What we don't learn from clinical trials in epilepsy.

Abstract:

:The randomized, double-blind trial design offers the most accurate data regarding the efficacy of antiepileptic treatments. However, translating the results of a trial into clinical care can be complex due to the intrinsic tension between the requirements for scientific methods that minimize systematic and random error, and the need for clinically relevant and generalizable data. The interpretation of the trial results is complicated further by the probable inaccuracy of self-reported seizure rates and spontaneously reported adverse effects in most trials. Patient preference may be a feasible outcome measure that allows patient-oriented validation of the results, and also inherently weighs the positive and negative effects of a treatment in a single endpoint.

journal_name

Epilepsia

journal_title

Epilepsia

authors

Gilliam F

doi

10.1046/j.1528-1157.44.s7.2.x

subject

Has Abstract

pub_date

2003-01-01 00:00:00

pages

51-4

eissn

0013-9580

issn

1528-1167

pii

7002

journal_volume

44 Suppl 7

pub_type

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