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1.
Neurology ; 67(3): 400-6, 2006 Aug 08.
Article in English | MEDLINE | ID: mdl-16894098

ABSTRACT

OBJECTIVE: To compare the cognitive effects of lamotrigine vs topiramate as adjunctive therapy in adults with epilepsy. METHODS: A multicenter, double-blind, randomized, prospective study was conducted in adults with partial seizures. Lamotrigine or topiramate was introduced as an adjunctive therapy to carbamazepine or phenytoin and titrated over 8 weeks to target doses. These drugs were maintained another 8 weeks (maintenance phase) without dosage changes. The primary endpoint was change from screening to the end of the maintenance phase in a combined analysis of standardized measures of cognition (Controlled Oral Word Association Task [COWA]; Stroop Color-Word Interference; Digit Cancellation; Lafayette Grooved Pegboard, dominant hand; Rey Auditory Verbal Learning Test, delayed recall; and Symbol-Digit Modalities test). RESULTS: For the primary endpoint, cognitive performance at the end of the maintenance phase was better with lamotrigine than with topiramate (415.3 vs 315.1; p < 0.001). On the individual cognitive tests, performance was better with lamotrigine than with topiramate in mean changes from screening on the COWA (p < 0.001), Stroop Color-Word Interference (p = 0.038), and Symbol-Digit Modalities tests (p < 0.001). The treatment effect exceeded the minimum clinically important difference for the COWA and the Symbol-Digit Modalities test. Mean changes from screening in the Performance-On-Line test simulating driving skills reflected better performance with lamotrigine than with topiramate (p = 0.021). The median percentage change from baseline in seizure frequency was lower with lamotrigine than with topiramate during the escalation phase (-80% vs -100%; p = 0.028) but not during the maintenance phase (-75% vs -100%; p = 0.062). The frequencies of cognitive adverse events and of premature withdrawals related to cognitive decline were higher with topiramate than with lamotrigine (6% vs 0%; p = 0.013). CONCLUSION: Lamotrigine had significantly less impact than topiramate on measures of cognition when used as adjunctive therapy for partial seizures.


Subject(s)
Anticonvulsants/pharmacology , Cognition/drug effects , Fructose/analogs & derivatives , Triazines/pharmacology , Adolescent , Adult , Aged , Anticonvulsants/therapeutic use , Double-Blind Method , Epilepsy/drug therapy , Female , Fructose/pharmacology , Fructose/therapeutic use , Humans , Lamotrigine , Male , Prospective Studies , Topiramate , Treatment Outcome , Triazines/therapeutic use
2.
Pediatr Neurol ; 25(5): 419-21, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11744321

ABSTRACT

The polyneuropathy caused by chronic gasoline inhalation is reported to be a gradually progressive, symmetric, sensorimotor polyneuropathy. We report unleaded gasoline sniffing by a female 14 years of age that precipitated peripheral neuropathy. In contrast with the previously reported presentation of peripheral neuropathy in gasoline inhalation, our patient developed multiple mononeuropathies superimposed on a background of sensorimotor polyneuropathy. The patient illustrates that gasoline sniffing neuropathy may present with acute multiple mononeuropathies resembling mononeuritis multiplex, possibly related to increased peripheral nerve susceptibility to pressure in the setting of neurotoxic components of gasoline. The presence of tetraethyl lead, which is no longer present in modern gasoline mixtures, is apparently not a necessary factor in the development of gasoline sniffer's neuropathy.


Subject(s)
Gasoline/adverse effects , Mononeuropathies/chemically induced , Neuritis/chemically induced , Substance-Related Disorders/diagnosis , Administration, Inhalation , Adolescent , Female , Humans , Mononeuropathies/diagnosis , Neural Conduction/drug effects , Neuritis/diagnosis , Neurologic Examination/drug effects , Reaction Time/drug effects
3.
J Clin Neurophysiol ; 18(2): 162-5, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11435807

ABSTRACT

Policies of administration and availability of EEG offered during nonbusiness hours vary widely among EEG laboratories. The authors surveyed medical directors of accredited EEG laboratories (n = 84) to determine the ranges of availability and clinical indications for approval of continuously available emergent EEG (E-EEG). Of 46 respondents, 37 (80%) offered E-EEG. Two centers recently lost funding for E-EEG. Availability was not associated with the total number of EEGs performed annually. The mean estimated response time from request to expert interpretation was 3 +/- 4 hours (range, 1-24 hours). The five clinical indications for which most respondents approved E-EEGs were possible nonconvulsive status epilepticus (100%), treatment of status epilepticus (84%), cerebral death exam (81%), diagnosis of convulsive status epilepticus (79%), and diagnosis of coma or encephalopathy (70%). Respondents disagreed widely when asked which clinical situations merited E-EEG, with some approving all requests and others denying all except for nonconvulsive status epilepticus. The wide range of current practice suggests that research focused on outcomes of aggressive, EEG-aided patient evaluation and treatment are needed to define better the costs and benefits of a continuously available EEG service.


Subject(s)
Electroencephalography/statistics & numerical data , Emergency Treatment/standards , Health Services Accessibility/statistics & numerical data , Laboratories, Hospital/organization & administration , Practice Patterns, Physicians'/statistics & numerical data , Brain Death/diagnosis , Brain Diseases/diagnosis , Canada , Coma/diagnosis , Electroencephalography/economics , Health Care Surveys , Health Services Accessibility/trends , Humans , Laboratories, Hospital/statistics & numerical data , Practice Patterns, Physicians'/trends , Referral and Consultation/statistics & numerical data , Status Epilepticus/diagnosis , Time and Motion Studies , United States , Workforce
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