02544nas a2200349   4500000000100000008004100001100001700042700001300059700001300072700001600085700001700101700001600118700001700134700001300151700001500164700001600179700001900195700001700214700001700231700001600248700001700264700001300281700001400294700001300308245021900321250001500540300000800555490000700563050001600570520155700586020005102143       2016                            d1 aFinfer Simon1 aMehta S.1 aArabi Y.1 aAlsolamy S.1 aAl-Dawood A.1 aAl-Omari A.1 aAl-Hameed F.1 aBurns K.1 aAlmaani M.1 aLababidi H.1 aA. Bshabshe Al1 aAl-Aithan A.1 aMandourah Y.1 aMekhlafi G.1 aAbdukahil S.1 aAfesh L.1 aDbsawy M.1 aSadat M.00aThromboprophylaxis using combined intermittent pneumatic compression and pharmacologic prophylaxis versus pharmacologic prophylaxis alone in critically ill patients: study protocol for a randomized controlled trial  a2016/08/05  a3900 v17  a[IF]: 1.7313 a<p>
BACKGROUND: Venous thromboembolism (VTE) remains a common problem in critically ill patients. Pharmacologic prophylaxis is currently the standard of care based on high-level evidence from randomized controlled trials. However, limited evidence exists regarding the effectiveness of intermittent pneumatic compression (IPC) devices. The Pneumatic compREssion for preventing VENous Thromboembolism (PREVENT trial) aims to determine whether the adjunct use of IPC with pharmacologic prophylaxis compared to pharmacologic prophylaxis alone in critically ill patients reduces the risk of VTE. METHODS/DESIGN: The PREVENT trial is a multicenter randomized controlled trial, which will recruit 2000 critically ill patients from over 20 hospitals in three countries. The primary outcome is the incidence of proximal lower extremity deep vein thrombosis (DVT) within 28 days after randomization. Radiologists interpreting the scans are blinded to intervention allocation, whereas the patients and caregivers are unblinded. The trial has 80 % power to detect a 3 % absolute risk reduction in proximal DVT from 7 to 4 %. DISCUSSION: The first patient was enrolled in July 2014. As of May 2015, a total of 650 patients have been enrolled from 13 centers in Saudi Arabia, Canada and Australia. The first interim analysis is anticipated in July 2016. We expect to complete recruitment by 2018. TRIAL REGISTRATION: Clinicaltrials.gov: NCT02040103 (registered on 3 November 2013). Current controlled trials: ISRCTN44653506 (registered on 30 October 2013).
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