Everything about Blood Serum totally explained
Blood plasma is the
liquid component of
blood, in which the
blood cells are suspended. It makes up about 55% of total blood
volume. It is comprised of mostly water (90% by volume), and contains dissolved proteins, glucose, mineral ions, hormones, carbon dioxide (plasma being the main medium for excretory product transportation), as well as the actual blood cells. Blood plasma is prepared simply by spinning a tube of fresh blood in a
centrifuge until the blood cells fall to the bottom of the tube. The blood plasma is then poured or drawn off. Blood serum is blood plasma without
fibrinogen or the other clotting factors.
Plasmapheresis is a type of medical therapy involving separation of plasma from red blood cells.
Fresh frozen plasma
"Fresh frozen plasma" (FFP) is prepared from a single
unit of blood or by
apheresis, drawn from a single person. It is frozen (-40F Degrees) after collection and can be stored for ten
years from date of collection. FFP contains all of the coagulation factors and proteins present in the original unit of blood. It is used to treat
coagulopathies from
warfarin overdose,
liver disease, or dilutional coagulopathy. FFP which has been stored more than the standard
length of time is sometimes re-classified as simply "frozen plasma," which is identical except that the coagulation factors are no longer considered completely
viable.
Plasma which has been used as a source of
Cryoprecipitate (Plasma, Cryoprecipitate Reduced) is more limited, but still acceptable for many uses. The term "FFP" is sometimes used informally to mean any frozen transfusable plasma product, including products which don't meet the standards for FFP
Dried plasma
"Dried plasma" was developed and first used in
WWII. Prior to the
United States' involvement in the war, liquid plasma and "whole blood" were used. The "
Blood for Britain" program during the early
1940s was quite successful (and popular in the United States) based in part on Dr.
Charles Drew's contribution. A large
project was begun in
August of the year
1940 to collect blood in
New York City hospitals for the export of plasma to
Britain. Dr. Drew was appointed
medical supervisor of the "Plasma for Britain" project. His notable contribution at this time was to transform the
test tube methods of many blood
researchers, including himself, into the first successful
mass production techniques.
Nonetheless, the decision was made to develop a
dried plasma package for the
armed forces as it would reduce breakage and make the transportation, packaging, and storage much simpler.
The resulting
Army-
Navy dried plasma package came in two
tin cans containing 400
cc bottles. One bottle contained enough
distilled water to completely reconstitute the dried plasma contained within the other bottle. In about three
minutes, the plasma would be ready to use and could stay fresh for around four
hours.
Following the "Plasma for Britain" invention, Dr. Drew was named
director of the
Red Cross blood bank and assistant director of the
National Research Council, in charge of blood collection for the United States Army and Navy. Dr. Drew argued against the armed forces
directive that blood/plasma was to be separated by the
race of the
donor. Dr. Drew argued that there was no racial difference in
human blood and that the
policy would lead to needless
deaths as
soldiers and
sailors were required to wait for "same race" blood.
By the end of the war the American Red Cross had provided enough blood for over six million plasma packages. Most of the
surplus plasma was returned to the United States for
civilian use.
Serum albumin replaced dried plasma for
combat use during the
Korean War.
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