The impact of renal dysfunction on outcomes in the ExTRACT-TIMI 25 trial

被引:75
作者
Fox, Keith A. A.
Antman, Elliott M. [1 ]
Montalescot, Gilles
Agewall, Stefan
SomaRaju, Bhupathi
Verheugt, Freek W. A.
Lopez-Sendon, Jose
Hod, Hanoch
Murphy, Sabina A.
Braunwald, Eugene
机构
[1] Univ Edinburgh, Edinburgh, Midlothian, Scotland
[2] Brigham & Womens Hosp, Dept Med, Cardiovasc Div, TIMI Study Grp, Boston, MA USA
[3] Harvard Univ, Sch Med, Boston, MA USA
[4] Pitie Salpetriere Univ Hosp, Inst Cardiol, Paris, France
[5] Karolinska Univ Hosp, Karolinska Inst, Coronary Care Unit, Stockholm, Sweden
[6] CARE Hosp, Hyderabad, Andhra Pradesh, India
[7] Univ Hosp Nijmegen, Nijmegen, Netherlands
[8] Hosp Univ La Paz Madrid, Madrid, Spain
[9] Chaim Sheba Med Ctr, Heart Inst, Tel Hashomer, Israel
关键词
D O I
10.1016/j.jacc.2006.12.049
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives The ExTRACT-TIMI 25 (Enoxaparin and Thrombolysis Reperfusion for Acute Myocardial Infarction Treatment-Thrombolysis In Myocardial Infarction 25) trial provided the opportunity to evaluate the impact of renal dysfunction on outcomes in patients with ST-segment elevation myocardial infarction (STEMI) and compare enoxaparin (ENOX) and unfractionated heparin (UFH). Background It is unclear how renal dysfunction influences the balance between benefit and risk of antithrombotic therapy. Methods In the ExTRACT-TIMI 25 trial, 20,479 patients were randomized to UFH or ENOX A reduced ENOX dose was administered to patients age >= 75 years and those with an estimated creatinine clearance (CrCI) <30 ml/min. Results A powerful relationship was observed between the severity of renal dysfunction (per 10 ml/min decrement in CrCl) and death, stroke, intracranial hemorrhage, and major and minor bleeding (p < 0.001 for each). There was a progressive increase in the treatment benefit with ENOX on death or nonfatal myocardial infarction (p < 0.01) with better renal function. Net clinical benefit (death, nonfatal MI, or nonfatal major bleeding) was significantly superior with ENOX (p < 0.001) for patients with a CrCI >60 ml/min (79.1% of the study population). Major bleeding and intracranial hemorrhage did not differ for patients with preserved renal function (CrCl >90 ml/ min), but in those with renal dysfunction there was a progressively greater increase in the risk of major and minor bleeding with ENOX. Conclusions Enoxaparin was superior to UFH for the majority of subjects. With more severe renal dysfunction, the net clinical benefit between ENOX and UFH did not differ, despite the rise in adverse events in both treatment groups. Future studies should take renal dysfunction into account when assessing antithrombotic regimens.
引用
收藏
页码:2249 / 2255
页数:7
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