Dalteparin versus Unfractionated Heparin in Critically Ill Patients

被引:317
作者
Cook, Deborah [1 ]
Meade, Maureen
Guyatt, Gordon
Walter, Stephen
Heels-Ansdell, Diane
Warkentin, Theodore E.
Zytaruk, Nicole
Crowther, Mark
Geerts, William [2 ]
Cooper, D. Jamie [3 ]
Vallance, Shirley [3 ]
Qushmaq, Ismael [4 ]
Rocha, Marcelo [5 ]
Berwanger, Otavio [6 ]
Vlahakis, Nicholas E. [7 ]
机构
[1] McMaster Univ, Hlth Sci Ctr, Dept Med, Hamilton, ON L8N 3Z5, Canada
[2] Univ Toronto, Toronto, ON, Canada
[3] Alfred Hosp, Melbourne, Vic, Australia
[4] King Faisal Specialist & Res Ctr, Jeddah, Saudi Arabia
[5] Santa Casa Hosp, Porto Alegre, RS, Brazil
[6] Hosp Coracao, Sao Paulo, Brazil
[7] Mayo Clin, Rochester, MN USA
基金
加拿大健康研究院;
关键词
DEEP-VEIN THROMBOSIS; MOLECULAR-WEIGHT HEPARIN; VENOUS THROMBOSIS; CLINICAL-TRIALS; PROPHYLAXIS; THROMBOEMBOLISM; PREVENTION; RISK;
D O I
10.1056/NEJMoa1014475
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND The effects of thromboprophylaxis with low-molecular-weight heparin, as compared with unfractionated heparin, on venous thromboembolism, bleeding, and other outcomes are uncertain in critically ill patients. METHODS In this multicenter trial, we tested the superiority of dalteparin over unfractionated heparin by randomly assigning 3764 patients to receive either subcutaneous dalteparin (at a dose of 5000 IU once daily) plus placebo once daily (for parallel-group twice-daily injections) or unfractionated heparin (at a dose of 5000 IU twice daily) while they were in the intensive care unit. The primary outcome, proximal leg deep-vein thrombosis, was diagnosed on compression ultrasonography performed within 2 days after admission, twice weekly, and as clinically indicated. Additional testing for venous thromboembolism was performed as clinically indicated. Data were analyzed according to the intention-to-treat principle. RESULTS There was no significant between-group difference in the rate of proximal leg deep-vein thrombosis, which occurred in 96 of 1873 patients (5.1%) receiving dalteparin versus 109 of 1873 patients (5.8%) receiving unfractionated heparin (hazard ratio in the dalteparin group, 0.92; 95% confidence interval [CI], 0.68 to 1.23; P = 0.57). The proportion of patients with pulmonary emboli was significantly lower with dalteparin (24 patients, 1.3%) than with unfractionated heparin (43 patients, 2.3%) (hazard ratio, 0.51; 95% CI, 0.30 to 0.88; P = 0.01). There was no significant between-group difference in the rates of major bleeding (hazard ratio, 1.00; 95% CI, 0.75 to 1.34; P = 0.98) or death in the hospital (hazard ratio, 0.92; 95% CI, 0.80 to 1.05; P = 0.21). In prespecified per-protocol analyses, the results were similar to those of the main analyses, but fewer patients receiving dalteparin had heparin-induced thrombocytopenia (hazard ratio, 0.27; 95% CI, 0.08 to 0.98; P = 0.046). CONCLUSIONS Among critically ill patients, dalteparin was not superior to unfractionated heparin in decreasing the incidence of proximal deep-vein thrombosis.
引用
收藏
页码:1305 / 1314
页数:10
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