Evidence map›Paper›PMID 36177517›Full record

ArticleEpilepsia open2022

Therapeutic drug monitoring of perampanel in children diagnosed with epilepsy: Focus on influencing factors on the plasma concentration-to-dose ratio.

Yue Li, Na Dong, Yu-Xin Qin, Hao-Ran Dai, Ya-Hui Hu, Yue-Tao Zhao, Hong-Li Guo, Yuan-Yuan Zhang, Jing Chen, Xiao-Peng Lu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Epilepsia open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Observational
  7. Article
  8. Article
  9. Article
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 at 3 institutions in 1 country.

Yue LiDepartment of Pharmacy, Pharmaceutical Sciences Research Center, Children's Hospital of Nanjing Medical University, Nanjing, China.ORCID 0000-0003-3176-150X
Na DongInstitute of Pharmaceutical Sciences, China Pharmaceutical University, Nanjing, China.ORCID 0000-0002-0047-4068
Yu-Xin QinKangda College of Nanjing Medical University, Lianyungang, China.
Hao-Ran DaiSchool of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, China.ORCID 0000-0002-2084-0862
Ya-Hui HuDepartment of Pharmacy, Pharmaceutical Sciences Research Center, Children's Hospital of Nanjing Medical University, Nanjing, China.ORCID 0000-0002-8895-2350
Yue-Tao ZhaoSchool of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, China.
Hong-Li GuoDepartment of Pharmacy, Pharmaceutical Sciences Research Center, Children's Hospital of Nanjing Medical University, Nanjing, China.ORCID 0000-0002-6660-8145
Yuan-Yuan ZhangDepartment of Pharmacy, Pharmaceutical Sciences Research Center, Children's Hospital of Nanjing Medical University, Nanjing, China.
Jing ChenDepartment of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, China.
Xiao-Peng LuDepartment of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, China.
Feng ChenDepartment of Pharmacy, Pharmaceutical Sciences Research Center, Children's Hospital of Nanjing Medical University, Nanjing, China.ORCID 0000-0003-4800-6762
Second Affiliated Hospital of Nanjing Medical University · CNChina Pharmaceutical University · CNKangda College of Nanjing Medical University

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to investigate the efficacy and tolerability of perampanel (PER) therapy and to optimize a specific plasma reference range for PER in children. Another major aim was to evaluate the potential determinators of PER concentration.

methodsConcentrations obtained from 80 children were analyzed for routine therapeutic drug monitoring (TDM) between 2021 and 2022. We retrospectively reviewed the clinical data of these patients and assessed the efficacy at 3 months after treatment initiation. Trough concentration-to-dose ratio (C

resultsA 3-month PER therapy produced a ≥50% reduction in seizure frequency in 58.8% of patients. Twelve patients reported at least one adverse effect (AE), mainly dizziness. The monitoring data showed that the median C SIGNIFICANCE: In this study, PER treatment showed acceptable efficacy and tolerance in Chinese children with epilepsy. Contributing factors like age to variable C

Indexed as

Drug MonitoringEpilepsyAnticonvulsantsChildHumansNitrilesPyridonesRetrospective StudiesSeizuresAnticonvulsantsNitrilesperampanelPyridoneschildrenepilepsyperampanelplasma concentration rangetherapeutic drug monitoring

Identifiers

PMID36177517
PMCPMC9712465
OpenAlexW4298086680

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.