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首页> 外文期刊>Japanese journal of infectious diseases >Evaluation of the efficacy of ribavirin therapy on survival of Crimean-Congo hemorrhagic fever patients: a case-control study.
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Evaluation of the efficacy of ribavirin therapy on survival of Crimean-Congo hemorrhagic fever patients: a case-control study.

机译:利巴韦林疗法对克里米亚-刚果出血热患者生存的疗效评估:一项病例对照研究。

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The mortality rate resulting from Crimean-Congo hemorrhagic fever (CCHF) has been reported in different epidemics to range from 5% to more than 70%. While ribavirin has been recommended as the drug of choice in the treatment of CCHF, no consistent study has unequivocally demonstrated its effectiveness. Using the case-control method, we attempted to evaluate the efficacy of ribavirin in reducing mortality among CCHF cases admitted to Boo-Ali Educational Hospital in Zahedan, Iran, during the years 2000 to 2006. Sixteen deaths among CCHF cases were compared with 47 cases of survival. All patients had a definitive diagnosis based on the results of IgG and IgM capture ELISA tests recorded in their files. Ribavirin therapy for patients who survived had begun on average approximately 24 h earlier than the initiation of ribavirin therapy in the cases of death (P=0.033), and about 2 days earlier in non-bleeding survivors than in bleeding survivors (P=0.013). Based on the results of a multivariable analysis, themost important variables found to enhance survival were the time interval between the disease onset and ribavirin prescription (P=0.004), the time interval between bleeding onset and ribavirin prescription (P=0.037), and the time interval between disease onset and bleeding onset (P=0.014). Based on our findings, ribavirin appears to exert a marked effect on disease outcome, especially when it is prescribed within the first 4 days of the disease.
机译:据报道,在不同的流行病中,克里米亚-刚果出血热(CCHF)导致的死亡率在5%至70%以上。尽管利巴韦林已被推荐作为治疗CCHF的首选药物,但尚无一致的研究明确证明其有效性。使用病例对照方法,我们尝试评估利巴韦林在降低2000年至2006年伊朗扎赫丹Boo-Ali教育医院收治的CCHF病例中死亡率的功效。将CCHF病例中的16例死亡与47例进行了比较生存所有患者均根据其文件中记录的IgG和IgM捕获ELISA检测结果进行了明确的诊断。对于死亡患者,利巴韦林治疗的平均开始时间比开始利巴韦林治疗的时间早约24小时(P = 0.033),非出血幸存者比出血幸存者提前约2天(P = 0.013) 。根据多变量分析的结果,发现提高生存率的最重要变量是疾病发作和利巴韦林处方之间的时间间隔(P = 0.004),出血发作和利巴韦林处方之间的时间间隔(P = 0.037)以及疾病发作与出血发作之间的时间间隔(P = 0.014)。根据我们的发现,利巴韦林似乎对疾病的结果有明显的影响,尤其是在疾病的前4天内开具处方时。

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