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N-乙酰半胱氨酸和蜂胶治疗对慢性阻塞性肺疾病(COPD)患者症状、生活质量和加重影响的析因分析:一项随机、双盲、安慰剂对照试验。

Factorial analysis of N-acetylcysteine and propolis treatment effects on symptoms, life quality and exacerbations in patients with Chronic Obstructive Pulmonary Disease (COPD): a randomized, double-blind, placebo-controlled trial.

机构信息

Medical Faculty Novi Sad, University of Novi Sad, Novi Sad, Serbia.

出版信息

Eur Rev Med Pharmacol Sci. 2022 May;26(9):3192-3199. doi: 10.26355/eurrev_202205_28737.

Abstract

OBJECTIVE

Standard treatment for chronic obstructive pulmonary disease (COPD) includes inhalation therapy along with mucoactive drugs. The aim of this study was to assess the efficacy and safety of orally administered mucolytic N-acetylcysteine and propolis (NACp) in COPD patients.

PATIENTS AND METHODS

A randomized, double-blind, prospective, interventional, 6 months study was conducted at the Institute for Pulmonary Diseases of Vojvodina, Sremska Kamenica, Serbia. Effects of daily NACp administration (600 mg, 1200 mg or placebo) on exacerbation, life quality (St. George's Respiratory Questionnaire-SGRQ), symptoms (COPD assessment test-CAT; Visual analogue cough scale-VAS; Leicester Cough Questionnaire-LCQ; Medical Research Council Dyspnoea scale-mMRC) and spirometric parameters in 120 COPD patients were assessed. Tests were conducted at three-time points: baseline, after three months and after 6 months of NACp treatment.

RESULTS

Repeated measures ANOVA showed that pulmonary function parameters, 6-minute walk test and mMRC score did not significantly change during the study. Cough VAS and CAT scores were significantly different between groups as within experimental groups. LCQ and SGRQ scores did not differ between placebo, and both examined groups, but within each examined group statistically significant difference was confirmed in observed parameters during therapy. Factorial analysis and subsequent binary logistic regression revealed "Symptoms related factor" as the strongest predictor of exacerbation for supplemented groups (p<0.01).

CONCLUSIONS

Treatment with high NACp for 6 months is safe and beneficial for cough and expectoration symptoms and improves the life quality. NACp significantly reduces acute exacerbation frequency in COPD patients by controlling COPD related symptoms.

摘要

目的

慢性阻塞性肺疾病(COPD)的标准治疗包括吸入疗法和黏液溶解药物。本研究旨在评估口服黏液溶解剂 N-乙酰半胱氨酸和蜂胶(NACp)在 COPD 患者中的疗效和安全性。

患者和方法

在塞尔维亚伏伊伏丁那肺病研究所,Sremska Kamenica 进行了一项随机、双盲、前瞻性、干预性、6 个月的研究。评估了每天给予 NACp(600mg、1200mg 或安慰剂)对恶化、生活质量(圣乔治呼吸问卷-SGRQ)、症状(COPD 评估测试-CAT;咳嗽视觉模拟量表-VAS;莱斯特咳嗽问卷-LCQ;医学研究委员会呼吸困难量表-mMRC)和 120 例 COPD 患者的肺功能参数的影响。在三个时间点进行了测试:基线、三个月后和 NACp 治疗 6 个月后。

结果

重复测量方差分析显示,在研究期间,肺功能参数、6 分钟步行试验和 mMRC 评分没有显著变化。咳嗽 VAS 和 CAT 评分在组间差异显著,而在实验组内差异显著。LCQ 和 SGRQ 评分在安慰剂组和两个实验组之间没有差异,但在每个实验组中,在观察到的参数在治疗期间都有统计学差异。因子分析和随后的二元逻辑回归显示,对于补充组,“症状相关因素”是恶化的最强预测因子(p<0.01)。

结论

用高剂量 NACp 治疗 6 个月是安全的,对咳嗽和排痰症状有益,并改善了生活质量。NACp 通过控制 COPD 相关症状,显著降低 COPD 患者急性加重的频率。

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