<?xml version="1.0"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://dirros.openscience.si/IzpisGradiva.php?id=31978"><dc:title>Symptom improvement with BDP/FF/G fixed triple inhalation powder in moderate to severe COPD patients uncontrolled with dual therapies</dc:title><dc:creator>Harlander,	Matevž	(Avtor)
	</dc:creator><dc:creator>Šubic,	Tjaša	(Avtor)
	</dc:creator><dc:creator>Eržen,	Renato	(Avtor)
	</dc:creator><dc:creator>Maček Cafuta,	Arjana	(Avtor)
	</dc:creator><dc:creator>Lopert,	Anton	(Avtor)
	</dc:creator><dc:creator>Horvat,	Alojz	(Avtor)
	</dc:creator><dc:creator>Božič,	Dušan	(Avtor)
	</dc:creator><dc:creator>Klobučar,	Albert	(Avtor)
	</dc:creator><dc:creator>Krstić,	Zoran	(Avtor)
	</dc:creator><dc:creator>Todorović,	Nataša	(Avtor)
	</dc:creator><dc:creator>Sobotkiewicz,	Nina	(Avtor)
	</dc:creator><dc:creator>Kirbiš,	Simona	(Avtor)
	</dc:creator><dc:creator>Novakovič,	Ana	(Avtor)
	</dc:creator><dc:creator>Šegota,	Nikša	(Avtor)
	</dc:creator><dc:creator>Červenjak,	Branislav	(Avtor)
	</dc:creator><dc:creator>Panjan Avramovič,	Jasmina	(Avtor)
	</dc:creator><dc:creator>Paun,	Kata	(Avtor)
	</dc:creator><dc:creator>Gabršček,	Lucija	(Avtor)
	</dc:creator><dc:subject>chronic obstructive pulmonary disease</dc:subject><dc:subject>therapy</dc:subject><dc:subject>COPD Assessment Tool</dc:subject><dc:description>People living with COPD are frequently inadequately treated due to underdiagnosis ormisdiagnosis. The aim of this study was to evaluate the real-world performance of thebeclomethasone dipropionate/formoterol fumarate/glycopyrronium (BDP/FF/G) fixed triplecombination formulated in a dry powder inhaler (DPI) in improving symptoms, lungfunction, and adherence in moderate to severe COPD patients uncontrolled on dualtherapies. We conducted a non-interventional, open-label, single-arm, multicenter,prospective study across 19 outpatient centers in Slovenia. The primary objective was tomeasure symptom improvement with the COPD Assessment Tool (CAT). A total of 359patients with moderate to severe COPD (97% classified as GOLD E, frequent exacerbators)were followed for 24 weeks. There was a significant 6-point reduction in the CAT score afterswitching from dual therapies to BDP/FF/G inhalation powder (95% CI: −7.0 to −5.5;p &lt; 0.0001). FEV1 increased by 110 mL (95% CI: 90–130; p &lt; 0.0001) and FVC by 95 mL (95%CI: 65–120; p &lt; 0.0001), reaching a statistically significant improvement of 2.5 percentagepoints in the FEV1/FVC quotient. The net improvement in dyspnea severity was 50.9%(95% CI 44.7%–57.2%), as assessed using the modified Medical Research Council (mMRC)Scale. Treatment adherence improved significantly after 6 months of triple therapy. In ourcohort, switching uncontrolled moderate-to-severe COPD patients from dual therapy toBDP/FF/G fixed triple inhalation powder led to significant improvements in symptoms,lung function, dyspnea, sleep quality, and treatment adherence.</dc:description><dc:date>2026</dc:date><dc:date>2026-08-24 09:31:36</dc:date><dc:type>Neznano</dc:type><dc:identifier>31978</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
