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430  Part V:  Therapeutic Principles  Chapter 28:  Therapeutic Apheresis: Indications, Efficacy, and Complications    431





                    100                                                      RED CELL APHERESIS
                                                                        Red cell exchange refers to the removal of a patient’s red cells in exchange
                     80                  y  = y e –x                    for donor red cells. When red cells are removed for therapeutic pur-
                                             0
                                          t
                   Percent remaining (y t )  60                         erythrocytapheresis. Red cell exchange is employed in settings where a
                                                                        poses, but not replaced with donor red cells, the process is referred to as
                                                                        clinical disorder is caused by an abnormality (inherited or acquired) of
                                                                        the patient’s red blood cells, and erythrocytapheresis may be employed
                     40
                                                                        in situations characterized by an untoward elevation in circulating red
                                                                        cell volume or in iron-overload states.
                                                                                                    48
                     20
                                                                        RED CELL EXCHANGE
                      0
                                                                        Therapeutic red cell exchange can be performed manually (i.e.,
                                                                        “exchange transfusion”) or by apheresis using automated programma-
                        0.0    0.5    1.0    1.5    2.0    2.5    3.0   ble blood-processing equipment. 49–51  This discussion focuses on auto-
                                   Plasma volumes processed (x)         mated red cell exchange. The programming functions of automated
                                                                        apheresis instruments are used to determine the parameters of red cell
                  Figure 28–2.  Depletion of soluble substances from the intravascular   exchange  procedures.  Data  that  include  the  patient’s  gender,  height,
                  compartment by plasma exchange according to the One Compart-  and weight are used to calculate the patient’s total blood volume.
                                                                                                                          52
                  ment Model. With each incremental volume of plasma removed (and   Also programmed into the machine are the patient’s starting hema-
                  replaced) from the intravascular compartment, a fixed proportion of   tocrit, the desired ending hematocrit, the average hematocrit of the
                  the remaining intravascular content of a soluble substance of interest is   replacement red cell units, and the desired fluid balance (typically 100
                  removed. The processing of 1.0 plasma volume depletes the intravascu-  percent). The desired fraction of the patient’s own red cells remaining
                  lar substance of interest by approximately two thirds. Processing of the   in the circulation at the end of the procedure (fraction of cells remain-
                  next half plasma volume furthers the depletion to almost 80 percent.
                                                                        ing [FCR]) is also programmed into the instrument. The instrument’s
                                                                        computer can thus determine how many units of red cells are to be
                                                                        used to obtain the desired hematocrit and FCR. The desired FCR is
                                                                        calculated based on the therapeutic end point targets of the red cell
                  thienopyridine derivatives ticlopidine and clopidogrel.  Autoanti-  exchange procedure 49,53–55 :
                                                            41
                  bodies to ADAMTS-13 are seen in ticlopidine-associated TTP, and
                  the contribution of TPE to the survivability of ticlopidine-associated
                                                                                =
                  TTP is similar to what is seen in acquired idiopathic TTP. 41,42  Patients   FCR(as %) 100
                  with clopidogrel-associated TTP do not appear to benefit from plasma     starting hematocrit  desiredend pointparameter 
                  exchange. 41                                                   ×     desiredendinghematocrit  ×  starting parametre   

                  ADVERSE EFFECTS OF THERAPEUTIC                        where the specified starting and end point parameters may be the per-
                  PLASMA EXCHANGE                                       cent  hemoglobin  S,  the  percent  parasitized  red  cells  counted  on  the
                  Two large studies identified adverse effects in 40 percent of patients   blood film, etc.
                  but only 12 percent of plasma exchange procedures and in 49 percent
                  of patients but only 17 percent of plasma exchange procedures, respec-  Red Cell Exchange in Sickle Cell Disease
                  tively. 43,44  This indicates that although a plurality of patients may experi-  Chapter  49  discusses  sickle  cell  anemia  and  related  abnormalities  in
                  ence an adverse effect during a course of plasma exchange, they will not   greater detail.
                  necessarily experience them in every procedure during the prescribed   In general, clinical studies of the role of transfusion therapy in
                  course. In both studies, most adverse effects were classified as mild or   sickle cell disease have focused mostly on simple transfusion or manual
                  moderate and did not prevent the successful completion of the pro-  exchange transfusion (reviewed in Ref. 56). Manual versus automated
                  cedure. The majority of adverse effects consisted of muscle cramps or   red cell exchange have not been directly compared in a clinical trial,
                  paresthesias, transient hypotension, mild nausea, or, in patients receiv-  although automated red cell exchange can be completed more efficiently
                  ing plasma as the colloid exchange fluid, fever, chills or urticaria. Muscle   and quickly than manual exchange transfusion.  Automated red cell
                                                                                                            49
                  cramps, paresthesias, and mild nausea can be attributed to hypocalcemic   exchange mitigates the accumulation of iron while maintaining a low
                  toxicity that occurs when plasma ionized calcium decreases as a result   level of hemoglobin S in patients receiving chronic treatment and, thus,
                  of the rapid infusion of calcium-free pharmaceutical albumin and, in   has entered into routine use where available. 57–59  Manual or automated
                  part, to the use of calcium chelating agents as anticoagulants in plasma   red cell exchange can be initiated using isotonic saline, rather than
                  exchange procedures. 45,46  A large national survey reported similar find-  packed red cells, as the replacement fluid during the early part of the
                  ings but with a lower rate of adverse effects during plasma exchange   procedure in order to maximize the removal of hemoglobin S–containing
                  (3.3 percent of procedures without plasma as the colloid replacement   red cells and avoid the gratuitous removal of normal red cells. 57,59,60  As
                  fluid, 7.8 percent of procedures with plasma as the colloid replacement   shown in Table  28–2, red cell exchange is indicated as first-line therapy
                  fluid) because adverse effects that did not compromise the completion of   in acute vasoocclusive stroke, and may be used in acute chest syndrome
                  the procedure were not included.  Very few adverse effects are seen as   refractory to standard management or in prophylaxis (primary or sec-
                                          47
                  caused by complications of peripheral venous access ; however, adverse   ondary) for vasoocclusive stroke.  In the latter two instances, red cell
                                                       47
                                                                                                56
                  effects of central venous access placement, although relatively rare, can   exchange may not be superior to simple transfusion. 56,61  In addition,
                  be severe. 45,47                                      red cell exchange may not be superior to simple transfusion, as needed,





          Kaushansky_chapter 28_p0427-0436.indd   431                                                                   9/17/15   6:05 PM
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