Hilde M. Braakman , Joke Creemers , Danny M. Hilkman , Sylvia Klinkenberg , Suzanne M. Koudijs , Mariette Debeij-van Hall , Erwin M. Cornips
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引用次数: 4
Abstract
We report a child with Lennox–Gastaut syndrome with an increase in seizure frequency and loss of psychomotor skills due to a disintegrated cervical VNS lead, not detected during standard device monitoring. The lead was completely removed and replaced by a new 303 lead on the same nerve segment. After reinitiating VNS, side effects forced us to switch it off, resulting in immediate seizure recurrence. EEG recording demonstrated a non-convulsive status epilepticus that was halted by reinitiating VNS therapy. Thereafter, he remained seizure free for eight months, and regained psychomotor development.
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