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实验室发现、同情使用法匹拉韦和 2015 年几内亚埃博拉病毒病患者的结局:一项回顾性观察研究。

Laboratory Findings, Compassionate Use of Favipiravir, and Outcome in Patients With Ebola Virus Disease, Guinea, 2015-A Retrospective Observational Study.

机构信息

Bernhard Nocht Institute for Tropical Medicine, Hamburg.

European Mobile Laboratory Consortium, Hamburg.

出版信息

J Infect Dis. 2019 Jun 19;220(2):195-202. doi: 10.1093/infdis/jiz078.

DOI:10.1093/infdis/jiz078
PMID:30788508
原文链接:
https://pmc.ncbi.nlm.nih.gov/articles/PMC6581890/
Abstract

BACKGROUND

In 2015, the laboratory at the Ebola treatment center in Coyah, Guinea, confirmed Ebola virus disease (EVD) in 286 patients. The cycle threshold (Ct) of an Ebola virus-specific reverse transcription-polymerase chain reaction assay and 13 blood chemistry parameters were measured on admission and during hospitalization. Favipiravir treatment was offered to patients with EVD on a compassionate-use basis.

METHODS

To reduce biases in the raw field data, we carefully selected 163 of 286 patients with EVD for a retrospective study to assess associations between potential risk factors, alterations in blood chemistry findings, favipiravir treatment, and outcome.

RESULTS

The case-fatality rate in favipiravir-treated patients was lower than in untreated patients (42.5% [31 of 73] vs 57.8% [52 of 90]; P = .053 by univariate analysis). In multivariate regression analysis, a higher Ct and a younger age were associated with survival (P < .001), while favipiravir treatment showed no statistically significant effect (P = .11). However, Kaplan-Meier analysis indicated a longer survival time in the favipiravir-treated group (P = .015). The study also showed characteristic changes in blood chemistry findings in patients who died, compared with survivors.

CONCLUSIONS

Consistent with the JIKI trial, this retrospective study revealed a trend toward improved survival in favipiravir- treated patients; however, the effect of treatment was not statistically significant, except for its influence on survival time.

摘要

背景

2015 年,科亚埃博拉治疗中心的实验室确诊了 286 例埃博拉病毒病(EVD)患者。入院时和住院期间测量了埃博拉病毒特异性逆转录-聚合酶链反应检测的循环阈值(Ct)和 13 项血液化学参数。根据同情用药原则向 EVD 患者提供了法匹拉韦治疗。

方法

为了减少原始现场数据中的偏差,我们精心挑选了 286 例 EVD 患者中的 163 例进行回顾性研究,以评估潜在危险因素、血液化学发现改变、法匹拉韦治疗和结局之间的关联。

结果

法匹拉韦治疗组患者的病死率低于未治疗组(42.5%[73 例中的 31 例] vs. 57.8%[90 例中的 52 例];单因素分析 P=0.053)。多变量回归分析显示,Ct 值较高和年龄较小与生存相关(P<0.001),而法匹拉韦治疗无统计学意义(P=0.11)。然而,Kaplan-Meier 分析表明,法匹拉韦治疗组的生存时间更长(P=0.015)。该研究还显示了死亡患者与幸存者之间血液化学发现的特征性变化。

结论

与 JIKI 试验一致,这项回顾性研究显示法匹拉韦治疗组患者的生存率有所提高,但治疗效果除了对生存时间的影响外,没有统计学意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f513/6581890/3dfe99462685/jiz078f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f513/6581890/b76eb4b82c05/jiz078f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f513/6581890/0b904e86c1cd/jiz078f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f513/6581890/3dfe99462685/jiz078f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f513/6581890/b76eb4b82c05/jiz078f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f513/6581890/0b904e86c1cd/jiz078f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f513/6581890/3dfe99462685/jiz078f0003.jpg

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