Literature DB >> 8784211

Efficacy and adverse effects of established and new antiepileptic drugs.

R H Mattson1.   

Abstract

Antiepileptic drug (AED) selection is based primarily on efficacy for specific seizure types and epileptic syndromes. However, efficacy is often similar for the different AEDs, and other properties such as adverse effects, pharmacokinetic properties, and cost may also be of importance. For idiopathic generalized epilepsies with absence, tonic-clonic, and myoclonic seizures, the AED of choice is valproate (VPA). Secondarily generalized epilepsies with tonic, atonic, and other seizure types are difficult to treat with any single AED or combination of AEDs. The AEDs of choice for absence seizures are ethosuximide (ESM) and VPA. For control of primary generalized tonic-clonic seizures, any of the other major AEDs can be effective. If VPA cannot be prescribed, carbamazepine (CBZ), phenobarbital (PB), phenytoin (PHT), or primidone (PRM) may be effective, but ESM or a benzodiazepine (BZD) must be added to control associated absence or myoclonic seizures. The AEDs of first choice for partial epilepsies with partial and secondarily generalized tonic-clonic seizures are CBZ and PHT. Increasing evidence suggests that VPA is a good alternative when CBZ and PHT fail. PB and PRM are second-choice selections because of adverse effects. A combination of two of the five standard AEDs may be necessary to treat intractable seizures, but no studies have been done to indicate an optimal combination. Other epilepsy syndromes such as neonatal and infantile epilepsies, febrile epilepsy, alcoholic epilepsy, and status epilepticus require specific AED treatment. Ultimately, AED selection must be individualized. No "drug of choice" can be named for all patients. The expected efficacy for the seizure type, the importance of the expected adverse effects, the pharmacokinetics, and the cost of the AEDs all must be weighed and discussed with the patient before a choice is made. A number of new AEDs with unique mechanisms of action, pharmacokinetic properties, and fewer adverse effects hold important promise of improved epilepsy treatment.

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Year:  1995        PMID: 8784211     DOI: 10.1111/j.1528-1157.1995.tb05995.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  13 in total

1.  Volume-selective 1H MR spectroscopy for in vivo detection of valproate in patients with epilepsy.

Authors:  S Seyfert; J Bernarding; J Braun
Journal:  Neuroradiology       Date:  2003-03-27       Impact factor: 2.804

2.  Hypersensitivity to topiramate sprinkle capsules does not preclude the use of topiramate tablets.

Authors:  Dorothy Marsden; Susan E Libretto
Journal:  Paediatr Drugs       Date:  2004       Impact factor: 3.022

Review 3.  Treatment of concomitant illnesses in patients receiving anticonvulsants: drug interactions of clinical significance.

Authors:  P Loiseau
Journal:  Drug Saf       Date:  1998-12       Impact factor: 5.606

4.  The importance of drug adverse effects compared with seizure control for people with epilepsy: a discrete choice experiment.

Authors:  Andrew Lloyd; Emma McIntosh; Martin Price
Journal:  Pharmacoeconomics       Date:  2005       Impact factor: 4.981

Review 5.  A comparative review of the adverse effects of anticonvulsants in children with epilepsy.

Authors:  S J Wallace
Journal:  Drug Saf       Date:  1996-12       Impact factor: 5.606

6.  Anticonvulsant activity of fraction isolated from ethanolic extract of heartwood of Cedrus deodara.

Authors:  Daniel Dhayabaran; Ebinezar Jeyaseeli Florance; Krishnadas Nandakumar; Alagarsamy Shanmugarathinam; Ayarivan Puratchikody
Journal:  J Nat Med       Date:  2014-04       Impact factor: 2.343

7.  Cognitive Adverse Effects of Antiepileptic Drugs : Incidence, Mechanisms and Therapeutic Implications.

Authors:  R Kälviäinen; M Äikiä; P J Riekkinen
Journal:  CNS Drugs       Date:  1996-05       Impact factor: 5.749

8.  Anti-seizure activity of the aqueous leaf extract of Solanum nigrum linn (solanaceae) in experimental animals.

Authors:  Noel N Wannang; Joseph A Anuka; Helen O Kwanashie; Steven S Gyang; Asa Auta
Journal:  Afr Health Sci       Date:  2008-06       Impact factor: 0.927

9.  Comparative Molecular Similarity Indices Analysis of 1-(Naphthylalky1)-1H-imidazole Analogs with Antiepileptic Activity.

Authors:  S Ganguly; R Mishra
Journal:  J Young Pharm       Date:  2010-10

10.  Evaluation of antiepileptic activity of chloroform extract of Acalypha fruticosa in mice.

Authors:  Sumalatha Govindu; Sreedevi Adikay
Journal:  Pharmacognosy Res       Date:  2014-04
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