In vitro interference of the red cell substitute pyridoxalated hemoglobin-polyoxyethylene with blood compatibility, coagulation, and clinical chemistry testing
| Autor: | Robert H. Christenson, Mahmoud D. Elfath, Linda C. Gregory, Benjamin F. Trump, Show-Hong Duh, Colin F. Mackenzie, Gladys L. Alonsozana |
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| Rok vydání: | 1997 |
| Předmět: |
Rouleaux
Prothrombin time medicine.diagnostic_test business.industry Pharmacology Fibrinogen Polyethylene Glycols Hemoglobins Anesthesiology and Pain Medicine Blood Grouping and Crossmatching Blood Substitutes ABO blood group system Chemistry Clinical Immunology medicine Coagulation testing Humans Liver function Cardiology and Cardiovascular Medicine Liver function tests business Blood Coagulation medicine.drug Partial thromboplastin time |
| Zdroj: | Journal of cardiothoracic and vascular anesthesia. 11(7) |
| ISSN: | 1053-0770 |
| Popis: | Objectives: Pyridoxalated hemoglobin-polyoxyethylene (PHP) is a prototypical red cell substitute approved for phase I studies. Peripheral blood smears of human blood mixed with PHP in 1 to 4 g/dL concentrations showed dose-dependent red cell aggregation and rouleaux. Whether this aggregation limits interpretation of blood compatibility testing and whether the intense coloration of serum or plasma containing PHP affects routine coagulation and clinical chemistry measurements was tested. Design: In vitro studies. Setting: University hospital laboratory. Participants: Four healthy volunteers, blood types A, B, AB, and O. All were Rh+. Measurements and Main Results: ABO typing, Rh typing, and antibody screening and coagulation studies were performed on blood: PHP admixtures having final concentrations of 1, 2, and 4 g/dL. For clinical chemistry interference studies, known concentrations of analytes were added to a serum matrix containing PHP ABO (forward) and Rh typing showed no interference in the three concentrations tested. Reverse ABO typing and antibody screening showed rouleaux at 4 g/dL, which corrected with routine saline replacement. Partial thromboplastin time (PTT), prothrombin time (PT), and fibrinogen showed no clinically significant differences from the controls. Results for electrolytes, renal function analytes, and markers of cardiac injury were acceptable by standard laboratory methods. However, results of liver function tests were unacceptable in PHPcontaining specimens. Conclusions: PHP-induced aggregation was observed with high PHP concentration; however, compatibility testing was not affected because agglutination was corrected by saline replacement, which is standard practice. Although routine blood banking, coagulation, and most clinical chemistry analytes can be measured reliably, alternative methods and strategies are needed for assessing liver function in the presence of PHP. |
| Databáze: | OpenAIRE |
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