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首页> 外文期刊>Journal of viral hepatitis. >Cirrhosis but not neutropenia is associated with the development of infection in patients with chronic hepatitis C undergoing treatment with pegylated interferon-alpha and ribavirin
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Cirrhosis but not neutropenia is associated with the development of infection in patients with chronic hepatitis C undergoing treatment with pegylated interferon-alpha and ribavirin

机译:接受聚乙二醇干扰素-α和利巴韦林治疗的慢性丙型肝炎患者,肝硬化而非中性粒细胞减少与感染的发展有关

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Peginterferon-alpha (PegIFNa) frequently causes neutropenia, mainly due to bone marrow suppression. The aim of this study was to explore factors that are associated with infections during antiviral treatment. We analysed data from 275 chronic hepatitis C (CHC) patients with compensated liver disease who underwent 318 courses of PegIFNa and ribavirin. Neutropenia was defined as neutrophils <1000 cells/μL. Mean leucocytes count significantly decreased from baseline to treatment nadir (7081 ± 2182 vs 3293 ± 1331 cells/μL, P < 0.001), while neutropenia was observed in 32% during treatment. Thirty-one infections were observed. The incidence rate for infection was assessed at 1.46 infections per 100 person-months of therapy. The hazard rate for infection did not correlate with the neutrophils' nadir or the decrease in white blood cells. In multivariate Cox's regression analysis, cirrhosis was the only factor that was significantly associated with the occurrence of infection. Our data show that the development of bacterial infections during treatment with PegIFNa and ribavirin in patients with compensated CHC is not associated with reduction or the nadir of white cells or neutrophil counts. Baseline cirrhosis is the only factor related with infection during treatment. The common practice of dose adjustment or discontinuation of interferon should be revised; careful assessment of liver damage before therapy and close monitoring during therapy are essential in all patients receiving interferon-based regimes, to minimize the detrimental consequences of infections.
机译:聚乙二醇干扰素-α(PegIFNa)经常引起中性粒细胞减少,主要是由于骨髓抑制。这项研究的目的是探讨抗病毒治疗期间与感染相关的因素。我们分析了来自275名接受代偿性肝病的慢性丙型肝炎(CHC)患者的数据,这些患者接受了318疗程的PegIFNa和利巴韦林治疗。中性粒细胞减少症定义为中性粒细胞<1000个细胞/μL。从基线到治疗最低点,平均白细胞计数显着降低(7081±2182 vs 3293±1331细胞/μL,P <0.001),而在治疗期间观察到中性白细胞减少症的发生率为32%。观察到三十一次感染。感染的发生率估计为每100人-月治疗1.46感染。感染的危险率与中性粒细胞的最低点或白细胞的减少无关。在多因素Cox回归分析中,肝硬化是与感染发生显着相关的唯一因素。我们的数据表明,代偿性CHC患者在接受PegIFNa和利巴韦林治疗期间细菌感染的发展与白细胞减少或最低点或中性粒细胞计数无关。基线肝硬化是与治疗期间感染相关的唯一因素。应当调整剂量调整或停用干扰素的常规做法;对于所有接受基于干扰素治疗的患者,治疗前对肝损害的仔细评估和治疗期间的密切监测对于将感染的有害影响降至最低至关重要。

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