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1.
Epilepsy Behav ; 24(4): 426-9, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22683245

ABSTRACT

The objective of this study was to determine prevalence and predictive risk factors of suicidality in a large sample of epilepsy outpatients. We prospectively examined 193 consecutive adult epilepsy outpatients for depression, including suicidal ideation. Demographic and epilepsy factors, medication toxicity and health-related quality of life were also evaluated. The prevalence of suicidal ideation within the past two weeks was 11.9%. Although medication toxicity, health-related quality of life and BDI scores were each associated with suicidal ideation in the bivariate analyses, only the BDI remained significant in the logistic regression analysis. About one-fourth of the subjects with suicidal ideation had no significant symptoms of depression. Recent thoughts of suicide are a common occurrence in the outpatient epilepsy clinic setting, but these are not predicted by gender, age, seizure factors, medication toxicity or self-perceived quality of life. Although depression is associated with suicidal ideation, about one-fourth of the suicidal subjects were euthymic or only mildly depressed.


Subject(s)
Depression/epidemiology , Depression/psychology , Epilepsy/epidemiology , Epilepsy/psychology , Quality of Life , Suicide/psychology , Adult , Anticonvulsants/therapeutic use , Epilepsy/drug therapy , Female , Humans , Male , Middle Aged , Psychiatric Status Rating Scales , Regression Analysis , Seizures/epidemiology , Seizures/psychology , Suicide/statistics & numerical data , Surveys and Questionnaires
2.
Epilepsy Behav ; 14(3): 459-64, 2009 Mar.
Article in English | MEDLINE | ID: mdl-19130899

ABSTRACT

OBJECTIVE: Clinicians monitor cognitive effects of drugs primarily by asking patients to describe their side effects. We examined the relationship of subjective perception of cognition to mood and objective cognitive performance in healthy volunteers and neurological patients. METHODS: Three separate experiments used healthy adults treated with lamotrigine (LTG) and topiramate (TPM), adults with epilepsy on LTG or TPM, and patients with idiopathic Parkinson's disease. Correlations were calculated for change scores on and off drugs in the first two experiments and for the single assessment in Experiment 3. RESULTS: Across all three experiments, significant correlations were more frequent (chi(2)=259, P < or = 0.000) for mood versus subjective cognitive perception (59%) compared with subjective versus objective cognition (2%) and mood versus objective cognitive performance (2%). CONCLUSIONS: Subjective perception of cognitive effects is related more to mood than objective performance. Clinicians should be aware of this relationship when assessing patients' cognitive complaints.


Subject(s)
Affect/physiology , Anticonvulsants/pharmacology , Cognition/physiology , Epilepsies, Partial/psychology , Parkinson Disease/psychology , Psychomotor Performance/physiology , Self Concept , Adult , Affect/drug effects , Anticonvulsants/therapeutic use , Cognition/drug effects , Cross-Over Studies , Depression/psychology , Double-Blind Method , Epilepsies, Partial/drug therapy , Female , Fructose/analogs & derivatives , Fructose/pharmacology , Fructose/therapeutic use , Humans , Lamotrigine , Male , Neuropsychological Tests , Parkinson Disease/drug therapy , Psychomotor Performance/drug effects , Quality of Life , Topiramate , Triazines/pharmacology , Triazines/therapeutic use
3.
Epilepsy Res ; 80(2-3): 158-62, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18485669

ABSTRACT

BACKGROUND: Psychiatric disorders may occur in patients with intractable partial epilepsy after surgical treatment. Previous reports attributed the presence of psychological adverse events to specific pathological entities such as dysembryoplastic neuroepithelial tumors (DNETs) and gangliogliomas. The rationale for the present study is to evaluate the importance of the surgical pathology in individuals undergoing epilepsy surgery. METHODS: The patients were separated into three groups based on the surgical pathology: group I ganglioglioma (N=25), group II DNETs (N=25), and group III mesial temporal sclerosis (N=25). Thirteen of the 75 patients (17.3%) had a preexisting psychiatric disorder. The most common preoperative psychiatric diagnosis was depression (N=4). Sixty-three of the lesions (84%) were restricted to the temporal lobe. The operative strategy included resection of the lesion and epileptogenic cortex. Sixty-two of the 75 patients (83%) were rendered seizure-free. RESULTS: Eight of the 75 patients (10.7%) had an acquired psychiatric illness following surgical treatment. A mood disorder developed in three patients after surgery. No statistical difference emerged in preoperative psychiatric co-morbidity (no group difference; p=1.0) or in newly diagnosed postoperative psychiatric disease (group I vs. II, p=0.67; group I vs. III, p=1.0; and group II vs. III, p=0.67) within the three surgical pathology groups. CONCLUSION: This study indicates that the presence of psychiatric disease before and after surgery for intractable partial epilepsy, predominantly of temporal lobe origin, was independent of the pathological findings.


Subject(s)
Epilepsies, Partial/epidemiology , Epilepsies, Partial/pathology , Mental Disorders/epidemiology , Mental Disorders/etiology , Adolescent , Adult , Anterior Temporal Lobectomy/adverse effects , Child , Comorbidity , Epilepsies, Partial/surgery , Female , Follow-Up Studies , Functional Laterality , Ganglioglioma/epidemiology , Ganglioglioma/pathology , Ganglioglioma/surgery , Humans , Intelligence , Intelligence Tests , Male , Mental Disorders/pathology , Neuropsychological Tests , Retrospective Studies
4.
Neurology ; 64(12): 2108-14, 2005 Jun 28.
Article in English | MEDLINE | ID: mdl-15985582

ABSTRACT

BACKGROUND: The relative cognitive and behavioral effects of lamotrigine (LTG) and topiramate (TPM) are unclear. METHODS: The authors directly compared the cognitive and behavioral effects of LTG and TPM in 47 healthy adults using a double-blind, randomized crossover design with two 12-week treatment periods. During each treatment condition, subjects were titrated to receive either LTG or TPM at a target dose of 300 mg/day for each. Neuropsychological evaluation included 17 measures yielding 41 variables of cognitive function and subjective behavioral effects. Subjects were tested at the end of each antiepileptic drug (AED) treatment period and during two drug-free conditions (pretreatment baseline and 1 month following final AED withdrawal). RESULTS: Direct comparison of the two AEDs revealed significantly better performance on 33 (80%) variables for LTG, but none for TPM. Even after adjustment for blood levels, performance was better on 19 (46%) variables for LTG, but none for TPM. Differences spanned both objective cognitive and subjective behavioral measures. Comparison of TPM to the non-drug average revealed significantly better performance for non-drug average on 36 (88%) variables, but none for TPM. Comparison of LTG to non-drug average revealed better performance on 7 (17%) variables for non-drug average and 4 (10%) variables for LTG. CONCLUSIONS: Lamotrigine produces significantly fewer untoward cognitive and behavioral effects compared to topiramate (TPM) at the dosages, titrations, and timeframes employed in this study. The dosages employed may not have been equivalent in efficacy. Future studies are needed to delineate the cognitive and behavioral effects of TPM at lower dosages.


Subject(s)
Anticonvulsants/administration & dosage , Cognition Disorders/chemically induced , Fructose/analogs & derivatives , Mood Disorders/chemically induced , Triazines/adverse effects , Adult , Anticonvulsants/adverse effects , Brain/drug effects , Brain/physiopathology , Cognition Disorders/physiopathology , Cognition Disorders/psychology , Cross-Over Studies , Dose-Response Relationship, Drug , Double-Blind Method , Epilepsy/drug therapy , Female , Fructose/administration & dosage , Fructose/adverse effects , Humans , Lamotrigine , Male , Memory/drug effects , Memory Disorders/chemically induced , Memory Disorders/physiopathology , Memory Disorders/psychology , Middle Aged , Mood Disorders/physiopathology , Mood Disorders/psychology , Neuropsychological Tests , Psychomotor Performance/drug effects , Reaction Time/drug effects , Reference Values , Topiramate , Treatment Outcome , Triazines/administration & dosage , Verbal Behavior/drug effects
5.
Neurology ; 62(1): 23-7, 2004 Jan 13.
Article in English | MEDLINE | ID: mdl-14718691

ABSTRACT

OBJECTIVE: To determine the effectiveness of systematic screening with a brief 19-item self-report instrument, the Adverse Events Profile (AEP), to reduce adverse effects of antiepileptic drugs (AEDs) and improve subjective health status. METHODS: The authors performed a prospective randomized trial comparing the use of the AEP with usual care without the AEP. Sixty-two patients with an AEP score of >or=45 were enrolled from a consecutive group of 200 consenting adults with epilepsy. RESULTS: The mean percent improvement in AEP scores was greater in the patient group for which clinicians received the AEP compared with the usual care group (25% vs 5%; p < 0.01). Mean change in Quality of Life in Epilepsy Inventory (QOLIE)-89 total scores was not different between groups, but for the entire sample QOLIE-89 change was greater for patients having a 15-point improvement in AEP scores than for those with a 0- to 15-point improvement or a worsened score (24 vs 12 vs 3; analysis of variance, p < 0.008). More patients in the AEP group had a >15-point improvement in QOLIE-89 score (p < 0.03). Use of the AEP was associated with a 2.8-fold increase (95% CI, 1.7 to 4.8) in AED modifications. No difference in seizure rates was observed. CONCLUSIONS: Systematic screening for antiepileptic drug side effects may increase identification of toxicity and guide medication changes to reduce adverse effects and possibly improve subjective health status.


Subject(s)
Adverse Drug Reaction Reporting Systems/statistics & numerical data , Anticonvulsants/adverse effects , Drug Evaluation/methods , Drug Evaluation/statistics & numerical data , Surveys and Questionnaires , Academic Medical Centers/statistics & numerical data , Adult , Anticonvulsants/therapeutic use , Female , Health Status , Humans , Male , Missouri , Outpatients/statistics & numerical data , Prospective Studies , Quality of Life , Reproducibility of Results , Seizures/drug therapy , Treatment Outcome
6.
Vet Hum Toxicol ; 45(6): 294-8, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14640477

ABSTRACT

Phosphate mining operations in southeastern Idaho have exposed selenium (Se) that was originally sequestered in the subsurface. Sheep grazing in these areas have died as a result of high Se concentrations in forage and water. This study was designed to monitor the health status of sheep grazing in a natural environment with known elevated levels of Se. A total of 72 Columbia x Suffolk sheep were divided into 3 treatment groups that included control (Con), low selenium (LoSe) and high selenium (HiSe). The baseline phase of the study was conducted in an area with normal background Se levels in forage and water, and was grazed for 3 w by all sheep groups. The sheep then were moved onto reclaimed mine areas to begin the 4-w exposure phase. This was followed by a 2-w depuration phase where sheep again received normal Se levels in forage and water. The Con group was held on areas with normal Se levels of forage (< 0.32 ppm Se dw) and water (< 1.70 ppb Se). The LoSe group was held in an area of elevated forage Se (< 13.0 ppm Se dw) and normal Se levels in their water (< 1.70 ppb Se) during the exposure phase. The HiSe group was held on mining areas with elevated Se forage (< 49.0 ppm Se dw) and drinking water (340 to 415 ppb Se). Whole blood and serum levels in the HiSe group peaked at 1.32 and 0.99 ppm mean Se, respectively. The LoSe group had mean whole blood and serum Se levels of 0.75 ppm on day 42 and 0.32 ppm on day 35 respectively. The Con group maintained low Se levels in both whole blood and serum that ranged from 0.05 to 0.14 ppm and 0.06 to 0.13 ppm respectively. The Se exposure in the HiSe group was estimated 0.26 mg Se/kg body weight/d. One sheep in the HiSe group died and was diagnosed with Se toxicosis based on clinical signs, histopathology and tissue Se levels. Se in liver (3.90 ppm), kidney (1.90 ppm) and skeletal muscle (0.70 ppm) were indicative of high to toxic Se exposure. Two other sheep necropsied after the exposure phase also had Se concentrations in liver, kidney and skeletal muscle representative of high or toxic Se exposure (5.50, 3.50 and 1.10 ppm Se), but these sheep had no gross or histopathological signs of illness. More research is needed on the toxicology of Se in sheep grazing natural settings.


Subject(s)
Chemical and Drug Induced Liver Injury/veterinary , Diet , Environmental Pollutants/toxicity , Selenium/toxicity , Sheep Diseases/blood , Alanine Transaminase/blood , Alkaline Phosphatase/blood , Animal Husbandry , Animals , Animals, Newborn , Aspartate Aminotransferases/blood , Chemical and Drug Induced Liver Injury/blood , Chemical and Drug Induced Liver Injury/etiology , Female , Idaho , Kidney/metabolism , Liver/drug effects , Liver/enzymology , Liver/metabolism , Mining , Muscle, Skeletal/metabolism , Selenium/blood , Selenium/metabolism , Serum Albumin , Sheep , Sheep Diseases/chemically induced
7.
Epilepsia ; 42(10): 1340-4, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11737170

ABSTRACT

PURPOSE: High-dose i.v. opioids (e.g., alfentanil, 50 microg/kg bolus) are known to increase the intraoperative reading of epileptiform activity during epilepsy surgery (ES), thereby facilitating localization of the epileptogenic zone (i.e., the site of ictal onset and initial seizure propagation). However, this phenomenon has not been studied with remifentanil (i.e., a novel ultra-short acting opioid). The purpose of the present study was to evaluate the effect of remifentanil on electrocorticography (ECoG) during ES. METHODS: After Institutional Review Board approval, 25 adult patients undergoing elective ECoG-guided anterior temporal corticectomy were enrolled. At the time of ECoG, anesthesia consisted of inhaled isoflurane < or =0.1% (end-tidal) in 50% N2O, and i.v. fentanyl, 2 microg/kg/h and vecuronium. Patients were maintained at normocapnia and normoxia during ECoG. After acquisition of baseline ECoG, bolus remifentanil, 2.5 microg/kg i.v., was administered. The number of epileptiform spikes occurring 5 min before and after this bolus were compared by using a one-sided sign test; p values < or =0.05 were considered statistically significant. RESULTS: When compared with baseline ECoG, bolus i.v. remifentanil significantly increased the frequency of single spikes or repetitive spike bursts in the epileptogenic zone while suppressing activity in surrounding normal brain. CONCLUSIONS: During ES, remifentanil enhanced epileptiform activity during intraoperative ECoG. Such observations facilitate localization of the epileptogenic zone while minimizing resection of nonepileptogenic eloquent brain tissue. Although not specifically evaluated in this study, we speculate that remifentanil's short elimination half-life will facilitate neurologic function testing immediately after ES. Should this be the case, we envision remifentanil has the potential to supplant other opioids (e.g., alfentanil) during ECoG-guided ES.


Subject(s)
Cerebral Cortex/drug effects , Electroencephalography/drug effects , Epilepsy, Temporal Lobe/surgery , Epilepsy/chemically induced , Monitoring, Intraoperative , Piperidines/adverse effects , Adult , Aged , Brain Mapping , Cerebral Cortex/surgery , Dose-Response Relationship, Drug , Epilepsy/surgery , Epilepsy, Temporal Lobe/chemically induced , Female , Humans , Infusions, Intravenous , Male , Middle Aged , Neurologic Examination/drug effects , Piperidines/administration & dosage , Psychosurgery , Remifentanil , Temporal Lobe/drug effects , Temporal Lobe/surgery
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