临床肺科杂志
臨床肺科雜誌
림상폐과잡지
JOUNAL OF CLINICAL PULMONARY MEDICINE
2014年
7期
1261-1263,1264
,共4页
舒利迭%思力华%稳定期COPD%疗效
舒利迭%思力華%穩定期COPD%療效
서리질%사력화%은정기COPD%료효
seretide%tiotropium%stable chronic obstructive pulmonary disease%curative effect
目的:探讨思力华联合舒利迭治疗稳定期慢性阻塞性肺病( chronic obstructive pulmonary disea-ses,COPD)的疗效及安全性。方法研究对象为2010年11月~2011年12月我院收治的258例稳定期COPD患者,随机分为治疗组(129例)、对照组(129例)。治疗组吸入舒利迭50μg/250μg/次,2次/d,思力华18μg/次,1次/d;对照组仅吸入舒利迭50μg/250μg/次,2次/d,用药12周,比较分析两组疗效。结果治疗组显效率(65.9%)及总有效率(93.8%)均显著高于对照组(27.9%,62.8%)(P<0.05),治疗后肺功能指标FEV1、FEV1/FVC及动脉血气PaO2均明显升高(P<0.05),且治疗组显著高于对照组(P<0.05),而动脉血气PaCO2明显降低(P<0.05),且治疗组显著低于对照组(P<0.05),两组不良反应发生率比较差异无统计学意义(P>0.05)。结论舒利迭联合思力华治疗稳定期COPD的临床疗效显著,优于单用舒利迭,可明显改善患者动脉血气及肺功能,是稳定期COPD患者的理想治疗方案。
目的:探討思力華聯閤舒利迭治療穩定期慢性阻塞性肺病( chronic obstructive pulmonary disea-ses,COPD)的療效及安全性。方法研究對象為2010年11月~2011年12月我院收治的258例穩定期COPD患者,隨機分為治療組(129例)、對照組(129例)。治療組吸入舒利迭50μg/250μg/次,2次/d,思力華18μg/次,1次/d;對照組僅吸入舒利迭50μg/250μg/次,2次/d,用藥12週,比較分析兩組療效。結果治療組顯效率(65.9%)及總有效率(93.8%)均顯著高于對照組(27.9%,62.8%)(P<0.05),治療後肺功能指標FEV1、FEV1/FVC及動脈血氣PaO2均明顯升高(P<0.05),且治療組顯著高于對照組(P<0.05),而動脈血氣PaCO2明顯降低(P<0.05),且治療組顯著低于對照組(P<0.05),兩組不良反應髮生率比較差異無統計學意義(P>0.05)。結論舒利迭聯閤思力華治療穩定期COPD的臨床療效顯著,優于單用舒利迭,可明顯改善患者動脈血氣及肺功能,是穩定期COPD患者的理想治療方案。
목적:탐토사력화연합서리질치료은정기만성조새성폐병( chronic obstructive pulmonary disea-ses,COPD)적료효급안전성。방법연구대상위2010년11월~2011년12월아원수치적258례은정기COPD환자,수궤분위치료조(129례)、대조조(129례)。치료조흡입서리질50μg/250μg/차,2차/d,사력화18μg/차,1차/d;대조조부흡입서리질50μg/250μg/차,2차/d,용약12주,비교분석량조료효。결과치료조현효솔(65.9%)급총유효솔(93.8%)균현저고우대조조(27.9%,62.8%)(P<0.05),치료후폐공능지표FEV1、FEV1/FVC급동맥혈기PaO2균명현승고(P<0.05),차치료조현저고우대조조(P<0.05),이동맥혈기PaCO2명현강저(P<0.05),차치료조현저저우대조조(P<0.05),량조불량반응발생솔비교차이무통계학의의(P>0.05)。결론서리질연합사력화치료은정기COPD적림상료효현저,우우단용서리질,가명현개선환자동맥혈기급폐공능,시은정기COPD환자적이상치료방안。
Objective To observe the curative effect and safety of tiotropium combined with seretide in the treatment of stable chronic obstructive pulmonary disease ( COPD) . Methods 258 patients with stable COPD were randomly divided into the treatment group and the control group, 129 cases in each group. The treatment group was given seretide (50μg/250μg) twice daily and tiotropium bromide (18μg) once daily, and the control group was giv-en seretide (50μg/250μg) twice daily. The treatment course was 12 weeks. Before and after the treatment, lung function and arterial blood gas of the two groups were examined and compared respectively. Results The effective rate was 65. 9% and the total effective rate was 93. 8% in the treatment group, which were significantly higher than that in the control group (27. 9%, 62. 8%) (P<0. 05). After the treatment, the levels of FEV1, FEV1/FVC and PaO2 increased significantly (P<0. 05), and the improvement was more pronounced in the treatment group than in the control group (P<0. 05). The level of PaCO2 decreased obviously (P<0. 05), and the decrease was more pro-nounced in the treatment group than in the control group (P<0. 05). There was no statistical difference in the inci-dence of adverse reactions (P>0. 05). Conclusion Seretide combined with tiotropium is effective in the treatment of stable COPD, which is better than seretide only and can obviously improve lung function and arterial blood gas.