人民卫生出版社系列期刊
ISSN 2096-2738 CN 11-9370/R

中国科技核心期刊(中国科技论文统计源期刊)
中国科学引文数据库(CSCD)来源期刊
《中国学术期刊影响因子年报》统计源期刊
美国化学文摘社(CAS)数据库收录期刊
日本科学技术振兴机构(JST)数据库收录期刊

新发传染病电子杂志 ›› 2026, Vol. 11 ›› Issue (2): 35-40.doi: 10.19871/j.cnki.xfcrbzz.2026.02.007

• 论著 • 上一篇    下一篇

更昔洛韦注射液联合重组人干扰素α-1b治疗呼吸道合胞病毒肺炎患儿的疗效研究

何耀红, 谭言国, 陈谨, 屈爽   

  1. 首都医科大学附属复兴医院呼吸科,北京 100038
  • 收稿日期:2025-04-17 出版日期:2026-04-30 发布日期:2026-05-18
  • 通讯作者: 何耀红,Email:fxbpnp@163.com
  • 基金资助:
    北京健康教育协会工作委托项目(BJK.JY202204)

Study on the effect of ganciclovir injection combined with recombinant human interferon α-1b in the treatment of RSV pneumonia in children

He Yaohong, Tan Yanguo, Chen Jin, Qu Shuang   

  1. Department of Respiratory Medicine, Fuxing Hospital, Capital Medical University, Beijing 100038, China
  • Received:2025-04-17 Online:2026-04-30 Published:2026-05-18

摘要: 目的 探究呼吸道合胞病毒(respiratory syncytial virus,RSV)肺炎患儿经更昔洛韦注射液联合重组人干扰素α-1b治疗的疗效分析,为临床RSV肺炎患儿治疗方案的选择提供参考依据。方法 选取2021年12月至2023年12月在首都医科大学附属复兴医院确诊的105例RSV肺炎患儿(年龄3~8岁)为研究对象,采用随机数字表法将其分为联合组(35例)、对照组(35例)、常规组(35例)。联合组给予更昔洛韦注射液联合重组人干扰素α-1b治疗,对照组给予重组人干扰素α-1b治疗,常规组接受常规治疗(如降温、祛痰、止咳、氧疗、基础抗病毒等)。结果 联合组总有效率(94.29%,33/35)显著高于对照组(68.57%,24/35)和常规组(57.14%,20/35)(均P<0.05)。联合组咳嗽[(3.96±0.88)d]、喘鸣音[(3.39±0.85)d]、呼吸困难[(1.62±0.30)d]等临床症状缓解时长,均显著短于对照组[分别为(6.35±1.17)d,(5.57±1.12)d,(3.27±0.69)d]和常规组[分别为(7.59±1.34)d,(6.89±1.27)d,(4.62±0.84)d](均P<0.05)。治疗后,三组患儿肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)、降钙素原(procalcitonin,PCT)、白介素(interleukin,IL)-10、CD8+T淋巴细胞、免疫球蛋白E(immunoglobulin E,IgE)水平均较治疗前降低,CD4+T淋巴细胞水平均较治疗前升高,且联合组上述指标的改善幅度更显著(均P<0.05)。结论 更昔洛韦注射液联合重组人干扰素α-1b能更好地改善RSV肺炎患儿的炎症反应以及临床症状,提高机体免疫功能,疗效确切且安全可靠。

关键词: 呼吸道合胞病毒肺炎, 重组人干扰素α-1b, 更昔洛韦注射液, 疗效

Abstract: Objective To investigate the therapeutic efficacy of ganciclovir injection combined with recombinant human interferon alpha-1b on children with respiratory syncytial virus (RSV) pneumonia, providing a basis for clinical diagnosis and treatment of RSV pneumonia. Method 105 pediatric patients with RSV pneumonia (admitted from December 2021 to December 2023, aged 3-8 years) were randomly separated into combination group (35 cases) , control group (35 cases), and regular group (35 cases) in Fu Xing Hospital, Capital Medical University. The regular group received conventional treatment, the control group was treated with recombinant human interferon α-1b, and the combination group was treated with ganciclovir injection combined with recombinant human interferon α-1b(including antipyretic, expectorant, antitussive, oxygen therapy and basic antiviral therapy). Result The total effective rate of the combination group (94.29%, 33/35) was higher than that of the control group (68.57%, 24/35) and regular group (57.14%, 20/35) (all P<0.05). The improvement of clinical indicators such as cough[(3.96±0.88)d], wheezing[(3.39±0.85)d], and dyspnea[(1.62±0.30)d] in the combination group was better than that in the control group[(6.35±1.17)d, (5.57±1.12)d, (3.27±0.69)d, respectively] and regular group[(7.59±1.34)d, (6.89±1.27)d, (4.62±0.84)d, respectively] (all P<0.05). After treatment, the levels of tumor necrosis factor alpha (TNF-α), procalcitonin (PCT), interleukin (IL)-10, CD8+, and immunoglobulin E (IgE) in both groups of children decreased, while CD4+ increased. And the improvement amplitude of the combination group was higher than that of the control group and regular group (all P<0.05). Conclusion The combination of ganciclovir injection and recombinant human interferon α-1b can improve the clinical symptoms, reduce inflammatory response and improve immune function in children with RSV pneumonia, the efficacy is certain, with definite efficacy and good safety.

Key words: Respiratory syncytial virus pneumonia, Recombinant human interferon α-1b, Ganciclovir injection, Efficacy

中图分类号: