Reliever salbutamol use as a measure of exacerbation risk in chronic obstructive pulmonary disease

被引:32
作者
Jenkins, Christine R. [1 ,2 ]
Postma, Dirkje S. [3 ]
Anzueto, Antonio R. [4 ,5 ]
Make, Barry J. [6 ]
Peterson, Stefan [7 ]
Eriksson, Goran [8 ]
Calverley, Peter M. [9 ]
机构
[1] Univ Sydney, Concord Hosp, Dept Thorac Med, Sydney, NSW 2139, Australia
[2] George Inst Global Hlth, Sydney, NSW 2139, Australia
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Pulm Med & TB, NL-9700 RB Groningen, Netherlands
[4] Univ Texas Hlth Sci Ctr San Antonio, Dept Med, Pulm Sect, San Antonio, TX 78229 USA
[5] South Texas Vet Hlth Care Syst, San Antonio, TX USA
[6] Univ Colorado, Denver Sch Med, Natl Jewish Hlth, Div Pulm Sci & Crit Care Med, Denver, CO 80206 USA
[7] Medicon Village AB, StatMind, S-22363 Lund, Sweden
[8] Univ Lund Hosp, Dept Resp Med & Allergol, S-22187 Lund, Sweden
[9] Aintree Univ Hosp NHS Fdn Trust, Inst Ageing & Chron Dis, Clin Sci Dept, Liverpool L9 7AL, Merseyside, England
关键词
COPD; Budesonide/formoterol; Exacerbation; Reliever medication; Predictor; METERED-DOSE INHALER; COPD EXACERBATIONS; ASTHMA CONTROL; HEALTH-STATUS; EFFICACY; BUDESONIDE/FORMOTEROL; MODERATE; THERAPY; BURDEN; SAFETY;
D O I
10.1186/s12890-015-0077-0
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Debate exists regarding which endpoints most sensitively reflect day-to-day variation in chronic obstructive pulmonary disease (COPD) symptoms and are most useful in clinical practice to predict COPD exacerbations. We hypothesized that short-acting beta(2)-agonist (SABA) reliever use would predict short-and long-term exacerbation risk in COPD patients. Methods: We performed a retrospective analysis of data from a study (ClinicalTrials.govregistration: NCT00419744) comparing budesonide/formoterol 320/9 mu g with formoterol 9 mu g (both twice daily) in patients with moderate-to-very-severe COPD; reliever salbutamol 90 mu g was provided. First occurrence of reliever use >4 (low), >10 (medium), and >20 (high) inhalations/day was assessed as a predictor of short-term (3-week) exacerbation risk. Mean daily reliever use in the week preceding the 2-month visit was investigated as a predictor of the long-term (10-month) exacerbation risk, using intervals of 2-5, 6-9, and = 10 inhalations/day. Results: Overall, 810 patients were included (61 % male; mean age 63.2 years; post-bronchodilator forced expiratory volume in 1 s 37.7 % of predicted). First occurrence of low, medium, or high reliever use was predictive of an exacerbation within the following 3 weeks; exacerbation risk increased significantly with increasing reliever use. Mean reliever use over 1 week was predictive of long-term exacerbation risk. Patients with mean use of 2-5, 6-9, and = 10 inhalations/day exhibited 21 %, 67 %, and 135 % higher exacerbation rates, respectively, in the following 10 months, compared with <2 inhalations/day. Budesonide/formoterol was associated with lower short-and long-term exacerbation risk than formoterol in all reliever-use groups. Conclusions: SABA reliever use is a predictor of short-and long-term exacerbation risk in moderate-to-very-severe COPD patients with a history of exacerbations receiving budesonide/formoterol or formoterol.
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