Volume 51, Issue s1 pp. 34S-37S

Improving the predictive value of red blood cell storage trials: lessons from the Biomedical Excellence for Safer Transfusion (BEST) Collaborative Trial 41

John R. Hess

John R. Hess

From the University of Maryland School of Medicine, University of Maryland Medical Center, Baltimore, Maryland.

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First published: 11 January 2011
Citations: 1
John R. Hess, MD, MPH, FACP, FAAAS, University of Maryland School of Medicine, c/o Blood Bank, N2W50a, University of Maryland Medical Center, 22 South Greene Street, Baltimore, MD 21201-1595; e-mail: [email protected].

Abstract

BACKGROUND: Storage system trials are conducted for the development and licensure of new red blood cell (RBC) storage systems or to validate new ways of using existing systems. Results from one laboratory are often difficult to reproduce in another laboratory, leading to confusion.

STUDY DESIGN AND METHODS: A large international trial was designed to test the warm overnight hold using common donor collection systems and pooling of units to reduce interlaboratory variability of measures of RBC storage. Methods of measurement were left to the individual laboratories. pH was measured on both laboratory pH meters and clinical blood gas machines. Adenosine 5′-monophosphate (ATP) was measured by a variety of methods.

RESULTS: Intralaboratory variability of measures of pH and ATP were small compared to interlaboratory variability. Initial pH measures between laboratories varied over 0.4 pH units, while RBC ATP concentrations varied 2 to 10 µMol/g hemoglobin. pH variability was partly related to temperature of measurement, but the variability in ATP measures was a problem of both methods and standards.

CONCLUSIONS: Common methods and shared standards between laboratories would improve the interpretation of RBC storage measurements. Improved comparability between major laboratories would speed the development of better RBC storage systems.

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