{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Ronn C"],"funding":["Novo Nordisk","Novo Nordisk Fonden"],"pagination":["e001929"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10928788"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["11(1)"],"pubmed_abstract":["<h4>Objectives</h4>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 <i>Stenotrophomonas maltophilia</i> and increasing ICS dosing in patients with COPD exists.<h4>Design</h4>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 µg), moderate ICS dose (400-800 µg) and high ICS dose (>800 µg). Dose-response relationship was investigated by a multivariable Cox proportional hazards regression.<h4>Results</h4>Of the total 22 689 patients, 459 had lower respiratory tract cultures positive for <i>S. maltophilia</i>. The HR of <i>S. maltophilia</i> 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).<h4>Conclusions</h4>We found that ICS was associated with a high, dose-dependent increased hazard of <i>S. maltophilia</i> 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."],"journal":["BMJ open respiratory research"],"pubmed_title":["Inhaled corticosteroids and <i>Stenotrophomonas maltophilia</i> in outpatients with chronic obstructive pulmonary disease: a retrospective cohort study."],"pmcid":["PMC10928788"],"funding_grant_id":["NNF20OC0060657"],"pubmed_authors":["Ostergaard C","Dessau RB","Boel JB","Sivapalan P","Ulrik CS","Heerfordt CK","Janner J","Moberg M","Kamstrup P","Jensen JS","Ronn C","Eklof J"],"additional_accession":[]},"is_claimable":false,"name":"Inhaled corticosteroids and <i>Stenotrophomonas maltophilia</i> in outpatients with chronic obstructive pulmonary disease: a retrospective cohort study.","description":"<h4>Objectives</h4>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 <i>Stenotrophomonas maltophilia</i> and increasing ICS dosing in patients with COPD exists.<h4>Design</h4>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 µg), moderate ICS dose (400-800 µg) and high ICS dose (>800 µg). Dose-response relationship was investigated by a multivariable Cox proportional hazards regression.<h4>Results</h4>Of the total 22 689 patients, 459 had lower respiratory tract cultures positive for <i>S. maltophilia</i>. The HR of <i>S. maltophilia</i> 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).<h4>Conclusions</h4>We found that ICS was associated with a high, dose-dependent increased hazard of <i>S. maltophilia</i> 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.","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Mar","modification":"2026-06-27T03:08:11.463Z","creation":"2026-06-27T03:05:43.281Z"},"accession":"S-EPMC10928788","cross_references":{"pubmed":["38460975"],"doi":["10.1136/bmjresp-2023-001929"]}}