Patient-Oriented Evidence That Matters
Pneumatic Compression in Addition to Pharmacologic Thromboprophylaxis Does Not Further Reduce DVT Risk
Am Fam Physician. 2019 Oct 1;100(7):440-441.
Does the addition of intermittent pneumatic compression to pharmacologic thromboprophylaxis further decrease the risk of deep venous thrombosis (DVT) in critically ill patients?
This study found no benefit to the addition of intermittent pneumatic compression to pharmacologic anticoagulation for the prevention of proximal DVT in critically ill patients. Although this finding was consistent across per-protocol and sensitivity analyses, the study itself was underpowered because of a low incidence of DVT in the control group. The possibility of a clinically important effect of the intervention, either benefit or harm, is not completely excluded. (Level of Evidence = 1b–)
Current guidelines recommend pharmacologic thromboprophylaxis in all critically ill patients. In this international multicenter study, researchers investigated whether the addition of mechanical thromboprophylaxis with intermittent pneumatic compression would further reduce the risk of DVT in these patients. Adult patients expected to be in the intensive care unit (ICU) for at least 72 hours were randomized, using concealed allocation, to receive pneumatic compression (n = 991) or pharmacologic thromboprophylaxis alone (n = 1,012). Both groups received pharmacologic thromboprophylaxis with unfractionated heparin or low-molecular-weight heparin. In the pneumatic compression group, patients also received intermittent compression to both lower limbs for at least 18 hours per day. Although sequential compression devices with thigh-length sleeves were preferred, nonsequential devices and knee-length sleeves, as well as foot pumps, were permitted. In the control group, pneumatic compression was only permitted during times when pharmacologic thromboprophylaxis was interrupted. Proximal venous ultrasonography of the lower limbs was performed 48 hours after randomization and then twice weekly if DVT was clinically suspected. The two groups were balanced at baseline: the mean age was 58 years, almost 80% of patients were medical admissions to the ICU, and two-thirds were receiving mechanical ventilation. The primary outcome of new proximal lower limb DVT did not differ significantly between the two groups (3.9% in the pneumatic compression group vs. 4.2% in the control group; relative risk = 0.93; 95% CI, 0.60 to 1.44; P = .74). There were no significant differences detected in any secondary outcomes, including pulmonary embolisms, death, or skin injuries related to pneumatic compression. Because the incidence of DVT in the control group was lower than an expected 7%, this trial was underpowered to detect a difference if it truly exists.
Study design: Randomized controlled trial (nonblinded)
Funding source: Government
Setting: Inpatient (ICU only)
Reference: Arabi YM, Al-Hameed F, Burns KE, et al.; Saudi Critical Care Trials Group. Adjunctive intermittent pneumatic compression for venous thromboprophylaxis. N Engl J Med. 2019;380(14):1305–1315.
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