Evidence map›Paper›PMID 40730937›Full record

ArticleEuropean journal of drug metabolism and pharmacokinetics2025

Evaluation of the Effect of Ticagrelor Dose Interruption and Treatment Resumption with or without Bolus Doses Through Population PK/PD Simulation.

Hiroyoshi Matsui, Le Thien Truc Pham, Eyob Adane

Abstract read
In one paragraph

Article in European journal of drug metabolism and pharmacokinetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Hiroyoshi MatsuiRaabe College of Pharmacy, Ohio Northern University, 525 S. Main St., Ada, OH, 45810, USA.
Le Thien Truc PhamRaabe College of Pharmacy, Ohio Northern University, 525 S. Main St., Ada, OH, 45810, USA.
Eyob AdaneRaabe College of Pharmacy, Ohio Northern University, 525 S. Main St., Ada, OH, 45810, USA. e-adane@onu.edu.ORCID http://orcid.org/0000-0002-2447-6113

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTicagrelor is an oral P2Y

objectivesThe objective of the current study was to simulate the impact of therapy interruption on the PK/PD of ticagrelor.

methodsThe oral absorption of ticagrelor was described by a transit compartment model, and population PK/PD parameters were obtained from published literature. The PD of ticagrelor was described using a sigmoidal direct-response I

resultsDuring uninterrupted ticagrelor use, median PRUs ranged between ~ 13 to ~ 40, with > 70% below low platelet reactivity (LPR). The % of PRUs below high platelet reactivity (HPR) drops to ~ 47%, ~ 11%, ~ 2% and 0% upon dose interruption of 1, 2, 3, and 5 days, respectively. Within 2 h of dose resumption with either the loading or the maintenance dose, > 94% of PRUs were below LPR.

conclusionOur results suggest the need for individualizing duration of dose interruption prior to surgery and its resumption afterwards.

Indexed as

Models, BiologicalPlatelet Aggregation InhibitorsPurinergic P2Y Receptor AntagonistsTicagrelorAcute Coronary SyndromeAdministration, OralComputer SimulationDose-Response Relationship, DrugFemaleHumansMaleThrombosisPlatelet Aggregation InhibitorsPurinergic P2Y Receptor AntagonistsTicagrelor

Identifiers

PMID40730937
PMCPMC12394376

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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.