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Adverse events and near miss reporting in the NHS
  1. R Shaw1,2,
  2. F Drever1,
  3. H Hughes1,
  4. S Osborn1,
  5. S Williams1
  1. 1National Patient Safety Agency, London, UK
  2. 2Hammersmith Hospitals NHS Trust, London, UK
  1. Correspondence to:
 Professor R Shaw

Abstract

Objectives: To conduct a multicentre study on adverse event and near miss reporting in the NHS and to explore the feasibility of creating a national system for collecting these data.

Design: Prospective voluntary reporting by staff with anonymised transfer of data was used by a national system to collect data from 18 NHS trusts.

Participants: Staff from 12 acute trusts, three mental health trusts, two ambulance trusts, and one primary care trust.

Main outcomes measured: Number of incidents, date and time of incident, patient age and sex, clinical speciality, location, outcome, risk rating, type and description of incident.

Results: A total of 28 998 incidents were reported including 11 766 (41%) slips, trips and falls, 2514 (9%) medication management incidents, 2429 (8%) resource issues, and 2164 (7%) treatment issues. 138 catastrophic and 260 major adverse outcomes were reported. Slips, trips and falls (n = 11 766) were the most common type of incident.

Conclusions: Voluntary reporting by staff when linked to a multicentre data collecting system can yield information on a large number of incidents. This provides support for the principle of creating a national IT system to collect and analyse incident data.

  • patient safety
  • incident reporting
  • adverse events

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Footnotes

  • Conflict of interest: none.

    These data have been made public in an appendix to the NPSA Business Plan 2002/3.