Jump to: Page Content, Site Navigation, Site Search,
You are seeing this message because your web browser does not support basic web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.
Leon G Fine a Department of Medicine, Royal Free and University
College Medical School, University College London, London WC1E
6JJ, b Department of
Cardiothoracic Surgery, Queen Elizabeth Hospital, Birmingham B15
2TH, c RAND Health, PO Box 2138 Santa Monica, CA
90407-2138, USA
Correspondence to: L G Fine l.fine{at}ucl.ac.uk
Objectives:
To assess the quality and
completeness of a database of clinical outcomes after cardiac surgery
and to determine whether a process of validation, monitoring, and
feedback could improve the quality of the database.
What is already know in this topic
The tacit assumption is that such outcomes data are accurate and can be
relied on by the public and by healthcare providers to guide
improvements What this study adds
An independent short process of monitoring, validation, and feedback
improved the quality of the database Such databases probably require an ongoing process of monitoring in
order to allow data of adequate quality to be generated for the purpose
of improving healthcare outcomes
Design:
Stratified sampling of retrospective data followed by prospective re-sampling of database after intervention of
monitoring, validation, and feedback.
Setting:
Ten tertiary care cardiac surgery centres in
the United Kingdom.
Intervention:
Validation of data derived from a
stratified sample of case notes (recording of deaths cross checked with
mortuary records), monitoring of completeness and accuracy of data
entry, feedback to local data managers and lead surgeons.
Main outcome measures:
Average percentage
missing data, average
coefficient, and reliability score by centre
for 17 variables required for assignment of risk scores. Actual minus
risk adjusted mortality in each centre.
Results:
The database was incomplete, with a mean
(SE) of 24.96% (0.09%) of essential data elements missing, whereas only 1.18% (0.06%) were missing in the patient records (P<0.0001). Intervention was associated with (a) significantly less
missing data (9.33% (0.08%) P<0.0001); (b) marginal
improvement in reliability of data and mean (SE) overall centre
reliability score (0.53 (0.15) v 0.44 (0.17)); and
(c) improved accuracy of assigned Parsonnet risk scores (
0.84 v 0.70). Mortality scores (actual minus risk adjusted
mortality) for all participating centres fell within two standard
deviations of the mean score.
Conclusion:
A short period of independent validation, monitoring, and feedback improved the quality of an outcomes database and improved the process of risk adjustment, but with substantial room
for further improvement. Wider application of this approach should
increase the credibility of similar databases before their public release.
Release of healthcare outcomes into the public domain has altered
referral patterns and has led to improvement in some centres and
elimination of others
Sampling of a published national cardiac surgery database in England
revealed it to be both incomplete and unreliable in its ability to
yield accurate, risk adjusted outcomes data
Read all Rapid Responses