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World Neurosurg ; 89: 320-8, 2016 May.
Artículo en Inglés | MEDLINE | ID: mdl-26805677

RESUMEN

OBJECTIVE: The α2 agonist dexmedetomidine (DEX) is an anesthetic agent that can provide sedation and analgesia without respiratory depression or changes in neuronal activity during microrecordings. The aim of our study was to confirm the efficacy and safety of anesthesia with DEX for unilateral deep brain stimulation of the subthalamic nucleus (STN) in patients with Parkinson disease. METHODS: In 2013 and 2014, a series of 11 consecutive patients received continuous low-dose DEX infusion during unilateral deep brain stimulation of the STN. Intraoperative microrecordings, stimulation results, and patient reaction times in executing verbal and motor tasks were retrospectively analyzed. Functional outcomes were evaluated by comparing preoperative and 1-year postoperative Unified Parkinson's Disease Rating Scale Part III scores. RESULTS: Typical activity of the STN was recorded in all patients, and the delay in the execution of both motor and verbal tasks was ≤2 seconds. No hemorrhagic complications occurred, and no postoperative side effects were observed. The mean percentage of Unified Parkinson's Disease Rating Scale Part III improvement at last follow-up was 39.01% (range, 23.70%-55.60%). The mean percentage of levodopa equivalent dose reduction was 45.86% (range, 21.50%-65.70%). CONCLUSIONS: The results of our study confirm that the use of DEX in managing patients with Parkinson disease during unilateral deep brain stimulation of the STN is safe and effective and can be considered a promising option for sedation during this type of procedure.


Asunto(s)
Estimulación Encefálica Profunda/métodos , Dexmedetomidina/uso terapéutico , Hipnóticos y Sedantes/uso terapéutico , Enfermedad de Parkinson/terapia , Núcleo Subtalámico/efectos de los fármacos , Núcleo Subtalámico/fisiopatología , Agonistas de Receptores Adrenérgicos alfa 2/uso terapéutico , Anciano , Antiparkinsonianos/uso terapéutico , Femenino , Estudios de Seguimiento , Humanos , Monitorización Neurofisiológica Intraoperatoria , Masculino , Persona de Mediana Edad , Actividad Motora/efectos de los fármacos , Actividad Motora/fisiología , Pruebas Neuropsicológicas , Enfermedad de Parkinson/fisiopatología , Tiempo de Reacción , Estudios Retrospectivos , Índice de Severidad de la Enfermedad , Habla/efectos de los fármacos , Habla/fisiología , Resultado del Tratamiento
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