Matar Charbel F, Kahale Lara A, Hakoum Maram B, Tsolakian Ibrahim G, Etxeandia-Ikobaltzeta Itziar, Yosuico Victor Ed, Terrenato Irene, Sperati Francesca, Barba Maddalena, Schünemann Holger, Akl Elie A
Department of Internal Medicine, American University of Beirut Medical Center, Riad El Solh, Beirut, Lebanon, 1107 2020.
Cochrane Database Syst Rev. 2018 Jul 11;7(7):CD009447. doi: 10.1002/14651858.CD009447.pub3.
The choice of the appropriate perioperative thromboprophylaxis for people with cancer depends on the relative benefits and harms of different anticoagulants.
To systematically review the evidence for the relative efficacy and safety of anticoagulants for perioperative thromboprophylaxis in people with cancer.
This update of the systematic review was based on the findings of a comprehensive literature search conducted on 14 June 2018 that included a major electronic search of Cochrane Central Register of Controlled Trials (CENTRAL, 2018, Issue 6), MEDLINE (Ovid), and Embase (Ovid); handsearching of conference proceedings; checking of references of included studies; searching for ongoing studies; and using the 'related citation' feature in PubMed.
Randomized controlled trials (RCTs) that enrolled people with cancer undergoing a surgical intervention and assessed the effects of low-molecular weight heparin (LMWH) to unfractionated heparin (UFH) or to fondaparinux on mortality, deep venous thrombosis (DVT), pulmonary embolism (PE), bleeding outcomes, and thrombocytopenia.
Using a standardized form, we extracted data in duplicate on study design, participants, interventions outcomes of interest, and risk of bias. Outcomes of interest included all-cause mortality, PE, symptomatic venous thromboembolism (VTE), asymptomatic DVT, major bleeding, minor bleeding, postphlebitic syndrome, health related quality of life, and thrombocytopenia. We assessed the certainty of evidence for each outcome using the GRADE approach (GRADE Handbook).
Of 7670 identified unique citations, we included 20 RCTs with 9771 randomized people with cancer receiving preoperative prophylactic anticoagulation. We identified seven reports for seven new RCTs for this update.The meta-analyses did not conclusively rule out either a beneficial or harmful effect of LMWH compared with UFH for the following outcomes: mortality (risk ratio (RR) 0.82, 95% confidence interval (CI) 0.63 to 1.07; risk difference (RD) 9 fewer per 1000, 95% CI 19 fewer to 4 more; moderate-certainty evidence), PE (RR 0.49, 95% CI 0.17 to 1.47; RD 3 fewer per 1000, 95% CI 5 fewer to 3 more; moderate-certainty evidence), symptomatic DVT (RR 0.67, 95% CI 0.27 to 1.69; RD 3 fewer per 1000, 95% CI 7 fewer to 7 more; moderate-certainty evidence), asymptomatic DVT (RR 0.86, 95% CI 0.71 to 1.05; RD 11 fewer per 1000, 95% CI 23 fewer to 4 more; low-certainty evidence), major bleeding (RR 1.01, 95% CI 0.69 to 1.48; RD 0 fewer per 1000, 95% CI 10 fewer to 15 more; moderate-certainty evidence), minor bleeding (RR 1.01, 95% CI 0.76 to 1.33; RD 1 more per 1000, 95% CI 34 fewer to 47 more; moderate-certainty evidence), reoperation for bleeding (RR 0.93, 95% CI 0.57 to 1.50; RD 4 fewer per 1000, 95% CI 22 fewer to 26 more; moderate-certainty evidence), intraoperative transfusion (mean difference (MD) -35.36 mL, 95% CI -253.19 to 182.47; low-certainty evidence), postoperative transfusion (MD 190.03 mL, 95% CI -23.65 to 403.72; low-certainty evidence), and thrombocytopenia (RR 3.07, 95% CI 0.32 to 29.33; RD 6 more per 1000, 95% CI 2 fewer to 82 more; moderate-certainty evidence). LMWH was associated with lower incidence of wound hematoma (RR 0.70, 95% CI 0.54 to 0.92; RD 26 fewer per 1000, 95% CI 39 fewer to 7 fewer; moderate-certainty evidence). The meta-analyses found the following additional results: outcomes intraoperative blood loss (MD -6.75 mL, 95% CI -85.49 to 71.99; moderate-certainty evidence); and postoperative drain volume (MD 30.18 mL, 95% CI -36.26 to 96.62; moderate-certainty evidence).In addition, the meta-analyses did not conclusively rule out either a beneficial or harmful effect of LMWH compared with Fondaparinux for the following outcomes: any VTE (DVT or PE, or both; RR 2.51, 95% CI 0.89 to 7.03; RD 57 more per 1000, 95% CI 4 fewer to 228 more; low-certainty evidence), major bleeding (RR 0.74, 95% CI 0.45 to 1.23; RD 8 fewer per 1000, 95% CI 16 fewer to 7 more; low-certainty evidence), minor bleeding (RR 0.83, 95% CI 0.34 to 2.05; RD 8fewer per 1000, 95% CI 33 fewer to 52 more; low-certainty evidence), thrombocytopenia (RR 0.35, 95% CI 0.04 to 3.30; RD 14 fewer per 1000, 95% CI 20 fewer to 48 more; low-certainty evidence), any PE (RR 3.13, 95% CI 0.13 to 74.64; RD 2 more per 1000, 95% CI 1 fewer to 78 more; low-certainty evidence) and postoperative drain volume (MD -20.00 mL, 95% CI -114.34 to 74.34; low-certainty evidence) AUTHORS' CONCLUSIONS: We found no difference between perioperative thromboprophylaxis with LMWH versus UFH and LMWH compared with fondaparinux in their effects on mortality, thromboembolic outcomes, major bleeding, or minor bleeding in people with cancer. There was a lower incidence of wound hematoma with LMWH compared to UFH.
为癌症患者选择合适的围手术期血栓预防措施取决于不同抗凝剂的相对获益和危害。
系统评价抗凝剂用于癌症患者围手术期血栓预防的相对疗效和安全性的证据。
本系统评价的更新基于2018年6月14日进行的全面文献检索结果,包括对Cochrane对照试验中心注册库(CENTRAL,2018年第6期)、MEDLINE(Ovid)和Embase(Ovid)进行的大型电子检索;查阅会议论文集;检查纳入研究的参考文献;搜索正在进行的研究;以及使用PubMed中的“相关引用”功能。
纳入接受手术干预的癌症患者的随机对照试验(RCT),并评估低分子量肝素(LMWH)与普通肝素(UFH)或磺达肝癸钠相比对死亡率、深静脉血栓形成(DVT)、肺栓塞(PE)、出血结局和血小板减少症的影响。
我们使用标准化表格,对研究设计、参与者、感兴趣的干预结局和偏倚风险进行了重复数据提取。感兴趣的结局包括全因死亡率、PE、有症状的静脉血栓栓塞(VTE)、无症状DVT、大出血、小出血、血栓后综合征、健康相关生活质量和血小板减少症。我们使用GRADE方法(GRADE手册)评估每个结局的证据确定性。
在7670条识别出的独特引文中,我们纳入了20项RCT,共9771名接受术前预防性抗凝的癌症随机患者。我们为本更新确定了7项新RCT的7份报告。荟萃分析未明确排除LMWH与UFH相比在以下结局方面的有益或有害影响:死亡率(风险比(RR)0.82,95%置信区间(CI)0.63至1.07;风险差(RD)每1000人少9例,95%CI每1000人少19例至多4例;中等确定性证据)、PE(RR 0.49,95%CI 0.17至1.47;RD每1000人少3例,95%CI每1000人少5例至多3例;中等确定性证据)、有症状DVT(RR 0.67,95%CI 0.27至1.69;RD每1000人少3例,95%CI每1000人少7例至多7例;中等确定性证据)、无症状DVT(RR 0.86,95%CI 0.71至1.05;RD每1000人少11例,95%CI每1000人少23例至多4例;低确定性证据)、大出血(RR 1.01,95%CI 0.69至1.48;RD每1000人少0例,95%CI每1000人少10例至多15例;中等确定性证据)、小出血(RR 1.01,95%CI 0.76至1.33;RD每1000人多1例,95%CI每1000人少34例至多47例;中等确定性证据)、因出血再次手术(RR 0.93,95%CI 0.57至1.50;RD每1000人少4例,95%CI每1000人少22例至多26例;中等确定性证据)、术中输血(平均差(MD)-35.36 mL,95%CI -253.19至182.47;低确定性证据)、术后输血(MD 190.03 mL,95%CI -23.65至403.72;低确定性证据)和血小板减少症(RR 3.07,95%CI 0.32至29.33;RD每1000人多6例,95%CI每1000人少2例至多82例;中等确定性证据)。LMWH与较低的伤口血肿发生率相关(RR 0.70,95%CI 0.54至0.92;RD每1000人少26例,95%CI每1000人少39例至多7例;中等确定性证据)。荟萃分析还发现了以下其他结果:术中失血量(MD -6.75 mL,95%CI -85.49至71.99;中等确定性证据);以及术后引流量(MD 30.18 mL,95%CI -36.26至96.62;中等确定性证据)。此外,荟萃分析未明确排除LMWH与磺达肝癸钠相比在以下结局方面的有益或有害影响:任何VTE(DVT或PE,或两者兼有;RR 2.51,95%CI 0.89至7.03;RD每1000人多57例,95%CI每1000人少4例至多228例;低确定性证据)、大出血(RR 0.74,95%CI 0.45至1.23;RD每1000人少8例,95%CI每1000人少16例至多7例;低确定性证据)、小出血(RR 0.83,95%CI 0.34至2.05;RD每1000人少8例,95%CI每1000人少33例至多52例;低确定性证据)、血小板减少症(RR 0.35,95%CI 0.04至3.30;RD每1000人少14例,95%CI每1000人少20例至多48例;低确定性证据)、任何PE(RR 3.13,95%CI 0.13至74.64;RD每1000人多2例,95%CI每1000人少1例至多78例;低确定性证据)和术后引流量(MD -20.00 mL,95%CI -114.34至74.34;低确定性证据)
我们发现,在癌症患者中,LMWH与UFH进行围手术期血栓预防以及LMWH与磺达肝癸钠进行围手术期血栓预防在对死亡率、血栓栓塞结局、大出血或小出血的影响方面没有差异。与UFH相比,LMWH的伤口血肿发生率较低。