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Trials / Completed

CompletedNCT01604083

European Transfusion Practice and Outcome Study

European Transfusion Practice and Outcome Study A Multi-central Evaluation of Standard of Transfusion Care and Clinical Outcome for Elective Surgical Patients. Observational Study.

Status
Completed
Phase
Study type
Observational
Enrollment
6,066 (actual)
Sponsor
European Society of Anaesthesiology · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of the ETPOS study is to describe differences in transfusion habits throughout Europe and to correlate these habits to perioperative outcome parameters. Special focus is put on the number of PRBCs (packed red blood cells) transfused and the ratio of PRBCs to other blood products or coagulation factors in the operating room. Furthermore the motivation of physicians to transfuse PRBC and blood products in the operating room will be investigated.

Detailed description

In European patients undergoing elective non-cardiac surgery receiving at least one PRBC(packed red blood cells) during their surgery it is proposed to: 1. Evaluate evidence of differences in the standard of peri-operative transfusion care in different healthcare systems within Europe, and the use of blood conserving techniques. 1. Evaluate the ratio of transfusion of PRBC to blood products in the operating room 2. Evaluate which factors determine transfusion of PRBC (is it patient's haemodynamics / haemoglobin threshold/ pressure from the surgeon / acute brisk bleeding / else) and blood products (ratio to PRBC / POC (point of care) monitoring/ per protocol/ else) in the operating room 2. Evaluate whether there are factors in transfusion therapy that are associated with outcome (in-hospital mortality and unplanned admission to ICU(Intensive Care Unit).)

Conditions

Timeline

Start date
2013-04-01
Primary completion
2013-10-01
Completion
2013-12-01
First posted
2012-05-23
Last updated
2019-05-01

Locations

9 sites across 8 countries: Croatia, Czechia, Estonia, Germany, Greece, Israel, Spain, Sweden

Source: ClinicalTrials.gov record NCT01604083. Inclusion in this directory is not an endorsement.