Blood Products in Cardiac Surgery

NCT02068755 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 31000

Last updated 2014-02-21

No results posted yet for this study

Summary

Blood transfusion is a common procedure essential for the treatment of patients undergoing cardiac surgery. Inappropriate transfusions, however, not only incur needless healthcare costs, but increase unnecessary risks due to transfusion reactions and infectious and immunomodulative causes. Safe and appropriate patient care requires evaluated blood component prescription practices.

Practically all patients undergoing cardiac surgery in Finland have a blood product booking from the Finnish Red Cross Blood Service. This registry contains large volumes of transfusion-related information on all Finnish patients undergoing cardiac surgery in Finnish centers. Participating hospitals were scattered to all geographical areas in Finland and concentrated to the most populated regions.

Data on the blood product use, laboratory findings one month pre-operatively and 12 months post-operatively were available.

Finnish hospitals have been required to provide information on hospital visits for the Finnish National Research and Development Centre for Welfare and Health for healthcare planning purposes. We used in part the original data sent by hospitals to the Finnish Hospital Discharge Register (FHDR).

Conditions

Sponsors & Collaborators

  • Finnish Red Cross Blood Service

    collaborator OTHER
  • Central Finland Hospital District

    collaborator OTHER
  • Turku University Hospital

    collaborator OTHER_GOV
  • Oulu University Hospital

    collaborator OTHER
  • Tampere University Hospital

    collaborator OTHER
  • Kuopio University Hospital

    collaborator OTHER
  • Helsinki University Central Hospital

    collaborator OTHER
  • Satakunta Central Hospital

    collaborator OTHER
  • University of Turku

    lead OTHER

Principal Investigators

  • Pirjo Mustonen, MD, PhD · Central Finland Central Hospital

  • Juhani Airaksinen, Prof · Turku University Hospital and University of Turku

  • Fausto Biancari, MD, PhD · Oulu University Hospital

  • Tuomas O Kiviniemi, Md, PhD · Turku University Hospital and University of Turku

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2002-01-31
Primary Completion
2012-12-31
Completion
2012-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02068755 on ClinicalTrials.gov