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2 mg/kg and then as an intravenous drip of 2 to 8 mg/kg/h is an effective alternative to midazolam, but after 24 h the drug behaves like a high dose of barbiturate and there may be dif culty due to hypotension If none of these measures controls the seizures, all medication except phenytoin should be discontinued and a more aggressive approach taken to subdue all brain electrical activity by the use of general anesthesia The preferred medications for this purpose have been pentobarbital and propofol, which, despite their poor record as primary anticonvulsants, are easier to manage than the alternative inhalational anesthetic agents An initial intravenous dose of 5 mg/kg pentobarbital or 2 mg/kg propofol is given slowly to induce an EEG burst-suppression pattern, which is then maintained by the administration of 05 to 2 mg/kg/h pentobarbital or up to 10 mg/kg/h of propofol Every 12 to 24 h, the rate of infusion is slowed to determine whether the seizures have stopped The experience of Lowenstein and colleagues, like our own, is that most instances of status epilepticus that cannot be controlled with the standard anticonvulsants and midazolam will respond to high doses of barbiturates or propofol, but that these infusions cause hypotension and cannot be carried out for long periods Should the seizures continue, either clinically or electrographically, despite all these medications, one is justi ed in the assumption that the convulsive tendency is so strong that it cannot be checked by reasonable quantities of anticonvulsants A few patients in this predicament have survived and awakened, even at times with minimal neurologic damage Iso urane (Forane) has been used in these circumstances with good effect, as we have reported (Ropper et al), but the continuous administration of such inhalational agents is impractical in most critical care units Halothane has been ineffective as an anticonvulsant, but ether, although impractical, has in the past been effective in some cases In the end, in these patients with truly intractable status, one usually depends on phenytoin, 05 g, and phenobarbital, 04 g/day (smaller doses in infants and children, as shown in Tables 16-9), and on measures that safeguard the patient s vital functions Valproate is available as an intravenous preparation, making it suitable for administration in status, but its potential role in this circumstance has not been extensively studied A word must be added concerning neuromuscular paralysis and continuous EEG monitoring in status epilepticus With failure of aggressive anticonvulsant and anesthetic treatment, there may be a temptation to paralyze all muscular activity, an effect easily attained with drugs such as pancuronium, while neglecting the underlying seizures The use of such neuromuscular blocking drugs without a concomitant attempt to suppress seizure activity is inadvisable If such measures are undertaken, continuous or frequent intermittent EEG monitoring is essential; this may also be also helpful in the early stages of status epilepticus in that it guides the dosages of anticonvulsants required to suppress the seizures In the related but less serious condition of acute repetitive seizures, in which the patient awakens between ts, a diazepam gel, which is well absorbed if given rectally, is available and has been found useful in institutional and home care of epileptic patients, although it is quite expensive A similar effect has been attained by the nasal or buccal (transmucosal) administration of midazolam, which is absorbed from these sites (5 mg/mL, 02 mg/ kg nasally; 2 mL to 10 mg buccally) These approaches have found their main use in children with frequent seizures who live in supervised environments, where a nurse or parent is available to administer the medication.

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Petit mal status should be managed by intravenous lorazepam, valproic acid, or both, followed by ethosuximide Nonconvulsive status is treated along the lines of grand mal status, usually stopping short of using anesthetic agents

The final formatting option is to change the dimensionality of the chart type or the shape of the chart types For column and bar charts, you can display the value ranges as rectangles, pyramids, cones, or cylinders, and for pie and doughnut charts, you can set the angle of

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The surgical excision of epileptic foci in simple and complex partial epilepsies that have not responded to intensive and prolonged medical therapy is being used with increasing effectiveness in a growing number of specialized epilepsy units At these centers, it has been estimated that approximately 25 percent of all patients with epilepsy are candidates for surgical therapy and more than half of these may bene t from surgery With increasing experience and standardized approaches, especially in patients with temporal lobe epilepsy, it has been suggested that many patients are waiting too long before the surgical option A perspective that may promote surgery in even more patients is the observation that about 60 percent of patients with partial seizures will respond to a conventional anticonvulsant but that among the remainder, few will respond to the addition of a second or third drug To locate the discharging focus requires a careful analysis of clinical and EEG ndings, often including those obtained by longterm video/EEG monitoring and, sometimes, intracranial EEG recording by means of intraparenchymal depth electrodes, subdural strip electrodes, and subdural grids Recently, functional imaging and specialized EEG analysis have been introduced to supplement these methods The most favorable candidates for surgery are those with complex partial seizures and a unilateral temporal lobe focus, in whom rates of cure and signi cant improvement approach 90 percent in some series, but overall, are probably closer to 50 percent after 5 years A randomized trial conducted by Wiebe and colleagues gave representative results after temporal lobectomy of 58 percent of 40 carefully studied patients remaining seizure-free after 1 year, in contrast to 8 percent on medication alone Furthermore, as reported by Yoon and colleagues, among those patients who remain free of seizures for 1 year after surgery, over half are still free of seizures after 10 years and most of the remainder had one or fewer episodes per year It should be emphasized that most patients undergoing surgery in all these studies still require some anticonvulsant medication Excision of cortical tissue outside of the temporal lobe accomplishes complete seizure-free states in about 50 percent Taking all seizure types together, only about 10 percent of patients obtain no improvement at all and less than 5 percent are worse Other surgical procedures of value in selected cases are section of the corpus callosum and hemispherectomy The most encouraging results with callosotomy have been obtained in the control of intractable partial and secondarily generalized seizures, particularly when atonic drop attacks are the most disabling seizure type Removal of the entire cortex of one hemisphere, in addition to the amygdala and hippocampus, has been of value in children and also in some adults with severe and extensive unilateral cerebral disease and intractable contralateral motor seizures and hemiplegia Rasmussen encephalitis, Sturge-Weber disease, and large porencephalic cysts at times fall into this category Surgical, focused radiation, or endovascular reduction of arteriovenous malformations may reduce the frequency of seizures, but the results in this regard are somewhat unpredictable (see Chap 34) Driving and Epilepsy Only a few states in the United States and most provinces of Canada mandate that physicians report patients.

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