From the University of Texas Southwestern Medical Center, Dallas, Texas; the University of New Mexico Health Sciences Center, Albuquerque, New Mexico; the University Hospitals Case Medical Center, Cleveland, Ohio; Women and Infants Hospital of Rhode Island/Brown Medical School, Providence, Rhode Island; Medical College of Wisconsin, Waukesha, Wisconsin; Hartford Hospital/University of Connecticut School of Medicine, Hartford, Connecticut; the University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania; Eastern Virginia Medical School, Norfolk, Virginia; and Tufts Medical Center, Boston, Massachusetts.
Obstet Gynecol. 2011 Nov;118(5):1111-1125. doi: 10.1097/AOG.0b013e318232a394.
To comprehensively review and critically assess the available gynecologic surgery venous thromboembolism prophylaxis literature and provide clinical practice guidelines.
MEDLINE and Cochrane databases from inception to July 2010. We included randomized controlled trials in gynecologic surgery populations. Interventions and comparators included graduated compression stockings, intermittent pneumatic compression, unfractionated heparin, and low molecular weight heparin; placebo and routine postoperative care were allowed as comparators.
One thousand two hundred sixty-six articles were screened, and 14 randomized controlled trials (five benign gynecologic, nine gynecologic oncology) met eligibility criteria. In addition, nine prospective or retrospective studies with at least 150 women were identified and provided data on venous thromboembolism risk stratification, gynecologic laparoscopy, and urogynecologic populations.
TABULATION, INTEGRATION, AND RESULTS: Two reviewers independently screened articles with discrepancies adjudicated by a third. Eligible randomized controlled trials were extracted for these characteristics: study, participant, surgery, intervention, comparator, and outcomes data, including venous thromboembolism incidence and bleeding complications. Studies were individually and collectively assessed for methodologic quality and strength of evidence. Overall incidence of clinical venous thromboembolism was 0-2% in the benign gynecologic population. With use of intermittent pneumatic compression for benign major procedures, venous thromboembolism incidence was less than 1%. No venous thromboembolisms were identified in prospective studies of benign laparoscopic procedures. Overall quality of evidence in the benign gynecologic literature was poor. Gynecologic-oncology randomized controlled trials reported venous thromboembolism incidence (including "silent" venous thromboembolisms) of 0-14.8% with prophylaxis and up to 34.6% without prophylaxis. Fair quality of evidence supports that unfractionated heparin and intermittent pneumatic compression are both superior to placebo or no intervention but insufficient to determine whether heparins are superior to intermittent pneumatic compression for venous thromboembolism prevention. Combining two of three risks (aged 60 years or older, cancer, or personal venous thromboembolism history) substantially elevated the risk of venous thromboembolism.
Intermittent pneumatic compression provides sufficient prophylaxis for the majority of gynecology patients undergoing benign surgery. Additional risk factors warrant the use of combined mechanical and pharmacologic prophylaxis.
全面回顾和评估现有的妇科手术静脉血栓栓塞预防文献,并提供临床实践指南。
从 MEDLINE 和 Cochrane 数据库的建立到 2010 年 7 月。我们纳入了妇科手术人群的随机对照试验。干预措施和比较包括梯度压缩袜、间歇性气动压缩、未分级肝素和低分子量肝素;允许安慰剂和常规术后护理作为比较。
筛选了 1266 篇文章,14 项随机对照试验(5 项良性妇科,9 项妇科肿瘤)符合入选标准。此外,还确定了 9 项前瞻性或回顾性研究,至少有 150 名女性提供了静脉血栓栓塞风险分层、妇科腹腔镜检查和尿妇科人群的数据。
表格、综合和结果:两位审查员独立筛选文章,有分歧的由第三位审查员裁决。提取合格的随机对照试验以获取以下特征:研究、参与者、手术、干预、比较和结局数据,包括静脉血栓栓塞发生率和出血并发症。对研究进行了个体和综合评估,以确定方法学质量和证据强度。良性妇科人群的临床静脉血栓栓塞总体发生率为 0-2%。使用间歇性气动压缩治疗良性大手术,静脉血栓栓塞发生率低于 1%。良性腹腔镜手术的前瞻性研究未发现静脉血栓栓塞。良性妇科文献的整体证据质量较差。妇科肿瘤学随机对照试验报告了预防措施下静脉血栓栓塞发生率(包括“沉默”静脉血栓栓塞)为 0-14.8%,无预防措施下高达 34.6%。有一定质量的证据支持未分级肝素和间歇性气动压缩均优于安慰剂或无干预,但不足以确定肝素是否优于间歇性气动压缩预防静脉血栓栓塞。将三个风险因素中的两个(年龄 60 岁或以上、癌症或个人静脉血栓栓塞史)结合起来,大大增加了静脉血栓栓塞的风险。
间歇性气动压缩为大多数接受良性手术的妇科患者提供了充分的预防措施。其他危险因素需要使用机械和药物联合预防。