Browsing by Author "Ringshausen, Felix C. (23005846300)"
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Publication Bronchiectasis and asthma: Data from the European Bronchiectasis Registry (EMBARC)(2024) ;Polverino, Eva (18837810800) ;Dimakou, Katerina (6506811930) ;Traversi, Letizia (57204862743) ;Bossios, Apostolos (6603430310) ;Haworth, Charles S. (7005598480) ;Loebinger, Michael R. (17135062600) ;De Soyza, Anthony (57205884258) ;Vendrell, Montserrat (7006288000) ;Burgel, Pierre-Régis (6603867674) ;Mertsch, Pontus (57191255944) ;McDonnell, Melissa (57197895491) ;Škrgat, Sabina (57191262713) ;Maiz Carro, Luis (7004344176) ;Sibila, Oriol (8761639900) ;van der Eerden, Menno (6603272611) ;Kauppi, Paula (7003745689) ;Hill, Adam T. (15041954900) ;Wilson, Robert (55822965649) ;Milenkovic, Branislava (23005307400) ;Menendez, Rosario (7102205716) ;Murris, Marlene (6506255606) ;Digalaki, Tonia (58943780500) ;Crichton, Megan L. (57159486200) ;Borecki, Sermin (58943409600) ;Obradovic, Dusanka (35092808200) ;Nowinski, Adam (7003378139) ;Amorim, Adelina (57205735223) ;Torres, Antoni (57205521091) ;Lorent, Natalie (6506890833) ;Welte, Tobias (57223621683) ;Blasi, Francesco (41761074200) ;Van Braeckel, Eva (8265309200) ;Altenburg, Josje (35733143500) ;Shoemark, Amelia (16246385000) ;Shteinberg, Michal (7004226287) ;Boersma, Wim (7004305076) ;Elborn, J. Stuart (57220451524) ;Aliberti, Stefano (9247687000) ;Ringshausen, Felix C. (23005846300) ;Chalmers, James D. (56648999600)Goeminne, Pieter C. (35811825700)Background: Asthma is commonly reported in patients with a diagnosis of bronchiectasis. Objective: The aim of this study was to evaluate whether patients with bronchiectasis and asthma (BE+A) had a different clinical phenotype and different outcomes compared with patients with bronchiectasis without concomitant asthma. Methods: A prospective observational pan-European registry (European Multicentre Bronchiectasis Audit and Research Collaboration) enrolled patients across 28 countries. Adult patients with computed tomography–confirmed bronchiectasis were reviewed at baseline and annual follow-up visits using an electronic case report form. Asthma was diagnosed by the local investigator. Follow-up data were used to explore differences in exacerbation frequency between groups using a negative binomial regression model. Survival analysis used Cox proportional hazards regression. Results: Of 16,963 patients with bronchiectasis included for analysis, 5,267 (31.0%) had investigator-reported asthma. Patients with BE+A were younger, were more likely to be female and never smokers, and had a higher body mass index than patients with bronchiectasis without asthma. BE+A was associated with a higher prevalence of rhinosinusitis and nasal polyps as well as eosinophilia and Aspergillus sensitization. BE+A had similar microbiology but significantly lower severity of disease using the bronchiectasis severity index. Patients with BE+A were at increased risk of exacerbation after adjustment for disease severity and multiple confounders. Inhaled corticosteroid (ICS) use was associated with reduced mortality in patients with BE+A (adjusted hazard ratio 0.78, 95% CI 0.63-0.95) and reduced risk of hospitalization (rate ratio 0.67, 95% CI 0.67-0.86) compared with control subjects without asthma and not receiving ICSs. Conclusions: BE+A was common and was associated with an increased risk of exacerbations and improved outcomes with ICS use. Unexpectedly we identified significantly lower mortality in patients with BE+A. © 2024 The Authors - Some of the metrics are blocked by yourconsent settings
Publication Bronchiectasis and asthma: Data from the European Bronchiectasis Registry (EMBARC)(2024) ;Polverino, Eva (18837810800) ;Dimakou, Katerina (6506811930) ;Traversi, Letizia (57204862743) ;Bossios, Apostolos (6603430310) ;Haworth, Charles S. (7005598480) ;Loebinger, Michael R. (17135062600) ;De Soyza, Anthony (57205884258) ;Vendrell, Montserrat (7006288000) ;Burgel, Pierre-Régis (6603867674) ;Mertsch, Pontus (57191255944) ;McDonnell, Melissa (57197895491) ;Škrgat, Sabina (57191262713) ;Maiz Carro, Luis (7004344176) ;Sibila, Oriol (8761639900) ;van der Eerden, Menno (6603272611) ;Kauppi, Paula (7003745689) ;Hill, Adam T. (15041954900) ;Wilson, Robert (55822965649) ;Milenkovic, Branislava (23005307400) ;Menendez, Rosario (7102205716) ;Murris, Marlene (6506255606) ;Digalaki, Tonia (58943780500) ;Crichton, Megan L. (57159486200) ;Borecki, Sermin (58943409600) ;Obradovic, Dusanka (35092808200) ;Nowinski, Adam (7003378139) ;Amorim, Adelina (57205735223) ;Torres, Antoni (57205521091) ;Lorent, Natalie (6506890833) ;Welte, Tobias (57223621683) ;Blasi, Francesco (41761074200) ;Van Braeckel, Eva (8265309200) ;Altenburg, Josje (35733143500) ;Shoemark, Amelia (16246385000) ;Shteinberg, Michal (7004226287) ;Boersma, Wim (7004305076) ;Elborn, J. Stuart (57220451524) ;Aliberti, Stefano (9247687000) ;Ringshausen, Felix C. (23005846300) ;Chalmers, James D. (56648999600)Goeminne, Pieter C. (35811825700)Background: Asthma is commonly reported in patients with a diagnosis of bronchiectasis. Objective: The aim of this study was to evaluate whether patients with bronchiectasis and asthma (BE+A) had a different clinical phenotype and different outcomes compared with patients with bronchiectasis without concomitant asthma. Methods: A prospective observational pan-European registry (European Multicentre Bronchiectasis Audit and Research Collaboration) enrolled patients across 28 countries. Adult patients with computed tomography–confirmed bronchiectasis were reviewed at baseline and annual follow-up visits using an electronic case report form. Asthma was diagnosed by the local investigator. Follow-up data were used to explore differences in exacerbation frequency between groups using a negative binomial regression model. Survival analysis used Cox proportional hazards regression. Results: Of 16,963 patients with bronchiectasis included for analysis, 5,267 (31.0%) had investigator-reported asthma. Patients with BE+A were younger, were more likely to be female and never smokers, and had a higher body mass index than patients with bronchiectasis without asthma. BE+A was associated with a higher prevalence of rhinosinusitis and nasal polyps as well as eosinophilia and Aspergillus sensitization. BE+A had similar microbiology but significantly lower severity of disease using the bronchiectasis severity index. Patients with BE+A were at increased risk of exacerbation after adjustment for disease severity and multiple confounders. Inhaled corticosteroid (ICS) use was associated with reduced mortality in patients with BE+A (adjusted hazard ratio 0.78, 95% CI 0.63-0.95) and reduced risk of hospitalization (rate ratio 0.67, 95% CI 0.67-0.86) compared with control subjects without asthma and not receiving ICSs. Conclusions: BE+A was common and was associated with an increased risk of exacerbations and improved outcomes with ICS use. Unexpectedly we identified significantly lower mortality in patients with BE+A. © 2024 The Authors - Some of the metrics are blocked by yourconsent settings
Publication Objective sputum colour assessment and clinical outcomes in bronchiectasis: data from the European Bronchiectasis Registry (EMBARC)(2024) ;Aliberti, Stefano (9247687000) ;Ringshausen, Felix C. (23005846300) ;Dhar, Raja (7006700626) ;Haworth, Charles S. (7005598480) ;Loebinger, Michael R. (17135062600) ;Dimakou, Katerina (6506811930) ;Crichton, Megan L. (57159486200) ;De Soyza, Anthony (57205884258) ;Vendrell, Montse (7006288000) ;Burgel, Pierre-Regis (6603867674) ;McDonnell, Melissa (57197895491) ;Skrgat, Sabina (57191262713) ;Carro, Luis Maiz (54915148800) ;de Roux, Andres (6602925494) ;Sibila, Oriol (8761639900) ;Bossios, Apostolos (6603430310) ;van der Eerden, Menno (6603272611) ;Kauppi, Paula (7003745689) ;Wilson, Robert (55822965649) ;Milenkovic, Branislava (23005307400) ;Menendez, Rosario (7102205716) ;Murris, Marlene (6506255606) ;Borekci, Sermin (15520550700) ;Munteanu, Oxana (26435358100) ;Obradovic, Dusanka (35092808200) ;Nowinski, Adam (7003378139) ;Amorim, Adelina (57205735223) ;Torres, Antoni (57205521091) ;Lorent, Natalie (6506890833) ;Van Braeckel, Eva (8265309200) ;Altenburg, Josje (35733143500) ;Shoemark, Amelia (16246385000) ;Shteinberg, Michal (7004226287) ;Boersma, Wim (7004305076) ;Goeminne, Pieter C. (35811825700) ;Elborn, J. Stuart (57220451524) ;Hill, Adam T. (15041954900) ;Welte, Tobias (57223621683) ;Blasi, Francesco (41761074200) ;Polverino, Eva (18837810800)Chalmers, James D. (56648999600)Background A validated 4-point sputum colour chart can be used to objectively evaluate the levels of airway inflammation in bronchiectasis patients. In the European Bronchiectasis Registry (EMBARC), we tested whether sputum colour would be associated with disease severity and clinical outcomes. Methods We used a prospective, observational registry of adults with bronchiectasis conducted in 31 countries. Patients who did not produce spontaneous sputum were excluded from the analysis. The Murray sputum colour chart was used at baseline and at follow-up visits. Key outcomes were frequency of exacerbations, hospitalisations for severe exacerbations and mortality during up to 5-year follow-up. Results 13 484 patients were included in the analysis. More purulent sputum was associated with lower forced expiratory volume in 1 s (FEV1), worse quality of life, greater bacterial infection and a higher bronchiectasis severity index. Sputum colour was strongly associated with the risk of future exacerbations during follow-up. Compared to patients with mucoid sputum (reference group), patients with mucopurulent sputum experienced significantly more exacerbations (incident rate ratio (IRR) 1.29, 95% CI 1.22–1.38; p<0.0001), while the rates were even higher for patients with purulent (IRR 1.55, 95% CI 1.44–1.67; p<0.0001) and severely purulent sputum (IRR 1.91, 95% CI 1.52–2.39; p<0.0001). Hospitalisations for severe exacerbations were also associated with increasing sputum colour with rate ratios, compared to patients with mucoid sputum, of 1.41 (95% CI 1.29–1.56; p<0.0001), 1.98 (95% CI 1.77–2.21; p<0.0001) and 3.05 (95% CI 2.25–4.14; p<0.0001) for mucopurulent, purulent and severely purulent sputum, respectively. Mortality was significantly increased with increasing sputum purulence, hazard ratio 1.12 (95% CI 1.01–1.24; p=0.027), for each increment in sputum purulence. Conclusion Sputum colour is a simple marker of disease severity and future risk of exacerbations, severe exacerbations and mortality in patients with bronchiectasis. © 2024 European Respiratory Society. All rights reserved.
