Evidence map›Paper›PMID 29701129›Full record

ArticlePharmacogenomics2018

Feasibility and implementation of CYP2C19 genotyping in patients using antiplatelet therapy.

Thomas O Bergmeijer, Gerrit Ja Vos, Daniël Mf Claassens, Paul Wa Janssen, Remko Harms, Richard van der Heide, Folkert W Asselbergs, Jurriën M Ten Berg, Vera Hm Deneer

Open access · greenAbstract read
In one paragraph

Article in Pharmacogenomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 5 pooled it
2.0field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 5 syntheses or guidelines pooled it, 27 citations in OpenAlex.

  1. Pooled it
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  14. PInterventional neuroradiology : journal of peritherapeutic neuroradiology, surgical procedures and related neurosciences · 2021
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  15. Novel associations betweenPharmacogenomics · 2021
    Observational
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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

9 authors at 3 institutions in 2 countries.

Thomas O BergmeijerDepartment of Cardiology, St Antonius Hospital, 3435 CM, Nieuwegein, The Netherlands.
Gerrit Ja VosDepartment of Cardiology, St Antonius Hospital, 3435 CM, Nieuwegein, The Netherlands.
Daniël Mf ClaassensDepartment of Cardiology, St Antonius Hospital, 3435 CM, Nieuwegein, The Netherlands.
Paul Wa JanssenDepartment of Cardiology, St Antonius Hospital, 3435 CM, Nieuwegein, The Netherlands.
Remko HarmsDepartment of Clinical Pharmacy, St Antonius Hospital, 3435 CM, Nieuwegein, The Netherlands.
Richard van der HeideDepartment of Clinical Pharmacy, St Antonius Hospital, 3435 CM, Nieuwegein, The Netherlands.
Folkert W AsselbergsDepartment of Cardiology, Division Heart & Lungs, UMC Utrecht, 3584 CX, Utrecht, The Netherlands.
Jurriën M Ten BergDepartment of Cardiology, St Antonius Hospital, 3435 CM, Nieuwegein, The Netherlands.
Vera Hm DeneerDepartment of Clinical Pharmacy, University Medical Center Utrecht, 3584 CX, Utrecht, The Netherlands.
St. Antonius Ziekenhuis · NLNetherlands Heart Institute · NLUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimA tailored antiplatelet strategy based on CYP2C19 genotype may reduce atherothrombotic and bleeding events. We describe our experience with CYP2C19 genotyping, using on-site TaqMan or Spartan genotyping or shipment to a central laboratory. METHODOLOGY: Data from two ongoing projects were used: Popular Risk Score project (non-urgent percutaneous coronary intervention patients) and the Popular Genetics study (ST-segment elevation myocardial infarction patients). For both projects, the time to genotyping result was calculated.

resultsIn the Popular Risk Score project (n = 2556), median time from blood collection to genotyping result was 4:04 h. In the Popular Genetics study (n = 1038), median time from randomization to genotyping result was 2:24 h.

conclusionCYP2C19 genotyping is feasible in everyday clinical practice, both in the acute and non-acute settings.

Indexed as

Cytochrome P-450 CYP2C19Drug-Related Side Effects and Adverse ReactionsFeasibility StudiesGenotypeHumansMyocardial InfarctionPercutaneous Coronary InterventionPharmacogenomic TestingPlatelet Aggregation InhibitorsPrecision MedicineTime FactorsCYP2C19 protein, humanCytochrome P-450 CYP2C19Platelet Aggregation InhibitorsclopidogrelCYP2C19genotypingPCIpersonalized medicinepharmacogenomicsSTEMIticagrelor

Identifiers

PMID29701129
PMCPMC6021912
OpenAlexW2800634735

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.