Revista brasileira de anestesiologia
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Rev Bras Anestesiol · Aug 2007
[Comparison of the bispectral index in awake patients with cerebral palsy].
The EEG-BIS was created after studies in healthy adult subjects, and studies in children were first published in 1998. Cerebral palsy (CP) is secondary to a static lesion of the developing brain. The need to perform exams and surgical procedures to correct deformities, under anesthesia or sedation, is common in these patients. The need for monitoring of the hypnotic state in anesthetized patients has increased; patients with cerebral palsy can be included in this group of patients. The objective of this study was to evaluate the efficacy of the awake EEG-BIS in patients with cerebral palsy (CP) by comparing it with patients without neurological disorders (without CP). ⋯ The signals of the EEG are captured normally and the values of the awake EEG-BIS of CP patients are similar to that of non-CP patients.
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Rev Bras Anestesiol · Aug 2007
[Temporary lingual nerve dysfunction following the use of the laryngeal mask airway: report].
The laryngeal mask has been frequently used in Anesthesiology. Although the rate of complications with this technique is smaller than that of the endotracheal tube, it is not devoid of risks, especially in cases of difficult airways. The objective of this study was to report a case of unilateral lingual nerve damage after the use of the laryngeal mask airway. ⋯ Although complications after the use of the laryngeal mask airway are rare, they do occur, and neuropraxis of the lingual nerve is one of them. The diagnosis is clinical and it has a good outcome, with resolution of the symptoms within a few weeks or months.
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The Marshall-Smith Syndrome is a rare disease characterized by facial dysmorphism, accelerated osseous maturation, retarded neuropsychomotor development, and abnormalities of the airways. Patients with this syndrome have a high risk of developing anesthetic complications, especially concerning the maintenance of the airways. There are very few data in the anesthetic literature regarding this syndrome. The objective of this report was to show the difficulties and anesthetic management in a 28-day old child with this syndrome, who underwent surgery for correction of choanal atresia under general anesthesia. ⋯ In cases of anesthetic-surgical emergencies, in which the child does not ventilate and tracheal intubation is not possible, there is desaturation and bradycardia, requiring fast and appropriate decision making to guarantee adequate pulmonary ventilation. These patients need careful evaluation of the airways to identify upper and lower airways obstruction. During anesthesia, spontaneous ventilation should be maintained during induction until control of the airways is possible, avoiding the use of neuromuscular blockers.