Garrett J E, Lanes S F, Kolbe J, Rea H H
Respiratory Services, Green Lane Hospital, Auckland, New Zealand.
Thorax. 1996 Nov;51(11):1093-9. doi: 10.1136/thx.51.11.1093.
A study was undertaken to test the hypothesis that a particular inhaled beta agonist, fenoterol, increases the incidence of severe life threatening asthma.
A retrospective cohort was assembled comprising 655 patients with asthma aged 15-55 years who attended a single Auckland hospital for acute asthma between 1 January 1986 and 31 December 1987 (the "index event"). Patients were followed for the occurrence of death from asthma or admission to the intensive care unit for asthma, until death or 31 May 1989. Data on asthma medications and asthma severity were obtained from forms used specifically for managing patients with acute asthma in the emergency department and maintained as part of the hospital record and/or from the hospital record (when patients were admitted).
Following the index event 90 admissions to the intensive care unit (ICU) and 15 asthma deaths were identified. Before adjusting for asthma severity, patients using inhaled fenoterol had a greater incidence of severe life threatening asthma than patients using inhaled salbutamol (RR = 2.1, 95% CI 1.4 to 3.1). After controlling for two markers of severe asthma used in previous studies-a hospital admission in the previous year and prescribed oral corticosteroids-the relative risk estimate declined to 1.5 (95% CI 1.0 to 2.3). After controlling further for the number of hospital admissions during the study period, continuous oral corticosteroid use rather than short courses of treatment, severity of the previous attack requiring a hospital visit, and race, fenoterol was not associated with severe life threatening asthma at the time of attendance for a previous hospital visit (RR = 1.0, 95% CI 0.6 to 1.7).
Fenoterol is used more often by patients with severe asthma and, after adjusting for differences in baseline risk, it does not increase the risk of severe life threatening asthma.
开展了一项研究以检验以下假设:一种特定的吸入型β受体激动剂非诺特罗会增加严重危及生命的哮喘发病率。
组建了一个回顾性队列,包括655名年龄在15至55岁之间的哮喘患者,他们于1986年1月1日至1987年12月31日期间在奥克兰的一家医院就诊急性哮喘(“索引事件”)。对患者进行随访,观察哮喘死亡或因哮喘入住重症监护病房的情况,直至死亡或1989年5月31日。哮喘药物和哮喘严重程度的数据来自专门用于急诊科管理急性哮喘患者的表格,并作为医院记录的一部分保存,和/或来自医院记录(当患者入院时)。
在索引事件后,确定有90人入住重症监护病房(ICU)以及15例哮喘死亡。在未对哮喘严重程度进行校正时,使用吸入型非诺特罗的患者发生严重危及生命的哮喘的发生率高于使用吸入型沙丁胺醇的患者(相对危险度=2.1,95%可信区间1.4至3.1)。在对先前研究中使用的两个严重哮喘标志物(前一年的住院情况和处方口服糖皮质激素)进行控制后,相对危险度估计值降至1.5(95%可信区间1.0至2.3)。在进一步对研究期间的住院次数、持续口服糖皮质激素的使用而非短期疗程治疗、上次因哮喘发作严重程度需住院就诊情况以及种族进行控制后,非诺特罗与上次医院就诊时严重危及生命的哮喘无关(相对危险度=1.0,95%可信区间0.6至1.7)。
重度哮喘患者更常使用非诺特罗,在对基线风险差异进行校正后,它不会增加严重危及生命的哮喘风险。