Evidence map›Paper›PMID 41484505›Full record

ArticleEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2026

Evaluation of clinical efficacy and safety of T-705 (Favipiravir) in the treatment of fever with thrombocytopenia syndrome: a propensity score matching study.

Fei Zhao, Quanman Hu, Anmin Ge, Yan Hu, Yanyan Yang, Jundong Chen, Saiwei Lu, Yangfan Ou, Wenyao Su, Li Zhang and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Fei Zhao *College of Public Health, Zhengzhou University, Zhengzhou, 450001, China.
Quanman Hu *College of Public Health, Zhengzhou University, Zhengzhou, 450001, China.
Anmin GeCollege of Public Health, Zhengzhou University, Zhengzhou, 450001, China.
Yan HuDisease Control and Prevention Center, Xinyang, 463600, China.
Yanyan YangDisease Control and Prevention Center, Xinyang, 463600, China.
Jundong ChenDisease Control and Prevention Center, Xinyang, 463600, China.
Saiwei LuCollege of Public Health, Zhengzhou University, Zhengzhou, 450001, China.
Yangfan OuCollege of Public Health, Zhengzhou University, Zhengzhou, 450001, China.
Wenyao SuCollege of Public Health, Zhengzhou University, Zhengzhou, 450001, China.
Li ZhangDisease Control and Prevention Center, Xinyang, 463600, China. zhangli6688@126.com.
Shuaiyin ChenCollege of Public Health, Zhengzhou University, Zhengzhou, 450001, China. sychen@zzu.edu.cn.

Funding

the Henan Province Science and Technology Research Project 242102311147the National Natural Science Foundation of China 82073618the soft Science Research Program of Xinyang City 20240044
6 · The paper itself

Abstract

objectiveSevere Fever with Thrombocytopenia Syndrome (SFTS), an emerging infectious disease of essential public health concern, currently lacks specific antiviral treatments, This study evaluated the efficacy of the broad-spectrum antiviral drug T-705 (Favipiravir).

methodsUsing propensity score matching (PSM) to minimize confounding factors between T-705 and Non-T-705 groups, Absolute Shrinkage and Selection Operator (LASSO) regression and multivariate logistic regression were used to screen the factors affecting the efficacy of T-705.

resultsAnalysis revealed a consistently higher disease improvement rate in the T-705 group (82.3% Pre-PSM, 80.6% Post-PSM) compared to Non-T-705 group (67.3%), with the difference remaining statistically significant (P = 0.032) after PSM. The results demonstrated that Ct values (1.397, 1.168-1.671, P < 0.001), lactate dehydrogenase (LDH) (1.002, 1.001-1.003, P = 0.027) and albumin (ALB) (1.153, 1.001-1.330, P = 0.050) levels were the protective factor for disease improvement, while clinical type (0.146, 0.045-0.477, P = 0.001), age (0.942, 0.893-0.994, P = 0.030), activated partial thromboplastin time (APTT) (0.917, 0.873-0.963, P < 0.001), total bilirubin (TBIL) (0.867, 0.752-0.999, P= 0.048), creatinine (CREA) (0.992, 0.985-0.999, P = 0.038) and uric acid (UA) (0.994, 0.990-0.999, P = 0.017) levels were risk factors for disease improvement.

conclusionsThe study demonstrated that T-705 exhibited significant efficacy and favorable safety in the treatment of SFTS patients. Furthermore, a multivariate logistic regression verified its clinical significance, thereby providing robust evidence to support its inclusion in treatment guidelines.

Indexed as

Antiviral AgentsSevere Fever with Thrombocytopenia SyndromeAdultAgedAmidesFemaleHumansMaleMiddle AgedPropensity ScorePyrazinesRetrospective StudiesTreatment OutcomeAmidesAntiviral AgentsfavipiravirPyrazinesHeterogeneity of treatment effectPredictive factorsPropensity score matchingSevere fever with thrombocytopenia syndromeT-705 (Favipiravir)

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.