Diagnostic accuracy and effectiveness of automated electronic sepsis alert systems: A systematic review

Abstract
BACKGROUND Although timely treatment of sepsis improves outcomes, delays in administering evidence‐based therapies are common. PURPOSE To determine whether automated real‐time electronic sepsis alerts can: (1) accurately identify sepsis and (2) improve process measures and outcomes. DATA SOURCES We systematically searched MEDLINE, Embase, The Cochrane Library, and Cumulative Index to Nursing and Allied Health Literature from database inception through June 27, 2014. STUDY SELECTION Included studies that empirically evaluated 1 or both of the prespecified objectives. DATA EXTRACTION Two independent reviewers extracted data and assessed the risk of bias. Diagnostic accuracy of sepsis identification was measured by sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and likelihood ratio (LR). Effectiveness was assessed by changes in sepsis care process measures and outcomes. DATA SYNTHESIS Of 1293 citations, 8 studies met inclusion criteria, 5 for the identification of sepsis (n = 35,423) and 5 for the effectiveness of sepsis alerts (n = 6894). Though definition of sepsis alert thresholds varied, most included systemic inflammatory response syndrome criteria ± evidence of shock. Diagnostic accuracy varied greatly, with PPV ranging from 20.5% to 53.8%, NPV 76.5% to 99.7%, LR+ 1.2 to 145.8, and LR− 0.06 to 0.86. There was modest evidence for improvement in process measures (ie, antibiotic escalation), but only among patients in non–critical care settings; there were no corresponding improvements in mortality or length of stay. Minimal data were reported on potential harms due to false positive alerts. CONCLUSIONS Automated sepsis alerts derived from electronic health data may improve care processes but tend to have poor PPV and do not improve mortality or length of stay. Journal of Hospital Medicine 2015;10:396–402. © 2015 Society of Hospital Medicine
Funding Information
  • National Center for Advancing Translational Sciences (KL2TR001103)
  • Agency for Healthcare Research and Quality (R24HS022428-01)
  • National Institutes of Health (T32 HP19025-07-00)
  • National Heart, Lung, and Blood Institute (K24HL098372)