Non-access site bleeding associated with increased mortality in STEMI
One-year mortality was increased nearly threefold in a cohort of patients with non-access site bleeding after PCI in patients with STEMI.
The researchers aimed to evaluate whether access site bleeding or non-access site bleeding can predict outcomes in STEMI. The analysis included 2,002 patients who underwent primary PCI. The study also included a meta-analysis of studies investigating access site bleeding status in patients undergoing primary PCI for STEMI.
Outcome measures included 1-year mortality, recurrent MI, stent thrombosis and stroke.
Radial access was used in 3.7% of patients.
The rate of access site bleeding was 6.3%, while the rate of non-access site bleeding was 5.2%.
Multivariate analysis indicated no association between access site bleeding and 1-year mortality risk (HR=1.03; P=.89). Recurrent MI (HR=1.16; P=.64), stent thrombosis (HR=0.55; P=.42) and stroke (HR=0.47; P=.31) also demonstrated no association with access site bleeding.
However, an independent association between non-access site bleeding and 1-year mortality was reported (HR=2.77; P<.001). Non-access site bleeding was also associated with stent thrombosis (HR=3.10; P=.021), but not with recurrent MI or stroke.
In addition, a meta-analysis of 495,630 patients indicated a higher risk of 1-year mortality among those who experienced non-access site bleeding (HR=1.66; 95% CI, 1.56-1.76) compared with access site bleeding (HR=1.21; 95% CI, 1.11-1.31).
“These results taken together with those of previous studies indicate a greater risk of subsequent mortality in patients with non-[access site bleeding],” the researchers concluded.
Disclosure: The researchers report financial disclosures with Abbott Vascular, AstraZeneca, Boston Scientific, Covidien, CSL Behring, Eli Lilly/Daiichi Sankyo, Endothelix, Janssen Pharmaceuticals, Maya Medical, Merck & Co., Regado Biosciences, Sanofi Aventis and The Medicines Company.