Risk of active tuberculosis among COPD patients treated with fixed combinations of long-acting beta2 agonists and inhaled corticosteroids
Autor: | Tsan-Ming Huang, Kuan-Chih Kuo, Ya-Hui Wang, Cheng-Yi Wang, Chih-Cheng Lai, Hao-Chien Wang, Likwang Chen, Chong-Jen Yu, On the behalf of Taiwan Clinical Trial Consortium for Respiratory Diseases (TCORE) |
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Rok vydání: | 2020 |
Předmět: |
Male
Budesonide Pulmonary Disease Chronic Obstructive 0302 clinical medicine immune system diseases Adrenal Cortex Hormones Risk Factors Budesonide Formoterol Fumarate Drug Combination Medicine 030212 general & internal medicine Fluticasone education.field_of_study COPD Incidence respiratory system Middle Aged Fluticasone-Salmeterol Drug Combination Infectious Diseases Fluticasone/salmeterol Female Salmeterol hormones hormone substitutes and hormone antagonists circulatory and respiratory physiology Research Article medicine.drug medicine.medical_specialty Population Taiwan lcsh:Infectious and parasitic diseases 03 medical and health sciences Internal medicine Statistical significance Administration Inhalation Tuberculosis Humans lcsh:RC109-216 Propensity Score education Budesonide/formoterol Adrenergic beta-2 Receptor Agonists Aged business.industry Mycobacterium tuberculosis medicine.disease respiratory tract diseases 030228 respiratory system Formoterol business Follow-Up Studies |
Zdroj: | BMC Infectious Diseases BMC Infectious Diseases, Vol 20, Iss 1, Pp 1-8 (2020) |
ISSN: | 1471-2334 |
Popis: | Objectives To investigate the incidence of active tuberculosis (TB) among COPD patients using fluticasone/salmeterol or budesonide/formoterol, and to identify any differences between these two groups of patients. Methods The study enrolled COPD patients from Taiwan NHIRD who received treatment with fluticasone/salmeterol or budesonide/formoterol for > 90 days between 2004 and 2011. The incidence of active TB was the primary outcome. Results Among the intention-to-treat population prior to matching, the incidence rates of active TB were 0.94 and 0.61% in the fluticasone/salmeterol and budesonide/formoterol groups, respectively. After matching, the fluticasone/salmeterol group had significantly higher rates of active TB (adjusted HR, 1.41, 95% CI, 1.17–1.70) compared with the budesonide/formoterol group. The significant difference between these two groups remained after a competing risk analysis (HR, 1.45, 95% CI, 1.21–1.74). Following propensity score matching, the fluticasone/salmeterol group had significantly higher rates of active TB compared with the budesonide/formoterol group (adjusted HR, 1.45, 95% CI, 1.14–1.85). A similar trend was observed after a competing risk analysis (HR, 1.44, 95% CI, 1.19–1.75). A higher risk of active TB was observed in the fluticasone/salmeterol group compared with the budesonide/formoterol group across all subgroups, but some differences did not reach statistical significance. Conclusion Fluticasone/salmeterol carried a higher risk of active TB compared with budesonide/formoterol among COPD patients. |
Databáze: | OpenAIRE |
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