TY - JOUR
T1 - Identifying patients at risk of late recovery (≥8 days) from acute exacerbation of chronic bronchitis and COPD
AU - Anzueto, Antonio
AU - Miravitlles, Marc
AU - Ewig, Santiago
AU - Legnani, Delfino
AU - Heldner, Stephanie
AU - Stauch, Kathrin
N1 - Funding Information:
Antonio Anzueto has participated as a speaker in scientific meetings or courses organized and financed by pharmaceutical companies including: Boehringer Ingelheim, Bayer Schering Pharma, Pfizer, GlaxoSmithKline, and the Schering Plough Corporation. He has also provided consultancy services to Boehringer Ingelheim, Bayer Schering Pharma, Pfizer, GlaxoSmithKline and the Schering Plough Corporation. He has been the principal investigator for research grants and the University of Texas Health Science Center at San Antonio was paid for participating in multi-center clinical trials sponsored by: C R Bard, Lilly, GSK, Pfizer, and the National Institutes of Health, National Heart, Lung and Blood Institute.
Funding Information:
This study was supported by a research grant from Bayer Schering Pharma (BSP). Project Management including the set-up and conduct of the study was supervised by Kathrin Stauch and Stephanie Heldner from Global Non-Interventional Studies at BSP. The contract research organisation (CRO) Institute Dr. Schauerte (Oberhaching, Germany) was responsible for data capture and data management. The CRO Kantar Health (Munich, Germany) was responsible for statistical analysis and reporting of study results. Highfield Communication Consultancy (funded by Bayer Schering Pharma) provided editorial assistance in the preparation of this manuscript.
PY - 2012/9
Y1 - 2012/9
N2 - Objectives: To identify factors associated with late recovery (≥8 days from exacerbation start) in patients with acute exacerbations of chronic bronchitis/COPD (AECB/AECOPD). Methods: An international, observational, non-interventional study in outpatients with AECB/AECOPD who received treatment for their exacerbation with the antibiotic moxifloxacin. Factors analyzed for late recovery included patient demographic characteristics, geographic region and disease severity. Additionally, logistic regression analysis was undertaken to identify factors associated with late recovery. Results: The analysis population was 40,435 patients aged ≥35 years, from Asia-Pacific, Europe, the Americas and Middle East/Africa. Most were male (63.1%), mean age 60.4 years and current or ex-smokers (60.6%) with history of ≥2 exacerbations in the previous year. Patients who underwent spirometry (n = 6408, 19.7%) had moderate airflow obstruction (mean FEV1 1.7 L). Both clinicians and patients reported that moxifloxacin provided clinical improvement in a mean of 3 days and recovery in 6 days. Clinical factors significantly associated with late recovery were: age ≥65 years, duration of chronic bronchitis >10 years, cardiac comorbidity, >3 exacerbations in the previous 12 months, current exacerbation type (Anthonisen I/II) and hospitalization in the last 12 months. Conclusions: In a large cohort of patients, all treated with the same antibiotic for an exacerbation of chronic bronchitis or COPD, the main factors associated with late recovery (≥8 days) were: older age, history of frequent exacerbations, current exacerbation type of Anthonisen I/II, history of prior hospitalizations and cardiac comorbid conditions.
AB - Objectives: To identify factors associated with late recovery (≥8 days from exacerbation start) in patients with acute exacerbations of chronic bronchitis/COPD (AECB/AECOPD). Methods: An international, observational, non-interventional study in outpatients with AECB/AECOPD who received treatment for their exacerbation with the antibiotic moxifloxacin. Factors analyzed for late recovery included patient demographic characteristics, geographic region and disease severity. Additionally, logistic regression analysis was undertaken to identify factors associated with late recovery. Results: The analysis population was 40,435 patients aged ≥35 years, from Asia-Pacific, Europe, the Americas and Middle East/Africa. Most were male (63.1%), mean age 60.4 years and current or ex-smokers (60.6%) with history of ≥2 exacerbations in the previous year. Patients who underwent spirometry (n = 6408, 19.7%) had moderate airflow obstruction (mean FEV1 1.7 L). Both clinicians and patients reported that moxifloxacin provided clinical improvement in a mean of 3 days and recovery in 6 days. Clinical factors significantly associated with late recovery were: age ≥65 years, duration of chronic bronchitis >10 years, cardiac comorbidity, >3 exacerbations in the previous 12 months, current exacerbation type (Anthonisen I/II) and hospitalization in the last 12 months. Conclusions: In a large cohort of patients, all treated with the same antibiotic for an exacerbation of chronic bronchitis or COPD, the main factors associated with late recovery (≥8 days) were: older age, history of frequent exacerbations, current exacerbation type of Anthonisen I/II, history of prior hospitalizations and cardiac comorbid conditions.
KW - AECB
KW - AECOPD
KW - Exacerbation
KW - Moxifloxacin
KW - Non-interventional
KW - Observational
UR - http://www.scopus.com/inward/record.url?scp=84864602576&partnerID=8YFLogxK
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U2 - 10.1016/j.rmed.2012.06.002
DO - 10.1016/j.rmed.2012.06.002
M3 - Article
C2 - 22749710
AN - SCOPUS:84864602576
SN - 0954-6111
VL - 106
SP - 1258
EP - 1267
JO - Respiratory Medicine
JF - Respiratory Medicine
IS - 9
ER -