Evidence map›Paper›PMID 36225581›Full record

ArticleFrontiers in pharmacology2022

Population pharmacokinetics of voriconazole and initial dosage optimization in patients with talaromycosis.

Zhiwen Jiang, Yinyi Wei, Weie Huang, Bingkun Li, Siru Zhou, Liuwei Liao, Tiantian Li, Tianwei Liang, Xiaoshu Yu, Xiuying Li and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

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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

13 authors at 4 institutions in 1 country.

Zhiwen JiangDepartment of Dermatology and Venereology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Yinyi WeiDepartment of Pharmacy, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Weie HuangDepartment of Infectious Diseases, Baise People's Hospital, Baise, China.
Bingkun LiDepartment of Dermatology and Venereology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Siru ZhouDepartment of Pharmacy, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Liuwei LiaoDepartment of Dermatology and Venereology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Tiantian LiGuangxi Health Commission Key Lab of Fungi and Mycosis Research and Prevention, Nanning, China.
Tianwei LiangDepartment of Dermatology and Venereology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Xiaoshu YuDepartment of Infectious Diseases, Baise People's Hospital, Baise, China.
Xiuying LiDepartment of Dermatology and Venereology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Changjing ZhouDepartment of Infectious Diseases, Baise People's Hospital, Baise, China.
Cunwei CaoDepartment of Dermatology and Venereology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
TaoTao LiuDepartment of Pharmacy, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Guangxi Medical University · CNBaise University · CNFirst Affiliated Hospital of GuangXi Medical University · CNGuangxi Center for Disease Prevention and Control · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The high variability and unpredictability of the plasma concentration of voriconazole (VRC) pose a major challenge for clinical administration. The aim of this study was to develop a population pharmacokinetics (PPK) model of VRC and identify the factors influencing VRC PPK in patients with talaromycosis. Medical records and VRC medication history of patients with talaromycosis who were treated with VRC as initial therapy were collected. A total of 233 blood samples from 69 patients were included in the study. A PPK model was developed using the nonlinear mixed-effects models (NONMEM). Monte Carlo simulation was applied to optimize the initial dosage regimens with a therapeutic range of 1.0-5.5 mg/L as the target plasma trough concentration. A one-compartment model with first-order absorption and elimination adequately described the data. The typical voriconazole clearance was 4.34 L/h, the volume of distribution was 97.4 L, the absorption rate constant was set at 1.1 h

Indexed as

C- reactive protein (CRP)dosage optimizationMonte Carlo simulationpopulation pharmacokineticstalaromycosisvoriconazole

Identifiers

PMID36225581
PMCPMC9549404
OpenAlexW4297225254

What OpenQuestion holds

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LicenceCC BY
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.