Blood products use in France: a nationwide cross-sectional survey
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Titre | Blood products use in France: a nationwide cross-sectional survey |
Type de publication | Journal Article |
Year of Publication | 2016 |
Auteurs | Fillet A-M, Desmarets M, Assari S, Quaranta J-F, Francois A, Pugin A, Schuhmacher A, Lassale B, Monnet E, Cabre P, Legrand D, Binda D, Djoudi R |
Journal | TRANSFUSION |
Volume | 56 |
Pagination | 3033-3041 |
Date Published | DEC |
Type of Article | Article |
ISSN | 0041-1132 |
Résumé | BACKGROUNDBlood products use has increased in France between 2000 and 2011. To understand the reasons for this increase, data about transfused patients and transfusion practices needed to be updated. STUDY DESIGN AND METHODSA nationwide cross-sectional survey was performed with health care establishments. Diagnoses and indication for the transfusion, pretransfusion laboratory results, and blood products used were collected during a randomly selected 24-hour period in 2011. All patients who received at least one blood product delivered on the survey day were included. RESULTSA total of 10,794 blood products were requested for 4720 patients: 8688 red blood cell (RBC) units, 842 platelet (PLT) concentrates, and 1264 fresh-frozen plasma (FFP) units. Hematologic and cancer pathologies included 46% of transfused patients, 34% of the patients had transfusions in a surgical context, and 32.4% of transfused patients were receiving medication with an impact on transfusion. Nearly half of RBC transfusions were performed with hemoglobin levels of less than 8 g/dL. PLT transfusions for prophylactic indication were prescribed with PLT counts of less than 20 x 10(9) and 50 x 10(9)/L in 56.9 and 86.6% of patients, respectively. RBCs and PLTs transfusion practices were in agreement with national guidelines. FFP units were involved in 8.0% of all prescriptions. Among these, 57.4% were requested in the context of an acute hemorrhage and 8.4% for plasma exchange. The median of FFP use (n=2) in a nonsurgical context, excluding plasma exchange, suggests an insufficient dosing of FFP. CONCLUSIONExcept for insufficient FFP dosing per patient and limitations on assessment of indications for prescribing, transfusion practices were in agreement with national guidelines. |
DOI | 10.1111/trf.13887 |