首页|期刊导航|广州中医药大学学报|加味八珍汤改善聚乙二醇干扰素α-2b相关白细胞减少的临床观察

加味八珍汤改善聚乙二醇干扰素α-2b相关白细胞减少的临床观察OA

Clinical Observation on Modified Bazhen Decoction in Improving PEG-IFN Alpha-2b Related Leukopenia

中文摘要英文摘要

[目的]探讨加味八珍汤对聚乙二醇干扰素α-2b(PEG-IFN α-2b,以下统称干扰素)所致白细胞减少及临床症状的改善疗效.[方法]纳入2023年7月1日至2025年5月30日在广州中医药大学附属宝安中医院(深圳市宝安区中医院)肝病科接受干扰素治疗后出现白细胞减少的76例慢性乙型肝炎(CHB)气血两虚证患者,根据治疗方案的不同,分为试验组39例和对照组37例.对照组给予核苷(酸)类似物、鲨肝醇联合干扰素治疗,试验组在对照组的基础上加用加味八珍汤治疗,2组疗程均为8周.对比2组患者治疗前后血常规指标[白细胞计数(WBC)、中性粒细胞计数(NE)、血小板计数(PLT)]、乙肝表面抗原(HBsAg)、慢性肝病问卷(CLDQ)评分及中医证候积分的变化情况,观察2组患者治疗过程中不良事件发生情况,评估2组患者的白细胞改善疗效与用药安全性.[结果](1)脱落情况方面,研究过程中,试验组4例患者和对照组2例患者因存在主要数据缺失而剔除,故最终纳入70例患者,其中,试验组和对照组各35例.(2)白细胞改善疗效方面,治疗8周后,试验组的总有效率为57.14%(20/35),对照组为34.43%(11/35),组间比较(χ2检验),试验组的白细胞改善疗效明显优于对照组(P<0.05).(3)血常规方面,治疗后,2组患者的WBC、NE水平和试验组的PLT水平均较治疗前升高(P<0.05),而对照组的PLT水平治疗前后比较差异无统计学意义(P>0.05);治疗后组间比较,试验组对WBC、PLT水平的升高幅度均明显优于对照组(P<0.05).(4)HBsAg水平方面,治疗后,2组患者的血清HBsAg水平均较治疗前明显降低(P<0.05),但组间比较差异无统计学意义(P>0.05).(5)CLDQ评分方面,治疗后,试验组CLDQ量表的腹部症状、疲劳、全身症状、活动能力、情感功能及焦虑等6个维度评分均较治疗前明显改善(P<0.05),而对照组仅焦虑评分较治疗前改善(P<0.05);治疗后组间比较,试验组对CLDQ量表的6个维度评分的改善幅度均明显优于对照组(P<0.05).(6)中医证候方面,治疗后,试验组患者的中医证候积分较治疗前明显降低(P<0.05),而对照组较治疗前无明显降低(P>0.05);治疗后组间比较,试验组对中医证候积分的降低幅度明显优于对照组(P<0.05).(7)安全性方面,治疗过程中,试验组出现食欲不振等消化道症状、焦虑及情绪低落等精神异常频率明显低于对照组(P<0.05);而2组患者在皮疹、甲状腺功能异常、脱发、体质量下降方面均无显著性差异(P>0.05).[结论]加味八珍汤能够改善CHB患者干扰素治疗过程中出现的白细胞减少及临床症状,提升患者生活质量,可为CHB的中西医结合治疗提供循证医学证据.

Objective To investigate the therapeutic effect of Modified Bazhen Decoction on leukopenia and clinical symptoms induced by pegylated interferon alpha-2b(PEG-IFN α-2b,hereinafter referred to as interferon)in the treatment of chronic hepatitis B(CHB).Methods A total of 76 CHB patients of qi and blood deficiency type who developed leukopenia after interferon treatment at the Department of Hepatology,Bao'an Traditional Chinese Medicine Hospital Affiliated to Guangzhou University of Chinese Medicine(Shenzhen Bao'an Traditional Chinese Medicine Hospital)from July 1,2023 to May 30,2025 were enrolled.According to the treatment protocol,76 patients were divided into an trial group(39 cases)and a control group(37 cases).The control group received nucleos(t)ide analogues and batilol combined with interferon treatment,while the trial group received Modified Bazhen Decoction in addition to the control group's regimen.Both groups were treated for 8 weeks.Changes in blood routine parameters[white blood cell count(WBC),neutrophil count(NE),and platelet count(PLT)],hepatitis B surface antigen(HBsAg)levels,chronic liver disease questionnaire(CLDQ)scores,and traditional Chinese medicine(TCM)syndrome scores were compared between the two groups before and after treatment.Adverse events during treatment were observed,and the efficacy of leukopenia improvement and medication safety were evaluated.Results(1)Regarding dropout,4 patients in the trial group and 2 patients in the control group were excluded due to missing primary data during the study,resulting in 70 patients finally included,with 35 cases in each group.(2)In terms of leukopenia improvement efficacy,after 8 weeks of treatment,the total effective rate in the trial group was 57.14%(20/35),significantly higher than 34.43%(11/35)in the control group(by chi-square test,P<0.05).(3)Regarding blood routine parameters,after treatment,WBC and NE levels in both groups and PLT levels in the trial group were significantly increased compared with before treatment(P<0.05),while PLT levels in the control group showed no statistically significant difference before and after treatment(P>0.05).Intergroup comparison after treatment showed that the trial group had significantly greater increases in WBC and PLT levels than the control group(P<0.05).(4)Regarding HBsAg levels,after treatment,serum HBsAg levels in both groups were significantly decreased compared with before treatment(P<0.05),but there was no statistically significant difference between the two groups(P>0.05).(5)Regarding CLDQ scores,after treatment,the trial group showed significant improvements in the scores of all six dimensions of the CLDQ scale,including abdominal symptoms,fatigue,systemic symptoms,activity,emotional function,and anxiety(P<0.05),while the control group only showed improvement in anxiety scores(P<0.05).Intergroup comparison after treatment demonstrated that the trial group had significantly greater improvements in the scores of all six dimensions of the CLDQ scale than the control group(P<0.05).(6)Regarding TCM syndromes,after treatment,TCM syndrome scores in the trial group were significantly decreased compared with before treatment(P<0.05),while no significant decrease was observed in the control group(P>0.05).Intergroup comparison after treatment showed that the trial group had a significantly greater reduction in TCM syndrome scores than the control group(P<0.05).(7)Regarding safety,during treatment,the frequency of gastrointestinal symptoms such as poor appetite and psychiatric symptoms such as anxiety and low mood in the trial group was significantly lower than that in the control group(P<0.05).There were no significant differences between the two groups in rash,thyroid dysfunction,alopecia,or weight loss(P>0.05).Conclusion Modified Bazhen Decoction can improve interferon-induced leukopenia and clinical symptoms in CHB patients,enhance patients'quality of life,and provide evidence-based medical evidence for the integrated traditional Chinese and western medicine treatment of CHB.

朱琴艳;欧阳子琛;陈欣怡;孙姮辉;鲁艳平;胡敬宝

广州中医药大学第七临床医学院,广东 深圳 518100广州中医药大学附属宝安中医院,广东 深圳 518100广州中医药大学第七临床医学院,广东 深圳 518100广州中医药大学第七临床医学院,广东 深圳 518100广州中医药大学附属宝安中医院,广东 深圳 518100广州中医药大学附属宝安中医院,广东 深圳 518100

医药卫生

加味八珍汤慢性乙型肝炎PEG-IFN α-2b白细胞减少气血两虚证临床症状生活质量

Modified Bazhen Decoctionchronic hepatitis B(CHB)PEG-IFN alpha-2bleukopeniaqi and blood deficiency syndromeclinical symptomsquality of life

《广州中医药大学学报》 2026 (6)

1495-1502,8

国家中医药管理局综合司·国家卫生健康委办公厅·中央军委后勤保障部卫生局联合资助项目—强化建设的重大疑难疾病(肝硬化)中西医临床协助项目(编号:ZDYN-2024-B-012)

10.13359/j.cnki.gzxbtcm.2026.06.010

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