The prophylactic treatment of chronic daily headache

被引:49
作者
Mathew, Ninan T. [1 ]
机构
[1] Houston Headache Clin, Houston, TX 77004 USA
来源
HEADACHE | 2006年 / 46卷 / 10期
关键词
chronic daily headache; prophylaxis; botulinum toxin type A; double-blind; placebo-controlled trials; active comparator-controlled trials;
D O I
10.1111/j.1526-4610.2006.00621.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Chronic daily headache (CDH), a heterogeneous group of headache disorders occurring on at least 15 days per month, affects up to 4% to 5% of the general population. CDH disorders include transformed (or chronic) migraine, chronic tension-type headache, new daily persistent headache, and hemicrania continua. Patients with CDH have greater disability and lower quality of life than episodic migraine patients and often overuse headache pain medications. To date, only topiramate, gabapentin, tizanidine, fluoxetine, amitriptyline, and botulinum toxin type A (BoNTA) have been evaluated as prophylactic treatment of CDH in randomized, double-blind, placebo-controlled, or active comparator-controlled trials. The evidence supporting the use of BoNTA as prophylaxis of CDH is composed of larger and longer trials, as over 1000 patients were evaluated for up to 11 months duration. Compared with placebo BoNTA has significantly reduced the frequency of headache episodes, a recommended efficacy measure for headache trials and has been demonstrated to be safe and very well tolerated with few discontinuations due to adverse events. Side effects are generally transient, mild to moderate, and nonsystemic. The results of clinical trials using traditional oral pharmacotherapy, while supportive of their use as prophylactic treatment of CDH, are limited by several factors, including small numbers of patients, the choice of efficacy measures, and short treatment periods. The use of oral agents was associated with systemic side effects, which may limit their effectiveness as prophylactic treatment of CDH.
引用
收藏
页码:1552 / 1564
页数:13
相关论文
共 46 条
[1]   FLUOXETINE PROPHYLAXIS OF MIGRAINE [J].
ADLY, C ;
STRAUMANIS, J ;
CHESSON, A .
HEADACHE, 1992, 32 (02) :101-104
[2]  
Aoki KR, 2003, HEADACHE, V43, pS9
[3]  
Barrientos N., 2003, J HEADACHE PAIN, V4, P146, DOI [DOI 10.1007/S10194-003-0049-2, 10.1007/s10194-003-0049-2]
[4]   Transformed migraine and medication overuse in a tertiary headache centre - clinical characteristics and treatment outcomes [J].
Bigal, ME ;
Rapoport, AM ;
Sheftell, FD ;
Tepper, SJ ;
Lipton, RB .
CEPHALALGIA, 2004, 24 (06) :483-490
[5]   Assessment of migraine disability using the Migraine Disability Assessment (MIDAS) Questionnaire: A comparison of chronic migraine with episodic migraine [J].
Bigal, ME ;
Rapoport, AM ;
Lipton, RB ;
Tepper, SJ ;
Sheftell, FD .
HEADACHE, 2003, 43 (04) :336-342
[6]   Gabapentin in postamputation phantom limb pain: A randomized, double-blind, placebo-controlled, cross-over study [J].
Bone, M ;
Critchley, P ;
Buggy, DJ .
REGIONAL ANESTHESIA AND PAIN MEDICINE, 2002, 27 (05) :481-486
[7]   Topiramate for migraine prevention - A randomized controlled trial [J].
Brandes, JL ;
Saper, JR ;
Diamond, M ;
Couch, JR ;
Lewis, DW ;
Schmitt, J ;
Neto, W ;
Schwabe, S ;
Jacobs, D .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 291 (08) :965-973
[8]   Tbe development of cutaneous allodynia during a migraine attack - Clinical evidence for the sequential recruitment of spinal and supraspinal nociceptive neurons in migraine [J].
Burstein, R ;
Cutrer, MF ;
Yarnitsky, D .
BRAIN, 2000, 123 :1703-1709
[9]   Deconstructing migraine headache into peripheral and central sensitization [J].
Burstein, R .
PAIN, 2001, 89 (2-3) :107-110
[10]   Epidemiology of chronic daily headache in the general population [J].
Castillo, J ;
Muñoz, P ;
Guitera, V ;
Pascual, J .
HEADACHE, 1999, 39 (03) :190-196