2012Zhongguo huxi yu weizhong jianhu zazhiRequires access

Salmeterol/Fluticasone Propionate Combined with Tiotropium in Treatment of Severe to Very Severe Stable COPD Patients

Wang Xiang-ron

Open publisher page 0 citations

Abstract

Objective To observe the effects of salmeterol/fluticasone combined with tiotropium in the treatment of sever to very sever COPD.Methods Eighty patients with severe to very severe stable COPD were recruited from outpatient of Central Hospital of Cangzhou between May 2008 and October 2009.The subjects were randomly divided into a salmeterol/fluticasone group and a combination group.The salmeterol/fluticasone group received salmeterol/fluticasone propionate,and the combination group received the combination therapy of tiotropium and salmeterol/fluticasone propionate.All patients had received the treatment for 12 months.At baseline and at the end of 1-month,3-month,6-month,12-month,lung function(FEV1,IC and FVC),six-minute walk distance and the St.George's Respiratory Questionnaire(SGRQ) score were assessed.The number of exacerbations and the time to the first exacerbation were also recorded.Results At every visit,lung function(FEV1,IC and FVC),six-minute walk distance and the SGRQ score were improved in both groups compared with baseline(P0.05),especially in the combination group(P0.05).Compared with the salmeterol/fluticason,the combination therapy with tiotropium significantly decreased the incidence of exacerbations and prolonged the time to the first exacerbation(P0.05).And there was no significant difference between two groups in adverse effects(P0.05).Conclusions The combination therapy with salmeterol/fluticasone propionate and tiotropium was superior to salmeterol/fluticasone propionate in treatment of sever to very severe stable COPD patients in improving lung function,exercise tolerance,and quality of life,without additional adverse effects.

About this research paper

What this paper is about

Objective To observe the effects of salmeterol/fluticasone combined with tiotropium in the treatment of sever to very sever COPD.Methods Eighty patients with severe to very severe stable COPD were recruited from outpatient of Central Hospital of Cangzhou between May 2008 and October 2009.The subjects were randomly divided into a salmeterol/fluticasone group and a combination group.The salmeterol/fluticasone group received salmeterol/fluticasone propionate,and the combination group received the combination therapy of tiotropium and salmeterol/fluticasone propionate.All patients had received the treatment for 12 months.At baseline and at the end of 1-month,3-month,6-month,12-month,lung function(FEV1,IC and FVC),six-minute walk distance and the St.George's Respiratory Questionnaire(SGRQ) score were assessed.The number of exacerbations and the time to the first exacerbation were also recorded.Results At every visit,lung function(FEV1,IC and FVC),six-minute walk distance and the SGRQ score were improved in both groups compared with baseline(P0.05),especially in the combination group(P0.05).Compared with the salmeterol/fluticason,the combination therapy with tiotropium significantly decreased the incidence of exacerbations and prolonged the time to the first exacerbation(P0.05).And there was no significant difference between two groups in adverse effects(P0.05).Conclusions The combination therapy with salmeterol/fluticasone propionate and tiotropium was superior to salmeterol/fluticasone propionate in treatment of sever to very severe stable COPD patients in improving lung function,exercise tolerance,and quality of life,without additional adverse effects.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To observe the effects of salmeterol/fluticasone combined with tiotropium in the treatment of sever to very sever COPD.Methods Eighty patients with severe to very severe stable COPD were recruited from outpatient of Central Hospital of Cangzhou between May 2008 and October 2009.The subjects were randomly divided into a salmeterol/fluticasone group and a combination group.The salmeterol/fluticasone group received salmeterol/fluticasone propionate,and the combination group received the combination therapy of tiotropium and salmeterol/fluticasone propionate.All patients had received the treatment for 12 months.At baseline and at the end of 1-month,3-month,6-month,12-month,lung function(FEV1,IC and FVC),six-minute walk distance and the St.George's Respiratory Questionnaire(SGRQ) score were assessed.The number of exacerbations and the time to the first exacerbation were also recorded.Results At every visit,lung function(FEV1,IC and FVC),six-minute walk distance and the SGRQ score were improved in both groups compared with baseline(P0.05),especially in the combination group(P0.05).Compared with the salmeterol/fluticason,the combination therapy with tiotropium significantly decreased the incidence of exacerbations and prolonged the time to the first exacerbation(P0.05).And there was no significant difference between two groups in adverse effects(P0.05).Conclusions The combination therapy with salmeterol/fluticasone propionate and tiotropium was superior to salmeterol/fluticasone propionate in treatment of sever to very severe stable COPD patients in improving lung function,exercise tolerance,and quality of life,without additional adverse effects.

Key concepts: Salmeterol, Medicine, Fluticasone propionate, Fluticasone, Exacerbation, COPD, Adverse effect, Internal medicine

Related papers

Back to paper searchBrowse research topicsOriginal source
Salmeterol/Fluticasone Propionate Combined with Tiotropium in Treatment of Severe to Very Severe Stable COPD Patients — Research Paper | ScholarLens