首页|参芪补肺汤联合孟鲁司特钠片治疗非小细胞肺癌术后慢性咳嗽的临床研究

参芪补肺汤联合孟鲁司特钠片治疗非小细胞肺癌术后慢性咳嗽的临床研究

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目的 观察参芪补肺汤联合孟鲁司特钠片治疗非小细胞肺癌(NSCLC)术后慢性咳嗽的临床疗效.方法 将100 例NSCLC术后慢性咳嗽患者按照随机数字表法分为2 组,对照组50 例予孟鲁司特钠片治疗,治疗组50 例在对照组治疗基础上联合参芪补肺汤治疗.2 组均治疗 4 周.比较 2 组治疗前后咳嗽症状、莱彻斯特咳嗽生命质量问卷(LCQ-MC)评分、肺功能指标[用力肺活量(FVC)、第1s用力呼气容积(FEV1)、FEV1/FVC、呼气峰流量(PEF)]、炎症指标[白细胞介素8(IL-8)、肿瘤坏死因子α(TNF-α)、降钙素原(PCT)、白细胞介素6(IL-6)]、中医证候评分,并统计2 组不良反应发生率、复发率和疗效.结果 治疗组总有效率98.00%(49/50),对照组总有效率82.00%(41/50),治疗组临床疗效优于对照组(P<0.05).2 组治疗后日间与夜间咳嗽症状评分均较本组治疗降低(P<0.05),且治疗组治疗后均低于对照组(P<0.05),2 组治疗后LCQ-MC评分均升高(P<0.05),且治疗组治疗后高于对照组(P<0.05).2组治疗后FVC、FEV1、FEV1/FVC、PEF均较本组治疗前升高(P<0.05),且治疗组治疗后均高于对照组(P<0.05).2 组治疗后IL-8、TNF-α、PCT、IL-6 均较本组治疗降低(P<0.05),且治疗组治疗后均低于对照组(P<0.05).2 组治疗后中医证候各项评分均较本组治疗前降低(P<0.05),且治疗组治疗后均低于对照组(P<0.05).治疗组不良反应发生率4.00%(2/50),对照组不良反应发生率18.00%(9/50),治疗组不良反应发生率低于对照组(P<0.05).治疗组复发率4.08%(2/49),对照组24.39%(10/41),治疗组复发率低于对照组(P<0.05).结论 参芪补肺汤联合孟鲁司特钠片治疗NSCLC术后慢性咳嗽患者疗效显著,能够有效缓解咳嗽症状,改善患者肺功能,提升LCQ-MC评分,且不良反应发生率与复发率降低,具有临床应用价值.
Clinical study of Shenqi Bufei Decoction combined with Montelukast sodium tablets in treating post-operative chronic cough in patients with non-small cell lung cancer
Objective To explore the clinical efficacy of Shenqi Bufei Decoction combined with Montelukast sodium tab-lets in treating post-operative chronic cough in patients with non-small cell lung cancer(NSCLC).Methods A total of 100 NSCLC patients with post-operative chronic cough were randomized 1∶1 to receive Montelukast sodium tablets(the control group)or Shenqi Bufei Decoction plus Montelukast sodium tablets(the treatment group).A 4-week treatment was performed in the both groups,aiming to compare cough symptoms,Leicester Cough Questionnaire in Mandarin-Chinese(LCQ-MC)score,lung function index(forced vital capacity[FVC],forced expiratory volume in the first second[FEV1],FEV1/FVC,peak ex-piratory flow[PEF]),inflammatory markers(interleukin-8[IL-8],tumor necrosis factor-α[TNF-α],procalcitonin[PCT],interleukin-6[IL-6]),traditional Chinese medicine(TCM)syndrome score,and the incidence of adverse reac-tions,recurrence rate and efficacy of the two groups were statistically analyzed.Results The total effective rate of the treatment group was better than that of the control group(98.00%[49/50]vs 82.00%[41/50],P<0.05).After treatment,the day-time and nighttime cough symptom scores in the both groups were significantly lower than those before treatment(P<0.05),but the LCQ-MC scores in the both groups were significantly increased(P<0.05),and the improvements were more common in the treatment group relative to the control group(both P<0.05).Af-ter treatment,the levels of FVC,FEV1,FEV1/FVC,and PEF in the both groups were significantly higher than those before treat-ment(P<0.05),and the increases were significantly higher in the treatment group compared to the control group(P<0.05).After treatment,the levels of IL-8,TNF-α,PCT,and IL-6 in the both groups were significantly lower than those before treatment(P<0.05),and which were significantly lower in the treatment group than in the control group(P<0.05).After treatment,the TCM syndrome scores of the both groups were significantly lower than those before treatment(P<0.05),which in the treatment group were significantly lower than those of the control group(P<0.05).The incidence of adverse reactions(4.00%[2/50]vs 18.00%[9/50])and the recurrence rate(4.08%[2/49]vs 24.39%[10/41])in the treatment group were significantly lower than those of the control group(both P<0.05).Conclusion Shenqi Bufei Decoction combined with Menelukast sodium tablet has a significant effect in NSCLC patients with post-operative chronic cough.It can effectively relieve cough symptoms,improve patients'pulmonary function,and improve the LCQ-MC score,decrease the incidence of adverse re-actions and recurrence rate.It has clinical application value.

Lung cancer,Non-small cell typePostoperativeChronic coughIntegrative traditional Chinese and Western medicine therapy

李晓娣、谢佳佳、王明选、杨双、易超、文琪

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四川省遂宁市中心医院中医及中西医结合科,四川 遂宁 629000

肺癌,非小细胞型 术后 慢性咳嗽 中西医结合疗法

四川省中医药管理局科学技术研究专项

2021MS377

2024

河北中医
河北省医学情报研究所,河北省中医药学会

河北中医

CSTPCD
影响因子:0.951
ISSN:1002-2619
年,卷(期):2024.46(8)
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