Ticagrelor monotherapy in patients with chronic kidney disease undergoing percutaneous coronary intervention: TWILIGHT-CKD

Eur Heart JPublished Secondary analysis of the TWILIGHT randomised trial

Authors' conclusion

Among CKD patients undergoing PCI, ticagrelor monotherapy reduced the risk of bleeding without a significant increase in ischaemic events as compared with ticagrelor plus aspirin.

Study context

Population
High-risk patients undergoing percutaneous coronary intervention (PCI) with drug-eluting stent, event-free after 3 months of ticagrelor plus aspirin; Chronic kidney disease (CKD) = estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m²1,111 (16.3%) with CKD
Participants
6,835 patients
Comparison
Ticagrelor plus placebo vs ticagrelor plus aspirin, by CKD status
Primary endpoint
Bleeding Academic Research Consortium (BARC) type 2, 3, or 5 bleeding
Methodological detailsprespecified subanalysis, placebo-controlled
  • Prespecified subanalysis
  • Placebo-controlled

Primary result

As reported in the abstract

BARC type 2, 3, or 5 bleeding, by CKD (subgroups)
Ticagrelor plus placebo vs Ticagrelor plus aspirinHazard ratio (95% CI)
CKD: 4.6% vs. 9.0%
0.50(0.31–0.80)
No CKD: 4.0% vs. 6.7%
0.59(0.47–0.75)

Further findings

OutcomeTicagrelor plus placeboTicagrelor plus aspirinHR (95% CI)
Death, MI, or stroke, by CKD (subgroups)CKD7.9%5.7%1.40 (0.88–2.22)
Death, MI, or stroke, by CKD (subgroups)No CKD3.2%3.6%0.90 (0.68–1.20)
  • Death, MI, or stroke, by CKD (subgroups): Pinteraction = 0.111

Death, MI, or stroke, by CKD (subgroups)

Not significantly different between randomized groups

Original publication

Ticagrelor monotherapy in patients with chronic kidney disease undergoing percutaneous coronary intervention: TWILIGHT-CKD. Eur Heart J. Published 23 August 2021. doi:10.1093/eurheartj/ehab533

Summarised from the published abstract; every number is checked against it

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