Antithrombotic therapy for non-ST-segment elevation acute coronary syndromes

被引:116
作者
Harrington, Robert A. [1 ]
Becker, Richard C. [2 ]
Cannon, Christopher P. [3 ]
Gutterman, David [4 ]
Lincoff, A. Michael [5 ]
Popma, Jeffrey J. [3 ]
Steg, Gabriel [6 ]
Guyatt, Gordon H. [7 ]
Goodman, Shaun G. [8 ]
机构
[1] Duke Univ, Med Ctr, Duke Clin Res Inst, Durham, NC 27705 USA
[2] Duke Clin Res Inst, Duke Cardiovasc Thrombosis Ctr, Durham, NC USA
[3] Brigham & Womens Hosp, Boston, MA 02115 USA
[4] Med Coll Wisconsin, Milwaukee, WI 53226 USA
[5] Cleveland Clin Fdn, Cleveland, OH 44195 USA
[6] Hop Bichat Claude Bernard, F-75877 Paris, France
[7] McMaster Univ, Hlth Sci Ctr, Hamilton, ON, Canada
[8] Univ Toronto, St Michaels Hosp, Toronto, ON M5B 1W8, Canada
关键词
acute coronary syndromes; anticoagulants; antiplatelet therapies; myocardial infarction;
D O I
10.1378/chest.08-0691
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
This chapter about antithrombotic therapy for coronary artery disease is part of the Antithrombotic and Thrombolytic Therapy: American College of Chest Physicans Evidence-Based Clinical Practice Guidelines (8th Edition). Grade 1 recommendations are strong and indicate that the benefits do, or do not, outweigh risks, burden, and costs. Grade 2 suggestions are weaker as there is uncertainty regarding the benefits, risks and costs such that individual patients' values may lead to different choices (for a full understanding of the grading see the "Grades of Recommendation for Antithrombotic Agents" chapter by Guyatt et al, CHEST 2008; 133[suppl]:123S-131S). Among the key recommendations are the following: for all patients presenting with non-ST-segment elevation (NSTE) acute coronary syndrome (ACS), without a clear allergy to aspirin, we recommend immediate aspirin (162 to 325 mg po) and then daily oral aspirin (75 to 100 mg) [Grade 1A]. For NSTE ACS patients who are at at least moderate risk for an ischemic event and who will undergo an early invasive management strategy, we recommend "upstream" treatment either with clopidogrel (300 mg po bolus, followed by 75 mg/d) or a small-molecule IV glycoprotein (GP) IIb/IIIa inhibitor (eptifibatide or tirofiban) [Grade 1A]. For NSTE ACS patients who are at least moderate risk for an ischemic event and for whom an early conservative or a delayed invasive strategy of management is to be used, we recommend "upstream" treatment with clopidogrel (300 mg oral bolus, followed by 75 mg/d) [Grade 1A]. For NSTE ACS patients who undergo PCI, we recommend treatment with both clopidogrel and an IV GP IIb/IIIa inhibitor (Grade 1A). We recommend a loading dose of 600 mg of clopidogrel given at least 2 h prior to planned PCI followed by 75 mg/d (Grade 1B). For all patients presenting with NSTE ACS, we recommend anticoagulation with UFH or LMWH or bivahrudin or fondaparinux over no anticoagulation (Grade 1A). For NSTE ACS patients who will undergo an early invasive strategy of management, we recommend UFH (with a GP IIb/IIIa inhibitor) over either LMWH or fondaparinux (Grade 1B). For NSTE ACS patients in whom an early conservative or a delayed invasive strategy of management is to be used, we recommend fondaparinux over enoxaparin (Grade 1A) and LMWH over UFH (Grade 1B). We recommend continuing LMWH during PCI treatment of patients with NSTE ACS when it has been started as the "upstream" anticoagulant (Grade 1B). In low- to moderate-risk patients with NSTE ACS undergoing PCI, we recommend either bivalirudin with provisional ("bail-out") GP IIb/IIIa inhibitors or UFH plus a GP IIb/IIIa inhibitor over alternative antithrombotic regimens (Grade 1B).
引用
收藏
页码:670S / 707S
页数:38
相关论文
共 160 条
[41]  
Collet JP, 2001, CIRCULATION, V103, P658
[42]   BLOOD-PRESSURE, STROKE, AND CORONARY HEART-DISEASE .2. SHORT-TERM REDUCTIONS IN BLOOD-PRESSURE - OVERVIEW OF RANDOMIZED DRUG TRIALS IN THEIR EPIDEMIOLOGIC CONTEXT [J].
COLLINS, R ;
PETO, R ;
MACMAHON, S ;
HEBERT, P ;
FIEBACH, NH ;
EBERLEIN, KA ;
GODWIN, J ;
QIZILBASH, N ;
TAYLOR, JO ;
HENNEKENS, CH .
LANCET, 1990, 335 (8693) :827-838
[43]   Enoxaparin versus unfractionated heparin in patients treated with tirofiban, aspirin and an early conservative initial management strategy: results from the A phase of the A-to-Z trial [J].
de Lemos, JA ;
Blazing, MA ;
Wiviott, SD ;
Brady, WE ;
White, HD ;
Fox, KAA ;
Palmisano, J ;
Ramsey, KE ;
Bilheimer, DW ;
Lewis, EF ;
Pfeffer, M ;
Califf, RM ;
Braunwald, E .
EUROPEAN HEART JOURNAL, 2004, 25 (19) :1688-1694
[44]   PREVALENCE OF TOTAL CORONARY-OCCLUSION DURING THE EARLY HOURS OF TRANSMURAL MYOCARDIAL-INFARCTION [J].
DEWOOD, MA ;
SPORES, J ;
NOTSKE, R ;
MOUSER, LT ;
BURROUGHS, R ;
GOLDEN, MS ;
LANG, HT .
NEW ENGLAND JOURNAL OF MEDICINE, 1980, 303 (16) :897-902
[45]   Adverse impact of bleeding on prognosis in patients with acute coronary syndromes [J].
Eikelboom, John W. ;
Mehta, Shamir R. ;
Anand, Sonia S. ;
Xie, Changchun ;
Fox, Keith A. A. ;
Yusuf, Salim .
CIRCULATION, 2006, 114 (08) :774-782
[46]  
Ellis SG, 1999, CIRCULATION, V100, P799
[47]   LOW-MOLECULAR-WEIGHT HEPARIN IN PREVENTION OF RESTENOSIS AFTER ANGIOPLASTY - RESULTS OF ENOXAPARIN RESTENOSIS (ERA) TRIAL [J].
FAXON, DP ;
SPIRO, TE ;
MINOR, S ;
COTE, G ;
DOUGLAS, J ;
GOTTLIEB, R ;
CALIFF, R ;
DOROSTI, K ;
TOPOL, E ;
GORDON, JB ;
OHMEN, M ;
RAIZNER, A ;
PAR, T ;
CURRIER, J ;
HANKIN, B .
CIRCULATION, 1994, 90 (02) :908-914
[48]   Combining enoxaparin and glycoprotein IIb/IIIa antagonists for the treatment of acute coronary syndromes: Final results of the National Investigators Collaborating on Enoxaparin-3 (NICE-3) study [J].
Ferguson, JJ ;
Antman, EM ;
Bates, ER ;
Cohen, M ;
Every, NR ;
Harrington, RA ;
Pepine, CJ ;
Theroux, P .
AMERICAN HEART JOURNAL, 2003, 146 (04) :628-634
[49]  
Ferguson JJ, 2004, JAMA-J AM MED ASSOC, V292, P45
[50]   A RANDOMIZED COMPARISON OF CORONARY-STENT PLACEMENT AND BALLOON ANGIOPLASTY IN THE TREATMENT OF CORONARY-ARTERY DISEASE [J].
FISCHMAN, DL ;
LEON, MB ;
BAIM, DS ;
SCHATZ, RA ;
SAVAGE, MP ;
PENN, I ;
DETRE, K ;
VELTRI, L ;
RICCI, D ;
NOBUYOSHI, M ;
CLEMAN, M ;
HEUSER, R ;
ALMOND, D ;
TEIRSTEIN, PS ;
FISH, RD ;
COLOMBO, A ;
BRINKER, J ;
MOSES, J ;
SHAKNOVICH, A ;
HIRSHFELD, J ;
BAILEY, S ;
ELLIS, S ;
RAKE, R ;
GOLDBERG, S .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (08) :496-501