Coronary disease & ACS

Fibrin clot properties independently predict adverse clinical outcome following acute coronary syndrome: a PLATO substudy

Eur Heart JPublished Secondary analysis of the PLATO randomised trial

Authors' conclusion

Fibrin clots that are resistant to lysis independently predict adverse outcome in ACS patients.

Study context

Population
Acute coronary syndrome (ACS) patients randomised to clopidogrel or ticagrelor in PLATO, plasma sampled at hospital discharge
Participants
4,354 patients
Comparison
Fibrin clot properties and 1-year outcomes
Primary endpoint
CV death, spontaneous myocardial infarction (MI) and PLATO-defined major bleeding
Follow-up
1 year after sample collection

Primary result

As reported in the abstract

Association per 50% increase in clot property (adjusted for CV risk factors) · 1 year
Hazard ratio (95% CI)P value
Lysis time (per 50% increase)CV death/spontaneous MI
1.17(1.05–1.31)
P < 0.01
Lysis time (per 50% increase)CV death
1.36(1.17–1.59)
P < 0.001
Maximum turbidity (per 50% increase)CV death
1.24(1.03–1.50)
P = 0.024

Per 50% increase, as printed

Further findings

OutcomeHR (95% CI)P value
CV death, after adjustment for other prognostic biomarkers · 1 yearPer 50% increase in lysis time1.2 (1.01–1.42)P = 0.042
  • Cardiovascular (CV) death, after adjustment for other prognostic biomarkers: adjusted for leukocyte count, hs-CRP, hs-troponin T, cystatin C, NT-proBNP and GDF-15

CV death, after adjustment for other prognostic biomarkers · 1 year

Association with CV death not significant for maximum turbidity after biomarker adjustment

Consistency by randomised antiplatelet treatment

Associations consistent regardless of randomised antiplatelet treatment
all interaction P > 0.05

Safety

PLATO-defined major bleeding

Neither lysis time nor maximum turbidity associated with major bleeding

Original publication

Fibrin clot properties independently predict adverse clinical outcome following acute coronary syndrome: a PLATO substudy. Eur Heart J. Published 29 January 2018. doi:10.1093/eurheartj/ehy013

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