Jump to content

National Congenital Heart Disease Audit

Add links
From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by BrownHairedGirl (talk | contribs) at 02:42, 25 April 2022 (add {{Use dmy dates}}). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

National Congenital Heart Disease Audit (NCHDA) (formerly called the Central Cardiac Audit Database) is a database established in 2000 for quality assurance purposes, to monitor the outcome for an individual who has undergone cardiac treatment.[1] It comprises six national heart disease audits. Each audit enables health professionals to continually measure and improve care by comparing their work to specific standards and national trend. These audits from 2011 are part of the National Institute for Cardiovascular Outcomes Research formerly at University College London and in April 2015 moved to St. Bartholomew's Hospital.[2]

Audits

The following audits are available within the CCAD:

References

  1. ^ Paul R. Barach; Jeffery P. Jacobs; Steven E. Lipshultz; Peter C. Laussen (4 December 2014). Pediatric and Congenital Cardiac Care: Volume 1: Outcomes Analysis. Springer. p. 219. ISBN 978-1-4471-6587-3. Retrieved 27 January 2021.
  2. ^ Denne, Lin; Alam, H. (21 November 2017). The National Congenital Heart Disease Audit - Data Quality Audit 2016/17. National Institute for Cardiovascular Outcomes Research. p. 2. {{cite book}}: |website= ignored (help)


Retrieved from "https://en.wikipedia.org/w/index.php?title=National_Congenital_Heart_Disease_Audit&oldid=1084538382"