Transfusion Error Surveillance System (TESS), 2022

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Organization: Public Health Agency of Canada

Published: 2024-07-12

TESS Project

The Transfusion Error Surveillance System (TESS) collects non-nominal data on errors that occur during the transfusion process for improving transfusion practices and patient safety. The surveillance system was initiated in 2005. TESS now monitors four provinces and territories and 16% of blood transfusion activities in Canada. Detailed methods of TESS can be found in the Transfusion error surveillance system (TESS) : 2012-2016 report.

Surveillance data summary

  • 9,746Footnote 1ErrorsFootnote 2 (e.g. blood sample labelled with incorrect patient identification) were reported in the year of 2022.
  • 0.03% of all reported errors (e.g. 3 / 9, 746) resulted in harmFootnote 3 to the patient.

Overall counts of reported errors for 2022Footnote 4

  • All ErrorsFootnote 2 (9,746; 100%)
    • Near Miss (8,959; 91.9%)
      • Planned Discovery (8,879; 99.1%)
      • Unplanned Discovery (80; 0.9%)
    • Actual Event (787; 8.1%)
      • Harm (3; 0.4%)
      • No Harm (784; 99.6%)

Location of error occurrence

  • Transfusion laboratory 19%
  • Outpatient clinics /procedures 15%
  • Operating room 12%
  • Obstetrics 2%
  • Medical/ surgical ward 20%
  • ICU 12%
  • Emergency 17%
  • Others 3%

Harm caused by errors, TESS 2022

Implication

Reporting and investigating errors in both transfusion services and clinical settings help identify and control risks before resulting in harm to the patient, thus providing valuable opportunities to improve transfusion safety.

Learn more about TESS

Visit Canada.ca and search "Transfusion Error Surveillance System" and Follow us on Twitter @GovCanHealth

Footnotes

Footnote 1

As a result of comparing dynamic data extracted from web-based databases, small discrepancies between PHAC and provincial or territorial numbers are expected.

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Footnote 2

The Transfusion Error Surveillance System (TESS): 2012-2016 report contains the definition of "error", "harm", "near miss", "actual event", "planned discovery", and "unplanned discovery"

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Footnote 3

"Harm": the patient had an unintended or inadequate response to transfusion or suffered a negative impact or adverse transfusion reaction as a result of the error.

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Footnote 4

Due to rounding, percentages may not always add up to 100%.

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Footnote 5

FNHR: febrile non-hemolytic reaction.

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Footnote 6

Other includes: 1 case of harm was associated with transfusion delay

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Footnote 7

TACO: transfusion-associated circulatory overload

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