A randomized, double-blind comparison of antiepileptic drug treatment in the elderly with new-onset focal epilepsy

被引:135
作者
Werhahn, Konrad J. [1 ,3 ,10 ]
Trinka, Eugen [2 ,3 ]
Dobesberger, Judith [2 ,3 ]
Unterberger, Iris
Baum, Petra [4 ]
Deckert-Schmitz, Maria [5 ]
Kniess, Tobias [6 ]
Schmitz, Bettina [7 ]
Bernedo, Viviane [1 ]
Ruckes, Christian [8 ]
Ehrlich, Anne [8 ]
Kraemer, Guenter [9 ,11 ]
机构
[1] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Neurol, D-55122 Mainz, Germany
[2] Paracelsus Med Univ, Dept Neurol, Salzburg, Austria
[3] Med Univ Innsbruck, Dept Neurol, A-6020 Innsbruck, Austria
[4] Univ Leipzig, Dept Neurol, D-04109 Leipzig, Germany
[5] Harlaching Hosp, Dept Neurol, Munich, Germany
[6] Rhon Klinikum, Neurol Clin, Bad Neustadt an der Saale, Germany
[7] Vivantes Humboldt Klinikum, Dept Neurol, Berlin, Germany
[8] Johannes Gutenberg Univ Mainz, Interdisciplinary Ctr Clin Trials, Univ Med Ctr, D-55122 Mainz, Germany
[9] Swiss Epilepsy Ctr, Zurich, Switzerland
[10] UCB Pharma, Brussels, Belgium
[11] Neurozentrum Bellevue, Zurich, Switzerland
关键词
Elderly; Monotherapy; Antiepileptic drugs; Levetiracetam; Carbamazepine; NEWLY-DIAGNOSED EPILEPSY; NURSING-HOME RESIDENTS; RELEASE CARBAMAZEPINE; UNPROVOKED SEIZURES; LAMOTRIGINE; LEVETIRACETAM; MONOTHERAPY; MULTICENTER; TRIAL; ILAE;
D O I
10.1111/epi.12926
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To compare the effectiveness of controlled-released carbamazepine (CR-CBZ) to levetiracetam (LEV) and to lamotrigine (LTG) in elderly patients with newly diagnosed focal epilepsy. Methods: Randomized, double-blind, parallel-group trial conducted between January 2007 and August 2011, in 47 ambulatory or hospital sites in Germany, Austria, or Switzerland. Eligible participants were aged >= 60, had new-onset epilepsy, had no acute illness as the cause of their seizures, and had no contraindication to the drugs in the trial. Patients were randomized 1: 1: 1 to CR-CBZ, LTG, or LEV. Doses were up-titrated for 6 weeks and could be maintained or adjusted depending on seizure relapse or tolerability over an additional period of 52 weeks. Primary outcome was the retention to treatment at week 58; secondary measures related to seizure and adverse event frequency. Results: Of 361 randomized patients, 359 were included (CR-CBZ n = 121, LTG n = 117, LEV n = 122) in the modified intent-to-treat population (mean age [range] 71.4 [60-95] years). At week 58, the retention rate for LEV was significantly higher than for CR-CBZ (61.5% vs. 45.8%, p = 0.02), and similar to LTG (55.6%). Seizure freedom rates at weeks 30 and 58 were not different across the groups. Twice as many patients receiving CR-CBZ discontinued due to adverse events or death compared to those in the LEV group (32.2% vs. 17.2%; odds ratio 2.28, 95% confidence interval [CI] 1.25-4.19, p = 0.007), whereas discontinuation was intermediate for LTG (26.3%). Median daily doses of completers (n = 195) were CR-CBZ 380.0 mg/day (333.0-384.0), LTG 95 mg/day (94.0-97.0), and LEV 950 mg/day (940.0-985.0). Significance: In the initial monotherapy of focal epilepsy in the elderly, 1-year retention to LEV was higher compared to CR-CBZ due to better tolerability. Retention of LTG was intermediate and close to LEV, but did not differ significantly from either comparators. NCT00438451, www.clinicaltrials.gov.
引用
收藏
页码:450 / 459
页数:10
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