Reporting of near-miss events for transfusion medicine: improving transfusion safety

J L Callum1, H S Kaplan, L L Merkley

  • 1Sunnybrook and Women's College Health Sciences Centre, and The University of Toronto, Toronto, Ontario, Canada. jeannie.callum@swchsc.on.ca

Transfusion
|October 19, 2001
PubMed
Abstract

Insights

A no-fault medical-event reporting system for transfusion medicine (MERS-TM) captured 819 transfusion errors and near-misses, identifying critical patient safety issues. Innovative error prevention is needed, as current methods are insufficient.

Area of Science:

  • Transfusion Medicine
  • Patient Safety
  • Medical Error Analysis

Background:

  • Medical errors contribute to serious adverse events in transfusion medicine.
  • A no-fault medical-event reporting system for transfusion medicine (MERS-TM) was developed to capture and analyze transfusion-related errors and near-misses.

Purpose of the Study:

  • To evaluate the effectiveness of the MERS-TM in identifying the frequency and patterns of transfusion-related errors.
  • To assess the types and origins of errors within the transfusion process.

Main Methods:

  • A prospective audit of transfusion-related errors was conducted over 19 months.
  • The MERS-TM was utilized to record events and near-misses.
  • Data analysis focused on error frequency, patterns, and severity.

Main Results:

  • 819 events and near-misses were recorded, with a median of 51 per month.
  • 61 events (7.4%) were potentially life-threatening, including sample collection/labeling errors and incorrect blood requests.
  • Near-misses were five times more frequent than errors, and 68% were detected before blood issuance.

Conclusions:

  • The MERS-TM effectively identified and analyzed transfusion errors, revealing patterns and enabling monitoring.
  • Despite no permanent injuries from recorded events, current error-detection mechanisms are inadequate.
  • Innovative strategies are required to prevent transfusion errors proactively.

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