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Effect of Treatment with Mucoactive Drugs on COPD Exacerbations During 5 years of Follow-up in the Czech Republic: A Real-World Study
J. Zatloukal, C. Page, K. Brat, M. Svoboda, E. Voláková, M. Plutinský, M. Kopecký, V. Koblížek
Language English Country United States
Document type Journal Article, Observational Study, Multicenter Study
Grant support
FNOl no. 00098892
Ministerstvo Zdravotnictví Ceské Republiky
no. 15/14/NAP
Ministerstvo Zdravotnictví Ceské Republiky
FNOl no. 00098892
Ministerstvo Zdravotnictví Ceské Republiky
FNBr no. 65269705
Ministerstvo Zdravotnictví Ceské Republiky
UHHK no. 00179906
Ministerstvo Zdravotnictví Ceské Republiky
UHHK no. 00179906
Ministerstvo Zdravotnictví Ceské Republiky
Research Area INDI
Cooperatio Charles University, Czechia
Research Area INDI
Cooperatio Charles University, Czechia
- MeSH
- Acetylcysteine * therapeutic use MeSH
- Time Factors MeSH
- Pulmonary Disease, Chronic Obstructive * drug therapy physiopathology diagnosis MeSH
- Expectorants * therapeutic use MeSH
- Middle Aged MeSH
- Humans MeSH
- Follow-Up Studies MeSH
- Disease Progression MeSH
- Prospective Studies MeSH
- Aged MeSH
- Forced Expiratory Volume MeSH
- Treatment Outcome MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Observational Study MeSH
- Geographicals
- Czech Republic MeSH
INTRODUCTION: Studies indicate that chronic treatment with mucoactive drugs may reduce COPD exacerbation rates. This real-world, multicenter, prospective, observational study aimed to determine the effect of long-term mucoactive treatment on exacerbations in patients with COPD in the Czech Republic. METHODS: 452 adult patients on the Czech Multicenter Research Database of COPD with post-bronchodilator FEV1 ≤ 60% of predicted value received standard of care and were followed up for 5 years. For the first 24 months, 81 patients received regular thiol-based mucoactive drugs (77 erdosteine, 4 N-acetylcysteine) at the discretion of the treating physician and 371 patients had no mucoactive treatment (control group). Erdosteine was fully reimbursed, and NAC was partially reimbursed for COPD patients. The annual number/rate of COPD exacerbations over 5 years was monitored. RESULTS: Patients receiving mucoactive treatment for 24 months had a significantly larger reduction from baseline in all exacerbations compared to the control group (- 0.61 vs - 0.18, p = 0.026; - 0.54 vs - 0.09, p = 0.007; - 0.55 vs 0.04, p = 0.005; - 0.67 vs 0.13, p = 0.002; - 0.53 vs 0.10, p = 0.019 in the first to fifth year, respectively). The reduction in moderate exacerbations was also significantly larger in those receiving mucoactive treatment versus no mucoactive treatment. The exacerbation rate was reduced to a greater extent in the subgroups with cough or with stage 3‒4 COPD who received mucoactive treatment but was independent of the use of inhaled corticosteroids (ICS). CONCLUSION: Mucoactive treatment for two years reduced the number of COPD exacerbations (all, moderate) over five years of follow-up. The reduction in exacerbations was more pronounced in patients with cough or with stage 3‒4 COPD but was independent of the use of ICS.
Department of Pneumology University Hospital Hradec Kralove Czech Republic
Department of Pulmonary Diseases and Tuberculosis Masaryk University Brno Czech Republic
Department of Respiratory Medicine University Hospital Olomouc Olomouc Czech Republic
Faculty of Medicine and Dentistry Palacky University Olomouc Czech Republic
Faculty of Medicine in Hradec Kralove Charles University Prague Czech Republic
Faculty of Medicine Masaryk University Brno Czech Republic
Institute of Biostatistics and Analyses Faculty of Medicine Masaryk University Brno Czech Republic
Institute of Biostatistics and Analyses Ltd Brno Czech Republic
Institute of Pharmaceutical Science King's College London London UK
References provided by Crossref.org
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