Skip Navigation

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow E-Letters: Submit a response to the article
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (2)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Bridgland, I. A.
Right arrow Articles by Menon, D. K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bridgland, I. A.
Right arrow Articles by Menon, D. K.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

British Journal of Anaesthesia, 2001, Vol. 87, No. 5 678-681
© 2001 The Board of Management and Trustees of the British Journal of Anaesthesia


Editorial

Editorial II

Monitoring medical devices: the need for new evaluation methodology

I. A. Bridgland and D. K. Menon

The publication of the document entitled ‘An organisation with a memory: report of an expert group on learning from adverse events in the NHS chaired by the Chief Medical Officer’1 by the Department of Health (DoH) last year has focused attention on preventable failures in NHS care. It was observed that the mechanisms for detecting, reporting and analysing failures were incomplete and frequently flawed. Following on from this, it was noted that, in cases where important lessons were learned, there was often a failure to embed these into future practice, resulting in repetition of the same failures. The National Patient Safety Agency2 has recently been created to address these issues.

The observations made in the DoH document are particularly true in the areas of perioperative medicine and critical care, where several factors predispose to failure of care. These factors include the proliferation of high-technology medical devices;3 the low signal provided . . . [Full Text of this Article]

Detecting failures attributable to poor usability

Difficulties in reporting and analysing usability problems

Implications for active learning

Strategic approaches to usability analysis: problems and potential solutions

Implications for equipment design

References


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
PerfusionHome page
C. Hamilton
Critical assessment of new devices
Perfusion, May 1, 2007; 22(3): 167 - 171.
[PDF]