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首页> 外文期刊>Journal of thrombosis and thrombolysis >Extended-duration versus short-duration pharmacological thromboprophylaxis in acutely Ill hospitalized medical patients: a systematic review and meta-analysis of randomized controlled trials
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Extended-duration versus short-duration pharmacological thromboprophylaxis in acutely Ill hospitalized medical patients: a systematic review and meta-analysis of randomized controlled trials

机译:延长持续时间对短持续时间药理血浆血栓药中急性病医疗患者:随机对照试验的系统评价和荟萃分析

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Extended- duration pharmacological thromboprophylaxis, for at least 28 days, is effective for the prevention of symptomatic venous thromboembolism (VTE) in high- risk surgical patients but is of uncertain benefit in hospitalized medical patients. We aimed to evaluate the efficacy and safety of extended- duration thromboprophylaxis in hospitalized medical patients. We conducted a systematic PubMed, Medline and EMBASE literature search until June 2016 and a meta- analysis of randomized controlled trials which compared extended- duration with short- duration thromboprophylaxis in hospitalized medical patients. Four randomized controlled trials comparing extendedduration prophylaxis (24- 47 days) with short- duration prophylaxis (6- 14 days) in a total of 34,068 acutely ill hospitalized medical patients were included. When compared with short- duration prophylaxis, extended- duration prophylaxis was associated with a decrease in symptomatic proximal or distal deep vein thrombosis (DVT) [relative risk (RR) = 0.52; 95% confidence interval (Cl): 0.35- 0.77: p = 0.001; absolute risk reduction (ARR) = 0.32%, number needed to treat (NNT) = 313], and symptomatic nonfatal pulmonary embolism (RR = 0.61; 95% Cl 0.38- 0.99: p = 0.04; ARR = 0.16%; NNT = 625), an increase in major bleeding (RR = 2.08; 95% Cl 1.50- 2.90: p < 0.0001, absolute risk increase = 0.41%, number needed to harm = 244), and no significant reduction in VTE- related mortality (RR = 0.69; 95% Cl 0.45- 1.06: p = 0.09) or all- cause mortality (RR = 1.00; 95% CI 0.89- 1.12; p = 0.95). There was heterogeneity for major bleeding due to results from the APEX trial (no difference between betrixaban and enoxaparin). Compared with short- duration thromboprophylaxis, extended- duration treatment reduces the risk for symptomatic DVT and non- fatal pulmonary embolism. Extended treatment with apixaban, enoxaparin and rivaroxaban but not betrixaban increases the risk for major bleeding.
机译:延长持续时间的药理学血浆丙基丙基脲至少28天对于预防高风险手术患者的症状静脉血栓栓塞(VTE)是有效的,但在住院医疗患者中是不确定的益处。我们旨在评估延长致癌血栓抑制在住院医疗患者中的疗效和安全性。我们在2016年6月进行了系统的PubMed,Medline和Embase文献搜索,并对随机对照试验的荟萃分析,其在住院医疗患者中与短期凝血性血栓血栓形成的延长持续时间。在共有34,068名急性病住院医疗患者中,四次随机受控试验比较延期预防预防(24-47天)的延期预防(6-14天)。与短期预防相比,延长持续时间预防与症状近端或远端深静脉血栓形成(DVT)的减少相关[相对风险(RR)= 0.52; 95%置信区间(CL):0.35- 0.77:P = 0.001;无能为止风险降低(ARR)= 0.32%,治疗(NNT)= 313]所需的数量,和症状非致肺栓塞(RR = 0.61; 95%CL 0.38- 0.99:P = 0.04; ARR = 0.16%; NNT = 625 ),主要出血增加(RR = 2.08; 95%Cl 1.50- 2.90:P <0.0001,绝对风险增加= 0.41%,危害= 244的数量,VTE-相关死亡率没有显着降低(RR = 0.69; 95%Cl 0.45- 1.06:p = 0.09)或所有导致死亡率(RR = 1.00; 95%CI 0.89- 1.12; P = 0.95)。由于APEX试验结果(Betrixaban和亚诺帕林之间没有差异),重大出血存在异质性。与短期凝血性血栓血管缺咽性相比,延长持续时间处理降低了症状DVT和非致命肺栓塞的风险。延长治疗含硒,脑诺卡林和Rivaroxaban,但不是Betrixaban增加了重大出血的风险。

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