Module 7 Part 2 - Blood Transfusion Therapy Flashcards

1
Q

We rarely give __ blood unless indicated?

A

whole blood

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2
Q

Blood is 1% RBC and 99% ___

A

plasma

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3
Q

Plasma is mostly ___

A

water

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4
Q

What is the bottom line regarding blood volume and what takes priority?

A

We always want to protect and reestablish circulating volume!

Without it we cannot get the functions of plasma

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5
Q

Major Functions of Blood Plasma

A

Maintenance of Blood volume

It suspends cellular elements like RBC, WBC, PLT

O2 and CO2 transport

Nutrient exchange

Hormone transport

Waste evacuation

Temperature regulation

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6
Q

There are at least __ different antigens on RBCs

A

80

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7
Q

ABO System

A

Way of designating blood as having A antigens, B antigens, both, or neither

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8
Q

How does dominance work in the AB System?

A

A and B are dominant over O

However, they are codominant to each other

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9
Q

Rh Factor System

A

Way of designating possession of the rH antigen or not

Positive = have the rH antigen

Negative = not present

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10
Q

How does dominance work for the rH system?

A

Positive rH is dominant over negative rH

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11
Q

Antibodies are in __; Antigens are on ___

A

Antibodies are in PLASMA and Antigens are on RBC!!!

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12
Q

If a person has A blood what kind of antibody is in their plasma? B blood? O Blood? AB Blood?

A

A = Anti B Antibody

B = Anti A Antibody

AB = No Antibody

O = Both A and B antibody

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13
Q

What are the rules for giving rH + and - blood?

A

We can give + blood people more + blood, but we cannot give a - person + blood since the - person will recognize the rH antigen on the transfusion as foreign and make antibodies against it

We can give rH - blood to positive and negative people because there is no antigen present to make antibodies against

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14
Q

What pattern of genetic inheritance can rH + blood be?

A

Homozygous dominant or Heterozygous

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15
Q

What pattern of genetic inheritance can rH - blood be?

A

Homozygous Recessive

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16
Q

Most common blood type? Least common blood type?

A

Common = O+

Least Common = AB-

This can make it hard to get the rarer blood types transfusions

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17
Q

Transfusion

A

Blood component therapy

Administration of whole blood or blood components directly into the bloodstream

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18
Q

What regulates the processes of blood products and transfusions?

A

The federal government through the American Association of Blood Banks (AABB) who have stringent requirements on collection, testing, storage, and distribution (not available in every country)

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19
Q

What are some options for blood transfusions?

A
  1. Homologous Blood
  2. Autologous Blood
  3. Designated (Directed) Blood
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20
Q

Homologous Blood Transfusion

A

transfusion of blood from random volunteer donors

There are rigid checks for risk factors

ex: blood drive

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21
Q

Autologous Blood Transfusion

A

Blood collected from the intended recipient (yourself) prior to a planned procedure or accident - OR - salvaged during surgery via “cell saver”

It eliminates the risk of alloimmunization, immune mediated transfusion reactions, and transmission of viral diseases

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22
Q

Alloimmunization

A

Risk for a transfusion reaction from blood of someone in the same species (ex: Human to Human)

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23
Q

Designated (Directed) Blood

A

Blood collected and transfused from a donor designated and picked by the recipient

ex: a family member of a proper blood type

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24
Q

Blood Components that are Available for Transfusion?

A

Whole Blood

Packed RBC

Modified RBC - Leukocyte-poor (Washed) or Irradiated

Platelets

Granulocytes

Fresh Frozen Plasma

Cryoprecipitate Antihemophilic Factor (AHF)

Coagulation Factor Concentrates

Albumin, Plasma Protein Fraction

Immune system globulin

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25
Whole Blood
RBC, plasma (plasma proteins, globulins, antibodies), stable clotting factors, and an anticoagulant/preservative It is the entirety of blood with a conservative that is given in emergency situations
26
Indications for Whole Blood Use
1. (Sometimes) Symptomatic Anemia and Major Volume Deficit 2. Massive Hemorrhaging with hypotension, tachycardia, SOB, pallor, low Hgb and Hct
27
Whole blood is ___ required and often medically ___
Whole blood is RARELY REQUIRED and often medically unnecessary
28
What could occur if whole blood is given to someone that does not need it?
Circulatory overload
29
Before giving blood products always...
check for ABO and Rh factor compatibility - TYPE AND CROSS
30
How should Whole blood be administered?
1. Initiate it slowly (70cc/hr) for 15 minutes at first 2. If there is no transfusion reaction then you can increase the rate and infuse for 2-4 hours
31
What is the exception to starting slow with the whole blood infusion?
It can be pushed as fast as tolerated in massive blood loss or shock scenarios Tolerance depends on comorbidities and other conditions - for example someone with Progressive Heart Failure cannot handle pushing whole blood usually unless it is dire
32
What is the cardinal rule of giving blood transfusions?
NEVER RUN WITH ANYTHING BUT NORMAL SALINE (not antibiotics, dextrose solution, electrolyte solution) because of interactions that can occur
33
Equipment needed to Transfuse Whole Blood
- Needle (19 gauge or larger; 23 in peds - bigger number = smaller lumen) - Standard straight or Y type blood infusion set with a 170 micron filter - 0.9% saline
34
Expected Outcomes of Giving Whole Blood
1. Resolution of symptoms and hypovolemic shock and anemia 2. increase in Hct and Hgb depending on number of units given
35
How much does 1 unit of whole blood increase Hct and Hgb?
1 unit = Hct increase by 3% and Hgb by 1 g/dL
36
If someone is given 3 units of whole blood what changes will be seen in their Hct and Hgb?
Hct will increase 9% and Hgb will increase byt 3 g/dL
37
Potential Complications from Whole Blood
Hemolytic Rxn Allergic Rxn (There is WBC in here) Hypothermia (from giving cold blood) Electrolyte Disturbances Citrate Intoxication Infectious Disease (Small but potential)
38
Citrate Intoxication
Citrate is a preservative in blood products that will metabolize to a base in the body If 5 units is given you could cause something like Metabolic Acidosis
39
You only have a __ hour window for use of blood products
4 hour window
40
Rules For Whole Blood Compatibility
* since it has both RBC and antibodies (plasma) these are the rules * 1. There is no universal donor or recipient 2. An ABO type must be given to the same ABO type (a to A, B to B, AB to AB, O to O) 3. Rh- blood can be given to Rh+ or Rh- blood, but Rh+ blood can only be given to Rh+ people
41
What sort of reaction occurs if someone is given the whole ABO or Rh blood?
A hemolytic transfusion reaction (They will attack one another)
42
Packed Red Blood Cells
RBCs centrifuged from whole blood with 80-90% of the plasma (antibodies and hidden viruses) removed Preservatives are added to increase viscosity (Hct increases) and increase shelf life
43
We give Packed RBCs to...
do the job of RBCs - getting increased oxygen carrying capability
44
2 Types of Packed RBC
1. Citrate Phosphate Dextrose Adenine (CPDA) 2. Additive Solution (100 mL) (AS-1, AS-3, or AS-5)
45
Indications to give Packed RBC
Increase O2 carrying capacity in symptomatic anemia d/t nutritional deficiencies or acute/chronic blood loss *This is only if they are without a need for volume expansion
46
What cases do NOT need packed red blood cells?
1. Need for volume expansion 2. Wound healing (albumin needed here) 3. General Wellbeing
47
First thing to do when you're going to administer Packed RBC
Check ABO and Rh compatibility - cross and test
48
How is Packed RBC administered?
1. Initially start slow (about 70 cc/hr) for 15 minutes 2. Increase rate as tolerates and infuse in 2-4 hours (never over 4) *you can subdivide it into aliquots *may need dilution with NS
49
Aliquots
A unit of the entire unit of blood we give (it is the same donor and blood product split into portions) It can be given to ease administration rate and is often used in Pediatric patients who cannot handle quick administration or heart failure patients
50
Why do we start infusing transfusions slow for 15 minutes?
To check if there is a transfusion reaction (we can tell because they will get a fever)
51
Equipment for Administering Packed RBC
1. Needle (19 gauge or larger; 23 gauge for peds) 2. Standard straight or Y type blood infusion set with 170 micron filter 3. 0.9% NS
52
Never do what with blood and other solutions?
never add medications or mix blood with other solutions
53
Expected outcome of Packed Red Blood Cell transfusion?
1. Resolution of Symptoms of Anemia 2. 1 Unit of blood will increase Hct by 3% and Hgb by 1 g/dL
54
Complications from Packed Red Blood Cell
Infectious Diseases Hemolytic Reaction Allergic Reaction (still a little plasma/WBC in here) Hypothermia Electrolyte Disturbances Citrate Intoxication
55
If we give 250 mL of packed red blood cells, and 500 mL of whole blood, is the patient receiving the same amount of RBC?
Yes, there is 250 mL in RBC in packed red blood cells, and in the whole blood it is 250mL of plasma and 250mL of RBC
56
Rules for Packed Red Blood Cell compatibility
*It is only cells here, no plasma antibodies* 1. O is a universal donor (no antigens on it) 2. AB is a universal recipient (no antibodies in their plasma to attack things) 3. A can be given to A, B can be given to B 4. Rh - can be given to Rh + or -, but Rh + can only be given to Rh +
57
Why is it a big problem to give an Rh- woman Rh+ blood?
The body will become sensitive to that agent, and if it does not cause a transfusion rxn now it can have impacts on if that woman has an Rh+ child later on (Erythroblastosis Fetalis)
58
Leukocyte Poor Red Blood Cells
A type of RBC given where WBC (responsible for allergic rxns) and plasma are washed out of the transfusion product to prevent further reactions It prevents alloimmunization
59
When is Leukocyte Poor RBC indicated?
If the patient has a history of blood transfusion reactions - non hemolytic allergic reactions (fever, rash, anaphylaxis)
60
Why is Leukocyte Poor RBC not just given to everyone if it can prevent allergic reactions?
It is very expensive
61
When and How is Washing Performed for Leukocyte Poor RBC ?
Washing is done at collection time It removes 80-95% of WBC and virtually all plasma It also removes potassium (K) Requites 1 hour to be processed Must be transfused within 24 hours if not frozen
62
What is storage like for Leukocyte Poor Red Blood Cells?
It is often frozen within 6 days of collection and has a high storage time of 10 years! Thawing and removal of cryoprotectant (glycerol) eliminates virtually all plasma and 99% of WBCs Needs 90 minutes to process and must be used in 24 hours
63
Alloimmunization
A transfusion reaction from receiving blood from the same species (ex: Human-Human) that could carry something like Cytomegalovirus
64
Expected Outcome of Leukocyte Poor Red Blood Cells
Prevention of rxn caused by infusion of WBCs and foreign proteins Removal of more (99.9%) of leukocytes may also decrease risk of alloimmunization and transmission of CMV
65
Complications from Leukocyte Poor RBC that can happen
Hemolytic Rxn (if not type and crossed) Hypothermia Electrolyte Disturbances Citrate Intoxication Infectious Disease (Still a very small risk)
66
Irradiated Red Blood Cells
RBC product exposed to a measured amount of ironizing (non harmful) radiation that stops donor lymphocytes from replicating and kill anything that could attack the recipient (viruses, bacteria, WBC, donor T cells, etc)
67
When is Irradiated RBC used?
Babies and Immunocompromised People
68
In order to use Irradiated RBC the bag must be labeled ...
IRRADIATED
69
Irradiated RBC carries no risk of what?
Radiation risk to transfusionist or recipient
70
What is the main goal of giving irradiated RBC?
to prevent Graft v Host Disease (Donor Attacks Receiver)
71
Indications for Irradiated RBC Use?
*To prevent post transfusion graft v host disease* Hodgkin's or Non Hodgkin's Lymphoma (Cancers) Acute Leukemia Congenital Immunodeficiency Disorders Low birth weight neonates Intrauterine Transfusions Bone marrow transplants
72
Expected Outcome of Irradiated RBC use?
Prevention of GVHD
73
Complications that can occur from Irradiated RBC use?
Hemolytic Rxn (if wrong type and cross) Hypothermia Electrolyte Disturbances Citrate Intoxication Infectious Disease
74
Platelet (Blood Product)
Removed form whole blood Still contains some RBCs (so it still must be type and crossed) Given to thrombocytopenic patients Can be gathered from pooled blood or apheresis (allowing it all to come from different people)
75
How many units of whole blood is needed to get one unit of platelets?
4-6 units of whole blood
76
Types of Platelet Transfusion
Random-Donor Single-Donor HLA-Matched (Human Leukocyte Antigen matched - still needs cross and test)
77
Indications to give Platelets
Thrombocytopenia (Chemotherapy induced too) Platelet Dysfunction PLT <10-20,000 or Active bleeding with PLT <50,000
78
Signs and Symptoms of PLT < 10-20,000
Petechiae Gum Bleeding Ecchymosis Hematuria Bloody Stool
79
Contraindications to give platelets?
Immune Thrombocytopenic Purpura Prophylaxis with massive blood loss or CABG
80
Why do we not give platelets to ITP patients?
The marker on the PLTs are "not you" and will be attacked
81
What should we give instead of PLTs to ITP patients
Steroids to increase immune response
82
Why do we not give PLT to massive blood loss patients?
It can actually decrease bone marrow function if too much- we do not want it to perceive there being enough platelets and to stop working
83
Monitor baby reticulocyte count because..
we should not give products like platelets if the bone marrow is able to make it itself - unless absolutely needed
84
Platelet Administration
ABO testing not necessary, but usually done Infuse at a rate of 10 mL/min and finish infusing within 4 hours
85
Platelets should not be ...
refrigerated
86
The max storage for platelets is ..
5 days
87
Equipment for a Platelet Transfusion
DO NOT USE AN RBC FILTER, use component with 170 micron filter from the blood bank (leukocyte poor filter) to catch leftover RBC and WBC 19 gauge or larger needle (like others) 0.9% NS!!
88
Expected Outcomes for Platelet Transfusion?
Prevention or resolution of bleeding d/t thrombocytopenia or PLT dysfunction
89
How often should we be rechecking PLT count with a PLT transfusion?
Within the first hour and every hour after to ensure the numbers rise
90
How does 1 unit of PLT change PLT count levels?
It increased PLT by 5000 cells/microL
91
If a patient has a PLT count of 5000, how many units of PLT will they need to get back to the 20,000 level?
3 units
92
Complications that can occur from PLT Transfusion
Infectious Diseases Allergic Rxns Febrile Rxns (Hemolytic is unlikely cause there are not really any RBC, but these are still possible from the RBC or WBC left)
93
Fresh Frozen Plasma (FFP)
Plasma very rich in clotting factors V, VIII, and IX with the platelets removed it is 91% water, 7% proteins, 2% carbohydrates Freezing it within 6 hours of collection preserves the clotting factors
94
Factor __ works with Factor ___ to turn prothrombin into thrombin
Factor V works With factor X
95
Low Factor V levels can mean what?
Inability to get a clot through the cascade
96
Low Factor VIII leads to?
Hemophilia A
97
Low Factor IX leads to?
Hemophilia B
98
Indications for Fresh Frozen Plasma Use?
A demonstrated deficiency of clotting factors: DIC, liver disease, coagulopathies, prior to invasive procedures PT or PTT >1.5 x the normal value
99
Clotting factors are made in the ___
liver
100
What is FFP NOT used for?
1. Volume expansion (use NS or albumin) 2. Nutritional Supplementation 3. Prophylaxis with massive blood loss or CABG
101
What value do we check if the patient is on Heparin ?
PTT
102
Albumin is a plasma protein that ...
maintains oncotic pressure - it helps pull fluids back to the vasculature at the venous end - this is why we need sufficient amounts of albumin
103
Administration of FFP
It contains no RBCs, but you must administer ABO and Rh compatible plasma after doing a cross and test because it is plasma (with antibodies in it) [Important to consider this because there are Rh antibodies in here an if we give Rh+ antibodies to a mom she could have an immune response against an Rh- baby later) Must be transfused within 24 hours of thawing Infused slower if there is risk for circulatory overload (200 mL/hour) Only give with NS
104
Why do we given a Mom Rogan mid pregnancy?
It gives metabolizable antibodies that will not be memorized by the immune system and thus can help prevent erythroblast fetalis
105
Equipment for FFP Transfusion
Do NOT use RBC filter Use component set with 170 micron filter obtains from Blood Bank 19 gauge or larger needle 0.9% NS (NEVER GIVE MEDS OR A DILUENT)
106
Expected outcome of FFP use
PT and PTT come down because we gave clotting factors Specific factor assays should be done to check specific levels
107
Complications from FFP
Allergic Rxn (WBC in plasma) Febrile Rxn (WBC in plasma) Circulatory Overload (biggest risk if done too fast) Infectious Disease
108
What is the biggest risk complication for FFP use?
Circulatory Overload
109
Plasma Compatibility rule for FFP?
*AB is now the universal donor (no antibodies) and O is the universal recipient (both antibodies)* Rh factor matters less, you can give Rh+ to + or - and vice versa because that antigen is usually on the RBC - exposure matters more A goes to A and B goes to B
110
Cryoprecipitate Antihemophilic Factor (AHF)
Lyophilized concentrate containing Factor VIII and VI, Fibrinogen, and mostly Factor XIII needed for the clotting cascade It is made from large pools of donor plasma
111
What is done to eliminate risk for viral transmission when using AHF?
It is heated or a solvent-detergent treatment is used
112
Lyophilization
Freeze Dried
113
Indications for AHF use
Factor VIII Problem: Hemophilia A (deficiency), von Willebrand's Disease, Hypofibrinogenemia, Factor XIII Deficiency Factor IX Problem: Hemophilia B (Deficiency)
114
Why does von Willebrand's Disease get AHF?
Factor VIII is carried by the von willebrand factor - without it the platelets cannot become sticky to form a clot
115
Factor XIII Deficiency
A rare autosomal recessive disorder that makes fibrin stabilizing factor deficiency - the clot will form without stabilizing fibrin so the clot will break down and bleeding will occur
116
AHF is only used ...
in life threatening emergencies when factor 13 concentrate is not available
117
Administration of AHF
- Dose is calculated based on plasma volume - 8-10 bags supply 2g fibrinogen (hemostatic dose) -Repeated doses may be needed to attain satisfactory serum levels Rate of infusion is quick here! because this is only really used in emergency scenarios (1-2mL per minute with 4 units (60 mL) in 15 minutes
118
Equipment for AHF administration?
Blood component administration set with 170 micron filter obtained from blood bank 19 gauge or larger needle 0.9% NS NEVER add anything to the NS
119
You must be familiar with what when giving blood?
Policies and procedures of your institution
120
Expected Outcomes after AHF treatment?
Hemostasis d/t increased levels of deficient factor Correction of factor and fibrinogen deficiencies Cessation of bleeding *Lab values are needed to assess effectiveness of treatment*
121
Complications of AHF use
Allergic Rxns Hepatitis potentially *Caused by WBC or IgA*
122
What are the rules of compatibility for AHF?
Same as with Fresh Frozen Plasma - *AB is now the universal donor (no antibodies) and O is the universal recipient (both antibodies)* Rh factor matters less, you can give Rh+ to + or - and vice versa because that antigen is usually on the RBC - exposure matters more A goes to A and B goes to B
123
Albumin Product
Products taken from plasma - 96% Albumin with 4% other plasma proteins and globulins
124
Plasma Protein Product
Products taken from plasma (like the Albumin Product) - 83% Albumin and 17% globulins
125
2 Available Forms of Albumin
1. 5% Iso Oncotic 2. 25% Solution
126
5% Iso-oncotic Albumin Solution
Solution w/ the same oncotic pressure as blood in a healthy person when given there will be no net movement of fluids unless there was very low albumin to begin with *Albumin controls oncotic pressure!*
127
25% Albumin Solution
Solutions 4x the oncotic pressure of the bloods normal oncotic pressure - because of this it pulls a lot more So be careful using this, can use with isotonic electrolyte solutions if there are not enough fluids (NS or Lactated ringers)
128
Indications to use Albumin and Plasma Protein Fraction
1. Volume Expansion (Protein exchange, shock, massive hemorrhage) 2. Acute Liver Failure (not making proteins) 3. Burns (everything is lost) 4. Hemolytic disease in the newborn
129
What may need to be given alongside Albumin and Plasma Protein Fraction until adequate circulating volume is established?
A diuretic
130
Since Albumin and Plasma Protein Fraction pulls fluids back into the vascular space what must we know?
KIDNEY FUNCTION
131
Hemolytic Disease in the Newborn
Immature baby liver leads to low albumin and plasma proteins, and d/t hemolysis you get RBC destruction leading to increased bilirubin levels The liver cannot conjugate the bilirubin in this state, so we give albumin to pull from the interstitial spaces in order to get rid of bilirubin and prevent newborn Jaundice (which can be dangerous)
132
Albumin and Plasma Protein Fraction Administration?
PPF is given 1-10 mL/min Albumin - 5% is given 1-10mL/min, but can be given faster; 25% is given slower at 0.2-0.4 mL/min\ ABO and Rh are not a factor in administration of this as there is no RBC or Plasma
133
When can 5% Albumin be given faster?
When the person is in shock with hypotension
134
Why is 25% albumin given much slower than 5%?
Its concentration It will cause significant increase in blood volume and blood pressure as it is given
135
Where can the RN find Albumin and Plasma Protein Fraction products?
NOT in the pharmacy and blood bank like other products It is already pasteurized, meaning any infectious disease causing things are dead, so it is in normal storage
136
Equipment for giving an Albumin or Plasma Protein Fraction Transfusion
19 gauge or larger needle Standard IV infusion set May require a specific filter Set and filter may be supplied alongside the solution in storage
137
Expected outcome of Albumin and PPF administration?
Acquire and maintain adequate BP and volume support
138
Complications of Albumin and PPF
Circulatory overload (a big one) Febrile Rxn (still possible regardless of pasteurization, so check vitals) *Compatibility does not matter in this cause and CANNOT transmit hepatitis or HIV since pasteurization process used to prepare products destroy viruses*
139
Fluid overload is a big problem, and if we give transfusions too quickly we can end up getting the signs and symptoms of...
heart failure
140
ISG - Immune Serum Globulins
Concentrated aqueous solution of gamma globulin containing a higher titer of antibodies It gives passive immunity via transfusion, but we also make this product with the liver (a large amount of this can be found in our plasma)
141
2 Types of ISG
Specific ISG Non Specific ISG
142
Non Specific ISG
Type of ISG obtained from a large pool of random donors It is used to increase Gamma Globulin levels and enhance the immune response via passive immunity
143
Specific ISG
Type of ISG prepared from donors with high antibody titer to known antigens (ex: Hep B Immune Glob (HBIG), Rh (D) Immune Glob (RhIG - RhoGAM), Varicella-Zoster Immune Glob (VZIG))
144
Why does ISG only give passive immunity
We give antibodies so the receiver does not have to and no memory cells are made as a result and eventually these will be metabolized - leaving no long lasting immunity So a snake or raccoon bite may need this
145
What is the downfall of ISG v a Vaccine for something like Hep B?
You will need more ISG if you are exposed again, but a vaccine can allow you to make your own antibodies in repeated exposure
146
Indications for ISG Transfusion
Passive Immune Protection against HBIG, RhIG, and VZIG Treatment for Hypogamma-globulinemia
147
HBIG
Immunoglobulin given following HBV exposure (Hep B)
148
RhIG
Immunoglobulin given following exposure to Rh (D) antigens through transfusion or pregnancy to prevent antibody development
149
VZIG
immunoglobulin given to immuno-compromised patients exposed to chicken pox
150
What sort of patient may get RhIG ISG?
A pregnant Rh - patient exposed to Rh+ blood
151
Who should not receive ISG?
Patients with a history of severe allergic reactions to plasma should not receive ISG
152
What can and cannot be transmitted via ISG?
Neither HIV nor Hep B is transmitted by ISG, however some IV gamma globulin solutions have been reported to transmit HEPATITIS C
153
Administration of ISG
Mostly given IM but IV also available Never give IM prep to IV d/t anaphylaxis risk Read package inserts carefully Give ISG prior to, or as soon after, exposure as possible
154
IM ISG Injections may be what and require what in response?
Painful and result in local irritation - they need a warm compress on the area
155
When must RhIG and VZIG be given to achieve optimal effect?
Within 72 hours of exposure
156
Administration of IV ISG
administer ONLY IV using a filter Do NOT administer with other medications Begin infusion within 2 hours of reconstitution
157
Most transfusion reactions result from ...
error, so know your stuff and double check
158
Expected Outcome of ISG Transfusion
Transient correction of gamma globulin deficiency OR prevention of disease through the passive administration of the antibody
159
Granulocyte Product
1 Unit: 10^10 granulocytes (WBC), variable amounts of lymphocytes (<10%), 30-50 mL of RBC, 100-400 mL of plasma, 6-10 units of platelets (optional) Volume w/ PLT is 200-400 mL, without is 100-200 mL It basically is WBC solution with basophils, neutrophils, and eosinophils
160
What is Granulocyte Product usually for?
A last ditch effort to stop infection
161
Indications for Granulocyte Transfusion
1. Acquired neutropenia from radiation or chemotherapy 2. Congenital WBC dysfunction 3. Serious infection unresponsive to conventional antibiotics
162
What about granulocyte product use is questionable?
its long term therapeutic benefit
163
How can we tell is Granulocyte product helped with an infection?
We cannot measure WBC count changes after giving, so the only way to know if it worked is if there is resolution of the infection (leading to its long term therapeutic use being questionable)
164
Granulocyte Administration
1 Unit is given daily and slowly over 1-4 hours It has a short survival time so it must be infused as soon as available (within 24 hours) *IT IS COLLECTED AND GIVEN QUICKLY/IMMEDIATELY
165
Equipment for Granulocyte Administration
Standard blood component set with 170 micron filter obtained from the blood bank 19 gauge of larger needle 0.9% saline DO NOT USE DEPTH TYPE MICROAGGREGATE OT LEUKOCYTE DEPLETION FILTER
166
Why should we not use microaggregate or leukocyte depletion filters with Granulocyte product?
Because it can trap WBC during infusion and then we are not giving what we are supposed to
167
With granulocyte product administration we have a very high risk for what?
Allergic and Febrile Reaction (so we must pre medicate)
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What do we use to premedicate with before giving Granulocyte Product?
Antihistamine Acetaminophen Steroids Meperidine
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Expected outcome of Granulocyte transfusion
Improvement in or resolution of infection No increase in peripheral WBC is seen in adults, but could be seen in children Improvement in clinical condition is the only measurement of treatment effectiveness
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Complications of Granulocyte Product Transfusion
Rash Febrile Reactions* Hepatitis *increased incidence of febrile, non hemolytic reactions with transfusion of granulocytes means you should infuse slowly and watch the patient closely Pulmonary Insufficiency if given with Amphotericin B
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Amphotericin B
Antifungal CANNOT BE GIVEN WITH GRANULOCYTES AS WITHIN 4 HOURS OF INFUSION THERE CAN BE A RISK FOR PULMONARY INSUFFICIENCY
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Compatibility Rules for Granulocytes
Since there is a little RBC in it, it follows packed RBC rules O is the universal donor AB is the universal receiver Rh- can be given to either Rh but Rh+ can only go to + A to A and B to B
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Transfusion Reaction
Antigens on the transfused product can be read and an antibody could be provided and produced causing an immune response and dangerous reaction
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2 Categories of Transfusion Reactions
Acute v Chronic
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Examples of Acute Transfusion Reactions
Acute Hemolytic Reaction Febrile Non Hemolytic Reaction (Most common) Mild allergic reaction Anaphylactic Reaction Circulatory Overload Sepsis Transfusion Related Acute Lung Injury (TRALI)
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Examples of Chronic Transfusion Reactions
Delayed hemolytic Hepatitis B Hepatitis C HIV-1 (AIDS virus) infection Iron overload Graft-versus-host disease (GVHD) Other: CMV, HTLV-I, malaria
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What are some of the General Manifestations of a Transfusion reaction
Fever (up 1-2 degrees C) chills muscle aches and pain back pain chest pain headache heat at site of infusion or along vein
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What are some of the Nervous System Manifestations of a Transfusion reaction
apprehension sense of impending doom tingling numbness
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What are some of the respiratory Manifestations of a Transfusion reaction
respiratory rate changes - tachy or bradypnea dyspnea cough wheezing rales
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What are some of the GIl Manifestations of a Transfusion reaction
nausea vomiting pain, abdominal cramping diarrhea (may be bloody)
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What are some of the renal Manifestations of a Transfusion reaction
changes in urine volume (oliguria, anuria, renal failure) Changes in urine color (dark, concentrated, shades of red brown and amber, may indicate the presence of Hgb or RBC in urine)
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What are some of the cardiovascular Manifestations of a Transfusion reaction
heart rate - tachy or bradycardia BP changes - hypotension and shock, hypertension Peripheral circulation - cyanosis, facial flushing Temp changes - cool and clammy or hot, flushed and dry Bleeding - generalized (DIC) or oozing at a surgical site
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What are some of the integumentary Manifestations of a Transfusion reaction
rashes hives (urticaria) swelling itching diaphoresis
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What are some of the Manifestations of a Transfusion reaction in an UNCONSCIOUS PATIENT
weak pulse fever hypotension visible hemoglobinuria increased operative bleeding (oozing at surgical site) vasomotor instability (tachycardia, bradycardia, hypotension) oliguria or anuria
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Reactions from different causes can exhibit similar manifestations, so...
every symptom should be considered potentially serious and transfusion should be discontinued until the cause is determined Assume the worse for safety reasons!!!
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Its important to get what before doing transfusions and during them?
Baseline vitals and 15 min in vitals and hourly after that maybe
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If a transfusion reaction begins, never do what?
Allow IV access to go away
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If a transfusion reaction begins what equipment needs to go back to the lab for testing?
Every piece of equipment: left over blood, tubing, urine, everything
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What to do when a transfusion reaction begins?
1. Stop Transfusion and keep the IV open with 0.9% NS 2. report rxn to both transfusion services and attending physician ASAP 3. Do clerical check at bedside of identifying tags and numbers 4. treat symptoms pre physicians orders and monitor vital signs 5. send blood bag with attached administration set and labels to the transfusion service 6. collect blood and urine samples and send to lab 7. document THOROUGHLY on transfusion reaction form and in the patients chart
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Acute Hemolytic Reaction
Acute Transfusion Rxn This occurs because of ABO INCOMPATIBLE whole blood, RBCs, or components containing 10 mL or more RBCs Antibodies in the recipients plasma attach to the antigens on transfused RBCs and cause RBC destruction
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Manifestations of an Acute Hemolytic Reaction
Chills and Fever LOWER BACK PAIN Flushing Tachycardia Tachypnea (comes with hypotension) Hypotension (comes with hypotension) Vascular Collapse Hemoglobinuria Hemoglobinemia Bleeding Acute renal failure Shock Cardiac arrest Death
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What are the most common symptoms of Acute Hemolytic Reaction? What is one of the unique symptoms?
Common: Fever and Chills Unique: Lower Back Pain
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How to manage an Acute hemolytic Reaction
treat shock if its present (priority is given to vascular stability always) Draw blood samples for serologic testing - do it slowly to prevent hemolysis send urine to the lab maintain BP with IV colloid solutions give diuretics as prescribed to maintain urine output (renal could fail in this case so maintain it) insert indwelling catheter or measure hourly input dialysis if renal failure occurs DOCUMENT!!!
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What not to do after an Acute Hemolytic Reaction?
DO NOT TRANSFUSE RBC CONTAINING COMPONENTS UNTIL TRANSFUSION SERVICE PROVIDES NEW CROSSMATCHED UNITS
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How to prevent Acute Hemolytic Reaction
Meticulously verify and document patient ID form sample collection to component transfusion
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Febrile Non Hemolytic Reaction
Acute Transfusion Reaction It is due to sensitization to donor WBC, PLTs, or plasma proteins RBC ARE NOT DESTROYED More common that Hemolytic reaction
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Manifestations of Febrile Non Hemolytic Reactions
Sudden chills Fever (increase more than 1 degree C) Headache flushing anxiety muscle pain
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How to manage a febrile non hemolytic reaction?
give antipyretics as prescribed AVOID aspirin in thrombocytopenic patients DO NOT restart transfusion
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Who is at highest risk for a Febrile Non Hemolytic Reaction
Anyone that has gotten a transfusion in the past
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Prevention for Febrile Non Hemolytic Reactions
Consider leukocyte poor blood products (filtered, washed, or frozen)
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Mild Allergic Reaction
Acute Transfusion rxn Sensitivity to foreign plasma proteins
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Manifestations of a Mild Allergic Reaction
Flushing itching Urticaria (Hives) NO FEVER
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Management for a Mild Allergic Reaction
Give antihistamine as directed If symptoms are mild and transient, transfusion may be restarted slowly (w/ benadryl) DO NOT restart transfusion if fever or pulmonary symptoms develop
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Prevention for Mild Allergic Reaction
Treat prophylactically with antihistamines
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Anaphylaxis and Anaphylactic Shock
Acute Transfusion reaction Caused by infusion of IgA proteins to IgA deficiency recipients who has developed an IgA antibody Very rare (1 in 40000 to 270000 transfusions) more severe - it is a massive histamine release
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What type of person may have an anaphylactic reaction?
IgA is low in people, so if they had a plasma transfusion before they could have made IgA antibodies causing this reaction A transfusion rxn in the past would set them up for a shock reaction now
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IgA
An immunoglobulin not found in great abundance in people it is in the GI tract, saliva, tears, body fluids
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Due to anaphylaxis, it is important to always as a transfusion patient...
If they have had a transfusion reaction in the past
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Manifestations of Anaphylaxis
Anxiety Urticaria Wheezing Throat Swelling Progresses to Shock - Cyanosis, Shock, Possible Cardiac Arrest
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Management for Anaphylactic Reaction
1. Initiate CPR if indicated 2. Have EP ready for injection (0.4 mL subQ or 0.1 mL diluted in 10 mL NS for IV) 3. DO NOT RESTART THIS TRANSFUSION
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Why is EP good for anaphylaxis?
EP can stop the mass histamine release that is occurring
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Prevention Measures for Anaphylactic Reaction
Transfuse extensively washed RBC products, from which all plasma has been removed Use blood from an IgA DEFICIENT DONOR (so no antibodies occur) Ask if they've had a reaction or transfusion before
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Circulatory Overload
Acute Transfusion Reaction Fluid is administered faster than the circulation can accommodate causing this reaction More common in kids and smaller people
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Circulatory overload causes ___ symptomology
Lung
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Manifestations of Circulatory Overload
Cough dyspnea pulmonary congestion (rales) HA HTN tachycardia distended neck veins
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Management for Circulatory overload
place patient upright with feet in dependent position to get fluid more to the periphery administer prescribed diuretics, oxygen, and morphine (to help breathing and dilate the venous system) Phlebotomy may be indicated (remove blood) Do an assessment every hour Next time, blood must be given in aliquats
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Crackles in the lung indicate...
pulmonary edema
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Prevention of Circulatory Overload
adjust transfusion volume and flow rate based on patient size and clinical status have transfusion service divide units into smaller aliquots for better spacing of fluid input may need to give a diuretic between units if more than 1 unit is being given
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Sepsis
Acute transfusion reaction this is transfusion of contaminated blood components
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Manifestations of Sepsis
Rapid onset of chills high fever vomiting diarrhea marked hypotension! *(d/t going into shock)* shock
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What 3 important things need to be documented due to sepsis reactions?
1. That blood is not expired 2. That blood was not sitting around for a long time 3. That we have not exceeded the 4 hour time frame
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Management of Sepsis
Obtain culture of patients blood and send bag with remaining blood to transfusion service for further study (to find the antibiotic against a specific organism needed) Treat septicemia as directed: antibiotics, IV fluids, vasopressors (increase BP to treat shock), steroids
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Prevention of Sepsis
Collect, process, store, and transfuse blood products according to blood banking standards and infuse them within 4 HOURS OF STARTING TIME
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TRALI
Acute transfusion reaction "Transfusion Related Acute Lung Injury" It occurs when transfused donor WBCs react with recipient WBCs resulting in agglutination and aggregation in the lungs and thus pulmonary damage
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Where does TRALI occur?
the lungs
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Manifestations of TRALI
dyspnea wheezing fever chills bronchospasms crackles restlessness non productive cough pulmonary infiltrates HTN or Hypotension systemic inflammatory symptoms
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What is TRALI NOT a sign of?
CHF or Volume Overload
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When unhooking a blood product what should be done for flushing?
The whole line should not be flushed because it still has product in it, it should be unhooked at site of insert
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Management of TRALI complications
1. STOP infusion and maintain patent IV line 2. Place in supine position 3. maintain open airway - mechanical ventilation if necessary (may need intubation) 4. Obtain VS and record 5. notify physician 6. administer fluids and EP, steroids, and diuretics per orders 7. Administer O2 8. Monitor VS and urine output (renal failure can occur with a perfusion problem) 9. Document event thoroughly
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how many cases of TRALI are fatal regardless of aggressive supportive care?
5-10 % (luckily PP of CO2 returns to pre transfusion levels in 48-96 hours and CXR returns normal in 98 hours so 90-95% of cases end well)
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Delayed hemolytic Reaction
Delayed Transfusion Reaction Causes RBC breakdown slowly leading to bilirubin wastes building up - can occur as early as 3 days to several months , but it is d/t the destruction of transfused RBCs by alloantibodies no detected during crossmatch HCT will drop from RBC lysis Usually occurs 1-2 weeks post transfusion
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Manifestations of Delayed hemolytic reaction
fever mild jaundice (waste - bilirubin buildup) decreased HCT
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Treatment for Delayed Hemolytic Reaction
generally, no acute treatment is required hemolysis that is severe enough can warrant further transfusions
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Hepatitis B
Delayed Transfusion Reaction involving inflammation of the liver (from elevated liver enzymes (AST and ALT) dying.
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Manifestations of Hep B
elevated liver enzymes (AST and ALT) anorexia malaise nausea and vomiting fever dark urine (increased from hemolysis occurring releasing heme) jaundice (increased bilirubin)
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Treatment for Hep B
usually resolve spontaneously within 4-6 weeks chronic carrier state can develop and can result in permanent liver damage though it should be treated symptomatically You can get passive IG for this but you can also get a vaccine for active immunity
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Hepatitis C
Delayed transfusion reaction Similar to Hep B (liver inflammation)
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How is Hep C different from Hep B?
Hep C usually has less severe symptoms (but could cause chronic liver disease and cirrhosis thus warranting a liver biopsy every 4-5 years)
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Treatment for Hep C
Before, anti-HCV test accounted for 90-95% of all post transfusion hepatitis - but now risk is low Treat symptomatically (treatment is worse for this than in B)
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HIV-1 (AIDS Virus) Infection
Delayed Transfusion reaction Can be asymptomatic for up to several years, with flu like symptoms 2-4 weeks after exposure, and alter symptomology and AIDS far out
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Later S/S of HIV-1
weight loss diarrhea fevers lymphadenopathy thrush pneumocystis pneumonia
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What is the current estimated risk of infection with HIV-1 from a blood transfusion?
1:30,000 to 1:1,500,000 depending on geographic area
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Iron Overload
Delayed transfusion reaction This is an increase in iron when you are NOT bleeding RBC is begin destroyed and heme is going to the liver and will be deposited around the body causing harm
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What is a potential cause for Iron Overload?
constant blood transfusions (like in chronic anemia or chronic renal patients)
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Manifestations of Iron Overload
congestive heart failure arrhythmias impaired thyroid and gonadal function diabetes cirrhosis commonly occurs in patients receiving >100 units for chronic anemia
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Treatment for Iron Overload
Treat Symptomatically One medicine is Deferoxamine (Desferal) which chelates and removes accumulated iron via the kidneys and can be administered IV or subQ
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Graft V Host Disease
Delayed Transfusion Reaction It is when the transfusions WBC attacks the receiver (unlike host v graft disease) - result of replication of donor lymphocytes (graft) in the transfusion recipient (host) that attack the recipient's RBC Common occurrence in an immunocompromised persons
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Manifestations of GVHD
fever rash diarrhea hepatitis
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Treatment for GVHD
there is no effective therapy so prevention is crucial with this
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How to prevent GVHD
1. Irradiate blood products intended for babies or immunocompromised patients 2. May want to use first degree family members donations
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What is one of the most important things to know when administering blood products?
KNOW HOSPITAL POLICY
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What must be gathered before any blood transfusion can occur?
INFORMED CONSENT (you as the nurse must gauge their understanding and obtain and record baseline vitals while the physicians gets the consent)
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What may need to be done to prepare for transfusion?
Get vitals Premedicate with prophylactic meds per physicians order Prep infusion site and start IV 0.9% NS Use appropriate needle size, filter, and administration set
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What sort of Special Administration Devices are needed for Blood Component Administration?
Electromechanical Infusion Devices (only if approved) External Pressure Infusion Cuffs (DO NOT USE BP CUFFS) Blood Warmers
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What is the benefit of blood warmers?
they decrease incidence of arrhythmias or cardiac arrest associated with massive infusion of cold blood components should be used rather than microwave, hot tap water, unmonitored water bath, etc
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If mult blood components are indicated...
check with the physician to establish an order of priority based on the situation *also may need lasix to prevent pulmonary edema*
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What to verify about components you want to transfuse?
1. Get from transfusion service and check for abnormalities - should be a deep red color 2. record name of person issuing blood, person to whom blood is issued, and date/time of issue 3. Read instruction on product label, check expiration date and time 4. recheck physicians order sheet to verify component ordered 5. compare ABO group and Rh type on the patients chart to that on bag tag and bag label LOTS OF CHECKING AND YOU NEED CONSENT
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What to do after doing checks for blood transfusion?
1. 2 qualified individuals should verify patient ID and documentation (most transfusion errors are a result of error in patient or component ID, so check name on bag bracelet, and have them say it) 2. Do NOT proceed until all comparisons match EXACLTY - contact transfusion service if any discrepancies 3. Sign transfusion form immediately prior to transfusion 4. document date and time transfusion started 5. keep all ID attached to blood container if paper BE METICULOUS
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What should be done upon Administration of blood components?
Start slow and observe closely for the first 15 minutes - educate patient and family what s/s to watch for Repeat vitals at 15 minutes and compare to baseline, can adjust flow if everything is ok monitor and record vitals per institution policy record this in the permanent record return empty blood containers and leftover product to transfusion service (never put it in fridges or freezers no monitored by them) *can get plasma derivatives from storage and pharmacy/central stores*
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What things should be record on transfusion permanent record?
patient name and ID # component and component #s initial of individuals verifying ID and starting/ending transfusion start and end times volume transfused and immediate response
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Who can confirm a transfusion?
2 people: 2 RNs OR 1 RN and an LPN OR 1 RN and 1 Physician
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Blood Administration Pitfalls to Avoid
Do NOT store component in nursing unit or other unmonitored refrigerator Do NOT keep blood out of a monitored refrigerator for more than 30 minutes before beginning transfusion Do NOT warm blood in an unmonitored bath or sink, or microwave oven Do NOT administer any blood component without a blood filter Do NOT use the same blood filter for more than 4 hours Do NOT transfuse a unit of blood for over 4 hours Do NOT add medications, including those intended for intravenous use, to blood or components or infuse through the same administration set as the blood component Do NOT allow any solution other than 0.9% Normal Saline to come in contact with the blood component or the administration set
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Universal Precautions
All patients should be assumed to be infectious for blood-borne pathogens Gloves MUST be worn when handling a patient’s body fluids Protective mask, eye goggles, and gown should also be worn if there is the potential for splash from or mucous membrane exposure to blood or other body fluids Take care to prevent injuries when using needles, scalpels, and other sharp instruments or devices NEVER recap needles ALWAYS dispose of needles immediately in a biohazard container Immediately & thoroughly wash hands and other skin surfaces that are contaminated with blood, body fluids containing visible blood, or other body fluids to which universal precautions apply Review your institutional guidelines for observing universal precautions *VERY IMPORTANT DURING THE COVID-19 PANDEMIC!!*