Evidence map›Paper›PMID 24127651›Full record

Trial reportPlatelets2014

Lower mortality following pulmonary adverse events and sepsis with ticagrelor compared to clopidogrel in the PLATO study.

Robert F Storey, Stefan K James, Agneta Siegbahn, Christoph Varenhorst, Claes Held, Joseph Ycas, Steen E Husted, Christopher P Cannon, Richard C Becker, Ph Gabriel Steg and 2 more

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Platelets, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% 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

76 citing papers in PubMed, 1 synthesis or guideline pooled it, 162 citations in OpenAlex.

  1. Antiplatelet agents for chronic kidney disease.The Cochrane database of systematic reviews · 2022
    Pooled it
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  7. Ticagrelor IncreasesInternational journal of molecular sciences · 2020
    Trial
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  14. Article
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  17. Review
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  19. Article
  20. Platelet P2YBritish journal of pharmacology · 2024
    Review

16 more citing papers are in PubMed but not listed here.

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

12 authors at 7 institutions in 5 countries.

Robert F StoreyDepartment of Cardiovascular Science, University of Sheffield , Sheffield , UK .
Stefan K James
Agneta Siegbahn
Christoph Varenhorst
Claes Held
Joseph Ycas
Steen E Husted
Christopher P Cannon
Richard C Becker
Ph Gabriel Steg
Nils Åsenblad
Lars Wallentin
Uppsala University · SEAarhus University Hospital · DKAstraZeneca (United States) · USBrigham and Women's Hospital · USDélégation Paris 7 · FRUniversity of Cincinnati Medical Center · USUniversity of Sheffield · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the PLATelet inhibition and patient Outcomes (PLATO) study of patients with acute coronary syndromes, ticagrelor reduced mortality compared to clopidogrel but the mechanisms for this mortality reduction remain uncertain. We analysed adverse events (AEs) consistent with either pulmonary infection or sepsis, and subsequent mortality, in 18,421 PLATO patients treated with ticagrelor or clopidogrel. AEs occurring within 7 days of last dose of study medication were defined as "on-treatment". Serial measurements of blood leukocyte counts, C-reactive protein and interleukin-6 were performed. Fewer on-treatment pulmonary AEs occurred in the ticagrelor compared to the clopidogrel group (275 vs. 331 respectively; p = 0.019), with fewer deaths following these AEs (33 vs. 71; p < 0.001), particularly in those who remained on study medication three days after AE onset (10 vs. 43; p < 0.001). There were fewer deaths attributed to sepsis in the ticagrelor group (7 vs. 23; p = 0.003). Leukocyte counts were lower in the clopidogrel group during treatment (p < 0.0001 at 1, 3 and 6 months) but not at 1 month post-discontinuation. C-reactive protein increased more at discharge in the ticagrelor group (28.0 ± 38.0 vs. 26.1 ± 36.6 mg/l; p < 0.001) and interleukin-6 remained higher during the first month of treatment with ticagrelor. We conclude that the mortality risk following pulmonary AEs and sepsis in acute coronary syndrome patients appears to be lower during ticagrelor compared to clopidogrel therapy. Further work should assess whether ticagrelor and clopidogrel have differential effects on immune signalling.

Indexed as

AdenosineAgedClopidogrelCoronary Artery DiseaseFemaleHumansMaleMiddle AgedPlatelet Aggregation InhibitorsPneumoniaSepsisTicagrelorTiclopidineTreatment OutcomeAdenosineClopidogrelPlatelet Aggregation InhibitorsTicagrelorTiclopidineClopidogrelcoronary artery diseaseplatelet aggregation inhibitorspneumoniasepsisticagrelor

Identifiers

PMID24127651
PMCPMC4220996
OpenAlexW2170741125

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.