Robbins Matthew S
Department of Neurology, Weill Cornell Medical College, New York, New York.
JAMA. 2021 May 11;325(18):1874-1885. doi: 10.1001/jama.2021.1640.
Approximately 90% of people in the US experience headache during their lifetime. Migraine is the second leading cause of years lived with disability worldwide.
Primary headache disorders are defined as headaches that are unrelated to an underlying medical condition and are categorized into 4 groups: migraine, tension-type headache, trigeminal autonomic cephalalgias, and other primary headache disorders. Studies evaluating prevalence in more than 100 000 people reported that tension-type headache affected 38% of the population, while migraine affected 12% and was the most disabling. Secondary headache disorders are defined as headaches due to an underlying medical condition and are classified according to whether they are due to vascular, neoplastic, infectious, or intracranial pressure/volume causes. Patients presenting with headache should be evaluated to determine whether their headache is most likely a primary or a secondary headache disorder. They should be evaluated for symptoms or signs that suggest an urgent medical problem such as an abrupt onset, neurologic signs, age 50 years and older, presence of cancer or immunosuppression, and provocation by physical activities or postural changes. Acute migraine treatment includes acetaminophen, nonsteroidal anti-inflammatory drugs, and combination products that include caffeine. Patients not responsive to these treatments may require migraine-specific treatments including triptans (5-HT1B/D agonists), which eliminate pain in 20% to 30% of patients by 2 hours, but are accompanied by adverse effects such as transient flushing, tightness, or tingling in the upper body in 25% of patients. Patients with or at high risk for cardiovascular disease should avoid triptans because of vasoconstrictive properties. Acute treatments with gepants, antagonists to receptors for the inflammatory neuropeptide calcitonin gene-related peptide, such as rimegepant or ubrogepant, can eliminate headache symptoms for 2 hours in 20% of patients but have adverse effects of nausea and dry mouth in 1% to 4% of patients. A 5-HT1F agonist, lasmiditan, is also available for acute migraine treatment and appears safe in patients with cardiovascular risk factors. Preventive treatments include antihypertensives, antiepileptics, antidepressants, calcitonin gene-related peptide monoclonal antibodies, and onabotulinumtoxinA, which reduce migraine by 1 to 3 days per month relative to placebo.
Headache disorders affect approximately 90% of people during their lifetime. Among primary headache disorders, migraine is most debilitating and can be treated acutely with analgesics, nonsteroidal anti-inflammatory drugs, triptans, gepants, and lasmiditan.
在美国,约90%的人在其一生中经历过头痛。偏头痛是全球导致失能生存年数的第二大原因。
原发性头痛疾病被定义为与潜在医疗状况无关的头痛,并分为4组:偏头痛、紧张型头痛、三叉自主神经性头痛和其他原发性头痛疾病。对超过10万人进行患病率评估的研究报告称,紧张型头痛影响了38%的人群,而偏头痛影响了12%的人群,且是最致残的。继发性头痛疾病被定义为由潜在医疗状况引起的头痛,并根据其病因是血管性、肿瘤性、感染性还是颅内压/容量性原因进行分类。出现头痛的患者应接受评估,以确定其头痛最可能是原发性还是继发性头痛疾病。应评估他们是否有提示紧急医疗问题的症状或体征,如突然发作、神经系统体征、年龄在50岁及以上、存在癌症或免疫抑制,以及身体活动或姿势改变引发头痛。急性偏头痛治疗包括对乙酰氨基酚、非甾体抗炎药以及含咖啡因的复方制剂。对这些治疗无反应的患者可能需要使用偏头痛特异性治疗药物,包括曲坦类药物(5-HT1B/D激动剂),2小时内可使20%至30%的患者疼痛缓解,但25%的患者会出现诸如上半身短暂潮红、紧绷或刺痛等不良反应。患有心血管疾病或有心血管疾病高风险的患者应避免使用曲坦类药物,因为其具有血管收缩特性。使用格派那类药物(炎症性神经肽降钙素基因相关肽受体拮抗剂,如瑞美吉泮或ubrogepant)进行急性治疗,可使20%的患者头痛症状在2小时内缓解,但1%至4%的患者会出现恶心和口干等不良反应。5-HT1F激动剂拉米地坦也可用于急性偏头痛治疗,且在有心血管危险因素的患者中似乎是安全的。预防性治疗包括抗高血压药、抗癫痫药、抗抑郁药、降钙素基因相关肽单克隆抗体和A型肉毒毒素,相对于安慰剂,这些药物可使偏头痛每月减少1至3天。
头痛疾病在约90%的人一生中都会出现。在原发性头痛疾病中,偏头痛最使人衰弱,可使用镇痛药、非甾体抗炎药、曲坦类药物、格派那类药物和拉米地坦进行急性治疗。