A prospective evaluation of standard versus battery-powered sequential compression devices in postsurgical patients

Am J Surg. 2015 Apr;209(4):675-81. doi: 10.1016/j.amjsurg.2014.06.017. Epub 2014 Aug 7.

Abstract

Background: Sequential compression devices (SCDs) reduce deep venous thrombosis in postsurgical patients, but the use is hindered by poor compliance.

Methods: General and orthopedic surgery patients (n = 67) were randomized to standard- or battery-powered SCDs. Compliance was documented hourly. Nurses and patients were issued a survey to assess barriers to compliance and device satisfaction.

Results: Compliance with standard SCDs was 47% compared with 85% with battery-powered SCDs (P < .001). The most common barriers identified by nurses and patients were ambulation and transfers, which were mitigated with the battery-powered device. A majority (79%) of those issued a battery-powered device reported no major problems compared with only 14% of patients issued a standard device (P < .005).

Conclusions: The dual venous thromboembolism prevention strategies of early mobilization and SCD utilization can be met with the appropriate equipment.

Keywords: Compression devices; Deep venous thrombosis; Prophylaxis; Quality improvement; Venous thromboembolism.

Publication types

  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Electric Power Supplies
  • Equipment Design
  • Female
  • Humans
  • Intermittent Pneumatic Compression Devices*
  • Male
  • Middle Aged
  • Patient Compliance / statistics & numerical data
  • Postoperative Complications / prevention & control*
  • Prospective Studies
  • Venous Thrombosis / prevention & control*