O'Toole Robert V, Stein Deborah M, O'Hara Nathan N, Frey Katherine P, Taylor Tara J, Scharfstein Daniel O, Carlini Anthony R, Sudini Kuladeep, Degani Yasmin, Slobogean Gerard P, Haut Elliott R, Obremskey William, Firoozabadi Reza, Bosse Michael J, Goldhaber Samuel Z, Marvel Debra, Castillo Renan C
From the Departments of Orthopedics (R.V.O., N.N.O., Y.D., G.P.S.) and Surgery (D.M.S.), R Adams Cowley Shock Trauma Center, the University of Maryland School of Medicine, Department of Health Policy and Management, Johns Hopkins Bloomberg School of Public Health (K.P.F., T.J.T., A.R.C., K.S., R.C.C.), the Department of Surgery, John Hopkins Hospital (E.R.H.), and the PREVENT CLOT Patient and Stakeholder Committee (D.M.) - all in Baltimore; the Department of Population Health Science, University of Utah, Salt Lake City (D.O.S.); the Department of Orthopaedic Surgery, Vanderbilt University Medical Center, Nashville (W.O.); the Department of Orthopaedics and Sports Medicine, University of Washington, Seattle (R.F.); the Department of Orthopaedic Surgery, Atrium Health Carolinas Medical Center, Charlotte, NC (M.J.B.); and the Department of Medicine, Harvard Medical School, Boston (S.Z.G.).
N Engl J Med. 2023 Jan 19;388(3):203-213. doi: 10.1056/NEJMoa2205973.
Clinical guidelines recommend low-molecular-weight heparin for thromboprophylaxis in patients with fractures, but trials of its effectiveness as compared with aspirin are lacking.
In this pragmatic, multicenter, randomized, noninferiority trial, we enrolled patients 18 years of age or older who had a fracture of an extremity (anywhere from hip to midfoot or shoulder to wrist) that had been treated operatively or who had any pelvic or acetabular fracture. Patients were randomly assigned to receive low-molecular-weight heparin (enoxaparin) at a dose of 30 mg twice daily or aspirin at a dose of 81 mg twice daily while they were in the hospital. After hospital discharge, the patients continued to receive thromboprophylaxis according to the clinical protocols of each hospital. The primary outcome was death from any cause at 90 days. Secondary outcomes were nonfatal pulmonary embolism, deep-vein thrombosis, and bleeding complications.
A total of 12,211 patients were randomly assigned to receive aspirin (6101 patients) or low-molecular-weight heparin (6110 patients). Patients had a mean (±SD) age of 44.6±17.8 years, 0.7% had a history of venous thromboembolism, and 2.5% had a history of cancer. Patients received a mean of 8.8±10.6 in-hospital thromboprophylaxis doses and were prescribed a median 21-day supply of thromboprophylaxis at discharge. Death occurred in 47 patients (0.78%) in the aspirin group and in 45 patients (0.73%) in the low-molecular-weight-heparin group (difference, 0.05 percentage points; 96.2% confidence interval, -0.27 to 0.38; P<0.001 for a noninferiority margin of 0.75 percentage points). Deep-vein thrombosis occurred in 2.51% of patients in the aspirin group and 1.71% in the low-molecular-weight-heparin group (difference, 0.80 percentage points; 95% CI, 0.28 to 1.31). The incidence of pulmonary embolism (1.49% in each group), bleeding complications, and other serious adverse events were similar in the two groups.
In patients with extremity fractures that had been treated operatively or with any pelvic or acetabular fracture, thromboprophylaxis with aspirin was noninferior to low-molecular-weight heparin in preventing death and was associated with low incidences of deep-vein thrombosis and pulmonary embolism and low 90-day mortality. (Funded by the Patient-Centered Outcomes Research Institute; PREVENT CLOT ClinicalTrials.gov number, NCT02984384.).
临床指南推荐使用低分子量肝素对骨折患者进行血栓预防,但缺乏与阿司匹林相比其有效性的试验。
在这项实用、多中心、随机、非劣效性试验中,我们纳入了18岁及以上因四肢骨折(从髋部至中足或肩部至腕部的任何部位)接受手术治疗或患有任何骨盆或髋臼骨折的患者。患者被随机分配在住院期间接受每日两次30mg剂量的低分子量肝素(依诺肝素)或每日两次81mg剂量的阿司匹林。出院后,患者继续根据各医院的临床方案接受血栓预防。主要结局是90天时任何原因导致的死亡。次要结局是非致命性肺栓塞、深静脉血栓形成和出血并发症。
共有12211名患者被随机分配接受阿司匹林(6101例)或低分子量肝素(6110例)。患者的平均(±标准差)年龄为44.6±17.8岁,0.7%有静脉血栓栓塞病史,2.5%有癌症病史。患者住院期间平均接受8.8±10.6次血栓预防剂量,出院时开具的血栓预防药物中位数为21天用量。阿司匹林组有47例患者(0.78%)死亡,低分子量肝素组有45例患者(0.73%)死亡(差异为0.05个百分点;96.2%置信区间为-0.27至0.38;非劣效性界值为0.75个百分点,P<0.001)。阿司匹林组2.51%的患者发生深静脉血栓形成,低分子量肝素组为1.71%(差异为0.80个百分点;95%CI为0.28至1.31)。两组的肺栓塞发生率(每组1.49%)、出血并发症及其他严重不良事件相似。
在接受手术治疗的四肢骨折或任何骨盆或髋臼骨折患者中,阿司匹林进行血栓预防在预防死亡方面不劣于低分子量肝素,且深静脉血栓形成和肺栓塞发生率低,90天死亡率也低。(由患者为中心的结果研究机构资助;PREVENT CLOT临床试验注册号,NCT02984384。)