Rozen T D
Department of Neurology, Jefferson Medical College, Thomas Jefferson University Hospital, Jefferson Headache Center, Philadelphia, PA, USA.
Headache. 2001 Nov-Dec;41 Suppl 1:S25-32. doi: 10.1046/j.1526-4610.2001.01154-5.x.
Cluster headache and trigeminal neuralgia are relatively rare but debilitating neurologic conditions. Although they are clinically and diagnostically distinct from migraine, many of the same pharmacologic agents are used in their management. For many patients, the attacks are so frequent and severe that abortive therapy is often ineffective; therefore, chronic preventive therapy is necessary for adequate pain control. Cluster headache and trigeminal neuralgia have several distinguishing clinical features. Cluster headache is predominantly a male disorder; trigeminal neuralgia is more prevalent in women. Individuals with cluster headaches often develop their first attack before age 25; most patients with trigeminal neuralgia are between age 50 and 70. Cluster headaches are strongly associated with tobacco smoking and triggered by alcohol consumption; trigeminal neuralgia can be triggered by such stimuli as shaving and toothbrushing. Although the pain in both disorders is excruciating, cluster headache pain is episodic and unilateral, typically surrounds the eye, and lasts 15 to 180 minutes; the pain of trigeminal neuralgia lasts just seconds and is usually limited to the tissues overlying the maxillary and mandibular divisions of the trigeminal nerve. Cluster headache is unique because of its associated autonomic symptoms. Although the pathophysiology of cluster headache and trigeminal neuralgia are not completely understood, both appear to have central primary processes, and these findings have prompted investigations of the effectiveness of the newer antiepileptic drugs for cluster headache prevention and for the treatment of trigeminal neuralgia. The traditional antiepileptic drugs phenytoin and carbamazepine have been used for the treatment of trigeminal neuralgia for a number of years, and while they are effective, they can sometimes cause central nervous system effects such as drowsiness, ataxia, somnolence, and diplopia. Reports of studies in small numbers of patients or individual case studies indicate that the newer antiepileptic drugs are effective in providing pain relief for trigeminal neuralgia and cluster headache sufferers, with fewer central nervous system side effects. Divalproex has been shown to provide effective pain control and to reduce cluster headache frequency by more than half in episodic and chronic cluster headache sufferers. Topiramate demonstrated efficacy in a study of 15 patients, with a mean time to induction of cluster headache remission of 1.4 weeks (range, 1 day to 3 weeks). In the treatment of trigeminal neuralgia, gabapentin has been shown to be effective in an open-label study. When added to an existing but ineffective regimen of carbamazepine or phenytoin, lamotrigine provided improved pain relief; it also may work as monotherapy. Topiramate provided a sustained analgesic effect when administered to patients with trigeminal neuralgia. The newer antiepileptic drugs show considerable promise in the management of cluster headache and trigeminal neuralgia.
丛集性头痛和三叉神经痛相对罕见,但却是使人衰弱的神经系统疾病。尽管它们在临床和诊断上与偏头痛不同,但在治疗中使用了许多相同的药物。对许多患者来说,发作过于频繁和严重,以至于发作期治疗往往无效;因此,慢性预防性治疗对于充分控制疼痛是必要的。丛集性头痛和三叉神经痛有几个明显的临床特征。丛集性头痛主要是男性疾病;三叉神经痛在女性中更为普遍。丛集性头痛患者通常在25岁之前首次发作;大多数三叉神经痛患者年龄在50至70岁之间。丛集性头痛与吸烟密切相关,并由饮酒引发;三叉神经痛可由剃须和刷牙等刺激引发。尽管这两种疾病的疼痛都极为剧烈,但丛集性头痛的疼痛是发作性的且为单侧性,通常围绕眼睛,持续15至180分钟;三叉神经痛的疼痛仅持续数秒,通常局限于三叉神经上颌支和下颌支上方的组织。丛集性头痛因其相关的自主神经症状而独特。尽管丛集性头痛和三叉神经痛的病理生理学尚未完全了解,但两者似乎都有中枢性原发过程,这些发现促使人们研究新型抗癫痫药物预防丛集性头痛和治疗三叉神经痛的有效性。传统抗癫痫药物苯妥英和卡马西平已用于治疗三叉神经痛多年,虽然它们有效,但有时会引起中枢神经系统效应,如嗜睡、共济失调、昏睡和复视。少数患者的研究报告或个案研究表明,新型抗癫痫药物对三叉神经痛和丛集性头痛患者有效,且中枢神经系统副作用较少。丙戊酸已被证明能有效控制疼痛,并使发作性和慢性丛集性头痛患者的丛集性头痛频率降低一半以上。托吡酯在一项针对15名患者的研究中显示出疗效,丛集性头痛缓解的平均诱导时间为1.4周(范围为1天至3周)。在治疗三叉神经痛方面,加巴喷丁在一项开放标签研究中已被证明有效。当添加到现有的但无效的卡马西平或苯妥英治疗方案中时,拉莫三嗪能更好地缓解疼痛;它也可作为单一疗法使用。托吡酯在给予三叉神经痛患者时能提供持续的镇痛效果。新型抗癫痫药物在丛集性头痛和三叉神经痛的治疗中显示出相当大的前景。