Decreasing clinically significant adverse events using feedback to emergency physicians of telephone follow-up outcomes
Study objective
We evaluate the effect on adverse events of a telephone follow-up quality improvement program.
Methods
This was a before-and-after intervention comparison based on prospectively collected data in a tertiary care hospital emergency department (ED) (82,000 visits per year). The first half (April 15 to July 31, 2001) served as control, and the second half (August 1 to November 15, 2001) served as intervention with feedback to physicians on telephone follow-up outcomes of discharged patients and resident training about the uncertain presentations of serious diseases and the need to use additional evaluation on selected patients (observation unit, hospital admission). Telephone follow-up of the high-risk patients and retrospective review of 3-day return visits were used to quantify outcome measures: return visits to EDs and clinically significant adverse events (return visits with serious misdiagnoses or an erroneous management plan). The differences in proportions of outcomes were measured with 95% confidence intervals (CIs).
Results
High-risk patients were enrolled: 566 (13.7%) of 4,139 discharged patients in the before-intervention period and 397 (11.3%) of 3,507 in the after-intervention period. The quality improvement initiative decreased return visits on enrolled patients from 10.1% (57/566) to 4.9% (19/397) (5.2% difference with 95% CI 1.8% to 8.8%) and decreased clinically significant adverse events from 4.1% (23/566) to 1.5% (6/397) (2.6% difference with 95% CI 0.3% to 4.8%). For all ED discharged patients, clinically significant adverse events decreased from 0.9% (39/4,139) to 0.4% (15/3,507) (0.5% difference with 95% CI 0.1% to 0.9%). During the study, the observation rate increased 4.3% (95% CI 2.8% to 5.7%), and the admission rate increased 3.4% (95% CI 2.1% to 4.8%).
Conclusion
A quality improvement program with feedback to physicians of telephone follow-up and resident education can decrease clinically significant adverse events in ED discharged patients.
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Author contributions: CHC conceived the study, designed the trial, and obtained the research funding. CHC, CKH, LMW, and CHL were involved in the performance of the trial and data collection. CHC analyzed the data. CHC and LG drafted the manuscript, and all authors contributed substantially to its revision. CHC takes responsibility for the paper as a whole.Presented at the American College of Emergency Physicians Research Forum, Seattle, WA, October 2002.This study was supported by 2001-2002 Education Improvement Grant of Veterans General Hospital–Taipei (grant numbers 375-6 and V90-439-3).
PII: S0196-0644(04)01288-0
doi:10.1016/j.annemergmed.2004.08.012
© 2005 American College of Emergency Physicians. Published by Elsevier Inc. All rights reserved.
