Skip to content

Patient Blood Management - Use and Outcome

Patient Blood Management - Use and Outcome

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02473666
Acronym
PBM-USZ
Enrollment
250000
Registered
2015-06-16
Start date
2012-01-31
Completion date
2019-12-31
Last updated
2020-11-12

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

Conditions

Hemorrhage

Keywords

Patient Blood Management, Red Blood Cells, Platelet

Brief summary

Study the influence of transfusion related Patient Blood Management Program actions on transfusion-related outcome measures and cost.

Detailed description

At the University Hospital of Zurich, an in-house designed monitoring and feedback system was introduced which electronically registers each transfusion of any allogeneic blood product, be it red blood cells, plasma or platelets as well as corresponding laboratory data. Results are reported quarterly to Department heads. The investigator analyzes whether the introduction of this monitoring and feedback system as part of a patient blood management Program has a significant influence on use of allogeneic blood product transfusions and transfusion-related costs, without compromising patient outcome.

Interventions

None listed

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Only case records, all discharged patients of the University Hospital of Zürich

Exclusion criteria

* Not discharged from our Hospital.

Design outcomes

Primary

MeasureTime frameDescription
Percentage of transfusions per participantparticipants will be followed form date of hospital entry until date of discharge or date of death up to 3 yearsParticipant wich had transfusion will be identified and the administrative, financial and clinical data will be compared to participants without transfusions

Secondary

MeasureTime frameDescription
Percentage of transfusion of any blood product per participantparticipants will be followed form date of hospital entry until date of discharge or date of death up to 3 yearsCount of any blood products per case, QM Data
Cost of any blood product per participantparticipants will be followed form date of hospital entry until date of discharge or date of death up to 3 yearscosts per case
Survey of Patient Blood Management Systemparticipants will be followed form date of hospital entry until date of discharge or date of death up to 3 yearsclinical, financial,and administrative data of all participants will be reviewed on the focus on transfusions

Countries

Switzerland

Outcome results

None listed

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