艾考恩丙替片对初治艾滋病患者的疗效及安全性评价

Efficacy and safety of Elvitegravir, Cobicistat, Emtricitabine and Tenofovir Alafenamide Fumarate Tablets in treatment-naive acquired immune deficiency syndrome patients

  • 摘要:
    目的 评价艾考恩丙替片对初治艾滋病患者的疗效及安全性。
    方法 选取80例初治艾滋病患者作为研究对象,随机分为对照组和观察组,每组40例。对照组采用免费抗病毒药物(替诺福韦+拉米夫定+依非韦伦)治疗,观察组采用艾考恩丙替片治疗。比较2组患者治疗前和治疗3、6、9、12个月后的CD4+、人类免疫缺陷病毒(HIV)载量、生化指标水平,并比较2组患者依从性、不良反应和生活质量。
    结果 治疗时,观察组有6例患者不依从,对照组有9例患者不依从; 随着治疗时间的延长, 2组患者CD4+水平逐渐升高, HIV载量逐渐降低,差异有统计学意义(P < 0.05); 治疗3、6、9、12个月后,观察组CD4+水平均高于对照组, HIV载量均低于对照组,差异有统计学意义(P < 0.05); 随着治疗时间的延长,对照组谷丙转氨酶、谷草转氨酶、尿素、肌酐、尿酸水平逐渐升高,且对照组治疗3、6、9、12个月后的随机血糖水平均高于治疗前,差异有统计学意义(P < 0.05); 治疗3、6、9、12个月后,观察组谷丙转氨酶、谷草转氨酶、尿素、肌酐、尿酸、随机血糖水平均低于对照组,差异有统计学意义(P < 0.05); 观察组不良反应发生率为2.94%(1/34), 低于对照组的90.00%(36/40), 差异有统计学意义(校正χ2=55.718, P < 0.001); 随着治疗时间的延长, 2组患者生活质量各维度评分逐渐升高,且观察组治疗后的生活质量各维度评分均高于对照组,差异有统计学意义(P < 0.05)。
    结论 与免费抗病毒药物方案相比,艾考恩丙替片对初治艾滋病患者的疗效更佳,可显著升高CD4+水平,降低HIV载量,且安全性高,可显著提高患者的生活质量。

     

    Abstract:
    Objective To evaluate the efficacy and safety of Elvitegravir, Cobicistat, Emtricitabine and Tenofovir Alafenamide Fumarate Tablets in initial treatment of acquired immune deficiency syndrome (AIDS) patients.
    Methods A total of 80 treatment-naive AIDS patients were selected as research subjects and randomly divided into control group and observation group, with 40 patients in each group. The control group was treated with free antiviral drugs (tenofovir + lamivudine + efavirenz), while the observation group was treated with Elvitegravir, Cobicistat, Emtricitabine and Tenofovir Alafenamide Fumarate Tablets. The CD4+ count, human immunodeficiency virus (HIV) viral load, and biochemical indicators were compared between the two groups before treatment and at 3, 6, 9, and 12 months after treatment. The adherence, adverse reactions, and quality of life were also compared between the two groups.
    Results During the treatment, six patients in the observation group and 9 patients in the control group had no compliance. With the extension of treatment time, the CD4+ level in both groups gradually increased, and the HIV viral load gradually decreased (P < 0.05). After 3, 6, 9, and 12 months of treatment, the CD4+ levels in the observation group were higher than those in the control group, and the HIV viral loads were lower than those in the control group (P < 0.05). With the extension of treatment time, the levels of alanine aminotransferase, aspartate aminotransferase, urea, creatinine, and uric acid in the control group gradually increased, and the random blood glucose levels after 3, 6, 9, and 12 months of treatment in the control group were higher than those before treatment (P < 0.05). After 3, 6, 9, and 12 months of treatment, the levels of alanine aminotransferase, aspartate aminotransferase, urea, creatinine, uric acid, and random blood glucose in the observation group were lower than those in the control group (P < 0.05). The incidence of adverse reactions in the observation group was 2.94% (1/34), which was lower than 90.00% (36/40) in the control group (corrected χ2=55.718, P < 0.001). With the extension of treatment time, the scores of various dimensions of quality of life in both groups gradually increased, and the scores of various dimensions of quality of life after treatment in the observation group were higher than those in the control group (P < 0.05).
    Conclusion Compared with the free antiviral drug regimen, Elvitegravir, Cobicistat, Emtricitabine and Tenofovir Alafenamide Fumarate Tablets shows better efficacy in the treatment of AIDS-naive patients, which can significantly increase the CD4+ level, and reduce the HIV viral load. Besides, it has high safety, and can significantly improve their quality of life.

     

/

返回文章
返回