Примери за използване на Stent thrombosis на Английски и техните преводи на Български
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Stent thrombosis.
Definite stent thrombosis d.
An additional retrospective analysis showed a nominally significant reduction in the incidence rates of stent thrombosis compared with placebo(see Table 4).
ST= stent thrombosis.
Prasugrel was associated with a 50% reduction in stent thrombosis through the 15 month follow-up period.
Coronary stent thrombosis including reports with fatal outcome c.
There was no statistically significant difference in the rates of stent thrombosis between treatment arms at 30 days(p=0.3257) and 1 year(p=0.7754).
The reduction in stent thrombosis with Efient was observed both early and beyond 30 days for both bare metal and drug eluting stents. .
OR= odds ratio; CI= confidence interval; IDR= ischaemia-driven revascularisation; MI= myocardial infarction; mITT= modified intent-to-treat;ST= stent thrombosis.
Acute stent thrombosis.
Patients≥ 75 years in whom the benefit with prasugrel wasmore evident included those with diabetes, STEMI, higher risk of stent thrombosis, or recurrent events.
Two deaths occurred after acute stent thrombosis, 1 in each arm of the study.
Efient showed superior efficacy compared to clopidogrel in reducing the primary composite outcome events as well as the pre-specified secondary outcome events,including stent thrombosis(see Table 3).
A total of 17 deaths occurred after subacute stent thrombosis, 3 in the bivalirudin arm and 14 in the UFH plus GP IIb/IIIa arm.
In TRITON-TIMI 38 and 3 of the cohort studies(Collet, Sibbing, Giusti) the combined group of patients with either intermediate or poor metaboliser status had a higher rate of cardiovascular events(death,myocardial infarction, and stroke) or stent thrombosis compared to extensive metabolisers.
Coronary artery thrombosis and coronary stent thrombosis with myocardial infarction, and catheter thrombosis have each been reported rarely.
The clinical benefit provided by the more potent P2Y12 inhibitors, ticagrelor and prasugrel,in their pivotal studies is related to a significant reduction in recurrent ischaemic events(including acute and subacute stent thrombosis(ST), myocardial infarction(MI), and urgent revascularization).
This increased risk of acute stent thrombosis was observed during the first 4 hours following the end of the procedure among patients who either discontinued the infusion of bivalirudin at the end of the procedure or received a continued infusion at the reduced dose of 0.25 mg/kg/h(see section 4.2).
Among post-MI or PAD patients without a history of stroke or TIA,Zontivity appeared to reduce the rate of definite stent thrombosis HR 0.71(0.51-0.99 for adjudicated“definite”) vs. placebo in subjects receiving any stent before or during the study.
In TRITON-TIMI 38 and 3 of the cohort studies(Collet, Sibbing, Giusti) the combined group of patients with either intermediate or poor metaboliser status had a higher rate of cardiovascular events(death,myocardial infarction, and stroke) or stent thrombosis compared to extensive metabolisers.
In TRITON-TIMI 38 and 3 of the cohort studies(n= 3,516; Collet, Sibbing, Giusti), patients with an impaired metaboliser status(intermediate and poor combined) had a higher rate of cardiovascular events(death,myocardial infarction, and stroke) or stent thrombosis compared to extensive metabolisers.
Thrombosis includes coronary artery thrombosis(blood clot in the heart arteries or within a stent being felt as a heart attack which can also be fatal) and/or thrombosis in the catheter, both of which are rare(may affect up to 1 in 1,000 people).
Thrombosis includes coronary artery thrombosis(blood clot in the heart arteries or within a stent being felt as a heart attack which can also be fatal) and/or thrombosis in the catheter, both of which are rare may affect up.