首页> 外文期刊>World journal of gastroenterology : >Granulocyte-colony stimulating factor therapy improves survival in patients with hepatitis B virus-associated acuteon-chronic liver failure
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Granulocyte-colony stimulating factor therapy improves survival in patients with hepatitis B virus-associated acuteon-chronic liver failure

机译:粒细胞集落刺激因子疗法可改善乙型肝炎病毒相关性急性慢性肝衰竭患者的生存

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AIM: To evaluate the safety and efficacy of granulocyte-colony stimulating factor (G-CSF) therapy in patients with hepatitis B virus (HBV)-associated acuteon-chronic liver failure (ACLF). METHODS: Fifty-five patients with HBV-associated ACLF were randomized into two groups: the treatment group and the control group. Twenty-seven patients in the treatment group received G-CSF (5 μg/kg per day, six doses) treatment plus standard therapy, and 28 patients in the control group received standard therapy only. The peripheral CD34+ cell count was measured consecutively by flow cytometry. Circulating white blood cell count, biochemical parameters, and other clinical data of these patients were recorded and analyzed. All patients were followed up for a period of 3 mo to evaluate the changes in liver function and survival rate. RESULTS: The peripheral neutrophil and CD34+ cell counts in the G-CSF group increased on day 3 from the onset of therapy, continued to rise on day 7, and remained elevated on day 15 compared to those of the control group. Child-Turcotte-Pugh score of patients in the treatment group was improved on day 30 from the onset of G-CSF therapy, compared to that in the controls (P = 0.041). Model for End-Stage of Liver Disease score of patients in the treatment group was improved on day 7 (P = 0.004) and remained high on day 30 from the onset of G-CSF therapy (P 0.001) compared to that in controls. After 3 mo of follow-up observation, the survival rate in the treatment group (48.1%) was significantly higher than that in the control group (21.4%) (P = 0.0181). CONCLUSION: G-CSF therapy promoted CD34+ cell mobilization in patients with HBV-associated ACLF, and improved the liver function and the survival rate of these patients.
机译:目的:评估粒细胞集落刺激因子(G-CSF)治疗乙型肝炎病毒(HBV)相关的急性慢性肝衰竭(ACLF)患者的安全性和有效性。方法:将55例HBV相关ACLF患者随机分为两组:治疗组和对照组。治疗组中的27例患者接受了G-CSF(每天5μg/ kg,六剂)治疗和标准疗法,对照组中的28例患者仅接受了标准疗法。通过流式细胞术连续测量外周CD34 +细胞计数。记录并分析这些患者的循环白细胞计数,生化参数和其他临床数据。所有患者均接受了3个月的随访,以评估其肝功能和存活率的变化。结果:与对照组相比,G-CSF组的中性粒细胞和CD34 +细胞计数在治疗开始的第3天开始增加,在第7天继续上升,并在第15天保持上升。与对照组相比,从G-CSF治疗开始的第30天,治疗组患者的Child-Turcotte-Pugh评分得到了改善(P = 0.041)。与对照组相比,治疗组患者的肝病终末期评分模型在第7天有所改善(P = 0.004),并且从G-CSF治疗开始的第30天仍保持较高水平(P <0.001)。随访3个月,治疗组生存率(48.1%)明显高于对照组(21.4%)(P = 0.081)。结论:G-CSF治疗可促进HBV相关ACLF患者的CD34 +细胞动员,并改善其肝功能和生存率。

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