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                  142    PA R T  II / Physiologic and Pathologic Responses



                  Table 6-4 ■ AGENTS USED TO PROMOTE COAGULATION BLOOD PRODUCTS
                  Product               Standard Volume               Administration                  Factor Replaced
                  Platelets (random donor)  Usually 8–10 donors/unit at 50–70 mL/unit  Rapid administration increases possible
                                                                        allergic reaction
                  Platelets (single donor)  One donor/200–300 mL      Rapid administration possible allergic reaction
                  Packed red blood cells (RBC)  250–350 mL/unit       Rapid administration; blood type mismatch
                  Fresh frozen plasma (FFP)  200–250 mL/unit          Rapid administration            II, V, VII, IX, X, XI, XII
                  Cryoprecipitate       Usually 8–10 donors/unit at 10–20 mL/unit  Rapid administration increases possible   I
                                                                        allergic reaction

                                                                                            th
                  Modified from Dzieczkowski J & Anderson K (2005) in Transfusion biology and therapy in Harrison’s principles of internal medicine (16 ed.). New York: McGraw-Hill Medical
                    Publishing Division.



                  implemented because ecchymotic areas under the cuff can de-  the number of various blood products received. RBC loss needs to
                  velop. Hemodynamic monitoring may be used and variations in  be replaced, but it is important to realize that a transfusion is not
                  indices may indicate cardiac failure, hypovolemia, or pulmonary  a benign intervention. Critically ill patients may be at risk for im-
                  complications such as PE. Monitoring urine output for at least   munosuppressive and microcirculatory complications with red
                  0.5 to 1 mL/kg per hour should be routine practice. Removal of  cell transfusions. 13  A restrictive transfusion strategy (transfuse
                  large catheters used for percutaneous interventions should al-  for a hemoglobin  7.0 g/dL) has been shown to be as effective
                  ways be performed with care. Achieving and maintaining hemo-  as a liberal strategy (transfuse for a hemoglobin  10 g/dL) with
                  stasis is dependent on technique. Manual pressure should be ap-  a decrease in mortality. 13  The only two groups of patients that
                  plied slightly above the insertion site of the vessel and minimal  may require the more liberal transfusion strategy are patients
                  padding should be used to control bleeding. This technique will  with an acute myocardial infarction or unstable angina.  13  In
                  allow visualization of the site for continual monitoring and  cases of massive bleeding that is not responsive to the usual in-
                  lessen the chance of hematoma formation. Once adequate he-  terventions as described above, recombinant factor VIIa has
                  mostasis is achieved, other devices can be applied to assure ade-  been used as an additional intervention. Originally used for
                  quate clot formation at the puncture site. Proper technique in  treatment of hemophilia, off-label use of factor VIIa has in-
                  hemostasis control is especially important for patients with a   creased markedly over the last 10 years. Recombinant factor
                  coagulopathy.                                       VIIa binds to the surface of activated platelets and promotes
                                                                                                               1
                     If hemorrhage is present, the priority should be volume resusci-  thrombin formation thereby enhancing clot formation. Dosing
                  tation. Blood products should be replaced depending on estimated  of this drug for off-label use varies greatly depending on the set-
                  blood loss and laboratory values. Aggressive fluid resuscitation  ting (surgery, trauma, hemorrhagic stroke, reversal of oral coag-
                  should be performed through short, large-bore venous access us-  ulation therapy, or impaired hepatic function). 14  Caution
                  ing pressure bags if the patient is hypotensive to assure fast in-  should be used when using factor VIIa due to the risk of throm-
                  travascular volume repletion. While infusing blood products, the  boembolic adverse events. 14,15  Observation for bleeding should
                  nurse should observe for allergic reactions (Tables 6-4 and 6-5).  include monitoring of all vascular accesses as well as the area
                  Continual bleeding may require massive blood product replace-  around the site. Vigilant surveys by the nurse of the skin surface
                  ment, which can cause a “washout” effect of most of the func-  and digits are necessary to observe for petechiae, ecchymosis,
                  tioning coagulation proteins, and paradoxically cause further   and other skin disruptions that may provide early warning signs
                  coagulopathy. It is also important to keep accurate records as to  of impending DIC (Display 6-3).






                  Table 6-5 ■ DRUGS USED TO PROMOTE COAGULATION
                  Drug                 Dose                        Side Effects            Mechanism
                  Protamine            1 mg for every 100 u of IV heparin  Hypotension; possible anaphylaxis  Binds heparin to neutralize
                                                                     if exposed to NPH       anticoagulant effect
                  Desarginine vasopressin   0.3  g/kg IV at 12- to 24-h interval  Mild flushing, headache, mild-to-  Temporarily improves platelet function
                    (DDAVP)                                          moderate abdominal pain  in patient with renal or liver disease;
                                                                                             mechanism not clear
                  Recombinant activated  Dose varies depending on indication;  Thrombotic events  Binds to surface of activated Platelets and
                    Human factor VII (rFVIIa)  most current use is off-label dose can        promotes Factor X activation and
                    (Novo-Seven)*        range from 5 to 300
 mcg/kg in                      thrombin generation where platelets
                                         varying number of doses                             are localized at a site of injury

                  *Goodnough, L., & Shander, A. (2007). Recombinant factor VIIa: Safety and efficacy. Current Opinion in Hematology, 14, 504–509.
                                                                                    4
                                                                                    4
                  Brunton, L., Lazo, J., & Parker, K. (2006). Goodman and Gilman’s the pharmacological basis of therapeutics. New York: McGraw-Hill Company.
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