Abstract
The national reference Center for blood groups checked samples of reagents and devices used in France for a definitive verification of pretransfusion ABO tests performed at the patient's bedside, as defined by French health authority regulations. The results of an initial inquiry was published in 1991. The new study shows no significant improvement of the quality of reagents and devices. This is a major concern considering the importance of ABO incompatibility in severe hemolytic transfusion reactions.
MeSH terms
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ABO Blood-Group System / analysis*
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Blood Banking / methods
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Blood Banks / statistics & numerical data*
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Blood Group Incompatibility / diagnosis*
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Blood Grouping and Crossmatching / instrumentation
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Blood Grouping and Crossmatching / methods
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Blood Grouping and Crossmatching / statistics & numerical data*
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Blood Transfusion
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Data Collection
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Erythrocyte Transfusion
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Evaluation Studies as Topic
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Forms and Records Control
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France
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Humans
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Indicators and Reagents
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Medical Records
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Reproducibility of Results
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Safety
Substances
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ABO Blood-Group System
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Indicators and Reagents