The donor's red cells are destroyed by the antibodies in the recipient's serum. The cause of this hemolysis is incompatibility of the transfused blood with the patient‘s blood. ABO incompatibility usually produces a violent reaction. The signs of an incompatible blood transfusion may be masked by general anesthesia. The blood pressure and the pulse rate must be checked every 5 minutes for the first 15 minutes after each new bottle of blood. A hemolytic reaction can be produced by just a small quantity of mismatched blood. Human error is frequently involved. Incorrect laboratory work; mislabeling of blood and misreading of the labels on blood bags and bottles, are frequently responsible. Take maximum care in checking the name of the patient, the blood group, the bottle number and expiry date as shown on the blood product, with the slip issued from the laboratory. The patient's name and hospital number on the label of the blood pack should match those on the identification tag worn by the patient. Checking must be done by the anesthetist and another responsible hospital staff member.
7.4.1.1 Signs of incompatible blood transfusion in the anesthetized patient: -Hypotension, tachycardia, cyanosis, skin rash, general oozing from the wound, later jaundice and oliguria (5 - 10% incidence). Acute circulatory collapse (cardiac arrest) and renal failure are the most serious complications and may lead to death. The effects vary with the amount of blood transfused, the degree of incompatibility and the physical state of the patient at the time of transfusion. Signs of incompatible blood transfusion in the conscious patient including feeling of pressure in the head, tingling of limbs, precordial pain, dyspnea, lumbar pain, restlessness, nausea and vomiting, could not be seen in anesthetized patient.
Diagnosis of transfusion reaction is established by hemoglobinuria; send to the laboratory the remaining blood in the bottle or bag, a sample of the patient's blood and sample of the patient's urine.
7.4.1.2 Treatment of a transfusion reaction
These may be caused by antibodies to white blood cells, platelets or immunoglobulin reactions between patient and donor. Mild urticaria is the commonest manifestation. More serious allergic reactions are: asthma, angioneurotic edema, laryngeal edema, cardiovascular collapse and anaphylactic reaction (rare). Some allergic reactions may be difficult to distinguish at an early stage from hemolytic reactions.
Treatment
Mild allergic reactions: give antihistamine e.g. chlorpheniramine 10-20mg IV or promethazine 25 to 50 mg IV.
Severe reactions:
Organisms may enter the blood by contamination through carelessness in collection or cross-matching. They will proliferate if blood is allowed to remain out of the refrigerator at room temperature. Blood that is left out of the refrigerator for more than 30 minutes should not be put back into storage. Some viral diseases may be transmitted in transfused blood especially where screening tests are not available.
During rapid transfusions there is always a risk of pulmonary edema and cardiac failure. This is referred to as circulatory overload. This danger is more common in:
Precautions: Slow the transfusion if the patient's blood pressure is normal.
Signs of circulatory overload
Treatment of circulatory overload
Whole blood is prevented from clotting (after collection), by the use of citrate. The citrate forms a complex with the calcium ions in the blood. Since calcium is necessary for the blood to clot and the calcium is not available (being tied up in a complex with citrate), the blood remains fluid. When the citrated blood is introduced into the patient's circulation, the citrate is quickly broken down into water and carbon dioxide and the calcium is set free. If for some reason the citrate persists in the circulation, signs of citrate intoxication are seen. These signs are essentially the signs of lack of calcium in the blood.
Signs of citrate intoxication (calcium lack)
Treatment: Give 10ml of 10% calcium gluconate or chloride for every 6 units of blood transfused.
The rapid administration of large volumes of blood or replacement fluids directly from the refrigerator can result in a significant reduction in body temperature. This can be prevented in the case of large transfusions
These may be caused by:
These problems may begin to occur after 6 (after transfusion of whole blood volume of the patient) units of packed cells or stored blood have been administered. Management explained on the following topics under precaution when transfusing large volume of blood
This is defined as the replacement of the total blood volume in less than 24 hours. Coagulation problems commonly result. Platelets and fresh blood or plasma are required.
Precautions when transfusing large volumes of blood:
Are composed of degenerated platelets, White blood cells, fibrin strands denatured proteins, damaged red blood cells (present especially after the first week of storage).
The rate of formation of micro-aggregates depends on length of storage, platelet and WBC count at time of collection and the anticoagulant used.
Effect of micro-aggregates: They are filtered by the pulmonary circulation and may cause histamine release and pulmonary insufficiency from increased pulmonary resistance and ventilation-perfusion mismatching. These pulmonary micro emboli can be prevented by transfusing blood that is as fresh as possible and by using membrane filters with a small pore size of 20 - 40 microns although this slows the rate of infusion. (Standard blood transfusion sets have a pore size of 170-260 microns).