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ΝΟΣΟΚΟΜΕΙΑΚΑ ΧΡΟΝΙΚΑ, ΤΟΜΟΣ 71, ΣΥΜΠΛΗΡΩΜΑ, 2009<br />

455<br />

Πiνακας 1. Major Changes in the 2007 ACC/AHA UA/NSTEMI Guidelines<br />

Pre-hospital management/emergency department<br />

Utilize 166 or ambulance (I-B), advise aspirin (IIa-B), nitroglycerin (IIa-C), perform & evaluate 12-lead ECGs (IIa-B)<br />

Coronary computed tomographic angiography in selected, lower-risk patients (IIa-B)<br />

Anti-ischemic/analgesics<br />

Avoid IV nitrates (III-C), ACE-I (III-B), β-blockers (III-A) in patients with hemodynamic instability<br />

ARBs may be substituted for ACE-I (I-A)<br />

Avoid NSAIDs (other than aspirin) during hospitalization (III-C)<br />

Antiplatelet therapy<br />

Drugs to minimize the risk of recurrent GI bleeding should be prescribed (I-B) in those with a prior history of GI bleeding<br />

May omit GPI in an invasive approach with bivalirudin and clopidogrel ≥6 h before PCI (IIa-B)<br />

Anticoagulant therapy<br />

Invasive strategy: fondaparinux or bivalirudin may be used as alternatives to UFH, enoxaparin (I-B)<br />

Conservative strategy: fondaparinux is acceptable (I-B), and preferred if an increased bleeding risk (I-B)<br />

Additional considerations for antithrombotic agents<br />

Conservative strategy (low risk): discontinue GPI (immediately), UFH (by 48 h), enoxaparin/ fondaparinux (by discharge or<br />

day 8) (I-A)<br />

CABG: Discontinue clopidogrel (5 to 7 days), short-acting GPIs (4 h), enoxaparin (12 to 24 h), fondaparinux (24 h), bivalirudin<br />

(3 h) before CABG (I-B)<br />

Urgent CABG: experienced surgeons may operate 50% may be performed in patients not eligible for CABG (IIa-B)<br />

Long-term medical therapy<br />

Lower-dose aspirin (75 to 162 mg) if no stenting (I-A), increased bleeding risk (IIa-C), and after an initial period after stenting<br />

(BMS 1 month [I-A], sirolimus-DES 3 months [I-B], paclitaxel-DES 6 months [I-B])<br />

Extended duration of clopidogrel to ideally 1 year after BMS and minimum of 12 months after DES (I-B)<br />

Aldosterone antagonists in addition to ACE-I in patients with LVEF

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