Quality and safety review for performance improvement is important for systems of care and is required for US academic emergency departments (EDs). Assessment of the impact of patient safety initiatives in the context of increasing burdens of quality measurement compels standardized, meaningful, high-yield approaches for performance review. Limited data describe how quality and safety reviews are currently conducted and how well they perform in detecting patient harm and areas for improvement. We hypothesized that decades-old approaches used in many academic EDs are inefficient and low yield for identifying patient harm.
We conducted a prospective observational study to evaluate the efficiency and yield of current quality review processes at five academic EDs for a 12-month period. Sites provided descriptions of their current practice and collected summary data on the number and severity of events identified in their reviews and the referral sources that led to their capture. Categories of common referral sources were established at the beginning of the study. Sites used the Institute for Healthcare Improvement's definition in defining an adverse event and a modified National Coordinating Council for Medication Error Reporting and Prevention (MERP) Index for grading severity of events.
Participating sites had similar processes for quality review, including a two-level review process, monthly reviews and conferences, similar screening criteria, and a grading system for evaluating cases. In 60 months of data collection, we reviewed a total of 4735 cases and identified 381 events. This included 287 near-misses, errors/events (MERP A–I) and 94 adverse events (AEs) (MERP E–I). The overall AE rate (event rate with harm) was 1.99 (95% confidence interval = 1.62%–2.43%), ranging from 1.24% to 3.47% across sites. The overall rate of quality concerns (events without harm) was 6.06% (5.42%–6.78%), ranging from 2.96% to 10.95% across sites. Seventy-two–hour returns were the most frequent referral source used, accounting for 47% of the cases reviewed but with a yield of only 0.81% in identifying harm. Other referral sources similarly had very low yields. External referrals were the highest yield referral source, with 14.34% (10.64%–19.03%) identifying AEs. As a percentage of the 94 AEs identified, external referrals also accounted for 41.49% of cases.
With an overall adverse event rate of 1.99%, commonly used referral sources seem to be low yield and inefficient for detecting patient harm. Approximately 6% of the cases identified by these criteria yielded a near miss or quality concern. New approaches to quality and safety review in the ED are needed to optimize their yield and efficiency for identifying harm and areas for improvement.
From the *Division of Emergency Medicine, Washington University in St. Louis, St. Louis, Missouri; †Department of Emergency Medicine, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin; ‡Department of Emergency Medicine, University of Colorado School of Medicine, Denver, Colorado; §Department of Emergency Medicine, Yale University School of Medicine, New Haven, Connecticut; ∥Department of Emergency Medicine, University of Missouri-Columbia School of Medicine, Columbia, Missouri; ¶Department of Emergency Medicine, Christiana Care, Wilmington, Delaware; **Department of Medicine, University of Central Florida; and ††Office of Clinical Effectiveness, Adventist Health System, Altamonte, Florida.
Correspondence: Richard T. Griffey, MD, MPH, FACEP, Division of Emergency Medicine, Associate Professor, Washington University School of Medicine, Washington University Institute for Public Health, Campus Box 8072, 660 S Euclid Ave, Barnes-Jewish Hospital, St. Louis, MO 63117 (e-mail: firstname.lastname@example.org).
The authors disclose no conflict of interest.