Inhaled corticosteroids and Stenotrophomonas maltophilia in outpatients with chronic obstructive pulmonary disease: a retrospective cohort study

被引:0
|
作者
Ronn, Christian [1 ]
Kamstrup, Peter [1 ]
Heerfordt, Christian Kjer [1 ]
Sivapalan, Pradeesh [1 ,2 ]
Eklof, Josefin [1 ]
Boel, Jonas Bredtoft [3 ]
Ostergaard, Christian [3 ]
Dessau, Ram Benny [4 ,5 ]
Moberg, Mia [6 ]
Janner, Julie [6 ]
Ulrik, Charlotte Suppli [2 ,6 ]
Jensen, Jens-Ulrik Staehr [1 ,2 ]
机构
[1] Univ Copenhagen, Dept Internal Med, Sect Resp Med, Hosp Gentofte, Copenhagen, Denmark
[2] Univ Copenhagen, Fac Hlth & Med Sci, Dept Clin Med, Copenhagen, Denmark
[3] Univ Copenhagen, Dept Clin Microbiol, Hosp Herlev, Herlev, Denmark
[4] Zealand Univ Hosp, Dept Clin Microbiol, Slagelse, Denmark
[5] Univ Southern Denmark, Dept Reg Hlth Res, Odense, Denmark
[6] Univ Copenhagen, Dept Resp Med, Hosp Hvidovre, Hvidovre, Denmark
关键词
COPD epidemiology; COPD Pathology; Pulmonary Disease; Chronic Obstructive; FLUTICASONE PROPIONATE/SALMETEROL 250/50; PNEUMONIA RISK; COPD;
D O I
10.1136/bmjresp-2023-001929
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Objectives Inhaled corticosteroids (ICS) are widely used in patients with chronic obstructive pulmonary disease (COPD). However, ICS are associated with an increased risk of adverse effects. We aimed to determine whether an association between a lower respiratory tract culture with Stenotrophomonas maltophilia and increasing ICS dosing in patients with COPD exists. Design An observational cohort study of outpatients with COPD in Denmark between 2010 and 2018. ICS exposure was categorised into four groups based on average daily consumption 1 year prior to inclusion: no use, low ICS dose (<= 400 mu g), moderate ICS dose (400-800 mu g) and high ICS dose (>800 mu g). Dose-response relationship was investigated by a multivariable Cox proportional hazards regression. Results Of the total 22 689 patients, 459 had lower respiratory tract cultures positive for S. maltophilia. The HR of S. maltophilia increased with increasing daily ICS dose: low ICS dose HR 2.6 (95% CI 1.6 to 4.0), moderate ICS dose HR 3.0 (95% CI 1.9 to 4.6) and high ICS dose HR 5.7 (95% CI 3.8 to 8.5). Conclusions We found that ICS was associated with a high, dose-dependent increased hazard of S. maltophilia in outpatients with COPD. High dose users had a nearly six times increased hazard compared with non-users of ICS. When appropriate, attempts at de-escalating ICS treatment should be made.
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