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An electronic trigger based on care escalation to identify preventable adverse events in hospitalised patients
  1. Viraj Bhise1,2,
  2. Dean F Sittig3,
  3. Viralkumar Vaghani1,2,
  4. Li Wei1,2,
  5. Jessica Baldwin1,2,
  6. Hardeep Singh1,2
  1. 1 Center for Innovations in Quality, Effectiveness, and Safety (IQuESt), Michael E DeBakey Veterans Affairs Medical Center, Houston, Texas, USA
  2. 2 Department of Medicine, Baylor College of Medicine, Houston, Texas, USA
  3. 3 School of Biomedical Informatics, University of Texas Health Science Center, Houston, Texas, USA
  1. Correspondence to Dr Hardeep Singh, Department of Medicine, Baylor College of Medicine, 2002 Holcombe Blvd, 152, Houston, Texas 77030, USA; hardeeps{at}bcm.edu

Abstract

Background Methods to identify preventable adverse events typically have low yield and efficiency. We refined the methods of Institute of Healthcare Improvement’s Global Trigger Tool (GTT) application and leveraged electronic health record (EHR) data to improve detection of preventable adverse events, including diagnostic errors.

Methods We queried the EHR data repository of a large health system to identify an ‘index hospitalization’ associated with care escalation (defined as transfer to the intensive care unit (ICU) or initiation of rapid response team (RRT) within 15 days of admission) between March 2010 and August 2015. To enrich the record review sample with unexpected events, we used EHR clinical data to modify the GTT algorithm and limited eligible patients to those at lower risk for care escalation based on younger age and presence of minimal comorbid conditions. We modified the GTT review methodology; two physicians independently reviewed eligible ‘e-trigger’ positive records to identify preventable diagnostic and care management events.

Results Of 88 428 hospitalisations, 887 were associated with care escalation (712 ICU transfers and 175 RRTs), of which 92 were flagged as trigger-positive and reviewed. Preventable adverse events were detected in 41 cases, yielding a trigger positive predictive value of 44.6% (reviewer agreement 79.35%; Cohen’s kappa 0.573). We identified 7 (7.6%) diagnostic errors and 34 (37.0%) care management-related events: 24 (26.1%) adverse drug events, 4 (4.3%) patient falls, 4 (4.3%) procedure-related complications and 2 (2.2%) hospital-associated infections. In most events (73.1%), there was potential for temporary harm.

Conclusion We developed an approach using an EHR data-based trigger and modified review process to efficiently identify hospitalised patients with preventable adverse events, including diagnostic errors. Such e-triggers can help overcome limitations of currently available methods to detect preventable harm in hospitalised patients.

  • diagnostic errors
  • triggers
  • adverse events
  • escalation of care
  • ICU
  • rapid response
  • patient safety

This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

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Footnotes

  • Twitter @HardeepSinghMD

  • Contributors Study concept and design: VB, HS, DFS. Acquisition of data: VB, LW. Statistical analysis: VB. Analysis and interpretation of data: VB, HS. Drafting of the manuscript: VB. Critical revision of the manuscript for important intellectual content: VB, DFS, VV, LW, JLB, HS. Administrative, technical or material support: VB, DFS, VV, LW, JLB, HS. Study supervision: VB, DFS, HS.

  • Funding Dr. Singh is supported by the VA Health Services Research and Development Service (CRE 12-033; Presidential Early Career Award for Scientists and Engineers USA 14-274), the VA National Center for Patient Safety, the Agency for Healthcare Research and Quality (R01HS022087 and R21HS023602), and the Houston VA HSR&D Center for Innovationsin Quality, Effectiveness and Safety (CIN 13-413).

  • Competing interests None declared.

  • Ethics approval Baylor College of Medicine IRB.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data sharing statement Sensitive data not available to be shared.