Evidence map›Paper›PMID 35193798›Full record

ArticleDiagnostic microbiology and infectious disease2022

Evaluation of risk factors for uric acid elevation in COVID-19 patients treated with favipiravir.

Yuki Hanai, Sadako Yoshizawa, Kazuhiro Matsuo, Shusuke Uekusa, Taito Miyazaki, Koji Nishimura, Takumi Mabuchi, Hayato Ohashi, Yoshikazu Ishii, Kazuhiro Tateda and 2 more

Open access · greenAbstract read
In one paragraph

Article in Diagnostic microbiology and infectious disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 29% of its field
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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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  4. Review
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

12 authors at 1 institution in 1 country.

Yuki HanaiDepartment of Pharmacy, Toho University Omori Medical Center, Tokyo, Japan; Department of Clinical Pharmacy, Faculty of Pharmaceutical Sciences, Toho University, Chiba, Japan. Electronic address: yuuki.hanai@med.toho-u.ac.jp.
Sadako YoshizawaClinical Research Center, Department of Microbiology and Infectious Diseases, Toho University School of Medicine, Tokyo, Japan.
Kazuhiro MatsuoDepartment of Clinical Pharmacy, Faculty of Pharmaceutical Sciences, Toho University, Chiba, Japan.
Shusuke UekusaDepartment of Clinical Pharmacy, Faculty of Pharmaceutical Sciences, Toho University, Chiba, Japan.
Taito MiyazakiDepartment of General Medicine and Emergency Care, Toho University School of Medicine, Tokyo, Japan.
Koji NishimuraDepartment of Pharmacy, Toho University Omori Medical Center, Tokyo, Japan.
Takumi MabuchiDepartment of Pharmacy, Toho University Omori Medical Center, Tokyo, Japan.
Hayato OhashiDepartment of Pharmacy, Toho University Omori Medical Center, Tokyo, Japan.
Yoshikazu IshiiDepartment of Microbiology and Infectious Diseases, Toho University School of Medicine, Tokyo, Japan.
Kazuhiro TatedaDepartment of Microbiology and Infectious Diseases, Toho University School of Medicine, Tokyo, Japan.
Takashi YoshioDepartment of Clinical Pharmacy, Faculty of Pharmaceutical Sciences, Toho University, Chiba, Japan.
Kenji NishizawaDepartment of Pharmacy, Toho University Omori Medical Center, Tokyo, Japan.
Toho University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objective of this retrospective study was to identify the clinical risk factor associated with uric acid elevation in coronavirus disease (COVID-19) patients treated with favipiravir. Uric acid elevation was defined as an unexplained increase of ≥1.5 times in the patient's uric acid level from baseline. Twenty-nine COVID-19 patients were included in the study. Uric acid elevation developed during favipiravir therapy in 12 (41.4%) patients and the median onset time was 4.5 days after starting favipiravir. In multiple logistic regression analysis, the favipiravir dosage (adjusted OR = 1.69 [1.02-2.81], P = 0.044) and younger patient age (adjusted OR = 0.91 [0.83-0.99], P = 0.040) were significant clinical risk factors for uric acid elevation. No significant between-group difference was noted in the uric acid elevation and non-elevation groups in the clinical recovery after favipiravir therapy. The uric acid levels of patients administered with favipiravir should be monitored closely.

Indexed as

COVID-19 Drug TreatmentUric AcidAmidesAntiviral AgentsHumansPyrazinesRetrospective StudiesRisk FactorsSARS-CoV-2Treatment OutcomeAmidesAntiviral AgentsfavipiravirPyrazinesUric AcidAntiviral therapyCOVID-19FavipiravirSARS-CoV-2Uric acid elevation

Identifiers

PMID35193798
PMCPMC8782729
OpenAlexW4206922184

What OpenQuestion holds

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Registered trials

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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.