avichai [1 ,4 ]
Kadmon, Gili [1 ,4 ]
Milkh, Rachel [2 ]
Nahum, Elhanan [1 ,4 ]
机构
[1] Schneider Childrens Med Ctr Israel, Pediat Intens Care Unit, Petah Tiqwa, Israel
[2] Schneider Childrens Med Ctr Israel, Pediat Sedat Serv, Petah Tiqwa, Israel
[3] Schneider Childrens Med Ctr Israel, Inst Neurol, Petah Tiqwa, Israel
[4] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
关键词
Autistic spectrum disorder; Dexmedetomidine; Electroencephalography; Pediatric sedation; Triclofos-sodium; CHLORAL HYDRATE; SPECTRUM DISORDER; EEG; MELATONIN;
D O I
10.1016/j.ejpn.2022.01.005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Sedation may be necessary for performing electroencephalograms in children with autistic spectrum disorder, however, our sedation success rate using triclofos sodium (TFS) is limited. Intra-nasal dexmedetomidine (IN-DEX) may be a superior sedative for these children. Objective: Compare IN-DEX with TFS for sedation efficacy, resistance to drug delivery and adverse events in children with autism undergoing an electroencephalogram. Study design: A single center, prospective observational study of children with autism sedated for electroencephalograms using IN-DEX compared to an age matched, historic group of children with autism, sedated for electroencephalograms using TFS. Results: Characteristics of 41 IN-DEX sedations were compared to 41 TFS sedations in 82 ASD children. Epileptiform discharges were demonstrated in 23/82 (28%) of children in the cohort. Sedation depth by UMSS was significantly deeper in the IN-DEX group (2.49 +/- 0.78 vs. 1.41 +/- 0.89, p < 0.001). Electroen-cephalogram quality demonstrated less motion artifact in the IN-DEX group (1.75 +/- 0.76 vs. 2.18 +/- 0.88, p < 0.001). The rate of very poor or sedation failure was significantly lower in the IN-DEX group (17% vs 56.1%, p < 0.001), RR = 0.3 (95% CI 0.15 to 0.63, p < 0.001). No major adverse events were documented in either group. Bradycardia occurred in 8/41(19.5%) of children in IN-DEX group and none in TFS group (p = 0.003). Hypotension or poor perfusion were not demonstrated in either group. Conclusion: In children with autism undergoing electroencephalograms, IN-DEX was more tolerable than TFS, induced deeper sedation with a greater success rate, and improved electroencephalogram quality. Both sedatives were equally safe in this population.(c) 2022 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:19 / 24
页数:6
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