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Ultrafiltration/Hemoconcentration
ULTRAFILTRATION/
HEMOCONCENTRATION, AN OFTEN OVERLOOKED AND UNDER UTILIZED METHOD OF
BLOOD MANAGEMENT, PROVIDING A MISSING KEY IN THE QUEST FOR AUTOLOGOUS
BLOOD CONSERVATION AND SALVAGING FOR SURGICAL PATIENTS
Also see ultrafiltration
literature
Ultrafiltration is a process of removing non-cellular water and
low molecular weight solutes including cytokines, anaphylatoxins and
platelet inhibitors from anticoagulated blood. This process has been
available for over twenty years. Ultrafiltration maintains all the formed
elements of whole blood such as red and white blood cells, platelets,
clotting factors, plasma proteins, antibodies, albumin, vitamins, minerals,
and most drugs or medications, all of which contribute to the stability,
hemostasis and overall homeostasis of the surgical patient.
Ultrafiltration can be applied to anticoagulated blood that is either in the
native circulation or in extracorporeal circuits, or blood that is collected
and held in reservoirs for salvaging and eventual return to the patient,
providing concentrated hyperoncotic autologous whole blood in a timely
fashion.
Traditionally, the more modern methods of blood salvaging today involve
direct infusion of diluted whole blood or the centrifugation of red cells or
cell processors and salvage devices that wash and save red blood cells,
i.e., "cell washers" or RBC-savers. These methods are efficient and readily
acceptable in almost all surgical arenas, but are not without limitations.
Direct infusion of diluted whole blood
produces hemodilution with crystalloid volume and lowers the viscosity and
COP. Such blood contains activated cytokines and anaphylatoxins, which
create abnormal volume kinetics and leads to organ edema and organ
dysfunction. The kidneys are then stressed even more to overcome the oncotic
challenge of diluted blood over an extended period of time (4–6+ hrs) to
restore normovolemic homeostasis at a critical time for the patient, thus
greatly increasing the risk of morbidity and mortality.
In contrast, RBC-savers are effective at
removing water and concentrating blood by tightly packing cells in a
centrifuge drawn from a reservoir. Subsequent washing removes cytokines,
anaphylatoxins, anticoagulants and other waste substances that may have been
collected in the reservoir suctioned from the surgical field.
The limitation is that cell savers also remove most of the other formed
elements found in whole blood except red blood cells. With large volumes
processed, this may lead to a coagulopathy, or worse, that of cell salvaged
syndrome or DIC requiring blood product usage and other interventions to
stabilize coagulation.
Ultrafiltration is not without its own
limitations. Careful attention must be applied to the blood that is going to
be hemoconcentrated, blood that it is anticoagulated and free of substances
not intended for reinfusion.
The end product of hemoconcentration is hyperoncotic whole blood that
increases the viscosity and COP, but is still anticoagulated and may need to
be reversed with the use of protamine. With this in mind, ultrafiltration
remains an untapped missing key that we can apply to better patient care
with the patient’s best interest first and paramount.
At a time in society when a patient’s own blood is at a premium,
ultrafiltration is rapidly gaining in popularity in the surgical arena. It
provides a quick, easy, and efficient way to save more of the
patient’s own blood and will help in the fight to reduce the use of
allogeneic blood products with their associated costs, fears, and morbidity
& mortality.
Ultrafiltration provides a viable alternative for blood salvaging and blood
management in surgery, offering an efficient way to achieve hyperoncotic
autologous whole blood for our patients and helping to stabilize the
patients quickly. This comes at a time when globally we all need to
reevaluate the use of allogeneic transfusions and the consequences of doing
so, and look for constructive, reliable and safe methods of managing
autologous blood, and avoid discarding viable and vital native cell
fractions.
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