Examples of using Stemi in English and their translations into Hungarian
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Colloquial
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Medicine
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Official
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Ecclesiastic
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Financial
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Programming
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Official/political
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Computer
What's a Stemi?
STEMI that cardiologists intend to treat with primary PCI; or.
Lead shows a stemi.
The presentation of unstable angina and NSTEMI may be indistinguishable,and also indistinguishable from acute STEMI.
Treatment in patients with acute STEMI.
Activate the STEMI protocol!
He's got acute chest pains, stemi.
Treatment of UA/ NSTEMI and STEMI- fondaparinux should not be used in patients with creatinine clearance< 20 ml/ min(see section 4.3).
EKG is consistent with an anterior wall stemi.
Immediate medical attention can increase the chances of survival, but STEMI carries a high risk of death and disability.
Intravenous(bolus) injection for acute STEMI indication only: Inhixa may be safely administered with sodium chloride 9 mg/ml(0.9%) solution for injection or 5% glucose in water.
Intravenous injection technique(for acute STEMI indication only).
To investigate TIT, 7146 STEMI patients were selected who were treated with percutaneous coronary intervention(PCI) within 24 hours of the beginning of the complaint and all of its components were known.
Intravenous(bolus) injection for acute STEMI indication only.
In STEMI or UA/ NSTEMI patients who are to undergo coronary artery bypass graft(CABG) surgery, fondaparinux where possible, should not be given during the 24 hours before surgery and may be ct.
The need of prehospital reanimation was high in our young STEMI population(11.5%).
Treatment of UA/ NSTEMI and STEMI- For the treatment of UA/ NSTEMI and STEMI, there are limited clinical data available on the use of fondaparinux 2.5mg once daily in patients with creatinine clearance between 20 and 30 ml/ min.
Possia reduced the occurrence of the primary composite endpoint compared to clopidogrel in both the UA/NSTEMI and STEMI population(Table 3).
Analysis of the composite endpoint in the All ACS population(combined UA/NSTEMI and STEMI cohorts) was contingent on showing statistical superiority of prasugrel versus clopidogrel in the UA/NSTEMI cohort(p< 0.05).
Hypersensitivity to rosiglitazone, glimepiride, other sulphonylureas or sulphonamides or to any of the excipients cardiac failure or history of cardiac failure(NYHA class I to IV) an Acute Coronary Syndrome(unstable angina,NSTEMI and STEMI)(see section 4.4).
For treatment of UA/NSTEMI and STEMI, fondaparinux should be used with caution in patients who are being treated concomitantly with other agents that increase the risk of haemorrhage(such as GPIIb/IIIa inhibitors or thrombolytics).
The rivaroxaban clinical program was designed to demonstrate the efficacy of Xarelto for the prevention of cardiovascular(CV) death,MI or stroke in subjects with a recent ACS(ST-elevation myocardial infarction[STEMI], non- ST-elevation myocardial infarction[NSTEMI] or unstable angina[UA]).
Treatment of UA/NSTEMI and STEMI- For the treatment of UA/NSTEMI and STEMI, there are limited clinical data available on the use of fondaparinux 2.5mg once daily in patients with creatinine clearance between 20 and 30 ml/min.
Thus, Brilique 90 mg twice daily together with low-dose ASA can be used in patients with ACS(unstable angina, non ST elevation Myocardial Infarction[NSTEMI]or ST elevation Myocardial Infarction[STEMI]); including patients managed medically, and those who are managed with percutaneous coronary intervention(PCI) or coronary artery by-pass grafting(CABG).
Treatment of ST segment elevation myocardial infarction(STEMI) OASIS 6 was a double blind, randomised study assessing the safety and efficacy of fondaparinux 2.5 mg once daily, versus usual care placebo(47%) or UFH(53%) in approximately 12,000 patients with STEMI.
Hypersensitivity to rosiglitazone, glimepiride, other sulphonylureas or sulphonamides or to any of the excipients- cardiac failure or history of cardiac failure( NYHA class I to IV)- an Acute Coronary Syndrome( unstable angina,NSTEMI and STEMI)( see section 4.4)- hepatic impairment- severe renal impairment i. e. creatinine clearance less than 30 ml/ min( including renal dialysis).- insulin dependant diabetes- diabetic ketoacidosis or diabetic coma.
The safety of Possia in patients with acute coronary syndromes( UA,NSTEMI and STEMI) was evaluated in the pivotal large phase 3 PLATO([ PLATelet Inhibition and Patient Outcomes] study, 18,624 patients), which compared patients treated with Possia( loading dose of 180 mg of Possia and a maintenance dose of 90 mg twice daily) to patients treated with clopidogrel( 300-600 mg loading dose followed by 75 mg once daily maintenance dose) both given in combination with acetylsalicylic acid( ASA) and other standard therapies.
