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Antiepileptic Drug Therapy And Its Effects On Pregnant Women

dc.contributor.authorAlshaqqabi, Hadeel .A.
dc.date.accessioned2019-04-20T10:36:28Z
dc.date.available2019-04-20T10:36:28Z
dc.date.issued2018-06-30
dc.identifier.urihttp://repository.limu.edu.ly/handle/123456789/734
dc.descriptionEpilepsy is a chronic disorder that causes unprovoked, recurrent seizures which are a sudden rush of electrical activity in the brain. A mild seizure may be difficult to recognize. It can last a few seconds during which you lack awareness. Stronger seizures can cause spasms and uncontrollable muscle twitches, and can last a few seconds to several minutes. During a stronger seizure, some people become confused or lose consciousness. Afterward you may have no memory of it happening The National Institute of Neurological Disorder and Stroke (NINDS) estimates epilepsy affects 1% of the United States population (about 2.5 million people).en_US
dc.description.abstractPregnant women with epilepsy constitute 0.5% of all pregnancies. Proper seizure control is the primary goal in treating women with epilepsy. The commonly used anticonvulsants are established human teratogens, factors such as epilepsy, anticonvulsant-induced teratogenicity, patient's genetic predisposition and the severity of convulsive disorder may attribute to adverse pregnancy outcome for the children of women with epilepsy Anticonvulsant interaction with folic acid and phytomenadione (vitamin K) metabolism may lead to an increased risk for neural tube defect and early neonatal bleeding. Preconceptional counselling should include patient education to ensure a clear understanding of risks of uncontrolled seizures and possible teratogenicity of anticonvulsants. Genetic counselling should be performed if both parents have epilepsy or the disease is inherited. Seizure control should be achieved at least 6 months prior to conception and, if clinically possible, by the lowest effective dose of a single anticonvulsant according to the type of epilepsy. The new anticonvulsants are not recommended in pregnancy and require further research to prove their safety in humans. Folic acid 5 mg/day should be administered 3 months before conception and during the first trimester to prevent folic acid deficiency-induced malformations Therapeutic drug monitoring should be performed monthly, or as clinically indicated. In order to prevent convulsions during labour, proper seizure control should be achieved during the third trimester. Benzodiazepines or phenytoin are found to be effective for seizure cessation during labour and delivery Phytomenadione should be administered immediately after birth to the newborn. The neonate should be assessed carefully for epilepsy and anticonvulsant-associated dysmorphology Advising the patient on postpartum management regarding contraception and breastfeeding will help maximise the best possible outcome for the newborn and mother. With proper preconceptional, antenatal and postpartum management up to 95% of these pregnancies have been reported to have favourable outcomes.en_US
dc.language.isoenen_US
dc.publisherfaculty of Basic Medical Science - Libyan International Medical Universityen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.titleAntiepileptic Drug Therapy And Its Effects On Pregnant Womenen_US
dc.typeOtheren_US


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Attribution 3.0 United States
Except where otherwise noted, this item's license is described as Attribution 3.0 United States