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      Treatment Outcomes in Patients With Newly Diagnosed Epilepsy Treated With Established and New Antiepileptic Drugs : A 30-Year Longitudinal Cohort Study

      research-article
      , PhD 1 , 2 , , MD 3 , , MD, PhD 4 , , MD, PhD 1 , 2 , 5 , 6 ,
      JAMA Neurology
      American Medical Association

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          Key Points

          Question

          Has the overall prognosis of epilepsy improved after the introduction of more than a dozen new antiepileptic drugs in the past 2 decades?

          Findings

          This longitudinal cohort study followed up a succession of newly diagnosed patients with epilepsy presenting at a single health care center over 30 years. The seizure-free rate observed was virtually unchanged over the study period, and the probability of achieving seizure freedom declined for each unsuccessful antiepileptic drug regimen prescribed.

          Meaning

          Despite availability of many new antiepileptic drugs with differing mechanisms of action, outcomes in newly diagnosed epilepsy have not improved; developing new disease-modifying compounds to current add to seizure-suppressing drug treatments may be necessary.

          Abstract

          This longitudinal cohort study assessed treatment outcomes in patients with newly diagnosed epilepsy and calculated the probability of achieving seizure freedom with first, second, and successive drug regimens prescribed.

          Abstract

          Importance

          A study published in 2000 showed that more than one-third of adults with epilepsy have inadequate control of seizures with antiepileptic drugs (AEDs). This study evaluates overall treatment outcomes in light of the introduction of more than 1 dozen new AEDs in the past 2 decades.

          Objective

          To assess long-term treatment outcome in patients with newly diagnosed and treated epilepsy.

          Design, Setting, and Participants

          This longitudinal observational cohort study was conducted at the Epilepsy Unit of the Western Infirmary in Glasgow, Scotland. A total of 1795 individuals who were newly treated for epilepsy with AEDs between July 1, 1982, and October 31, 2012, were included in this analysis. All patients were followed up for a minimum of 2 years (until October 31, 2014) or until death, whichever came sooner. Data analysis was completed between March 2015 and May 2016.

          Exposures

          Treatment with antiepileptic drugs for patients newly diagnosed with epilepsy.

          Main Outcomes and Measures

          Seizure control was assessed at the end of the study period. Probability of achieving 1-year seizure freedom was estimated for each AED regimen prescribed. Multivariable models assessed the associations between risk factors and AED treatment outcome after adjustments were made for demographic and clinical characteristics.

          Results

          Of the 1795 included patients, 964 (53.7%) were male; the median age was 33 years (range, 9-93 years). At the end of the study period, 1144 patients (63.7%) had been seizure free for the previous year or longer. Among those achieving 1-year seizure freedom, 993 (86.8%) were taking monotherapy and 1028 (89.9%) had achieved seizure control with the first or second AED regimens. Of the total patient pool, 906 (50.5%) remained seizure free for 1 year or longer with the initial AED. If this AED failed, the second and third regimens provided an additional 11.6% and 4.4% likelihoods of seizure freedom, respectively. Only 2.12% of patients attained optimal seizure control with subsequent AEDs. Epilepsy that was not successfully controlled with the first AED had 1.73 times greater odds of not responding to treatment for each subsequent medication regimen (odds ratio, 1.73; 95% CI, 1.56-1.91; P < .001).

          Conclusions and Relevance

          Despite the availability of many new AEDs with differing mechanisms of action, overall outcomes in newly diagnosed epilepsy have not improved. Most patients who attain control do so with the first or second AED. The probability of achieving seizure freedom diminishes substantially with each subsequent AED regimen tried. More than one-third of patients experience epilepsy that remains uncontrolled.

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          Author and article information

          Journal
          JAMA Neurol
          JAMA Neurol
          JAMA Neurol
          JAMA Neurology
          American Medical Association
          2168-6149
          2168-6157
          26 December 2017
          March 2018
          12 February 2018
          26 December 2018
          : 75
          : 3
          : 279-286
          Affiliations
          [1 ]Department of Medicine, The University of Melbourne, Parkville, Australia
          [2 ]Melbourne Brain Centre, Royal Melbourne Hospital, Parkville, Australia
          [3 ]West Glasgow Ambulatory Care Hospital, Yorkhill, Glasgow, Scotland
          [4 ]Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Australia
          [5 ]Department of Neurology, Royal Melbourne Hospital, Parkville, Australia
          [6 ]Department of Medicine and Therapeutics, Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China
          Author notes
          Article Information
          Corresponding Author: Patrick Kwan, MD, PhD, Department of Neurology, Royal Melbourne Hospital, Parkville VIC 3050, Australia ( patrick.kwan@ 123456unimelb.edu.au ).
          Accepted for Publication: August 3, 2017.
          Correction: This article was corrected on February 12, 2018, to remove typographical errors in the Treatment Outcomes subsection of the Results section and in the eAppendix of the Supplement.
          Published Online: December 26, 2017. doi:10.1001/jamaneurol.2017.3949
          Author Contributions: Drs Kwan and Brodie had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.
          Study concept and design: Brodie, Liew, Kwan.
          Acquisition, analysis, or interpretation of data: All authors.
          Drafting of the manuscript: Chen, Liew, Kwan, Brodie.
          Critical revision of the manuscript for important intellectual content: All authors.
          Statistical analysis: Chen, Liew.
          Obtained funding: Kwan, Brodie.
          Administrative, technical, or material support: Brodie.
          Study supervision: Brodie, Liew, Kwan.
          Conflict of Interest Disclosures: Outside the submitted work, Dr Brodie serves on the scientific advisory boards of Eisai Ltd, UCB Pharma, GlaxoSmithKline, Lundbeck, Bial, GW Pharmaceuticals, and Takeda; is on the speakers’ bureau for Eisai Ltd, UCB Pharma, GlaxoSmithKline, Lundbeck, Sanofi Aventis, and Abbott; and has accepted travel grants for scientific meetings from Eisai Ltd, UCB Pharma, and Lundbeck. Dr Liew has received research grants from the National Health and Medical Research Council of Australia, the Australian Research Council, and the National Heart Foundation of Australia. He and/or his institution has also received speaker or consultancy fees and/or research grants from Pfizer, AbbVie, Sanofi, AstraZeneca, GlaxoSmithKline, and Amgen. Dr Kwan has received research grants from the National Health and Medical Research Council of Australia, the Australian Research Council, the US National Institutes of Health, Hong Kong Research Grants Council, Innovation and Technology Fund, Health and Health Services Research Fund, and Health and Medical Research Fund. He and/or his institution also received speaker or consultancy fees and/or research grants from Eisai, GlaxoSmithKline, Johnson & Johnson, Pfizer, and UCB Pharma. No other disclosures are reported.
          Article
          PMC5885858 PMC5885858 5885858 noi170096
          10.1001/jamaneurol.2017.3949
          5885858
          29279892
          93dfb509-68e1-488b-b45b-5c0537d497bf
          Copyright 2017 American Medical Association. All Rights Reserved.
          History
          : 27 March 2017
          : 2 August 2017
          : 3 August 2017
          Categories
          Research
          Research
          Original Investigation
          Online First

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