Title |
Sedation with dexmedetomidine for conducting electroencephalogram in a patient with Angelman syndrome: a case report
|
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Published in |
Brazilian Journal of Anesthesiology, March 2014
|
DOI | 10.1016/j.bjane.2013.06.020 |
Pubmed ID | |
Authors |
Magda Lourenço Fernandes, Maria do Carmo Santos, Renato Santiago Gomez |
Abstract |
Angelman syndrome is characterized by severe mental retardation and speech and seizure disorders. This rare genetic condition is associated with changes in GABAA receptor. Patients with Angelman syndrome need to be sedated during an electroencephalogram ordered for diagnostic purposes or evolutionary control. Dexmedetomidine, whose action is independent of GABA receptor, promotes a sleep similar to physiological sleep and can facilitate the performing of this examination in patients with Angelman syndrome. Female patient, 14 years old, with Angelman syndrome; electroencephalogram done under sedation with dexmedetomidine. The procedure was uneventful and bradycardia or respiratory depression was not recorded. The examination was successfully interpreted and epileptiform activity was not observed. Dexmedetomidine promoted satisfactory sedation, was well tolerated and enabled the interpretation of the electroencephalogram in a patient with Angelman syndrome and seizure disorder. |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 36 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
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Unspecified | 8 | 22% |
Student > Master | 8 | 22% |
Student > Bachelor | 4 | 11% |
Student > Ph. D. Student | 3 | 8% |
Student > Doctoral Student | 2 | 6% |
Other | 5 | 14% |
Unknown | 6 | 17% |
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Medicine and Dentistry | 5 | 14% |
Neuroscience | 4 | 11% |
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Other | 7 | 19% |
Unknown | 5 | 14% |