ABSTRACT

A classification o f acute b lood loss is show n in Table 14.1. First, there is the im m ediate o r u rgen t need for red b lood cells and, in som e instances, o th er b lood products. Patients presenting w ith acute hem orrhage w ith loss o f less th an 40% o f the ir b lood volum e m ay tolerate fluid replacem ent w ith crystalloids, assum ing a n o rm al hem oglobin level before the acute event. A problem , however, m ay be estim ating the loss o f intravascular volum e and the po ten tial for fu rther red b lood cell loss. Ordinarily, for Class 1 and Class 2 acute trau m a patients (Table 14.1), red cell transfusions are n o t needed, particu larly in young patients w ho can adap t well to the acute b lood loss anem ia, assum ing th a t contro l o f hem orrhage has been, o r is likely to be, achieved. If in excess o f 40% blood volum e loss has oc­ cu rred in young patients, o r less in elderly people w ho m ay have pre-existing com ­ prom ised critical organ function , the u rgen t need for red b lood cell transfusions m ay exist. Two difficulties arise in this setting. ( 1 ) The circum stances m ay n o t allow the collection o f a sam ple for routine com patibility testing (C hapter 7). Trans­ fusion o f b lood g roup O red cells to these individuals is an appropria te early m ea­ sure. Rhesus negative units should be used, if possible, and in all situations for females o f child bearing age, arb itra rily u n d er the age o f 50 years. (2) If m ore tim e allows, a b lood sam ple can be collected. U nfortunately the no rm al identification m echanism s for insuring sam ple in tegrity m ay n o t be followed appropriately b e ­ cause o f pressures in dealing w ith p a tien t resuscitation. An inappropria tely la­ beled specim en o r a m isidentified specim en is then received in the b lood bank, resulting in frustra tion on the p a rt o f the em ergency room and b lood ban k p e r­ sonnel. For inappropria tely labeled specim ens, the con tinued release o f group O blood rem ains necessary. M islabeled specim ens are particu larly dangerous in this setting as the stage is set for an acute hem olytic reaction (C hapter 32). It is essen­ tial to collect and label the specim en correctly at the p o in t o f sam ple collection an d th e ph lebotom ist m u st sign (and date) the specim en. A specim en collected in to an unlabeled tube, w hich is rem oved from the p o in t o f collection and labeled elsewhere, is dangerous. In sum m ary, if tim e precludes adherence to correct label­ ing protocol, it is better to con tinue to transfuse g roup O (uncrossm atched) blood.