Evans J M, Hayes J L, Lipworth B J, MacDonald T M
Ninewells Hospital, Dundee.
Br J Gen Pract. 1996 Jul;46(408):423-5.
The aim of this study was to investigate the co-prescribing of beta-antagonists and beta-agonists in the community, and to assess the potential hazards of such co-prescribing.
The study was set in the population of Tayside, Scotland (population approximately 400,000), between January 1993 and March 1993. An automated person-specific prescribing database was used, which could also be linked to hospital admissions. Patients who were co-prescribed beta-antagonists and beta-agonists on the same day or within 30 days were selected. A model was used to identify those who showed an asthmatic profile, on the basis of age, and previous prescribing and hospitalization history, and for whom the co-prescribing was judged to be particularly hazardous.
Altogether, 0.9% of 15824 patients who received a beta-antagonist during the study period received a beta-agonist on the same day. This figure increased to 274 (1.7%) for 30-day co-prescription. A few instances of particularly hazardous co-prescribing were identified, which involved young people who had previously received prescriptions for corticosteroids and been hospitalized for asthma.
Potentially hazardous co-prescribing of beta-agonists and beta-antagonists occurs despite labelled warnings, even in patients who appear to be at high risk. These events are quite rare but probably should not occur at all.
本研究旨在调查社区中β受体拮抗剂和β受体激动剂的联合处方情况,并评估这种联合处方的潜在危害。
该研究于1993年1月至1993年3月在苏格兰泰赛德地区(人口约40万)进行。使用了一个自动化的个人特定处方数据库,该数据库还可与医院入院记录相链接。选择在同一天或30天内联合使用β受体拮抗剂和β受体激动剂的患者。基于年龄、既往处方和住院病史,使用一个模型来识别那些具有哮喘特征且联合处方被判定为特别危险的患者。
在研究期间接受β受体拮抗剂治疗的15824名患者中,共有0.9%在同一天接受了β受体激动剂治疗。30天联合处方的这一数字增至274例(1.7%)。识别出了一些特别危险的联合处方情况,涉及此前曾接受皮质类固醇处方并因哮喘住院的年轻人。
尽管有标签警示,但β受体激动剂和β受体拮抗剂的潜在危险联合处方仍会发生,即使在看似高危的患者中也是如此。这些事件相当罕见,但可能根本就不应发生。