A randomized, controlled multicentric study of inhaled budesonide and intravenous methylprednisolone in the treatment on acute exacerbation of chronic obstructive pulmonary disease. (December 2016)
- Record Type:
- Journal Article
- Title:
- A randomized, controlled multicentric study of inhaled budesonide and intravenous methylprednisolone in the treatment on acute exacerbation of chronic obstructive pulmonary disease. (December 2016)
- Main Title:
- A randomized, controlled multicentric study of inhaled budesonide and intravenous methylprednisolone in the treatment on acute exacerbation of chronic obstructive pulmonary disease
- Authors:
- Ding, Zhen
Li, Xiu
Lu, Youjin
Rong, Guangsheng
Yang, Ruiqing
Zhang, Ruixia
Wang, Guiqin
Wei, Xiqiang
Ye, Yongqing
Qian, Zhaoxia
Liu, Hongyan
Zhu, Daifeng
Zhou, Ruiqing
Zhu, Kun
Ni, Rongping
Xia, Kui
Luo, Nan
Pei, Cong - Abstract:
- Abstract: Background: Almost all international guidelines recommend corticosteroids for management of exacerbations of chronic obstructive pulmonary disease (COPD), because it leads to improved outcomes of acute exacerbations of chronic obstructive pulmonary disease (AECOPD). Nevertheless, due to its side effects, there are still concerns regarding the use of systemic corticosteroid (SC). Inhaled corticosteroids (IC) can be used as an alternative to SC, while reducing the risk of occurrence of side effects. Purpose: To measure the clinical efficacy and side effects of nebulized budesonide and systemic methylprednisolone in AECOPD. Methods: Valid data from 410 AECOPD patients in 10 hospitals was collected. Patients were randomly divided into 2 groups; budesonide group, treated with nebulized budesonide (2 mg 3 times/day); and methylprednisolone group, treated with intravenously injected methylprednisolone (40 mg/day). COPD assessment test (CAT), arterial blood gas analysis, hospitalization days, adverse effects, fasting blood glucose, serum creatinine, alanine aminotransferase levels, and blood drug were measured and analyzed in both groups. Results: Symptoms, pulmonary function and arterial blood gas analysis were significantly improved after treatment in both groups ( P < 0.05), with no significant differences between them ( P > 0.05), while incidence of adverse events in the budesonide group was lower ( P < 0.05). No significant differences in CAT score, days ofAbstract: Background: Almost all international guidelines recommend corticosteroids for management of exacerbations of chronic obstructive pulmonary disease (COPD), because it leads to improved outcomes of acute exacerbations of chronic obstructive pulmonary disease (AECOPD). Nevertheless, due to its side effects, there are still concerns regarding the use of systemic corticosteroid (SC). Inhaled corticosteroids (IC) can be used as an alternative to SC, while reducing the risk of occurrence of side effects. Purpose: To measure the clinical efficacy and side effects of nebulized budesonide and systemic methylprednisolone in AECOPD. Methods: Valid data from 410 AECOPD patients in 10 hospitals was collected. Patients were randomly divided into 2 groups; budesonide group, treated with nebulized budesonide (2 mg 3 times/day); and methylprednisolone group, treated with intravenously injected methylprednisolone (40 mg/day). COPD assessment test (CAT), arterial blood gas analysis, hospitalization days, adverse effects, fasting blood glucose, serum creatinine, alanine aminotransferase levels, and blood drug were measured and analyzed in both groups. Results: Symptoms, pulmonary function and arterial blood gas analysis were significantly improved after treatment in both groups ( P < 0.05), with no significant differences between them ( P > 0.05), while incidence of adverse events in the budesonide group was lower ( P < 0.05). No significant differences in CAT score, days of admission, blood gas analysis results and physiological and biochemical indexes were found between the two groups. Patients treated with methylprednisolone showed a higher degree of PaO2 level improvement. Conclusion: Results show that inhalation of budesonide (2 mg 3 times/day) and systemic methylprednisolone (40 mg/day) had similar clinical outcome in AECOPD. In conclusion, inhaled budesonide is an alternative to systemic corticosteroids in AECOPD treatment. Highlights: A multicentric, randomized controlled trials of inhaled budesonide in AECOPD. Inhaled budesonide resulted in similar efficacies as systematic methylprednisolone. Inhalation of budesonide could be an alternative treatment of AECOPD. … (more)
- Is Part Of:
- Respiratory medicine. Volume 121(2016)
- Journal:
- Respiratory medicine
- Issue:
- Volume 121(2016)
- Issue Display:
- Volume 121, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 121
- Issue:
- 2016
- Issue Sort Value:
- 2016-0121-2016-0000
- Page Start:
- 39
- Page End:
- 47
- Publication Date:
- 2016-12
- Subjects:
- Chronic obstructive pulmonary disease -- Exacerbation -- Inhaled corticosteroid -- Systemic corticosteroid
COPD chronic obstructive pulmonary disease -- AECOPD acute exacerbations of chronic obstructive pulmonary disease -- SC systemic corticosteroid -- IC inhaled corticosteroids -- CAT COPD assessment test -- FBG fasting blood glucose -- WBC white blood cell count -- ALT alanine aminotransferase -- SCr serum creatinine
Chest -- Diseases -- Periodicals
Chest -- Diseases -- Great Britain -- Periodicals
Respiratory organs -- Diseases -- Periodicals
Respiratory Tract Diseases -- Periodicals
Appareil respiratoire -- Maladies -- Périodiques
Thorax -- Maladies -- Périodiques
Appareil respiratoire -- Maladies -- Traitement -- Périodiques
Electronic journals
616.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09546111 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/09546111 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/09546111 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.rmed.2016.10.013 ↗
- Languages:
- English
- ISSNs:
- 0954-6111
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 7777.661900
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