Blood Bags

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Blood bags are made of polyvinyl chloride (PVC) plastic that contains di-(2-ethylhexyl) phthalate (DEHP)

to

make the containers pliable. The bag is flexible, tough, kink resistant and scratch-resistant. The
container’s

material should be able to withstand sterilization by gamma irradiation, ethylene oxide, electron beam
or

all of them. The plastic should allow adequate gas exchange for oxygen and carbon dioxide yet prevent

water evaporation from the blood component bags. Bags should be pyrogen-free and sterile. Besides a

statutory license for manufacturing blood bags, quality checks for standards by government-approved
testing

laboratories are mandatory before blood bags are put to use. Test reports should be ascertained before

acceptance of the bags in the blood centre inventory.

The different configurations of blood bags are single, double, triple, quadruple or quintuple bags. A
blood bag

with its tubing and venepuncture needle is a closed system. More recently, additional configurations for
blood

containers include in-line filters for removal of leukocytes from the whole blood (WB) or Red Blood Cell
(RBC)

units. For removing contaminants from skin flora, a diversion pouch is attached with the collection tube,
the

blood from which can be used for test samples.20 Blood collection bag design also includes safety
devices

such as the sliding sheath needle guard to prevent accidental needle-stick injuries. These devices allow

retraction of the needle into a safety guard after blood collection.

Blood bags are supplied in pouches and should be used within the shelf life prescribed by the
manufacturer.

The bags should be checked for a batch number, lot number and date of manufacture and expiry on the
bag.

Blood bags should be transported and stored between 20-240


C at all times before blood collection to maintain

the integrity and sterility of the preservative solution. The preservative solution in blood bags contains
an

30 TRANSFUSION MEDICINE TECHNICAL MANUAL Third Edition 2022

anticoagulant (AC) to prevent donor blood from clotting. The preservative solution also contains
nutrients for

the blood cells and an additive solution for red cells’ long-term storage. Table 2 discusses the details of
the

ingredients of an anticoagulant and its functions. The approved anticoagulant-preservative solutions


used in

the blood bag are as follows

• Acid-citrate-dextrose solution (ACD)

• Citrate-phosphate-dextrose solution (CPD)

• Citrate-phosphate-dextrose-dextrose solution (CP2D)

• Citrate-phosphate-dextrose-adenine solution (CPDA-1).

Table 2: Constituents of common anticoagulants (AC) and their functions

Solutions Function

Sodium Citrate (C) Binds with calcium ions and interferes with calcium-dependent steps in the clotting
cascade

Dextrose (D) Supports generation of ATP by glycolysis and supports red cell membrane to increase shelf

life

Citric Acid Prevents caramelisation of glucose during autoclaving

Phosphate (P) It supports the metabolism of the red cells during storage to ensure they release oxygen

readily at the tissue level

Adenine (A) Provides the source of energy

AS1 (SAGM) Saline (S)- Provides fluid for the suspension to maintain flow rate

Glucose (G)- Provides basic nutrients for glycolysis


Adenine (A) & Mannitol (M)- Provides ATP and Stabilizes RBC wall

Additive solutions (AS) are used to enhance the shelf life of RBC to 42 days. The three forms of addit

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