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1.
Epilepsy Behav ; 136: 108943, 2022 11.
Artículo en Inglés | MEDLINE | ID: mdl-36252288

RESUMEN

OBJECTIVE: We compared the relative occurrence of selected pregnancy outcomes and postpartum rehospitalizations among women with and without epilepsy and their infants. Using linked vital-hospital discharge records of women with deliveries in Washington State 1987-2014, comparisons were made overall, by epilepsy type, and by time periods related to antiepileptic drug (AED) marketing changes. METHODS: This population-based retrospective cohort study identified women with, and without epilepsy per diagnosis codes in the hospital discharge record from among all deliveries during 1987-2014 to examine maternal and infant outcomes, rehospitalization and mortality <2 years postpartum. Relative risks (RRs) and 95 % confidence intervals (CI) overall, and by epilepsy type were calculated using Poisson regression. We assessed the validity of epilepsy identification based on diagnosis codes by conducting a medical chart review for a sample of women. RESULTS: Women with epilepsy had increased risks of preeclampsia (RR 1.23; 95 % CI 1.08-1.41) and gestational diabetes (RR 1.18; 95 % CI 1.02-1.36). Their infants had increased malformation (RR 1.23; 95 % C: 1.08-1.42) and small for gestational age (SGA, RR 1.39; 95 % CI 1.25-1.54) risks, and were nearly three times as likely to not be breastfed. Affected mothers (RR 5.25; 95 % CI 2.46-11.23) and their infants (RR 1.64, 95 % CI 1.41-1.89) required more ICU admissions during the delivery hospitalizations, and more postpartum rehospitalization, with greatest risk in the first six months. Maternal mortality < 2 years after delivery was increased (RR 7.11; 95 % CI 2.47-20.49). Increased risks were observed for all epilepsy subtypes for nearly all outcomes examined. Risks of preterm delivery and low birthweight increased over time (p <.05). Suggestive, but not statistically significant temporal decreases in risks of gestational diabetes and malformations and increased risk of preterm labor were noted. We observed high sensitivity of diagnosis codes for identifying pregnant women with epilepsy. CONCLUSION: These population-based results emphasize the need for frequent postpartum monitoring of women with epilepsy. Increases in risks of low birthweight and preterm delivery over time are of concern. Possible temporal changes in other outcomes warrant further investigation.


Asunto(s)
Diabetes Gestacional , Epilepsia , Nacimiento Prematuro , Lactante , Recién Nacido , Embarazo , Femenino , Humanos , Diabetes Gestacional/epidemiología , Nacimiento Prematuro/epidemiología , Estudios Retrospectivos , Peso al Nacer , Periodo Posparto , Epilepsia/tratamiento farmacológico , Epilepsia/epidemiología , Morbilidad
4.
Neurodiagn J ; 53(2): 169-78, 2013 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-23833843

RESUMEN

A 29-year-old woman has a history of developmental delay and focal segmental glomerulosclerosis resulting in kidney failure. She underwent renal transplant which unfortunately failed, and is on hemodialysis as well as immunosuppression including tacrolimus. She was recently hospitalized for urosepsis requiring intensive treatment with vasopressors and multiple antibiotics. Soon after discharge, she was noted to have unstable gait, multifocal twitches, falls, and very brief episodes of staring or inattentiveness. She was readmitted. Her head CT was normal and lumbar puncture was negative. A bedside EEG was requested and showed an unusual response during photic stimulation.


Asunto(s)
Electroencefalografía/métodos , Epilepsias Mioclónicas/clasificación , Epilepsias Mioclónicas/diagnóstico , Estimulación Luminosa/métodos , Trastornos por Fotosensibilidad/clasificación , Trastornos por Fotosensibilidad/diagnóstico , Adulto , Diagnóstico Diferencial , Femenino , Humanos
7.
Expert Opin Pharmacother ; 8(12): 1931-40, 2007 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-17696794

RESUMEN

Rufinamide (1-[2,6-difluorobenzyl]-1H-1,2,3-triazole-4-carboxamide) is a new anti-epileptic drug with a novel triazole derivative structure. The suspected mechanism of action is limitation of sodium-dependent action potentials, thought to result in a membrane stabilizing effect. Rufinamide is extensively metabolized in the liver by non-CYP450 enzymes with an elimination half-life of 8 - 12 h. Three randomized, placebo-controlled trials have shown that rufinamide is effective against partial seizures in adults. Efficacy in the Lennox-Gastaut syndrome, a severe, disabling childhood onset epilepsy syndrome, was shown in a single, randomized, placebo-controlled trial. It has recently been approved for treatment of Lennox-Gastaut syndrome in Europe. In the US it is under regulatory review. Most common adverse effects are somnolence, fatigue, dizziness, dipolopia, nausea and ataxia. Rufinamide has shown promise as adjunctive treatment for Lennox-Gastaut syndrome and may have some role in localization related epilepsies as well.


Asunto(s)
Anticonvulsivantes/uso terapéutico , Epilepsia/tratamiento farmacológico , Triazoles/uso terapéutico , Adulto , Animales , Anticonvulsivantes/efectos adversos , Anticonvulsivantes/farmacocinética , Anticonvulsivantes/farmacología , Niño , Interacciones Farmacológicas , Humanos , Ensayos Clínicos Controlados Aleatorios como Asunto , Síndrome , Triazoles/efectos adversos , Triazoles/farmacocinética , Triazoles/farmacología
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