Evidence map›Paper›PMID 29962926›Full record

ArticleJournal of Korean medical science2018

Influence of

Eben Jung, Sunae Ryu, Zewon Park, Jong-Gu Lee, Jung-Yeon Yi, Doo Won Seo, Juhyun Lee, Ho-Sang Jeong, Jeong Mi Kim, Woo-Yong Oh

Open access · goldAbstract read
In one paragraph

Article in Journal of Korean medical science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. 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

10 authors at 1 institution in 1 country.

Eben JungClinical Research Division, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Cheongju, Korea.ORCID https://orcid.org/0000-0001-6614-3045
Sunae RyuClinical Research Division, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Cheongju, Korea.ORCID https://orcid.org/0000-0002-3817-2081
Zewon ParkClinical Research Division, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Cheongju, Korea.ORCID https://orcid.org/0000-0001-9385-8396
Jong-Gu LeeClinical Research Division, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Cheongju, Korea.ORCID https://orcid.org/0000-0002-0282-8720
Jung-Yeon YiClinical Research Division, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Cheongju, Korea.ORCID https://orcid.org/0000-0002-6030-2161
Doo Won SeoClinical Research Division, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Cheongju, Korea.ORCID https://orcid.org/0000-0002-9195-9975
Juhyun LeeClinical Research Division, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Cheongju, Korea.ORCID https://orcid.org/0000-0001-8623-0744
Ho-Sang JeongClinical Research Division, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Cheongju, Korea.ORCID https://orcid.org/0000-0002-2097-6479
Jeong Mi KimClinical Research Division, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Cheongju, Korea.ORCID https://orcid.org/0000-0002-5482-9899
Woo-Yong OhClinical Research Division, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Cheongju, Korea.ORCID https://orcid.org/0000-0001-7442-7128
Ministry of Food and Drug Safety · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCarvedilol is commonly used to treat hypertension as a β- and α

methodsA PK/PD study for a single and multiple dosing of carvedilol were conducted. All volunteers in 3 genotypic groups received single oral dose of carvedilol 12.5 mg for 3 days, then 25 mg QD for 5 days, and 12.5 mg QD for another 3 days. PK parameters for carvedilol and its three metabolites were determined using non-compartmental analysis. For PD properties, blood pressure, heart rate, and the chronotropic dose 25 (CD25) value were obtained.

resultsThe IM_2 group with two

conclusionThese findings showed that

Indexed as

AdultArea Under CurveBlood PressureCarbazolesCarvedilolCytochrome P-450 CYP2D6FemaleGenotypeHumansMaleMiddle AgedPolymorphism, GeneticPropanolaminesYoung AdultCarbazolesCarvedilolCytochrome P-450 CYP2D6PropanolaminesCarvedilolCYP2D6Genetic PolymorphismsKorean PopulationPharmacokinetic/Pharmacodynamic

Identifiers

PMID29962926
PMCPMC6021360
OpenAlexW2804867663

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.