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An adverse event screening tool based on routinely collected hospital-acquired diagnoses
Caroline Brand1, Joanne Tropea, Alexandra Gorelik
1Centre for Research Excellence in Patient Safety, Monash University, Melbourne, Victoria, Australia. caroline.brand@mh.org.au
Objective:
The aim was to develop an electronic adverse event (AE) screening tool applicable to acute care hospital episodes for patients admitted with chronic heart failure (CHF) and pneumonia.
Design:
Consensus building using a modified Delphi method and descriptive analysis of hospital discharge data.
Participants:
Consultant physicians in general medicine (n = 38).
Intervention:
In-hospital acquired (C-prefix) diagnoses associated with CHF and pneumonia admissions to 230 hospitals in Victoria, Australia, were extracted from the Victorian Admitted Episodes Data Set between July 2004 and June 2007. A 9-point rating scale was used to prioritize diagnoses acquired during hospitalization (routinely coded as a 'C-prefix' diagnosis to distinguish from diagnoses present on admission) for inclusion within an AE screening tool. Diagnoses rated a group median score between 7 and 9 by the physician panel were included.
Main Outcome Measures:
Selection of C-prefix diagnoses with a group median rating of 7-9 in a screening tool, and the level of physician agreement, as assessed using the Interpercentile Range Adjusted for Symmetry.
Results:
Of 697 initial C-prefix diagnoses, there were high levels of agreement to include 113 (16.2%) in the AE screening tool. Using these selected diagnoses, a potential AE was flagged in 14% of all admissions for the two index conditions. Intra-rater reliability for each clinician ranged from kappa 0.482 to 1.0.
Conclusions:
A high level of physician agreement was obtained in selecting in-hospital diagnoses for inclusion in an AE screening tool based on routinely collected data. These results support further tool validation.
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