Professional Documents
Culture Documents
UNIT-1
INTRODUCTION
Blood bank: : A place where blood is collected from donors, typed, separated into components, stored,
and prepared for transfusion to recipients. A blood bank may be a separate free-standing facility or part of
a larger laboratory in a hospital.
Separation of blood: Typically, each donated unit of blood (whole blood) is separated into multiple
components, such as red blood cells, plasma and platelets. Each component is generally transfused to a
different individual, each with different needs.
An increasingly common blood bank procedure is apheresis, or the process of removing a specific
component of the blood, such as platelets, and returning the remaining components, such as red blood
cells and plasma, to the donor. This process allows more of one particular part of the blood to be collected
than could be separated from a unit of whole blood. Apheresis is also performed to collect plasma (the
liquid part of the blood) and granulocytes (white blood cells).
BLOOD GROUPING
a method in which blood is characterized by the presence or absence of particular antgens on the surface
of red blood cells. The antigens can be recognised by their reaction to specific antibodies which causes ag
glutination to occur. Two well-known blood groupings are the abo blood group and rhesus blood
group systems.
ROULEAUX BLOOD
The stacking of cells (rouleaux formation) facilitates the rate of red cell sedimentation, a phenomenon
that may be seen on a peripheral smear. The appearance of rouleaux may be artificially caused by a poor
preparation of the smear or by viewing the slide in a thickened area. When rouleaux formation is truly
present, it is caused by an increase in cathodal proteins, such as immunoglobulins and fibrinogen.
Although myeloma and macroglobulinemias are first considered by hematologists, other causes occur
more frequently, such as acute and chronic infections, connective tissue diseases, and chronic liver
disease.
DEFINITIONS AND CLASSIFICATION OF AGGLUTINATION REACTIONS
Agglutination is defined as the formation of clumps of cells or inert particles by specific antibodies to
surface antigenic components (direct agglutination) or to antigenic components adsorbed or chemically
coupled to red cells or inert particles (passive hemagglutination and passive agglutination, respectively).
Erythrocytes are also agglutinated by non antibody substances such as plant proteins, viruses, salts of
heavy metals, inorganic colloidal acids and bases, and basic proteins (protamines, histones).
Agglutination inhibition or hemagglutination inhibition refers to the inhibition of these reactions by
soluble antigen which reacts with the combining sites of the antibodies and thereby prevents their binding
to and agglutination of the particles.
REVERSE GROUPING
In ABO grouping, the testing of the patient’s serum or plasma against, at minimum, A1 and B reagent
RBCs (the process is also known as “serum grouping” or the slang term “back typing“). The
interpretation of this part of the ABO test is usually simple: Reactions against the A1 cells only shows
that the person has anti-A and is therefore blood group B, for example. The blood group identified by the
reverse grouping should be the same as that identified by the “forward” (or “cell“) grouping; if not,
an ABO discrepancy is present.
SERUM GROUPING.
The currently favored term for the process of confirming a person's ABO type by checking the antibodies
in their serum (or plasma). ... However, the red cell type must be confirmed by the person's ABO
antibody profile, so we test the patients serum or plasma against both group A and group B red blood
cells.
Antibodies are heavy (~150 kDa) globular plasma proteins. The basic structure of all antibodies are same.
There are four polypeptide chains: two identical heavy chains and two identical light chains connected by
disulfide bonds. Light Chain (L) consists polypeptides of about 22,000 Da and Heavy Chain (H) consists
larger polypeptides of around 50,000 Da or more. There are five types of Ig heavy chain (in mammal)
denoted by the Greek letters: α, δ, ε, γ, and μ. There are two types of Ig light chain (in mammal), which
are called lambda (λ) and kappa (κ).
CLASSES/TYPES OF ANTIBODY
Serum containing antigen-specific antibodies is called antiserum. The 5 types – IgG, IgM, IgA, IgD, IgE
– (isotypes) are classified according to the type of heavy chain constant region, and are distributed and
function differently in the body.
FUNCTIONS OF ANTIBODY
1. IgG provides long term protection because it persists for months and years after the prescence of
the antigen that has triggered their production.
2. IgG protect against bacteris, viruses, neutralise bacterial toxins, trigger compliment protein
systems and bind antigens to enhance the effectiveness of phagocytosis.
3. Main function of IgA is to bind antigens on microbes before they invade tissues. It aggregates the
antigens and keeps them in the secretions so when the secretion is expelled, so is the antigen.
4. IgA are also first defense for mucosal surfaces such as the intestines, nose, and lungs.
5. IgM is involved in the ABO blood group antigens on the surface of RBCs.
6. IgM enhance ingestions of cells by phagocytosis.
7. IgE bind to mast cells and basophils wich participate in the immune response.
8. Some scientists think that IgE’s purpose is to stop parasites.
9. IgD is present on the surface of B cells and plays a role in the induction of antibody production.
HEMAGGLUTINATION
Hemagglutination is used for the diagnosis of some enveloped viruses such as influenza viruses. This
method relies on the specific feature of some enveloped viruses that can adsorb to red blood cells (RBCs).
Specifically, hemagglutinin5 (HA), an envelope glycoprotein of some enveloped viruses, imparts this
property.
DIAGNOSIS
Hemagglutination can be used to diagnose syndromes that are caused by the absence of a component
carrying blood group antigens (null phenotypes). For example, an absence of the Rh proteins
causes stomatocytosis and compensated hemolytic anemia (Rh syndrome), and an absence of Xk protein
causes the McLeod syndrome.
BLOOD TYPING
Blood typing is a method to tell what type of blood you have. Blood typing is done so you can safely
donate your blood or receive a blood transfusion. It is also done to see if you have a substance called Rh
factor on the surface of your red blood cells.
Your blood type is based on whether or not certain proteins are on your red blood cells. These proteins
are called antigens. Your blood type (or blood group) depends on what types your parents passed down to
you.
Blood is often grouped according to the ABO blood typing system. The 4 major blood types are:
Type A
Type B
Type AB
Type O
Rh typing uses a method similar to ABO typing. When blood typing is done to see if you have Rh factor
on the surface of your red blood cells, the results will be one of these:
RH FACTOR is a blood protein that plays a critical role in some pregnancies. People without Rh factor
are known as Rh negative, while people with the Rh factor are Rh positive. If a woman who is Rh
negative is pregnant with a fetus who is Rh positive, her body will make antibodies against the fetus's
blood. This can cause Rh disease, also known as hemolytic disease of the newborn, in the baby. In severe
cases, Rh disease leads to brain damage and even death. Since 1968, a vaccine has existed to prevent the
mother's body from making anti-bodies against the fetus's blood.
All people have a blood type (A, B, AB, or O). Everyone also has an Rh factor (positive or negative).
There can be a problem if a mother and baby have a different blood type and Rh factor.
HDN happens most often when an Rh negative mother has a baby with an Rh positive father. If the baby's
Rh factor is positive, like his or her father's, this can be an issue if the baby's red blood cells cross to the
Rh negative mother.
During pregnancy, you won't notice any symptoms. But your healthcare provider may see the following
during a prenatal test:
A yellow coloring of amniotic fluid. This color may be because of bilirubin. This is a substance that
forms as blood cells break down.
Your baby may have a big liver, spleen, or heart. There may also be extra fluid in his or her stomach,
lungs, or scalp. These are signs of hydrops fetalis. This condition causes severe swelling (edema).
DIAGNOSES
HDN can cause symptoms similar to those caused by other conditions. To make a diagnosis, your child’s
healthcare provider will look for blood types that cannot work together. Sometimes, this diagnosis is
made during pregnancy. It will be based on results from the following tests:
Blood test. Testing is done to look for for Rh positive antibodies in your blood.
Ultrasound. This test can show enlarged organs or fluid buildup in your baby.
Amniocentesis. This test is done to check the amount of bilirubin in the amniotic fluid. In this test, a
needle is put into your abdominal and uterine wall. It goes through to the amniotic sac. The needle takes a
sample of amniotic fluid.
Percutaneous umbilical cord blood sampling. This test is also called fetal blood sampling. In this test, a
blood sample is taken from your baby’s umbilical cord. Your child’s healthcare provider will check this
blood for antibodies, bilirubin, and anemia. This is done to check if your baby needs an intrauterine blood
transfusion.
HDN TREATMENT
Treatment will depend on your child’s symptoms, age, and general health. It will also depend on how
severe the condition is.
A healthcare provider will check your baby’s blood flow with an ultrasound.
This test puts red blood cells into your baby's circulation. In this test, a needle is placed through your
uterus. It goes into your baby’s abdominal cavity to a vein in the umbilical cord. Your baby may need
sedative medicine to keep him or her from moving. You may need to have more than 1 transfusion.
Early delivery
If your baby gets certain complications, he or she may need to be born early. Your healthcare provider
may induce labor may once your baby has mature lungs. This can keep HDN from getting worse.
Blood transfusions
Intravenous fluids
Phototherapy
In this test, your baby is put under a special light. This helps your baby get rid of extra bilirubin.
Your baby may need oxygen, a substance in the lungs that helps keep the tiny air sacs open (surfactant),
or a mechanical breathing machine to breathe better.
Exchange transfusion
This test removes your baby’s blood that has a high bilirubin level. It replaces it with fresh blood that has
a normal bilirubin level. This raises your baby’s red blood cell count. It also lowers his or her bilirubin
level. In this test, your baby will alternate giving and getting small amounts of blood
UNIT 2
Depending on how much blood you need, a transfusion can take between 1 and 4 hours. About 5 million
Americans need a blood transfusion every year, and the procedure is usually safe.
Red blood cells - cells that carry oxygen to and from tissues and organs
Platelets - cells that form clots to control bleeding
Plasma - the liquid part of the blood that helps clotting. You may need it if you have been badly burned,
have liver failure or a severe infection.
Most blood transfusions go very smoothly. Some infectious agents, such as HIV, can survive in blood and
infect the person receiving the blood transfusion. To keep blood safe, blood banks carefully screen
donated blood. The risk of catching a virus from a blood transfusion is low.
Sometimes it is possible to have a transfusion of your own blood. During surgery, you may need a blood
transfusion because of blood loss. If you are having a surgery that you're able to schedule months in
advance, your doctor may ask whether you would like to use your own blood, instead of donated blood. If
so, you will need to have blood drawn one or more times before the surgery. A blood bank will store your
blood for your use.
To minimize the chance of an adverse reaction during a transfusion, health care practitioners take
several precautions. Before starting the transfusion, usually a few hours or even a few days beforehand,
the patient is cross-matched with the donor blood (not done for transfusions of plasma or platelets).
After double-checking labels on the bags of blood that are about to be given to ensure the units are
intended for that recipient, the health care practitioner gives the blood to the recipient slowly, generally
over 1 to 4 hours for each unit of blood. Because most adverse reactions occur during the first 15
minutes of the transfusion, the recipient is closely observed at first. After that, a nurse checks on the
recipient periodically and must stop the transfusion if an adverse reaction occurs.
Most transfusions are safe and successful. However, mild reactions occur occasionally, and, rarely,
severe and even fatal reactions may occur.
Rare reactions include
Graft-versus-host disease (whereby transfused cells attack the cells of the person receiving a
transfusion)
Infections
Complications of massive transfusion (poor blood clotting, low body temperature, and low
calcium and potassium levels)
Fever
Fever may be caused by a reaction to the transfused white blood cells or to chemicals (cytokines)
released by the transfused white blood cells. For this reason, most hospitals in the United States remove
white blood cells from the transfused blood after it is collected.
In addition to an increase in temperature, the person has chills and sometimes headache or back pain.
Allergic reactions
Symptoms of an allergic reaction include itching, a widespread rash, swelling, dizziness, and headache.
Less common symptoms are breathing difficulties, wheezing, and airway obstruction. Rarely, an
allergic reaction is severe enough to cause low blood pressure and shock.
Fluid overload
Transfusion recipients can receive more fluid than their body can easily handle. Too much fluid may
cause swelling throughout the body or difficulty breathing. This complication is the most common
cause of transfusion-related death. Recipients who have heart disease are most vulnerable, so their
transfusions are given more slowly and they are monitored closely. People who receive too much fluid
are given a diuretic.
Lung injury
Another very rare reaction, called transfusion-related acute lung injury (TRALI), is caused by
antibodies in the donor's plasma. This reaction may cause serious breathing difficulties. This
complication is the second most common cause of transfusion-related death. It occurs in 1 in 5,000 to 1
in 10,000 cases, but many cases are mild and so may not be diagnosed.
Destruction of red blood cells
Despite careful typing and cross-matching of blood, mismatches due to subtle differences between
donor and recipient blood (and, very rarely, errors) can still occur. When such a mismatch occurs, the
recipient's body destroys the transfused red blood cells (a hemolytic reaction) shortly after the
transfusion.
The ‘Blood cold Chain’ is the systematic process for safe storage & transportation of blood & blood
components so that they are kept at the correct temperature at all times from blood collection from a
donor to administration of blood to a patient in need of transfusion.
cryoprecipitate needs to be s thawed at 30 degree to 37 degree C in a water bath for about 15-30
minutes
PLATELETS – PLATELET RICH PLASMA (PRP)/PLATELET CONCENTRATE (PC)
Blood transfusions are typically performed in a hospital, doctor's office, or other medical facility.
During a blood transfusion, an intravenous (IV) line is placed in a vein in your arm.
Blood or blood components that are stored in a plastic bag are delivered through the IV into your
bloodstream.
Tell your doctor or nurse immediately if you experience any of the following symptoms during your
transfusion:
Shortness of breath
Fever or chills
A sense of uneasiness
You won't need to change your diet or limit any activities before receiving a blood transfusion.
Let your doctor know if you've had a transfusion in the past that caused an adverse reaction.
After the procedure, you may develop bruising where the needle was inserted.
You may need more blood testing to check how your body is responding to the transfusion.
Blood transfusions are considered safe, but certain complications can happen during or after the
procedure. These include:
Fever
Lung injury
Acute immune hemolytic reaction (occurs when the body suddenly attacks donor red blood cells)
Delayed hemolytic reaction (occurs when the body gradually attacks donor red blood cells)
Graft-versus-host disease (occurs when donor white blood cells attack the recipient's bone marrow)
CRITERIA TO DONATE BLOOD
There are several parameters that determine the eligibility of an individual to donate blood. Guidelines
laid down by the Ministry of Health, Government of India have to be followed by blood banks and
organizations conducting blood donation camps
Overall health- The donor must be fit and healthy, and should not be suffering from
transmittable diseases.
Age and weight- The donor must be 18–65 years old and should weigh a minimum of 50 kg.
Pulse rate- Between 50 and 100 without irregularities.
Hemoglobin level- A minimum of 12.5 g/dL.
Blood pressure- Diastolic: 50–100 mm Hg, Systolic: 100–180 mm Hg.
Body temperature- Should be normal, with an oral temperature not exceeding 37.5 °C.
The time period between successive blood donations should be more than 3 months.
Individuals under certain conditions are deemed ineligible to donate blood:
Hepatitis B – HBsAg
Human immunodeficiency virus – anti-HIV 1 and 2 and HIV NAT (nucleic acid testing)
Hepatitis C – anti-HCV and HCV NAT
Human T-cell lymphotropic virus – anti-HTLV I and II
Syphilis – syphilis antibodies.
Some donations are tested for cytomegalovirus (CMV) antibodies to provide CMV negative blood for
patients with certain types of impaired immunity.
INFUSION RATE
An infusion rate of 17mL/min allows an entire unit of blood to be transfused in 30 minutes. The usual
recommended time period ranges between 1.5 and 2 hours per unit.
UNIT 3
Volunteer Donations
The standard or most common type of blood donation in which an individual donates one pint, which
goes to any patient in need.
Autologous Donations
Blood drawn from an individual prior to elective, non-urgent surgery during which loss of a lot of blood
is expected. The donated units are stored for up to 42 days and given back to the same individual when
and if a need for transfusion arises. This is very useful for patients with rare blood types who can be very
hard to support from the regular blood supply. Autologous donors must be healthy enough to donate
safely, so this is rarely an option for seriously ill patients.
There are two main methods of obtaining blood from a donor. The most frequent is to simply take the
blood from a vein as whole blood. This blood is typically separated into parts, usually red blood
cells and plasma,
The other method is to draw blood from the donor, separate it using a centrifuge or a filter, store the
desired part, and return the rest to the donor. This process is called apheresis, and it is often done with a
machine specifically designed for this purpose. This process is especially common
for plasma and platelets.
APHERESIS
An apheresis blood donation is the process of blood collected via a special machine to separate it during
the donation, so that only certain parts of the blood are collected and the remainder returned to the donor.
This allows more of a single component, such as red blood cells or platelets, to be collected in one sitting.
BLOOD BANK
A blood bank is a place where blood is collected and stored before it is used for transfusions. Blood
banking takes place in the lab. This is to make sure thet donated blood and blood products are safe before
they are used. Blood banking also determines the blood type. The blood is also tested for infectious
diseases.
BLOOD DONORS
Must be at least 16 years of age, or the minimum age set by state law
Must be in good health
Must weigh at least 110 pounds
Must pass the physical and health history exam given before donation
Some states let people younger than 16 or 17 years to donate blood, with parental consent.
Certain standard tests are done in the lab once blood is donated. These include:
Quality in transfusion practice must apply to the hospital blood bank or equivalent, because it plays a vital
role in ensuring that the correct blood component is supplied for the patient.
The laboratory aspect of the transfusion process is carried out in different ways across the countries of the
EU. In some settings a local hospital blood bank manages the blood component inventory and the clinical
blood transfusion laboratory services. Elsewhere, the blood establishment provides compatible blood
directly to hospitals.
Blood is composed of 55% plasma and 45% “formed elements,” including red blood cells, white blood
cells, and platelets. Because of these living cells suspended in the plasma, blood is considered a fluid
connective tissue (not a fluid). It is the only fluid tissue in the body.
2. Blood Provides the Body's Cells with Oxygen and Removes Carbon Dioxide
Blood absorbs oxygen from air in the lungs. It transports the oxygen to cells throughout the body, and it
removes waste carbon dioxide from the cells. In the lungs, the carbon dioxide moves from the blood to
the air and is exhaled.
3. Blood Transports Nutrients and Hormones
Blood plays a large role in digestion and endocrine system functions. Digested nutrients are absorbed into
the bloodstream through capillaries in the villi that line the small intestine. These nutrients include
glucose, amino acids, vitamins, minerals, and fatty acids. Blood also transports some hormones secreted
by endocrine system glands to target organs and tissues.
Blood absorbs and distributes heat throughout the body. It helps to maintain homeostasis through the
release or conservation of warmth. Blood vessels expand and contract when they react to outside
organisms, such as bacteria, and to internal hormone and chemical changes. These actions move blood
and heat closer to or farther from the skin surface, where heat is lost.
BACTERIAL CONTAMINATION
causes
Both gram-positive and gram-negative organisms have been implicated in transfusion transmitted
bacterial infection with serious morbidity and mortality occurring most frequently with gram-negative
bacteria.(1)
UNIT 4
CPD
citrate phosphate dextrose
(CPD) a solution containing citric acid, sodium citrate, monobasic sodium
phosphate, and dextrose that is the primary ANTICOAGULANT used for preservation of whole blood or red
blood cells for up to 21 days. The official USP name is anticoagulant citrate phosphate dextrose solution.
citrate phosphate dextrose adenine (CPDA1)
an ANTICOAGULANT solution, containing citric acid, sodium citrate, monobasic sodium
phosphate, dextrose, and adenine, used for the preservation of whole blood and red blood cells for up to 3
5 days; it extends red cell survival by providing adenine needed for the maintenance of red cell ATP level
s. The official USP name is anticoagulant citrate phosphate dextrose adenine solution.
CPDA-1
Citrate phosphate dextrose-adenine 1. A medium which supplies ATP, and extends the shelf life of packe
d red cells destined for transfusion to 35 days with a higher ATP level than earlier-generation red cell pres
ervation media.
SAGM
Additive solution containing combinations of Saline, Adenine, Glucose and Manitol (SAGM) provides
extended shelf life of RBC up to 42 days with increased functional viability. ... Reduced density of red
blood cell concentrate on addition of SAGM solution allows better flow property of Red blood cell and
better transfusion.
ACD (Acid Citrate Dextrose) Solution A and ACD (Acid Citrate Dextrose) Solution B are
anticoagulants for whole blood and also act as acidifying agents to platelet poor plasma.
In a method of separating different density fluid components, a fluid sample is placed in a first flexible
container. The container and its contents are then spun at high speed while controlling the shape of the
container so that its side walls spread apart and its bottom flattens to give the container and its contents a
relatively small aspect ratio whereby different density components of the fluid contents travel minimum
distances while separating in the container to achieve a density distribution in the container, with the
densest components of the fluid distal to the spin axis being distributed over a relatively large area surface
constituted by the container bottom
COMPATIBILITY TESTING
performed to determine if a particular unit of blood can be transfused safely into a certain patient. This
includes ABO-Rh blood typing (see above), antibody screening (for unexpected red blood cell antibodies
that could cause problem in the recipient), and cross-matching
Two antigens on blood cells (A and B) determine a person’s ABO blood type (either A, B, AB, or O). In
the United States, the most common blood type is O, followed closely by type A.
If you have type O blood, you can only get type O red blood cell transfusions. But you can give
your red blood cells to people with type A, B, AB, or O blood, which is why you are sometimes
called a universal donor. (Universal donor blood cells are typically only used in emergencies. For
example, if a person is bleeding severely and nearing death, there may no time for testing. In
everyday practice, people in the US are almost always given the exact same type of red blood
cells that they have.)
If you have type A blood, you cannot get either type B or AB red blood cells.
If you have type B blood, you cannot get type A or AB red blood cells.
If you have type AB blood, you can get transfusions of O, A, B, or AB red blood cells.
There are other types of allergic transfusion reactions that do not cause hemolysis.
Causes
Blood is classified into four different types: A, B, AB, and O.
Another way blood cells may be classified is by Rh factors. People who have Rh factors in their blood are
called "Rh positive." People without these factors are called "Rh negative." Rh negative people form
antibodies against Rh factor if they receive Rh positive blood.
There are also other factors to identify blood cells, in addition to ABO and Rh.
Your immune system can usually tell its own blood cells from those of another person. If you receive
blood that is not compatible with your blood, your body produces antibodies to destroy the donor's blood
cells. This process causes the transfusion reaction. Blood that you receive in a transfusion must be
compatible with your own blood. This means that your body does not have antibodies against the blood
you receive.
IMMUNE TRANSFUSION
Immune-mediated transfusion reactions occur when incompatible blood products are transfused into a
patient's circulation, triggering a response from the patient's immune system.
In general, the formation of this and other immune responses occur in three stages:
the immune system mounts a response to remove the antigen from the body
The immune response varies tremendously, depending on the individual (the health of his or her immune
system and genetic factors) and the antigen (how common it is and how "provocative" it is to the immune
system).
CROSS-MATCHING
Cross Matching is a procedure performed prior to a blood transfusion to determine whether donor blood
is compatible (or incompatible) with recipient blood.
Principle
Cross-matching will detect incompatibilities between the donor and recipient that will not be evident on
blood typing. There are two types of cross-matches: Major cross-match and Minor cross-match.
PROCEDURE
3. Major Crossmatch:
Label a test tube. Add two drops of the patient serum and one drop of the appropriate donor cell
suspension.
4. Minor Crossmatch:
Label a test tube. Add two drops of the appropriate donor serum and one drop of the patient cell
suspension.
After the transfusion is terminated (except for some types of mild reaction), you may be required by the
Transfusion Service Provider to send freshly collected blood and urine samples along with the blood pack
and IV line.
MINOR CROSSMATCH
Minor Crossmatch. In contrast to the “major” crossmatch (recipient serum vs. donor red blood cells), the
“minor” crossmatch is designed to test opposite compatibility: The donor's serum/plasma with the
recipient's red cells.
PLATELETS are essential for blood clotting. Platelet transfusions are routinely needed to support
patients undergoing cancer therapy, open-heart surgery, organ transplantation, and for patients with
bleeding disorders. Platelets have a very short shelf-life and must be transfused within five days of
collection.
RED BLOOD CELLS (RBCs) carry oxygen to all parts of the body. Red cell transfusions are most
needed after significant blood loss due to trauma, surgery, or to treat anemia. A single red blood cell
donation can be made every 8 weeks;
PLASMA is the liquid portion of the blood containing critical clotting factors. Plasma is used to treat
patients with coagulation factor deficiencies, such as patients with liver failure, and those patients with
certain bleeding disorders. Plasma donations can be made every 4 weeks. Type AB donors are in high
demand because they are “universal” plasma donors. Their plasma can be used to treat all patients.
FFP and Cryoprecipitate (often just called ‘cryo’) are both blood components made from plasma. Plasma
is the yellow liquid that carries red cells, white cells and platelets within the blood vessels around the
body. It contains vital proteins known as clotting factors
The primary purpose for a red blood cell transfusion is to increase the oxygen-carrying capacity of
the blood. Therefore, red blood cell transfusion is indicated in patients with anemia who have evidence
of impaired oxygen delivery