中国生化药物杂志
中國生化藥物雜誌
중국생화약물잡지
CHINESE JOURNAL OF BIOCHEMICAL PHARMACEUTICS
2015年
5期
140-142
,共3页
六君子汤%肺脾两虚%慢性阻塞性肺疾病%稳定期
六君子湯%肺脾兩虛%慢性阻塞性肺疾病%穩定期
륙군자탕%폐비량허%만성조새성폐질병%은정기
additive LiuJunZi decoction%both lung and spleen deficiency%chronic obstructive pneumonia%stable phase
目的:探讨六君子汤加减治疗肺脾两虚型慢性阻塞性肺疾病( chronic obstructive pneumonia,COPD)稳定期的疗效。方法选择杭州市余杭区第一人民医院门诊符合肺脾两虚型慢阻肺稳定期患者58例,用随机数字表法随机分为治疗组和对照组,每组29例,2组均给予沙美特罗替卡松粉吸入剂吸入,在此基础上,治疗组给予六君子汤加减口服,疗程为3个月,观察患者临床体征和症状改善情况,比较肺功能、痰液指标以及1年内急性发作比例。结果2组患者经不同治疗方案后,治疗组总有效率为93.1%,明显优于对照组的总有效率65.5%(P<0.05)。2组治疗后FEV1和FEV1/FVC均有提高(P<0.05),治疗组上述肺功能指标提高明显优于对照组(P<0.05)。2组HDACs活性、TNF-α及IL-8水平均有改善(P<0.05),治疗组明显优于对照组(P<0.05)。治疗组急性发作2例(6.9%),对照组急性发作7例(24.1%),差异无统计学意义。结论六君子汤加减治疗肺脾两虚型慢阻肺稳定期临床疗效确切,可明显改善患者临床症状以及实验室指标,控制病情发展,提高患者生存质量。
目的:探討六君子湯加減治療肺脾兩虛型慢性阻塞性肺疾病( chronic obstructive pneumonia,COPD)穩定期的療效。方法選擇杭州市餘杭區第一人民醫院門診符閤肺脾兩虛型慢阻肺穩定期患者58例,用隨機數字錶法隨機分為治療組和對照組,每組29例,2組均給予沙美特囉替卡鬆粉吸入劑吸入,在此基礎上,治療組給予六君子湯加減口服,療程為3箇月,觀察患者臨床體徵和癥狀改善情況,比較肺功能、痰液指標以及1年內急性髮作比例。結果2組患者經不同治療方案後,治療組總有效率為93.1%,明顯優于對照組的總有效率65.5%(P<0.05)。2組治療後FEV1和FEV1/FVC均有提高(P<0.05),治療組上述肺功能指標提高明顯優于對照組(P<0.05)。2組HDACs活性、TNF-α及IL-8水平均有改善(P<0.05),治療組明顯優于對照組(P<0.05)。治療組急性髮作2例(6.9%),對照組急性髮作7例(24.1%),差異無統計學意義。結論六君子湯加減治療肺脾兩虛型慢阻肺穩定期臨床療效確切,可明顯改善患者臨床癥狀以及實驗室指標,控製病情髮展,提高患者生存質量。
목적:탐토륙군자탕가감치료폐비량허형만성조새성폐질병( chronic obstructive pneumonia,COPD)은정기적료효。방법선택항주시여항구제일인민의원문진부합폐비량허형만조폐은정기환자58례,용수궤수자표법수궤분위치료조화대조조,매조29례,2조균급여사미특라체잡송분흡입제흡입,재차기출상,치료조급여륙군자탕가감구복,료정위3개월,관찰환자림상체정화증상개선정황,비교폐공능、담액지표이급1년내급성발작비례。결과2조환자경불동치료방안후,치료조총유효솔위93.1%,명현우우대조조적총유효솔65.5%(P<0.05)。2조치료후FEV1화FEV1/FVC균유제고(P<0.05),치료조상술폐공능지표제고명현우우대조조(P<0.05)。2조HDACs활성、TNF-α급IL-8수평균유개선(P<0.05),치료조명현우우대조조(P<0.05)。치료조급성발작2례(6.9%),대조조급성발작7례(24.1%),차이무통계학의의。결론륙군자탕가감치료폐비량허형만조폐은정기림상료효학절,가명현개선환자림상증상이급실험실지표,공제병정발전,제고환자생존질량。
Objective To investigate clinical efficacy of additive LiuJunZi decoction in treatment of patients with chronic obstructive pneumonia ( COPD) of both lung and spleen deficiency in stable phase.Methods A total of 58 patients with deficiency of both lung and spleen type stable COPD patients were randomly divided into treatment group and control group by a random number table, 29 cases in each group, patients in two groups were treated with salmeterol and fluticasone propionate powder for inhalation.On this basis, the treatment group were given additive Liujunzi Decoction, orally, with 3 months treatment.The clinical signs and symptoms of patients, pulmonary function, index of sputumand acute attack proportion in a year were observed and compared.Results After different treatment, total efficiency was 93.1% in treatment group, which was obviously higher than 65.5%in control group (P<0.05).After treatment, the values of FEV1 and FEV1/FVC improved compared with before treatment, and the above indexes of treatment group significantly improved compared with control group (P<0.05).The HDACs activety, levels of TNF-αand IL-8 mproved compared with before treatment, and the above indexes of treatment group significantly improved compared with control group (P<0.05).The acute attack was two cases in treatment group(6.9%), seven cases in control group(24.1%), but the difference had no statistically significant.Conclusion The additive Liujunzi decoction in the treatment of both lung and spleen deficiency type chronic obstructive pulmonary disease ( COPD) in stable phase has exact clinical curative effect, can significantly improve clinical symptoms and laboratory indexes, control the progression of the disease, and improve life quality of the patients.