Fillet Anne-Marie, Desmarets Maxime, Assari Suzanne, Quaranta Jean-François, François Anne, Pugin Aurore, Schuhmacher Anne, Lassale Bernard, Monnet Elisabeth, Cabre Philippe, Legrand Dominique, Binda Delphine, Djoudi Rachid
Medical Department, Etablissement Français du Sang, La Plaine Saint Denis, France.
Centre d'investigation clinique Inserm CIC1431, CHRU de Besançon, Besançon, France.
Transfusion. 2016 Dec;56(12):3033-3041. doi: 10.1111/trf.13887. Epub 2016 Nov 2.
Blood 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.
A 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.
A 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 × 10 and 50 × 10 /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.
Except for insufficient FFP dosing per patient and limitations on assessment of indications for prescribing, transfusion practices were in agreement with national guidelines.
2000年至2011年间,法国血液制品的使用量有所增加。为了解这种增长的原因,需要更新有关输血患者和输血实践的数据。
对医疗机构进行了一项全国性横断面调查。在2011年随机选择的一个24小时时间段内,收集了输血的诊断和指征、输血前实验室结果以及所使用的血液制品。纳入了所有在调查日接受至少一种血液制品输注的患者。
共为4720名患者申请了10794单位的血液制品:8688单位红细胞(RBC)、842单位血小板(PLT)浓缩物和1264单位新鲜冰冻血浆(FFP)。血液学和癌症病理患者占输血患者的46%,34%的患者在手术情况下接受输血,32.4%的输血患者正在接受对输血有影响的药物治疗。近一半的RBC输血是在血红蛋白水平低于8 g/dL时进行的。预防性PLT输血的患者中,分别有56.9%和86.6%的患者PLT计数低于20×10⁹/L和50×10⁹/L时进行了处方。RBC和PLT的输血实践符合国家指南。FFP单位占所有处方的8.0%。其中,57.4%是在急性出血情况下申请的,8.4%用于血浆置换。在非手术情况下(不包括血浆置换)FFP使用量的中位数(n = 2)表明FFP剂量不足。
除了每位患者FFP剂量不足以及处方指征评估存在局限性外,输血实践符合国家指南。