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C H A P T E R  121 


                                                               PEDIATRIC TRANSFUSION MEDICINE


                                                             Cassandra D. Josephson and Steven R. Sloan





            A variety of neonatal and pediatric patients require blood component   compound that intercalates with nucleic acid and, on activa-
            transfusions. This chapter focuses on aspects of blood-bank labora-  tion  with  ultraviolet  (UV)  light,  cross-links  pathogen  and
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            tory testing, blood products and components, transfusion indications,   white blood cell DNA, inhibiting replication.  Almost all of
            and potential adverse events that are specifically relevant to neonates   the  amotosalen,  a  potential  carcinogen,  is  removed  during
            and children.                                              processing.  However,  INTERCEPT  platelets  are  contraindi-
                                                                       cated for neonatal patients treated with phototherapy devices
                                                                       emitting  wavelengths  <425 nm  due  to  potential  erythema
            PEDIATRIC BLOOD BANKING                                    from interaction between UV light and amotosalen.
                                                                    •  Platelets  stored  in  a  Platelet  Additive  Solution  (PAS).  PAS
            Blood and Blood Components                                 platelets contain very little plasma, which reduces the risk of
                                                                       allergic  reactions  and  transfusion-related  acute  lung  injury
            Several different blood components, including whole blood, recon-  (TRALI),  but  also  lowers  the  dose  of  coagulation  factors
            stituted whole blood, red blood cells (RBCs), platelets, plasma, and   contained in the platelet component.
            cryoprecipitated  antihemophilic  factor  (CRYO)  may  be  available   •  Plasma is frozen to retain functional plasma proteins including
            from a blood bank for transfusion. Recently, additional components   clotting factors. Depending on the timing of freezing and thawing,
            have become available in the United States. They are photochemically-  the component may be called fresh frozen plasma (FFP) or another
            treated INTERCEPT platelets and plasma, and solvent detergent–  name. However, all of these plasma components contain all the
            treated plasma, Octaplas. The availability of specific component types   necessary  clotting  factors.  Two  pathogen-inactivated  plasma
            varies between blood suppliers.                         products,  that  had  been  available  in  several  countries,  are  now
                                                                    available in the United States:
            •  Whole blood is infrequently used and may not be available from   •  INTERCEPT(Cerus  Corporation,  Concord,  CA)  treated
              a particular blood bank or blood supplier, but it may be available   plasma using the same system as described above.
              on request and is used by some pediatric cardiac surgery services.   •  Octaplas  (Octapharma,  Hoboken,  NJ)  is  a  filtered  pooled
              Whole blood contains all RBCs, plasma, platelets, and an antico-  plasma  product  that  is  subjected  to  solvent/detergent  treat-
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              agulant preservative solution containing citrate, phosphate, dex-  ment  to  inactivate  lipid-enveloped  viruses.   Its  safety  and
              trose, and possibly adenine.                             efficacy  in  pediatric  patients  has  not  been  evaluated  which
            •  RBC units mostly contain RBCs but also contain some plasma   would  be  important  in  neonates  whose  coagulation  system
              and a preservative solution. Most RBC units contain an additive   regulation differs from adults. Specifically, Octaplas contains
              preservative solution that includes some combination of adenine,   low  concentrations  of  protein  S  and  α2-antiplasmin,  two
              dextrose, and mannitol. Additive solutions are safe for relatively   inhibitors  of  the  coagulation  system  that  are  present  in  low
              small  (≤20 mL/kg)  transfusions.  There  are  concerns  over  the   concentrations in neonates. 3,4
              safety of these additives given in large transfusions to neonates,   •  Cryoprecipitate is prepared from plasma and contains high con-
              and their safety in this setting has never been proven in a random-  centrations of fibrinogen.
              ized clinical trial. In view of this concern, some hospital blood   •  Because pediatric patients require smaller doses of blood compo-
              banks  provide  nonadditive  RBC  units  or  wash  additive  units   nents, they often require only a portion of a component.
              intended for large transfusions to neonates. Because many blood   •  RBCs are stored refrigerated and hence can be prepared in aliquots
              centers provide only additive RBC units to hospital blood banks   as needed if the blood bank has the necessary equipment. Alter-
              and  washing  an  RBC  unit  takes  approximately  1  hour,  blood   natively the blood center can collect RBC units into a collection
              banks have been unable to supply RBC units without additives in   system in which additional bags are attached for dispensing ali-
              many  situations.  Thus  many  institutions  now  have  significant   quots. Whole blood is also stored refrigerated, but its use is very
              experience  transfusing  large  volumes  of  additive  RBC  units  to   limited and it is almost never prepared in aliquots.
              neonates and have not noticed any problems.         •  All  platelet  components  are  stored  at  room  temperature  under
            •  Two  general  types  of  platelet  units  are  available  in  the  United   constant agitation and can be prepared in aliquots when needed
              States, although any one blood bank or hospital may stock only   in the blood bank if the blood bank has the necessary equipment
              one of these types. These two types, whole blood–derived platelets   and supplies. However, 1 unit of whole blood–derived platelets
              (platelets) and platelets collected by apheresis (pheresis platelets),   does not contain many doses, even for infants, and most blood
              differ in their size. A platelet unit contains approximately 5.5 to   banks do not aliquot them.
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              10 × 10  platelets in about 50 mL, whereas a pheresis platelet   •  All plasma products are stored frozen, and are not generally ali-
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              unit contains at least 3 × 10  platelets in about 200 mL. It is   quoted after thawing. However, many blood centers will prepare
              often easier to use platelet units for small children because pheresis   plasma aliquots before freezing.
              platelets usually need to be aliquoted to provide the correct dose.   •  Because  even  small  infants  rarely  require  less  than  1  unit  of
              However, many blood centers exclusively provide only one type   cryoprecipitate, this component is rarely prepared in aliquots.
              of  platelet  component.  Recently,  two  modifications  of  platelet
              components were approved in the United States, although these
              had been in use in other countries for several years.  Directed Donations
              •  Platelets that have undergone pathogen inactivation using the
                 INTERCEPT  Blood  System  (Cerus  Corporation,  Concord,   Families  often  prefer  to  donate  blood  for  their  children  using  a
                 CA)  which  mixes  amotosalen  HCl,  a  synthetic  psoralen   process  known  as  directed  donations,  and  some  blood  banks

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