Vagus nerve stimulation: Analysis of device parameters in 154 patients during the long-term XE5 study

被引:70
作者
DeGiorgio, CM
Thompson, J
Lewis, P
Arrambide, S
Naritoku, D
Handforth, A
Labar, D
Mullin, P
Heck, C
机构
[1] Olive View UCLA Med Ctr, Dept Neurol, Sylmar, CA 91342 USA
[2] SYNERGOS Inc, Springfield, IL USA
[3] So Illinois Univ, Springfield, IL USA
[4] Cornell Univ, Sch Med, Ithaca, NY 14853 USA
[5] Univ So Calif, Keck Sch Med, Dept Neurol, Los Angeles, CA USA
[6] Univ Calif Los Angeles, Sch Med, Los Angeles, CA USA
[7] Univ Calif Los Angeles, Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA
关键词
vagus nerve stimulation; device changes; duty cycle;
D O I
10.1046/j.1528-1157.2001.0420081017.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: To determine the effect of changes in device settings and duty cycle (on and off times) on the efficacy of vagus nerve stimulation (VNS) for refractory epilepsy. In the long-term XE5 study of VNS for intractable epilepsy, the median reduction in seizure frequency improved significantly after 1 year of follow-up, A central question is whether device changes improve efficacy. We analyzed the effects of device parameter changes on seizure frequency in 154 subjects who completed the study and who had complete data for analysis. Methods: Retrospective analysis of device changes during the XE5 long-term study of VNS. During the XE5 long-term follow-up study, the subject's device settings were modified within a Food and Drug Administration (FDA)-approved range of output current. pulse duration, frequency, on time, and off time. Significant changes in device settings occurred after 3 months. We investigated the relationship between percentage reduction in seizures and changes in device parameters between the 3- and 12-month visits. Within-group comparisons were performed for those who continued on standard on/off cycle of 30 s on and 5 min off, and those with the most common off times of 3, 1.8, and < 1.1 min. Results: Output current, pulse duration, frequency, and off time changed significantly between the 3- and 12-month longterm follow-ups. For the group as a whole. changes in device settings were not correlated with an improvement in efficacy. However, a significant improvement in efficacy occurred in a subgroup whose off time was reduced to less than or equal to1.1 min. In this group, the median reduction in seizures improved from 21% before the change in off time, to 39% after the change in off time (Wilcoxon Signed-Rank, p = 0.011), The responder rate (> 50% reduction in seizures) also significantly improved from 19 to 35% (McNemar's test, p = 0.046). Conclusions: The data from this retrospective analysis indicate that device changes were not the primary determinant of increased efficacy at 12 months of long-term follow-up. In general, patients who remained on the original settings of 30 s on and 5 min off continued to respond or improve in their response over the 1-year period. However, some patients may benefit from reductions in off time (increases in duty cycle). In a subgroup initially resistant to VNS. a change in off time to less than or equal to1.1 min off did result in significant improvements in efficacy.
引用
收藏
页码:1017 / 1020
页数:4
相关论文
共 15 条
[1]  
[Anonymous], REV ROUM NEUROL
[2]   Evaluation of refractory epilepsy treated with vagus nerve stimulation for up to 5 years [J].
Ben-Menachem, E ;
Hellström, K ;
Waldton, C ;
Augustinsson, LE .
NEUROLOGY, 1999, 52 (06) :1265-1267
[3]   Prospective long-term study of vagus nerve stimulation for the treatment of refractory seizures [J].
DeGiorgio, CM ;
Schachter, SC ;
Handforth, A ;
Salinsky, M ;
Thompson, J ;
Uthman, B ;
Reed, R ;
Collins, S ;
Tecoma, E ;
Morris, GL ;
Vaughn, B ;
Naritoku, DK ;
Henry, T ;
Labar, D ;
Gilmartin, R ;
Labiner, D ;
Osorio, I ;
Ristanovic, R ;
Jones, J ;
Murphy, J ;
Ney, G ;
Wheless, J ;
Lewis, P ;
Heck, C .
EPILEPSIA, 2000, 41 (09) :1195-1200
[4]   Reassessment: Vagus nerve stimulation for epilepsy - A report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology [J].
Fisher, RS ;
Handforth, A .
NEUROLOGY, 1999, 53 (04) :666-669
[5]   A RANDOMIZED CONTROLLED TRIAL OF CHRONIC VAGUS NERVE-STIMULATION FOR TREATMENT OF MEDICALLY INTRACTABLE SEIZURES [J].
GEORGE, R ;
SONNEN, A ;
UPTON, A ;
SALINSKY, M ;
RISTANOVIC, R ;
BERGEN, D ;
MIRZA, W ;
ROSENFELD, W ;
NARITOKU, D ;
MANONESPAILLAT, R ;
BAROLAT, G ;
WILLIS, J ;
STEFAN, H ;
TREIG, T ;
HUFNAGEL, A ;
KUZNIECKY, R ;
UTHMAN, B ;
WILDER, BJ ;
AUGUSTINSSON, L ;
BENMENACHEM, E ;
RAMSAY, E ;
WERNICKE, JF ;
TARVER, WB .
NEUROLOGY, 1995, 45 (02) :224-230
[6]   Vagus nerve stimulation therapy for partial-onset seizures - A randomized active-control trial [J].
Handforth, A ;
DeGiorgio, CM ;
Schachter, SC ;
Uthman, BM ;
Naritoku, DK ;
Tecoma, ES ;
Henry, TR ;
Collins, SD ;
Vaughn, BV ;
Gilmartin, RC ;
Labar, DR ;
Morris, GL ;
Salinsky, MC ;
Osorio, I ;
Ristanovic, RK ;
Labiner, DM ;
Jones, JC ;
Murphy, JV ;
Ney, GC ;
Wheless, JW .
NEUROLOGY, 1998, 51 (01) :48-55
[7]   Unexpected places - How did vagus nerve stimulation become a treatment for epilepsy? [J].
Lesser, RP .
NEUROLOGY, 1999, 52 (06) :1117-1118
[8]   FEASIBILITY AND SAFETY OF VAGAL-STIMULATION IN MONKEY MODEL [J].
LOCKARD, JS ;
CONGDON, WC ;
DUCHARME, LL .
EPILEPSIA, 1990, 31 :S20-S26
[9]   Vagus nerve stimulation [J].
Schachter, SC ;
Saper, CB .
EPILEPSIA, 1998, 39 (07) :677-686
[10]  
Stoica I., 1968, REV ROUM NEUROL, V5, P203