Coverage of incomplete stent apposition (ISA) is delayed compared to well-apposed struts in drug-eluting stents, with a risk ratio of 9.10 for noncoverage.
RCT (n=99)
Yes
Does incomplete stent apposition or side-branch location delay neointimal coverage compared to well-apposed struts in patients with drug-eluting stents?
Incomplete stent apposition and nonapposed side-branch struts in drug-eluting stents are associated with a significantly higher risk of delayed neointimal coverage compared to well-apposed struts at 9 to 13 months.
Effect estimate: RR 9.10 (95% CI 7.34 to 11.28)
Absolute Event Rate: 27.4% vs 94.9%
p-value: p=<0.001
Background— Pathology studies on fatal cases of very late stent thrombosis have described incomplete neointimal coverage as common substrate, in some cases appearing at side-branch struts. Intravascular ultrasound studies have described the association between incomplete stent apposition (ISA) and stent thrombosis, but the mechanism explaining this association remains unclear. Whether the neointimal coverage of nonapposed side-branch and ISA struts is delayed with respect to well-apposed struts is unknown. Methods and Results— Optical coherence tomography studies from 178 stents implanted in 99 patients from 2 randomized trials were analyzed at 9 to 13 months of follow-up. The sample included 38 sirolimus-eluting, 33 biolimus-eluting, 57 everolimus-eluting, and 50 zotarolimus-eluting stents. Optical coherence tomography coverage of nonapposed side-branch and ISA struts was compared with well-apposed struts of the same stent by statistical pooled analysis with a random-effects model. A total of 34 120 struts were analyzed. The risk ratio of delayed coverage was 9.00 (95% confidence interval, 6.58 to 12.32) for nonapposed side-branch versus well-apposed struts, 9.10 (95% confidence interval, 7.34 to 11.28) for ISA versus well-apposed struts, and 1.73 (95% confidence interval, 1.34 to 2.23) for ISA versus nonapposed side-branch struts. Heterogeneity of the effect was observed in the comparison of ISA versus well-apposed struts (H=1.27; I 2 =38.40) but not in the other comparisons. Conclusions— Coverage of ISA and nonapposed side-branch struts is delayed with respect to well-apposed struts in drug-eluting stents, as assessed by optical coherence tomography. Clinical Trial Registration— http://www.clinicaltrials.gov . Unique identifier: NCT00389220, NCT00617084.
Gutiérrez‐Chico et al. (Tue,) conducted a rct in nonapposed side-branch and incomplete stent apposition in drug-eluting stents (n=99). drug-eluting stents vs. well-apposed struts was evaluated on delayed neointimal coverage of ISA and nonapposed side-branch struts compared to well-apposed struts (RR 9.10, 95% CI 7.34 to 11.28, p=<0.001). Coverage of incomplete stent apposition (ISA) is delayed compared to well-apposed struts in drug-eluting stents, with a risk ratio of 9.10 for noncoverage.
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