Shalhoub J, Norrie J, Baker C, Bradbury A W, Dhillon K, Everington T, Gohel M S, Hamady Z, Heatley F, Hudson J, Hunt B J, Lawton R, Stansby G, Stephens-Boal A, Toh S, Warwick D, Davies A H
Academic Section of Vascular Surgery, Department of Surgery & Cancer, Imperial College London, UK.
Centre for Healthcare Randomised Trials, Health Services Research Unit, University of Aberdeen, UK.
Eur J Vasc Endovasc Surg. 2017 Jun;53(6):880-885. doi: 10.1016/j.ejvs.2017.02.013. Epub 2017 Apr 7.
The evidence base upon which current global venous thromboembolism (VTE) prevention recommendations have been made is not optimal. The cost of purchasing and applying graduated compression stockings (GCS) in surgical patients is considerable and has been estimated at £63.1 million per year in England alone.
The aim was to determine whether low dose low molecular weight heparin (LMWH) alone is non-inferior to a combination of GCS and low dose LMWH for the prevention of VTE.
The randomised controlled Graduated compression as an Adjunct to Pharmacoprophylaxis in Surgery (GAPS) Trial (ISRCTN 13911492) will randomise adult elective surgical patients identified as being at moderate and high risk of VTE to receive either the current "standard" combined thromboprophylactic LMWH with GCS mechanical thromboprophylaxis, or thromboprophylactic LMWH pharmacoprophylaxis alone. To show non-inferiority (3.5% non-inferiority margin) for the primary endpoint of all VTE within 90 days, 2236 patients are required. Recruitment will be from seven UK centres. Secondary outcomes include quality of life, compliance with stockings and LMWH, overall mortality, and GCS or LMWH related complications (including bleeding). Recruitment commenced in April 2016 with the seven UK centres coming "on-line" in a staggered fashion. Recruitment will be over a total of 18 months. The GAPS trial is funded by the National Institute for Health Research Health Technology Assessment in the UK (14/140/61).
当前全球静脉血栓栓塞症(VTE)预防建议所依据的证据并不理想。在外科手术患者中购买和使用分级压力弹力袜(GCS)的成本相当高,仅在英格兰每年估计就达6310万英镑。
旨在确定单独使用低剂量低分子量肝素(LMWH)在预防VTE方面是否不劣于GCS与低剂量LMWH联合使用。
“手术中药物预防辅助分级压力疗法”(GAPS)随机对照试验(ISRCTN 13911492)将把被确定为VTE中度和高度风险的成年择期手术患者随机分组,分别接受当前的“标准”联合血栓预防措施,即LMWH与GCS机械性血栓预防措施,或仅接受LMWH药物性血栓预防措施。为了在90天内所有VTE的主要终点上显示非劣效性(非劣效性界限为3.5%),需要2236名患者。招募将来自英国的七个中心。次要结局包括生活质量、对弹力袜和LMWH的依从性、总体死亡率以及与GCS或LMWH相关的并发症(包括出血)。招募于2016年4月开始,英国的七个中心将陆续“上线”。招募将持续18个月。GAPS试验由英国国家卫生研究院卫生技术评估机构资助(14/140/61)。