Adjunctive Intermittent Pneumatic Compression for Venous Thromboprophylaxis

Hassan Hawa, Sami Alsolamy, Yaseen M. Arabi, Ghaleb A. Almekhlafi, Abdulaziz Al‐Dawood, Lara Afesh, Yatin Mehta, Sangeeta Mehta, Ali Al Bshabshe, Karen E. A. Burns, Hani Lababidi, Simon Finfer, Sheryl Ann Abdukahil, Fahad Al-Hameed, Mohammed Alshahrani, Yasser Mandourah, Mohammed Almaani, Zia Arshad, Imran Khalid, Atul Gaur, Hergen Buscher, Abdulsalam Al Aithan, Jesna Jose
2019-02-18

SCID:  54.1/zum89xnd
BACKGROUND: Whether adjunctive intermittent pneumatic compression in critically ill patients receiving pharmacologic thromboprophylaxis would result in a lower incidence of deep-vein thrombosis than pharmacologic thromboprophylaxis alone is uncertain. METHODS: We randomly assigned patients who were considered adults according to the local standards at the participating sites (≥14, ≥16, or ≥18 years of age) within 48 hours after admission to an intensive care unit (ICU) to receive either intermittent pneumatic compression for at least 18 hours each day in addition to pharmacologic thromboprophylaxis with unfractionated or low-molecular-weight heparin (pneumatic compression group) or pharmacologic thromboprophylaxis alone (control group). The primary outcome was incident (i.e., new) proximal lower-limb deep-vein thrombosis, as detected on twice-weekly lower-limb ultrasonography after the third calendar day since randomization until ICU discharge, death, attainment of full mobility, or trial day 28, whichever occurred first. RESULTS: A total of 2003 patients underwent randomization - 991 were assigned to the pneumatic compression group and 1012 to the control group. Intermittent pneumatic compression was applied for a median of 22 hours (interquartile range, 21 to 23) daily for a median of 7 days (interquartile range, 4 to 13). The primary outcome occurred in 37 of 957 patients (3.9%) in the pneumatic compression group and in 41 of 985 patients (4.2%) in the control group (relative risk, 0.93; 95% confidence interval [CI], 0.60 to 1.44; P = 0.74). Venous thromboembolism (pulmonary embolism or any lower-limb deep-vein thrombosis) occurred in 103 of 991 patients (10.4%) in the pneumatic compression group and in 95 of 1012 patients (9.4%) in the control group (relative risk, 1.11; 95% CI, 0.85 to 1.44), and death from any cause at 90 days occurred in 258 of 990 patients (26.1%) and 270 of 1011 patients (26.7%), respectively (relative risk, 0.98; 95% CI, 0.84 to 1.13). CONCLUSIONS: Among critically ill patients who were receiving pharmacologic thromboprophylaxis, adjunctive intermittent pneumatic compression did not result in a significantly lower incidence of proximal lower-limb deep-vein thrombosis than pharmacologic thromboprophylaxis alone. (Funded by King Abdulaziz City for Science and Technology and King Abdullah International Medical Research Center; PREVENT ClinicalTrials.gov number, NCT02040103; Current Controlled Trials number, ISRCTN44653506.).
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2019-02-18
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Hassan Hawa
Sami Alsolamy
Yaseen M. Arabi
Ghaleb A. Almekhlafi
Abdulaziz Al‐Dawood
Lara Afesh
Yatin Mehta
Sangeeta Mehta
Ali Al Bshabshe
Karen E. A. Burns
Hani Lababidi
Simon Finfer
Sheryl Ann Abdukahil
Fahad Al-Hameed
Mohammed Alshahrani
Yasser Mandourah
Mohammed Almaani
Zia Arshad
Imran Khalid
Atul Gaur
Hergen Buscher
Abdulsalam Al Aithan
Jesna Jose
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