高级检索
    颜廷勇, 邵星星, 胡晓标. 不同剂量阿奇霉素联合N-乙酰半胱氨酸在稳定期COPD患者中的临床疗效对比[J]. 徐州医科大学学报, 2022, 42(1): 13-16. DOI: 10.3969/j.issn.2096-3882.2022.01.003
    引用本文: 颜廷勇, 邵星星, 胡晓标. 不同剂量阿奇霉素联合N-乙酰半胱氨酸在稳定期COPD患者中的临床疗效对比[J]. 徐州医科大学学报, 2022, 42(1): 13-16. DOI: 10.3969/j.issn.2096-3882.2022.01.003
    Clinical Application of Different Doses of Azithromycin Combined with N-acetylcysteine in the Treatment of COPD at Remission Stage[J]. Journal of Xuzhou Medical University, 2022, 42(1): 13-16. DOI: 10.3969/j.issn.2096-3882.2022.01.003
    Citation: Clinical Application of Different Doses of Azithromycin Combined with N-acetylcysteine in the Treatment of COPD at Remission Stage[J]. Journal of Xuzhou Medical University, 2022, 42(1): 13-16. DOI: 10.3969/j.issn.2096-3882.2022.01.003

    不同剂量阿奇霉素联合N-乙酰半胱氨酸在稳定期COPD患者中的临床疗效对比

    Clinical Application of Different Doses of Azithromycin Combined with N-acetylcysteine in the Treatment of COPD at Remission Stage

    • 摘要: 目的在稳定期慢性阻塞性肺疾病(chronic obstructive pulmonary disease, COPD)患者中比较不同剂量阿奇霉素联合N-乙酰半胱氨酸的临床疗效和安全性。方法回顾分析同期采用常规治疗方法(对照组,40例)和N-乙酰半胱氨酸联合阿奇霉素疗法(观察组,96例)的稳定期COPD患者病例资料。观察组患者均采用在常规治疗基础联用N-乙酰半胱氨酸和阿奇霉素,按阿奇霉素给药剂量观察组又分为A组(28例,0.5g/d)、B组(39例,0.25g/d)和C组(29例,0.125g/d),各组疗程均为6个月。对比4组患者治疗前后的肺功能各项检测指标、相关血清炎症因子及急性COPD发作次数,并对治疗期间各组不良反应情况进行比较。结果治疗前,4组患者的肺功能各检测指标、血清炎症因子和COPD急性发作次数比较差异均无统计学意义(P>0.05);治疗后,4组患者的肺功能各项指标、血清炎症因子和比治疗前均有明显改善(P<0.05),且观察组的改善程度均明显优于对照组(P<0.05);在观察组中A组和B组又优于C组(P<0.05);在COPD急性发作次数方面,治疗后4组均明显少于本组治疗前,但4组间差异无统计学意义(P>0.05)。结论对于稳定期COPD患者,采用N-乙酰半胱氨酸联合阿奇霉素的疗法,且阿奇霉素给药剂量在0.25g/d时,有较好的临床治疗效果和安全性,值得推广。

       

      Abstract: ob<x>jectIVE To compare the clinical efficacy and safety of N-acetylcysteine combined with different doses of azithromycin in the treatment of stably COPD. METHODS The data of patients with stable COPD treated with routine therapy and N-acetylcysteine combined with azithromycin were divided retrospectively into control group (40 cases) and observation group (96 cases). The patients in the observation group were treated with N-acetylcysteine combined with azithromycin ba<x>sed on conventional treatment. According to the dosage of azithromycin, the observation group was divided into three groups: group A (28 cases, 0.5g / d), group B (39 cases, 0.25g /d) and group C (29 cases, 0.125g /d). All group had a course of 6 months. the pulmonary function indexes, related serum inflammatory factors and the times of acute COPD attack were compared before and after treatment in four groups, and the side effects of each group during the treatment were compared. RESULTS Before the drug treatment, there was no significant difference in lung function, serum inflammatory factors and the number of COPD acute attack among the four groups (P>0.05); After the treatment, the pulmonary function indexes, serum inflammatory factors in all groups were significantly improved(P<0.05) than before; and the improvement degree of the observation group was significantly better than that of the control group (P<0.05). In the observation group, group A and group B were better than group C (P<0.05). In the comparison of the times of acute attack of COPD, the number of COPD in the four groups after treatment was significantly less than that before treatment, but there was no significant difference between the four groups(P>0.05). CONCLUSION In drug therapy for stable COPD patients, N-acetylcysteine combined with azithromycin is used and the azithromycin dosage is 0.25g/d. It has good clinical effect and safety, and it is worth popularizing.

       

    /

    返回文章
    返回