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Effect of oral ribavirin treatment on the viral load and disease progression in Crimean-Congo hemorrhagic fever

机译:口服利巴韦林治疗对克里米亚-刚果出血热病毒载量和疾病进展的影响

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Objectives: Crimean-Congo hemorrhagic fever (CCHF) is a lethal hemorrhagic disease. There is currently no specific antiviral therapy for CCHF approved for use in humans. In this study we aimed to investigate the effect of oral ribavirin treatment on the viral load and disease progression in CCHF. Methods: The study population was composed of patients who had a definitive diagnosis of CCHF by means of clinical presentation plus detection of viral RNA by reverse transcriptase polymerase chain reaction (RT-PCR). Ten patients who received oral ribavirin for 10 days and 40 control patients who received supportive treatment only were included in the study. Ribavirin treatment consisted of oral ribavirin 4g/day for 4 days and then 2.4g/day for 6 days. Viral load and hematological and biochemical laboratory parameters, which were measured daily, were analyzed. Results: Mean age (37.4 vs. 45.5, p=0.285), gender (male 50% vs. 62.5%, p=0.470), days from the appearance of symptoms to admission (4.3 vs.4.4 days, p=0.922), and initial complaints were similar between the ribavirin group and the control group. Upon hospital admission, mean viral load was 8.2x10^8 copies/ml in the ribavirin group and 8.3x10^8 copies/ml in the control group (p=0.994). During follow-up, no statistically significant differences were found between the groups with regard to the decrease in viral load, the reduction in alanine aminotransferase and aspartate aminotransferase levels, and the increase in platelet count. The case-fatality rate was 20% (2/10 patients) in the ribavirin group and 15% (6/40 patients) in the control group (p=0.509). Conclusion: In this study, oral ribavirin treatment in CCHF patients did not affect viral load or disease progression.
机译:目的:克里米亚-刚果出血热(CCHF)是一种致命的出血性疾病。目前尚无批准用于人类的CCHF特异性抗病毒治疗。在这项研究中,我们旨在研究口服利巴韦林治疗对CCHF病毒载量和疾病进展的影响。方法:研究人群包括通过临床表现明确诊断为CCHF并通过逆转录酶聚合酶链反应(RT-PCR)检测病毒RNA的患者。该研究包括10名接受口服利巴韦林治疗10天的患者和40名仅接受支持治疗的对照患者。利巴韦林治疗包括口服利巴韦林4g /天,持续4天,然后2.4g /天,持续6天。分析每天测量的病毒载量以及血液和生化实验室参数。结果:平均年龄(37.4 vs. 45.5,p = 0.285),性别(男性50%vs. 62.5%,p = 0.470),从出现症状到入院的天数(4.3 vs.4.4天,p = 0.922),利巴韦林组与对照组之间的最初主诉相似。入院后,利巴韦林组的平均病毒载量为8.2x10 ^ 8拷贝/ ml,对照组为8.3x10 ^ 8拷贝/ml(p=0.994)。在随访期间,两组之间在病毒载量降低,丙氨酸氨基转移酶和天冬氨酸氨基转移酶水平降低以及血小板计数增加方面没有统计学上的显着差异。利巴韦林组的病死率为20%(2/10例),对照组为15%(6/40例)(p = 0.509)。结论:在这项研究中,CCHF患者口服利巴韦林治疗不影响病毒载量或疾病进展。

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