Evidence map›Paper›PMID 30850677›Full record

Trial reportScientific reports2019

Determinants of high platelet reactivity in patients with acute coronary syndromes treated with ticagrelor.

Piotr Adamski, Katarzyna Buszko, Joanna Sikora, Piotr Niezgoda, Tomasz Fabiszak, Małgorzata Ostrowska, Malwina Barańska, Aleksandra Karczmarska-Wódzka, Eliano Pio Navarese, Jacek Kubica

Abstract readClinical Trial, Phase IVObservational StudyRandomized Controlled Trial
In one paragraph

Trial report in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

22 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
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  5. Review
  6. Article
  7. Clopidogrel resistance and its relevance: Current concepts.Journal of family medicine and primary care · 2024
    Review
  8. Platelet Reactivity in the Exacerbation of Psoriasis.Journal of clinical medicine · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Observational
  13. Review
  14. Review
  15. Article
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  17. Article
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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

10 authors.

Piotr AdamskiCollegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland. piotr.adamski@wp.eu.ORCID 0000-0001-9719-0987
Katarzyna BuszkoCollegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Joanna SikoraCollegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Piotr NiezgodaCollegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Tomasz FabiszakCollegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Małgorzata OstrowskaCollegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Malwina BarańskaCollegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.ORCID 0000-0002-2566-719X
Aleksandra Karczmarska-WódzkaCollegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Eliano Pio NavareseCollegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Jacek KubicaCollegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High platelet reactivity (HPR) is a risk factor for stent thrombosis, a potentially lethal complication of percutaneous coronary intervention. HPR is also associated with increased risk of myocardial infarction and death in invasively-treated patients with acute coronary syndrome (ACS). HPR occurs even in ACS patients treated with ticagrelor, a state-of-the-art antiplatelet agent, especially during the first hours of treatment. Patient-level pharmacodynamic data obtained from 102 ACS subjects enrolled in two prospective, pharmacodynamic trials were analysed in order to identify clinical features related with increased odds of on-ticagrelor HPR during the first two hours after ticagrelor loading dose in ACS patients. Presence of ST-segment elevation myocardial infarction (versus non-ST-segment elevation ACS) and morphine co-administration were the strongest predictors of HPR at 1 and 2 hours after ticagrelor loading dose according to linear regression analyses, multiple backward stepwise logistic regression analyses and generalized estimating equation model. By pinpointing simple to recognize clinical features, the results of this study facilitate identification of ACS patients who have the highest odds of HPR during the initial phase of treatment with ticagrelor, and who could potentially benefit from alternative treatment strategies.

Indexed as

Acute Coronary SyndromeAgedFemaleHumansMaleMiddle AgedModels, CardiovascularMorphinePercutaneous Coronary InterventionPlatelet ActivationPlatelet Aggregation InhibitorsProspective StudiesRegression AnalysisRisk FactorsST Elevation Myocardial InfarctionThrombosisMorphinePlatelet Aggregation InhibitorsTicagrelor

Identifiers

PMID30850677
PMCPMC6408477

What OpenQuestion holds

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Registered trials

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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.