Visser W H, Jaspers N M, de Vriend R H, Ferrari M D
Department of Neurology, University Hospital, Leiden, The Netherlands.
Cephalalgia. 1996 Dec;16(8):554-9. doi: 10.1046/j.1468-2982.1996.1608554.x.
To assess, in clinical practice, the (i) incidence, (ii) within-patient consistency, and (iii) clinical spectrum of chest symptoms (chest symptoms) after subcutaneous (sc) and oral sumatriptan, and (iv) to identify risk factors for chest symptoms.
Two-year retrospective survey with mailed self-administered questionnaire.
Neurology outpatient clinic of university hospital.
Migraine patients with or without aura (n = 869).
Incidence, within-patient consistency and characteristics of chest symptoms; demographic and clinical characteristics of patients.
There were 735 (85%) respondents. Sumatriptan was used by 453 patients, during 25 months (median), for 28000 attacks (median: 33 attacks/patient). Of sumatriptan users, 41% (sc) and 24% (oral) had chest symptoms in all attacks, 39% (sc) and 58% (oral) in none, and the remaining in some attacks. Because of chest symptoms, 10% discontinued sumatriptan. Chest symptoms mostly consisted of heavy arms and chest pressure, started within 5 (sc) to 30 (oral) min, and lasted 30 (sc) to 60 (oral) min. Compared with patients without chest symptoms, patients with chest symptoms more often were females and younger, and went to rest immediately after sumatriptan administration (all p < 0.001); they also tended to have lower body mass indices, more severe attacks and less efficacy of sumatriptan (all 0.001 < p < 0.05). Patients with chest symptoms had no higher incidence of cardiovascular symptoms or risk factors.
Chest symptoms are frequent, within-patients consistent, but rarely important, adverse events of (notably sc) sumatriptan. The risk of chest symptoms is patient-dependent and not related, even opposite, to cardiovascular disease. This contradicts the hypothesis that chest symptoms after sumatriptan are caused by cardiac ischemia. Patient acceptance of chest symptoms is improved by pre-advising on the risk and nature of chest symptoms.
在临床实践中评估皮下注射(sc)和口服舒马曲坦后(i)胸部症状的发生率、(ii)患者内一致性以及(iii)胸部症状的临床谱,以及(iv)确定胸部症状的危险因素。
通过邮寄自填问卷进行为期两年的回顾性调查。
大学医院神经内科门诊。
有或无先兆的偏头痛患者(n = 869)。
胸部症状的发生率、患者内一致性和特征;患者的人口统计学和临床特征。
有735名(85%)受访者。453名患者使用了舒马曲坦,在25个月(中位数)内用于28000次发作(中位数:每位患者33次发作)。在使用舒马曲坦的患者中,41%(皮下注射)和24%(口服)在所有发作中都有胸部症状,39%(皮下注射)和58%(口服)在任何发作中都没有胸部症状,其余患者在部分发作中有胸部症状。由于胸部症状,10%的患者停用了舒马曲坦。胸部症状主要包括手臂沉重和胸部压迫感,在皮下注射后5分钟至口服后30分钟内开始,持续30分钟(皮下注射)至60分钟(口服)。与没有胸部症状的患者相比,有胸部症状的患者更常为女性且更年轻,在服用舒马曲坦后立即休息(所有p < 0.001);他们的体重指数也往往较低,发作更严重且舒马曲坦的疗效较差(所有0.001 < p < 0.05)。有胸部症状的患者心血管症状或危险因素的发生率并不更高。
胸部症状是(尤其是皮下注射)舒马曲坦常见的、患者内一致但很少严重的不良事件。胸部症状风险因患者而异,与心血管疾病无关,甚至相反。这与舒马曲坦后胸部症状由心脏缺血引起的假设相矛盾。预先告知胸部症状的风险和性质可提高患者对胸部症状的接受度。