Skip to content

Common Causes of Blood Transfusion Events in a University Hospital: Analysis of Incident Reports

Common Causes of Blood Transfusion Events in a University Hospital: Analysis of Incident Reports.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01812499
Enrollment
131
Registered
2013-03-18
Start date
2013-01-31
Completion date
Unknown
Last updated
2013-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blood Transfusion Events

Keywords

blood transfusion, adverse event, incident reporting

Brief summary

Inhospital the blood transfusion process consists of many phases: ordering the blood product, analysis of the blood sample, delivery, transport and storage of the blood product and administration. In each of these phases (near) accidents may occur. A severe transfusion incident refers to the transfusion of a wrong blood product, whereas a near miss is detected before transfusion. In 2010 the University Hospitals Leuven introduced a new electronic patient incident report system for transfusion events. In this study the investigators will analyze the reported blood transfusion events to detect the most common causes of blood transfusion events and the weakest link in the blood transfusion chain.

Detailed description

A retrospective survey will be conducted of all transfusion events reported in the University Hospitals Leuven between January 2011 and July 2012. Both severe accidents and near misses will be included. Data will be drawn from the incident report system. Data concerning the number of transfused blood products will be required from the Medical Administration Service. Events will be classified according to the severity and the cause of the event. The different settings where the events took place will be compared using a chi-square test (p\<0,05).

Interventions

None listed

Sponsors

Universitaire Ziekenhuizen KU Leuven
Lead SponsorOTHER

Study design

Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* all transfusion events reported in the University Hospitals Leuven between January 2011 and July 2012 * Both severe accidents and near misses were included

Exclusion criteria

* Transfusion reactions

Design outcomes

Primary

MeasureTime frameDescription
Severity of inhospital blood transfusion eventsup to 1,5 yearsincluded events will be classified into near misses or severe incidents

Secondary

MeasureTime frameDescription
Causes of inhospital blood transfusion eventsup to 1,5 yearsEvents are classified into human error, technical problems, deficiency of the blood product and others. Events will also be classified considering the phase in the blood transfusion process. Causes will be studied hospital wide and per setting were the event took place.

Other

MeasureTime frameDescription
Incidence of inhospital blood transfusion eventsup to 1,5 yearsThe number of transfusion events divided by the total number of transfused blood products in the study period
Is there a relation between misidentification events and the setting where the event took place?up to 1,5 yearsThe different settings where the events took place will be compared using a chi-square test (p\<0,05).

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026