Blood Component Preparation and Storage Flashcards

(111 cards)

1
Q

After collection, a unit of WB intended for platelet production should be stored so that

a. the temperature cools towards 20-24C
b. the temperature cools towards 1-6C
c. the temperature cools towards 1-10C
d. there is no temperature requirement for storing WB prior to component production

A

Correct: the temperature cools towards 20-24C

Recall that platelets are optimally stored at 20-24C. If you intend to make platelets from the whole blood collected, then you should store the collected whole blood in a manner that will cool the blood towards 20-24C. It would be preferable to put the whole blood units in shipping containers that are NOT refrigerated, but are closer to a 20-24C range. The units will take some time to cool from body temperature (37.5C) to 20-24C

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2
Q

A unit of CP2D RBCs has a HCT of________, while a unit of AS-3 RBCs has a HCT of ____.

a. 90%, 55-65%
b. 80%, 55-65%
c. 55%, 80-90%
d. 50%, 75-85%

A

Correct: 80%, 55-65%

This question is written to mimic a question from the SBB exam. The correct answer is not an entire answer. The technical manual states that a unit of CP2D RBCs has a HCT of 65%-85% and a unit of AS-3 RBCs has a HCT of 55%-65%. None of the responses here match the Technical Manual exactly. When you take the SBB exam, you will quite often be in a position to choose the BEST response. Of the choices given, B is the best response.

To review the components, CP2D RBCs are red blood cells that are collected into a blood bag that contains CP2D anticoagulant. AS-3 RBC’s are Red Blood Cells to which the additive solution AS-3 is added to extend the life of the component.

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3
Q

A unit of whole blood collected from a volunteer whole blood donor is expected to yield how many units of factor VIII?

a. 40 IU
b. 80 IU
c. 150mg
d. 250mg

A

Correct: 80 IU

A unit of whole blood will produce one unit of Cryoprecipitate. The average unit of Cryoprecipitate has 80 IU of Factor VIII

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4
Q

Citrate-Phosphate-Dextorse-Dextrose (CP2D) is a common anticoagulant added to whole blood at the time of collection. The purpose of the DEXTROSE in this solution is:

a. to keep the blood from clotting
b. to extended the shelf life of the RBC to 42 days
c. to act as a buffer to control decrease of pH
d. to support ATP generation in RBC metabolism

A

Correct: to support ATP generation in RBC metabolism

Anticoagulant solutions typically contain Dextrose. The purpose of Dextrose is to support RBC metabolism which produces ATP for energy to maintain the RBC integrity

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5
Q

Quality Control is performed on Cryoprecipitated AHF. To perform the QC, 10 units of CRYO are pooled, and the fibrinogen and Factor VIII are assayed. The results are as follows:Total Factor VIII Activity = 910 IU Total Fibrinogen =2000 mg total. According to AABB, is this QC acceptable?

a. Yes. All values meet requirements
b. No. CRYO units may not be pooled when performing QC
c. NO. QC fails for Fibrinogen
d. NO. QC fails for Factor VIII activity

A

Correct: Yes. All values meet requirements

The AABB requires that Cryoprecipitate units are prepared in such a manner so that the final units of CRYO have a minimum of 80 IU and 150mg Fibrinogen. If you are testing a pool of 10 units, you would divide the assay result by 10 and compare it to the minimum standard. 910/10 = 91 IU Factor VIII and 2000/10 = 200mg Fibrinogen. Both results exceed the minimum QC requirements

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6
Q

Cryoprecipitated AHF contains all of the following EXCEPT:

a. Factor VIII
b. von Willebrand factor
c. Fibrinogen
d. Factor VII

A

Correct: Factor VII

CRYO does not contain Factor VII. That thaws into the plasma during component production of CRYO

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7
Q

Cryoprecipitated AHF should be stored at a temperature of ______ and has a shelf life of _____.

a. -18C or below; 1 year
b. -18C or below, 5 years
c. -65C or below, 1 year
d. -65C or below, 5 years

A

Correct: -18C or below; 1 year

This is straight out of the AABB standards. It is important that you know the storage temperatures and expiration dates for ALL components

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8
Q

Thawed Cryoprecipitated AHF has a shelf life of ______ if stored at _______.

(note: we are taking about CRYO that is prepared for transfusion-NOT during the initial component production)
a. 24 hours, 1-6C
b. 6 hours, 20-24C
c. 6 hours, 1-6C
d. 24 hours, 20-24C

A

Correct: 6 hours, 20-24C

When preparing CRYO for transfusion, the thawed product should be stored at room temperature and used within 6 hours. It is stored at room temperature to keep the cryo reconsituted. It has an expiration time of 6 hours. One thing to note is that we are talking about a CLOSED system here. If units of cryo are pooled in an open system, then the expiration time is lowered to 4 hours to limit the risk of bacterial contamination

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9
Q

The maximum shelf life of irradiated RBCs is:
a. 24 hours
b. 21 days
c. 28 days
d .No change from original expiration date

A

Correct: 28 days

Irradiation can accelerate the lesion of storage in RBCs, therefore the expiration date is shortened to 28 days or the date of the original expiration, whichever is shorter. That is to say that you can not exceed the original expiration date. So if you irradiate a unit of RBCs that is expiring in 5 days, the expiration date remains 5 days and is NOT extended to 28 days. Again, this question is a typical SBB type question. You might be tempted to select the option of “original expiration date” but choosing the maximum of 28 days is the more correct response.

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10
Q

RBC storage varies with the anticoagulant/preservative used. All of the following are properly paired items EXCEPT:

a. CPD: 21 days
b. AS: 42 days
c. CPDA1: 35 days
d. CP2D: 35 days

A

Correct: CP2D: 35 days

CP2D anticoagulant is 21 day expiration

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11
Q

If stored at 1-6C, thawed Fresh Frozen Plasma should be transfused within:

a. 4 hours
b. 6 hours
c. 24 hours
d. 5 days

A

Correct: 24 hours

You may have been tempted to select “5 days”. The reason that is not a correct answer is one of labeling. After the unit is thawed for 24 hours, it is no longer considered “Fresh Frozen Plasma”. It is now “Thawed Plasma”. While it may seem a minor issue of semantics, labeling confers a sense of what the component indications and uses are. “Fresh Frozen Plasma” is a product that is capabale of providing optimal levels of labile and stabile coagulation factors. Once it becomes “Thawed Plasma”, it is capable of providing only optimal amounts of STABILE coagulation factors.

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12
Q

Irradiated platelets have an expiration time of:

a. 4 hours from time of irradiation
b. 24 hours from time of irradiation
c. 3 days from date of irradiation
d. no shortened expiration time due to irradiation

A

Correct: no shortened expiration time due to irradiation

Because Platelets last only 5 days, there is no need to shorten the expiration date due to irradiation

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13
Q

he correct temperature for shipping Red Blood Cells (RBCs) is:

a. 1-6C
b. 1-10C
c. 20-24C
d. There is no specific temperature range for shipping RBCs

A

Correct: 1-10C

Shipping guidelines are more lenient than storage guidelines.

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14
Q

A unit of RBCs was returned to the blood bank at 10:45am from the oncology unit. The technologist who receives it inspects the unit, and determines that the container has not been penetrated, and 5 sealed segments remain attached to the RBC unit. She notes that the unit was issued from the blood bank at 7:45am. The technologist logs the unit back into the blood bank computer system, with a comment that the unit was issued and returned. She then places the RBC back in the available inventory. (note: the oncology unit does NOT have a monitored RBC storage refrigerator)The actions taken by this technologist can best be described by which statement below?

a. Actions are acceptable
b. Actions are unacceptable, since RBCs can never be returned once issued to the floor.
c. Actions are unacceptable, since RBC was out of a monitored refrigerator for too long a period
d. Actions are unacceptable, as the RBC should have had its labeling altered to reflect its return status.

A

Correct: Actions are unacceptable, since RBC was out of a monitored refrigerator for too long a period

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15
Q

Which of the following statements is TRUE?

a. To prepare Fresh Frozen Plasma (FFP), plasma must be separated from red blood cells within 24 hours
b. If an additive solution is used, the expiration date for RBCs stored at 1-6C is 42 days after phlebotomy
c. To prepare cryoprecipitated AHF, FFP is thawed at 20-24C.
d. The expiration date for RBCs that are frozen and stored at -65C or below is 5 years from date of freezing.

A

Correct: If an additive solution is used, the expiration date for RBCs stored at 1-6C is 42 days after phlebotomy

FFP must be prepared by separating the plasma from whole blood and placing into the freezer within 8 hours of collection (or less depending on the type of anticoagulant used-check the manufacturer;s product insert)

When preparing Cryoprecipitated AHF, the plasma is separated from the whole blood, frozen, then thawed at 1-6C and the residual plasma removed.

Frozen RBCs are stored at -65C or below and have an expiration date of 10 years

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16
Q

The preferred method for providing leukocyte reduced RBC components is:

a. use of cytomegalovirus CMV-negative units
b. use of a leukocyte reduction filter that leaves a residual of < 5.0 X 106 leukocytes
c. washing
d. irradiation

A

Correct: use of a leukocyte reduction filter that leaves a residual of < 5.0 X 106 leukocytes

Washing is not validated to remove adequate amounts of WBCs. Irradiation affects the WBCs so they can’t respond to the host, but does not actually remove them. CMV negative units are not necessarily WBC free. The units may be seronegative for CMV but still contain significant amounts of WBCs

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17
Q

To prepare a unit of platelets from whole blood, which method below is best?

a. two light spins
b. a hard spin followed by a light spin
c. a light spin followed by a hard spin
d. two hard spins.

A

Correct: a light spin followed by a hard spin

To prepare platelets from whole blood, first the whole blood unit is spun using a slower RPM (a “light” spin). This separates the whole blood into three layers: RBC layer, buffy coat, and platelet rich plasma. The blood bag is designed to allow the platelet rich plasma to be transferred in a closed system to another bag which has a satellite bag. The two bags are then heat sealed and separated. The two bags together are spun with a longer, faster spin (a “hard spin”) to pack the platelets into the lower portion of the bag. After the second centrifugation, most of the plasma is removed to the satellite bag, leaving the platelets suspended in enough plasma to maintain the component for 5 days.

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18
Q

Washed Red Blood Cells are ideal for a patient who requires:

a. RBCs free of leukocytes
b. RBCs that will not alloimmunize the patient
c. RBCs free of IgA proteins in the plasma
d. RBCs that are CMV negative

A

Correct: RBCs free of IgA proteins in the plasma

The other indications are not valid. Washing removes the plasma, but is not validated to remove WBCs, CMV or RBC antigens

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19
Q

What is the purpose of irradiating blood components?

a. To prevent CMV transmission
b. to prevent proliferation of transfused T lymphocytes
c. to remove lymphocytes from the components
d. To prevent HLA alloimmunization

A

Correct: to prevent proliferation of transfused T lymphocytes

The lymphocytes are still present, but they are inactivated

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20
Q

Which of the following RBC units would NOT be suitable for freezing using a high glycerol method?

a. RBCs from a donor who ingested aspirin 48 hours before phlebotomy.
b. RBCs from a donor who has sickle cell trait
c. RBCs from a donor who is CMV+
d. RBCs from a donor who had a HCT of 40% at time of phlebotomy

A

Correct: RBCs from a donor who has sickle cell trait

I marked this as an extra credit question, because I was not sure how well this would be conveyed in the readings. The statement is implied, but not stated directly in the Technical Manual. I included it to be sure that you would think about the suitability of RBCs for freezing, and to make sure that you learn this. The presence of the Hemoglobin S, even in a heterozygous state, means that the RBCS in a lowered concentration of oxygen can collapse on themselves and form “sickle” shapes. Adding glycerol to the RBCs for freezing maintains the integrity of normal RBC membranes, but the lowered oxygen can result in HbS RBCs to sickle

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21
Q

How many autologous units can one person donate before they lose 1 gram of iron?

a. 1 unit
b. 4 units
c. 10 units
d. 6 units

A

an average unit of RBCs contains approx 200-250mg of iron.

1000mg=1g

200-250mg iron content in one unit of RBCs = 0.20-0.25g iron content in one unit of RBCs

to reach 1g you’ll need 5-4 units

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22
Q

The rationale for deglycerolizing frozen RBCs with extensive washing is:

a. Glycerol is not approved by the Food and Drug Administration (FDA)
b. Glycerol is toxic to kidneys
c. Glycerol can cause anaphylaxis
d. Glycerol can cause hemolysis

A

Inadequately removed glycerol can cause in-vivo or in-vitro hemolysis. The presence of glycerol in the red cells renders them hypertonic relative to the solutions with physiologic osmolalities. If the cells are placed in these solutions, there is movement of water into the cells, resulting in their rupture. During the process of deglycerolization, solutions of prgressively lower osmolality are used to wash the red cells. This allows for the removal of the glycerol from the cells without excess hemolysis. Gloverol is approved by the FDA. It is unknown whether glycerol may cause renal toxicity, anaphylaxis or thrombocytopenia.

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23
Q

24 units of whole blood are collected at a mobile blood drive. They are placed into an igloo cooler, and transported to the component production laboratory for RBC production. When the units arrive, the igloo temperature is 18C. Which statement below represents the BEST course of action for these components?

a. make RBCs
b. quarantine all blood products and contact the supervisor
c. make platelets
d. discard all the whole blood units

A

Correct: Make RBCs.

AABB standards require a validated method to cool blood continuously toward 1-10C if transported from collection site. While there is no mandated temperature with which the components should be deemed acceptable upon arrival, an inspector of a blood collection facility would be more concerned with asking questions such as

How is blood stored and transported to ensure the integrity of the components to be manufactured?

What components does your facility make from whole blood units?

What is the process for qualifying the containers in use?

Take note that there are also requirements in place to cool products to a certain temperature within a particular time frame (for example, RBCs must be refrigerated between 1-6C within 8 hrs of collection) Thus, the above scenario, assuming all approved standard operating procedures of the facility are met, would allow for the production of RBCs. There is no evidence to suggest the whole blood was handled or processed inappropriately.

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24
Q

Which of the coagulation factors below will not be viable in a thawed unit of plasma frozen within 24 hours of phlebotomy?

a. V, VII, X
b. II, V, VIII, XI
c. I, V, VII, X
d. V, VIII

A

Correct: V, VIII

Remember that the labile clotting factors will remain active and at therapeutic levels only 24 hours after thawing. After that time period we can no longer use the component as FFP. We must now call it “plasma” and remove the words “Fresh Frozen”. Fresh Frozen Plasma is expected to have all coagulation factors viable and in the expected amounts present in a normal individual.

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25
A unit of CPDA-1 RBC expiring in 35 days is split into 5 small aliquots using a sterile pediatric quad set and prepared in a closed system. Each aliquot must be labeled as expiring in: a. 6 hours b. 24 hours c. 4 hours d. 35 days
Correct: 35 days Because the bags are aliquoted into a closed system, the expiration date does not change. Had you used an open system the expiration date would have been changed to 24 hours from the time the unit was spiked with the pedi-bags. It may be that you will not use the unit for babies after the 7 days have passed if your SOP requires that you use fresh RBCs. However, this does not affect the expiration date of the RBC units themselves.
26
The Code of Federal Regulations established by the FDA stresses the importance of ensuring blood products are safe, pure, and potent. An important QC test to assess platelet concentrate potency/viability is: a. plasma potassium concentration b. plasma pH c. prothrombin time d. bleeding time
Correct: Plasma pH The pH value is established as a quality parameter for stored platelet concentrates. pH values below 6.2 are associated with significant reduction of in vivo survival of the stored platelets. During storage, platelets generate metabolites, especially lactate which acidify the platelet concentrate. Plasma pH of platelets has to be maintained at 6.2 or greater during storage. While the other choices are factors that can shed light on the function and viability of platelets, only pH is included in the component QC testing on blood components. AABB Stds 32nd ed. 5.7.4.18 Validation and quality control of Platelets prepared from Whole Blood shall demonstrate that at least 90% of units sampled contain ≥5.5 × 1010 platelets and have a pH ≥6.2 at the end of allowable storage. FDA criteria apply
27
A unit of CP2D whole blood was collected for production of AS-3 LRBC. Due to a plastic shortage there is no more AS-3 available. The technologist has already separated plasma and RBC. What should be done with the final RBC (all testing acceptable)? a. Discard the RBC because the AS-3 could not be added b. Label the RBC with a 21 day expiration date c. Label the RBC with a 42 day expiration date d. Discard the units and consult MD
Correct: Label the RBC with a 21 day expiration date If the AS-3 cannot be added, the RBC is still acceptable but the expiration date is based on the original CP2D anticoagulant, so it should be labeled with a 21 day expiration date. There is no need to quarantine or discard the units if they can become a different type of product. This is the beauty of allowing for different variables in component production (ex thawing cryo in a cold water bath vs fridge)
28
A regular donor has been recruited to start giving double RBC donations because he is Yta(-). His last donation was an apheresis platelet donation on 04-05-22. The donor is schedule to donate the RBC pheresis on 04-13-22. On 04-05-22, his post-donation blood work gave the following results: Platelet count = 135,000/uL HCT = 38% Hgb = 13.0 Which statement below represents the correct way to handle this donor? a. The post-donation results qualify him to donate on 4/13/22. b. The platelet count must be retested and found acceptable prior to donating on 4/13/22. c. The HCT must be retested and found acceptable prior to donating on 4/13/22. d. The donor must be deferred for 16 weeks after the previous donation and is not qualified to donate on 4/13/22.
Correct: The HCT must be retested and found acceptable prior to donating on 4/13/22. Remember that RBC pheresis requires donors to have a minimum HCT of 40% The platelet count is not relevant to erythropheresis, and the deferral period is 48 hours. After he gives the erythropheresis, he will be deferred for 16 weeks.
29
A donor has given platelets pheresis 4 times in 2021, and the most recent donation was 12/30/21. He has been recruited to donate a unit of granlulocytes by apheresis on 04/08/22. His previous donor suitability questions were acceptable and his previous viral marker tests were all nonreactive. He donates on 04/08/22 and is found to be O Positive, with a negative antibody screen. What should be done concerning the viral marker testing for this donation? a. Viral marker testing is required before the unit is released to the patient b. Viral marker testing is not required because he has negative results within the past 6 months. c. Viral marker testing is not required for granulocyte pheresis collections. d. The unit may be emergency released to the patient before viral marker testing is performed.
Correct: The unit may be emergency released to the patient before viral marker testing is performed. Granulocyte pheresis have an outdate of 24 hours, which necessitates that units be emergency released before all testing is completed. We still must perform the testing, however, even if the unit is already released and transfused. The only exception to this is if the donor gave blood within the past 30 days. If the previous viral marker tests were nonreactive, then we could note that on the label that it was testing within the past 30 days.
30
A patient (born female) is scheduled to donate an autologous WB component. They are evaluated and the following information is noted: Hgb = 12.0 g/dL Oral Temperature 37.0F Medications: Accutane, Tegison, Plavix, Cephalosporin Donor questions: Donor mentions that they had a GI infection and is taking a 7-day course of antibiotics. They had two days of medications but is now asymptomatic. What action should be taken with this donor? a. Accept the donor because their oral temperature is normal and they are asymptomatic b. Defer the donor until they have finished the medication c. Defer the donor because their Hgb is too low d. Accept the donor and irradiate the unit as a precaution
Correct: Defer the donor until they have finished the medication We cannot draw a donor with an active infection currently taking antibiotics even if their symptoms have resolved and the oral temperature is normal. Irradiating the unit will not prevent bacterial contamination. The Hgb is acceptable, so that is not deferring.
31
Which of the following is proper procedure for preparation of platelet concentrates? a. One light spin followed by one hard spin b. One light spin followed by two hard spins c. two light spins d. two hard spins
a. One light spin followed by one hard spin Whole blood derived platelets are prepared by a light spin to separate the red blood cells from the platelet-rich plasma (PRP), followed by a hard spin of the PRP to concentrate platlets. Platelets are prepared by first centrifuging the whole blood with a light spin which pack the RBCs, but leave the platelets suspended in the plasma above as platelet rich plasma (PRP). The PRP is then separated, and centrifuged with a hard spin which will pack the platelets against the side of the bag, and then the excess plasma may be removed.
32
Irradiation of donor blood is intended to prevent which type of adverse transfusion reaction? a. Febrile Nonhemolytic (FNHTR) b. Transfusion Related Acute Lung Injury (TRALI) c. Transfusion Associated Graft vs Host Disease ( TA GVHD) d. Transfusion Associated Sepsis
Transfusion Associated Graft vs Host Disease ( TA GVHD) This disease occurs due ot the co-transfusion of viable lymphocytes in cellular blood products, such as whole blood, red blood cells, platelets, granulocytes, and fresh plasma. If the immune system of the recipient cannot recognize and destroy the co-transfused lymphocytes, they can engraft and mount an immunologic response against the host. A number of technologies can abrogate the risk of TA-GVHD in these include irradiation of the product and pathogen-reduction and both of these methods render the DNA in the co-transfused lymphocytes incapable of participating in cell division. Be aware of those products which would benefit from irradiation (cellular, rbc, platelet) vs those which would not (non-cellular, plasma, cryo)
33
A unit of whole blood collected should yield a minimum of..... a. 25 IU of Factor IX and 150 mg of Fibrinogen b. 80 IU of Factor VIII and 150 mg of Fibrinogen c. 80 IU of Factor VIII and 100 mg of Fibrinogen
b. 80 IU of Factor VIII and 150 mg of Fibrinogen AABB Standard 5.7.4.17 CRYOPRECIPITATED AHF Cryoprecipitated AHF shall be prepared by a method known to separate the cold insoluble portion from Fresh Frozen Plasma and result in a minimum of 150 mg of fibrinogen and and minimum of 80 IU of coagulation factor VIII per container or unit. In tests performed on pre-storage pooled components, the pool shall contain a minimum of 150 mg of fibrinogen and 80 IU of coagulation factor VIII times the number of components in the pool. On the SBB exam, you might see a varation of this question asking about a platelet yield. If you can remember the QC requirements for platelets and cryo derived from whole blood, then you can use recall abilities to answer this type of question.
34
What is the shelf life of pooled cryoprecipitate after thawing at 37 C if Cryo was pooled using a sterile connecting device. a. 4 hours b. 6 hours c. 12 hours d. 24 hours
b. 6 hours
35
What is the shelf life of liquid plasma recovered from an allogeneic whole blood unit? a. 5 days after expiration of whole blood unit b. It is the same as expiration of whole blood unit c. 10 days after expiration of whole blood unit d. 56 days after expiration of whole blood unit
a. 5 days after expiration of whole blood unit
36
At what temperature must packed red blood cells be shipped? a. 1-6 C b. 20-24 C c. 1-10 C d. 1-4 C
c. 1-10 C
37
A unit of apheresis platelets was irradiated for a transplant patient. How does the expiration deate change from the original outdate? a. There is no change. b. Expires 24 hours form date of irradiation c. Expires 8 hours from date of irradiation d. Expires in 3 days from date of irradiation
a. There is no change.
38
What is the expiration date of washed red blood cells? a. 48 hours b. 24 hours c. 8 hours d. 72 hours
b. 24 hours
39
Apheresis platelets were leukoreduced in the blood bank after they were collected from the donor. What is the expiration date? a. 5 days b. 24 hours c. 4 hours d. 6 hours
c. 4 hours
40
A whole blood unit was collected in CP2D. Packed red blood cells are made. What would be an acceptable hematocrit for the packed red blood cells? a. 85% b. 95% c. 75% d. 100%
c. 75%
41
What of the following blood products contain the most FVIII? a. Platelets b. Granulocytes c. Cryoprecipitate d. PF24
c. Cryoprecipitate
42
An apheresis unit has a pH of 6.0. Using a sterile connecting device additional compatible plasma was added to increase the pH. Is this an acceptable practice? a. No, volume should be decreased to increase the pH b. Yes c. No, apheresis platelets should be not be manipulated d. No, manipulation may only occur with random donor platelets
b. Yes
43
10 units of packed red blood cells are received by the transfusion service. 5 units were Rh positive and 5 units were Rh negative. Only the Rh negative units are confirmed with Anti-D reagent. What is the reason for this? a. The Rh-positive units will be given to Rh positive and Rh negative patients b.The Rh-negative units will only be given to Rh negative patients c. Rh negative units will be given to both Rh negative and Rh positive patients d. If there was a mistake in donor testing regarding Rh factor any adverse event would be limited to Rh negative units as Rh positive patients can receive either Rh negative or Rh positive blood
d. If there was a mistake in donor testing regarding Rh factor any adverse event would be limited to Rh negative units as Rh positive patients can receive either Rh negative or Rh positive blood
44
Quality control records regarding reagents must be kept for a minimum of: a. 10 years b. 5 years c. Indefinitely d. Permanently
a. 10 years
45
Packed red blood cells are stored in a refrigerator that does not have constant temperature recording. At what time interval must the temperature be documented? a. Every 6 hours b. Every 12 hours c. Every 4 hours d. Once a day
c. Every 4 hours
46
A lookback was initiated when the blood supplier notified the blood bank supervisor that a unit already shipped was found to be from a donor with hepatitis C virus. How long must the look back investigation be kept on file? a. 10 years b. 5 years c. Indefinitely d. Permanently
a. 10 years
47
How long must records of irradiating cellular components be kept on file in the transfusion service? a. 10 years b. 5 years c. Indefinitely d. Permanently
a. 10 years
48
How long must physician orders for blood components be kept on file? a. 10 years b. 5 years c. Indefinitely d. Permanently
b. 5 years
49
Patient samples and donor red cell segments must be kept for a minimum of: a. 7 days b. 7 days following transfusion c. 5 days d. 5 days following transfusion
b. 7 days following transfusion
50
What is the accepted time interval a patient sample may be used for crossmatching? a. 3 days b. 5 days c. 7 days d. 14 days
a. 3 days
51
A physician has placed an order to raise a patient's FVIII level from 3% to 50%. The patient's hematocrit is 40% and weight is 120 pounds. How many units of factor VIII are needed? a. 1400 b. 1435 c. 1390 d. 1075
d. 1075
52
A physician placed as order to raise the fibrinogen level in a patient from 20 mg/dL to 100 mg/dL. The patient's weight is 70 kg and hematocrit is 47%. Calculate the number of bags of cryoprecipitate that should be transfused. a. 9 b. 5 c. 2 d. 12
a. 9
53
Calculate the equivalent number of random platelets given the following platelet count in apheresis unit 5.1 x 10^11. a. 9 b. 12 c. 5 d. 2
a. 9
54
Indicate is the patient is refractory given the following: pretransfusion platelet count 5000, post transfusion platelet count 12,5000 u/L, BSA 2.0 m2. Unit contained 4 x 10^11 platelets. a. Yes, patient is refractory b. No, patient is not refractory
a. Yes, patient is refractory
55
Using a standard dose of 10-15 mL/kg, the hemoglobin in a neonate may be raised by: a. 2 g/dL b. 5 g/dL c. 7 g/dL d. 10 g/dL
a. 2 g/dL
56
A physician wishes to increase a patient's platelet count from 25,000 TO 100,000/uL. How many units of random donor platelets might achieve this? a. 8 b. 5 c. 2 d. 4
a. 8
57
Using a standard dose of 10-15 mL/kg, the hemoglobin in a neonate may be raised by: a. 2 g/dL b. 5 g/dL c. 7 g/dL d. 10 g/dL
a. 2 g/dL
58
How does AABB define irradiation? a. Exposure of blood components using gamma rays or x rays of 25 Gy to the central portion of irradiation canister or field to prevent the proliferation of T lymphocytes. b. Exposure of blood components using x rays of 25 Gy to the central portion of the irradiation canister or field to prevent the proliferation of lymphocytes. c.Exposure of blood components using gamma rays of 25 Gy to the central portion of the irradiation canister or field to prevent the proliferation of T lymphocytes d. Exposure of blood components using UV light of 25 Gy to the central portion of the irradiation canister or field to prevent the proliferation of B lymphocytes
a. Exposure of blood components using gamma rays or x rays of 25 Gy to the central portion of irradiation canister or field to prevent the proliferation of T lymphocytes.
59
What is the shelf life for a whole blood collection using CPDA-1 and AS-3 preservative solution? a. 35 days b. 42 days c. 21 days d. 56 days
b. 42 days
60
Which of the following is false regarding freezing red blood cells? a. May be frozen up to 6 days post expiration b. Must be frozen within 6 days of collection c. Can be frozen after 6 days of collection using rejuvenation d. Can use low or high glycerol concentrations
a. May be frozen up to 6 days post expiration
61
When would it be appropriate to label a unit of red blood cells as Low Volume? a. 350 mLs was collected into a 450 mL bag b. 450 mLs was collected into a 500 mL bag c. 420 mLs was collected into a 450 mL bag d. 455 mLs was collected into a 500 mL bag.
a. 350 mLs was collected into a 450 mL bag
62
For prestorage pooled cryoprecipitate, which of the following is true? a. Each pool must contain 80 IU antihemophilic factor b. Each pool must contain 200 mg/dL of fibrinogen c. Each pool must contain 150 mg/dL of fibrinogen d. Each pool must contain at least 150 mg/dL of fibrinogen and at least 80 IU of antihemophilic factor times the number of components in the pool.
d. Each pool must contain at least 150 mg/dL of fibrinogen and at least 80 IU of antihemophilic factor times the number of components in the pool.
63
A unit of apheresis granulocytes must contain a minimum of: a. 1 x 10^10 granulocytes in at least 75% of units tested b. 1 x 10^6 granulocytes in at least 75% of units tested c. 1 x 10^5 granulocytes in at least 75% of units tested d. 1 x 10^12 granulocytes in at least 75% of units tested
a. 1 x 10^10 granulocytes in at least 75% of units tested
64
Which of the following applies to quality control of random donor platelets? a. A minimum of 5.5 x 10^10 platelets and pH of >6.2 in at least 75% of units b. A minimum of 3.0 x 10^11 platelets and pH of >6.2 in at least 90% of units c. A minimum of 5.5 x 10^10 platelets and pH of >6.2 in at least 90% of units d. A minimum of 3.0 x 10^11 platelets and pH of >6.2 in at least 75% of units
c. A minimum of 5.5 x 10^10 platelets and pH of >6.2 in at least 90% of units
65
What must the leukocyte count be in a unit of pooled platelets leukocyte reduced? a. <5 x16^6 b. <8.3 x 10^5 c. <3 x 10^11 d. <5.5 x 10^10
a. <5 x16^6
66
FFP prepared from whole blood using CPDA-1 must be frozen within how many hours of collection? a. 6 a. <5 x16^6 c. 12 d. 24
a. <5 x16^6
67
From a managerial standpoint, why might medical directors prefer PF24 over FFP? a. PF24 is cheaper b. PF24 will contain all coagulation factors c. FFP will be devoid of factors V and VII d. PF24 has an expiration date of 48 hours once thawed
a. PF24 is cheaper
68
What is contained in Rejuvesol (PIPA)? a. Phosphate, inositol, pyruvate, adenine b. Phosphate, inositol, phenol, adolase c. Phosphate, imuxitab, phenol, adenine d. Phosphate, imuxitab, pyruvate, adenine
a. Phosphate, inositol, pyruvate, adenine
69
It is acceptable practice to use a sterile connecting device to replace incompatible plasma with normal sterile saline in a platelet unit for select transplant patients. a. True b. False
a. True
70
What is contained in the formula for relative centrifugal force? a. RPM and radius of rotor b. RPM and acceleration time c. RPM and de-acceleration time d. Radius of rotor and number of buckets
a. RPM and radius of rotor
71
In separating red blood cells from plasma in a whole blood unit, which of the following would be used? a. 5000 x g for 5 minutes b. 2000 x g for 5 minutes c. 1000 x g for 5 minutes d. 10000 x g for 5 minutes
a. 5000 x g for 5 minutes
72
What would be the best component for a patient with anti-IgA? a. packed red blood cells b. whole blood c. washed red blood cells d. leukopoor red blood cells
c. washed red blood cells
73
This product might be indicated for a patient with Chronic Granulomatous Disease. a. Granulocytes b. Irradiated RBCs c. Irradiated platelets d. Cryoprecipitate
a. Granulocytes
74
This product might be indicated for a patient with afibrinogenemia. a. Cryoprecipitate b. Apheresis platelets c. Normal serum albumin d. Red blood cells
a. Cryoprecipitate
75
This product might be indicated for a stem cell transplant patient. a. Leukoreduced platelets b. Irradiated red blood cells c. Cryoprecipitate d. Granulocytes
b. Irradiated red blood cells
76
This product might be indicated for a patient with anti-HLA A2 a. HLA matched platelets b. Leukocyte reduced platelets c. CMV negative red cells d. Irradiated granulocytes
a. HLA matched platelets
77
Which product might be useful for a patient with anti-k? a. Frozen red blood cells b. HLA matched platelets c. Leukocyte reduced red blood cells d. Cryo reduced FFP
a. Frozen red blood cells
78
What would be the best product to transfuse for a patient with Factor XIII decifiency? a. Cryoprecipitate b. FFP c. PF24 d. Cryo poor FFP
a. Cryoprecipitate
79
A plasma exchange may be employed for which of the following patient conditions? a. ITP b. TTP c. Iron decifiency anemia d. DIC
b. TTP
80
When preparing cryoprecipitate, FFP is thawed at what temperature? a. 22-24 C b. 1-6 C c. 30-37 C d. None of the above
b. 1-6 C
81
In deglycerolizing a unit of red blood cells, what concentration of sodium chloride is typically used first? a. 12% b. 0.9% c. 6% d. 9%
a. 12%
82
How many units would need to be screen if a patient had anti-K and the physician ordered 4 units of red blood cells? a. 2 b. 5 c. 7 d. 9
b. 5
83
How many units would need to be screened if a patient had anti-E and anti-Fya in their plasma and the physician ordered 4 units of red blood cells? a. 5 b. 20 c. 8 d. 15
b. 20
84
A patient with a warm autoantibody was recently transfused with 4 units of red blood cells. If an R1R2Jk(a+b-) cell was treated with ZZAP what antibodies might be left in absorbed plasma after performing an allogenic absorption? a. Anti-D, C, Jka, Fya, Fyb b. Anti-E,c, Jkb, Fya, M, N c. Anti-E, c, Jkb, Fya, Fyb d. Anti-C, E, Jkb, Fya Fyb
c. Anti-E, c, Jkb, Fya, Fyb
85
What would be the effect in infusing a unit of RBCs with ringers lactate? a. component would clot b. RBCs would swell c. ATP levels would decrease d. Calcium would decrease
a. component would clot
86
All of the following are exceptions to the rule that only isotonic saline can be administered with blood, except: a. ABO compatible plasma b. 5% albumin c. 25% albumin d. Plasma protein fraction
c. 25% albumin
87
Regarding QC, what platelet component does not require documentation of pH being 6.2 or greater? a. apheresis platelets b. random donor leukoreduced c. apheresis platelets leukoreduced d. apheresis platelets leukoreduced with additive solution
d. apheresis platelets leukoreduced with additive solution
88
In the eBDS for platelet bacterial testing a decrease in oxygen from the baseline reading indicates: a. bacteria has not been detected in platelet sample b. bacteria has been detected in platelet sample
b. bacteria has been detected in platelet sample
89
What is the principle of the INTERCEPT blood system for platelets in detecting bacteria before a decision is made to transfuse? a. amotosalen crosslinks nucleic acids of bacteria and enveloped viruses upon activation by illumination b. amotosalen crosslinks nucleic aids of bacteria and enveloped viruses c. bacteria in platelet sample consumes oxygen which can be measured d. bacteria in platelet sample produces oxygen which can be measured
a. amotosalen crosslinks nucleic acids of bacteria and enveloped viruses upon activation by illumination
90
All of the following is true regarding secondary testing of platelets for bacteria except: a. usually conducted late in storage period b. can only be conducted using a culture based bacterial detection device c. intended to detect bacterial contamination not revealed by primary testing d. intended to test a platelet unit which previously tested negative for bacteria on primary testing
b. can only be conducted using a culture based bacterial detection device
91
The FDA recommend testing pre-storage pooled platelets using an FDA cleared culture based bacterial detection device >24 hours after collection of the: a. oldest unit in the pool b. freshest unit in the pool
b. freshest unit in the pool
92
Detection of bacteria in post-storage platelets should be performed using a FDA cleared rapid bacterial detection test within how many hours prior to transfusion on whole blood derived platelets? a. 6 b. 1 c. 8 d. 4
d. 4
93
What should be done if a unit of irradiated RBCs has not been transfused in 24 hours from the time it was irradiated? a. irradiated again b. washed c. frozen d. rejuvenated
d. rejuvenated
94
platelet gel is produced when these substances are added to platelet rich plasma yielding a glue-like substance for surgical applications. a. thrombin and plasma b. calcium and antihemophilic factor c. activated protein c and fibrinogen d. calcium and thrombin
d. calcium and thrombin
95
Regarding shipping of platelets, the maximum time without agitation is: a. 1 hour b. 4 hours c. 8 hours d. 24 hours
d. 24 hours
96
A 2 year old female (weight 12 kg) with hypofibrinogenemia has a baseline fibronogen of 105 mg/dL. How many units of Cryo are needed to raise the fibrinogen to 170 mg/dL? a. 2 b. 5 c. 8 d. 10
a. 2
97
The purpose of irradiating blood product is to: a. Prevent post-transfusion purpura b. Prevent graft vs host disease c. Prevent virus transmission d. Prevent non-cardiogenic pulmonary edema
b. Prevent graft vs host disease Irradiation destroys the functionality of the nucleus, so that the transfused blood is not able to elicit an immune response against the patient.
98
Each unit of cryoprecipitate contains a minimum of: a. 150 Iu of Factor VIII and 80 mg of fibrinogen b. 25 IU of Factor IX and 150 mg of fibrinogen c. 80 IU of Factor VIII and 150 mg of fibrinogen d. 80 IU of Factor VIII and 100 mg of fibrinogen
c. 80 IU of Factor VIII and 150 mg of fibrinogen
99
Liquid plasma may be prepared from a whole blood unit until: a. WB expiration date b. 1 day after expiration c. 3 days after expiration d. 5 days after expiration
d. 5 days after expiration This is an AABB standard for components. See AABB standards 23rd ed reference standard 5.1.8A
100
At what factor level do hemophilia patients experience profuse bleeding after surgery or trauma? a. 0-1% b. 6-30% c. 40-65% d. 2-5%
d. 2-5%
101
How much Fibrinogen is in the average unit of whole blood? a. 25 mg b. 80 mg c. 150 mg d. 1500 mg
c. 150 mg Each unit of whole blood will produce one unit of cryoprecipitate, which typically has 150 mg of fibrinogen.
102
A 70 kg patient with severe hemophilia has a hematocrit of 40% and an inititial factor VIII level of 2 units/dl (0.02 units/ml). How many bags of cryoprecipitate should be given to raise the factor VIII level to 50 units/dl (0.5 units/ml). a. 10 b. 14 c. 18 d. 22
18 bags Calculation as follows: Patient weight (kg) x 70 ml/kg = total blood volume x (1-hct) = plasma volume Plasma Volume x (desired concentration - initial concentration) = # units Favor VIII Therefore, 70 x 70 = 4900 (blood volume) 4900 x (1-.40) = 2940 ml plasma volume 2940 x (0.50-0.0.2) = 1411 units of Factor VIII needed 1411/80 = 17.64 bags, but round up to 18
103
A unit of RBCs in prepared in CP2D with an AS-3 additive. What is the expiration date of the RBCs? a. 24 hours b. 21 days c. 35 days d. 42 days
42 days CP2D units are good for 21 days. If you add the additive solution, then the expiration is extended to 42 days.
104
Which of teh following HIV western blood patterns should be interpreted as positive? a. p24 and gp41 bands are present b. p31, p17, p55 bands are present c. p24, p31, p55 bands are present d. gp 120/160, p31, p55 bands are present
a. p24 and gp41 bands are present Interpretation is as follows for HIV western blot: Negative: No bands present Positive at least two bands from p24, gp41 or gp120/160 Indeterminate: presence of bands, but do not fulfill criteria for positive result
105
A patient has a height of 72 inches an a weight of 175 lbs. His pre-transfusion platelet count is 10,000/uL. He was transfused with 6 units of platelet concentrates. The 1 hour post transfusion platelet count is 50,000/uL. What is the corrected count increment (CCI) for the platelets transfusion? a. 15,758 b. 21,456 c. 24,242 d. 25,525
c. 24,242 BSA (meters squared) = The square root of [height (cm) x Weight (kg)] divided by 3600. Corrected Count Increment (CCI) = [Post transfusion Platelet Count - Pre transfusion Platelet Count]xBSA] divided by the number of platelets transfused. First calculate the BSA 1 inch =2.2 pounds The patient is 175/2.2=79.5 kg (80 kg) BSA in meters squared = the square root of [height (cm) x weight (kg)] divided by 3600 So (183 x 80)/3600 = 4.066(4) The square root of 4=2 So the BSA = 2m(2) represents "squared" Now that we have the BSA we can do the rest of the calculation. The calculation for corrected count increment is: Absolute platelet increment/ul x body surface area (m2) divided by the number of platelets transfused. The absolute platelet increment is the post-transfusion minus the pretransfusion count. The pretransfusion count was 10,000 and the post transfusion count was 50,000. 50,000-10,000 = 40,000 absolute platelet count. So if we put these numbers in our formula we now have: [40,000 x 2] = divided by the number of platelets transfused. To get the number of platelets transfused, we look again at the question. The patient received 6 units of random platelets. The average platelet has 5.5 x 10(10) platelets. We want this number in the exponent of 10(11) so the average value is then 0.55 x 10(11) 6x0.55 = 3.3 x 10(11) platelets transfused Now, our calculation for CCI has all the numbers we need, so we can perform the math. Corrected Count Increment (CCI) = [Post transfusion Platelet Count - Pre transfusion Platelet Count]xBSA] divided by the number of platelets transfused. [40,000x2] divided by 3.3 = 24,242
106
According to AABB standards, what is the correct interpretation of the plateletpheresis quality control results below? Unit# Platelet Count pH 1 3.2 x 10^11 6.2 2 3.0 x 10^11 6.4 3 3.4 x 10^10 6.4 5 3.0 x 10^11 6.4 a. QC passes b. QC fails for platelet count c. QC fails for pH d. QC results are invalid
b. QC fails for platelet count Unit#3 fails for platelet count, and as such, the QC does not have a 90% pass rate for platelet count.
107
A hospital orders 20 units of group O RBCs from the blood supplier. Upon arrival to the hospital transfusion service, the technologist reads the thermometer in the RBC shipping container and it reads 9 C. What is the correct course of action? a. refuse delivery of the RBCs because the temperature is too high. b. accept delivery of the RBCs, but they must be used within 24 hours of arrival time. c. Quarantine the units for 24 hours and observe them for hemolysis. If the visual inspection is acceptable, the units may be released from quarantine and used. d. Accept the units and process as per SOP
d. Accept the units and process as per SOP AABB standards states that whole blood and RBC components may be transported (Shipped) at 1-10 C. Therefore the shipment is acceptable.
108
RBC storage times vary with the anticoagulant/preservative used. Which of the following is properly paired? a. Citrate-phosphate-dextrose (CPD): 35 days b. Additive solution (AS): 47 days c. Citrate-phosphate-dextrose-adenine (CPDA)-1: 21 days d. Citrate-phosphate-dextrose-dextrose (CP2D): 21 days
d. citrate-phosphate-dextrose-dextrose (CP2D): 21 days CP2D is an anticoagulant and preservative used for collection of WB from donors, but it is only licensed for storage for 21 days at 1-6 C. Citrate-phosphate-dextrose (CPD) is also only licensed for 21 day storage. (If you add the preservative solution to this you can extend the life to 42 days). Additive solution (AS) is licensed to extend the expiration to 42 days. Citrate-phosphate-dextrose-adenine (CPDA)-1 has an expiration of 35 days. AABB Standards 30th ed section 5.1.6A is a chart of storage, transport and expiration for various components.
109
Which of the following statements concerning West Nile Virus (WNV) is true? a. Infected humans can transmit the virus to mosquitos, completing the virus's life cycle. b. West Nile Virus testing is performed via NAT for all US blood donors c. The main reservoir for the virus is rodents d. West Nile Virus testing via ELISA is mandated by the FDA
b. West Nile Virus testing is performed via NAT for all US blood donors Since 2003, West Nile Virus testing via NAT has been performed on blood donors "Infected humans can transmit the virus to mosquitos, completing the virus's life cycle" and "The main reservoir for the virus is rodents" are not true statements. Mosquitos feed off infected birds and then bite humans, injecting them with WNV. "West Nile Virus testing via ELISA is mandated by the FDA" is not a true statement because testing is performed via NAT, which is more sensitive.
110
Which of the following statements about transfusion transmitted Trypanosoma Cruzi and testing for T. cruzi is true? a. T. cruzi can be transmitted via transfusion of RBCs Frozen/Deglycerlyzed RBCs and platelets. b. T. cruzi is a retrovirus endemic in North America c. The Center for Biologics Evaluation and Research (CBER) has licensed a T. cruzi NAT for the detection of the parasite d. T. cruzi is not a concern for peripheral blood progenitor cell products as it does not survive freezing in 5% dimethyl sulfoxide (DMSO)
a. T. cruzi can be transmitted via transfusion of RBCs Frozen/Deglycerlyzed RBCs and platelets. Trypanosoma cruzi is a flagellate protozoan that causes Chagas Disease, and the CDC estimated in 2013 that over 300,000 people living in the US are infected with T cruzi. Chagas disease is endemic in Central and South America and it is estimated that population has 8 million infected people. T. cruzi can survive at room temperature, in refrigerated products and even can survive freezing and thawing, so the risk is very real for all blood components and transplants organs and tissues. Current blood donor testing gin the US is via ELISA
111
Fresh frozen plasma that was thawed but not used in 24 hours should be relabeled as______? a. recovered plasma b. source plasma c. thawed plasma d. FFP can retain its labeling if it is refrozen within 24 hours
thawed plasma If not used within 24 hours of thawing, FFP can be relabeled as thawed plasma. The words "fresh frozen" must be removed because the labile clotting factors, V and VIII are no longer at therapeutic, viable levels. Recovered plasms is obtained as a by-product when making cryoprecipitate. Source plasma is a term used by the FDA for those products collected from paid plasma donors. It is not acceptable to re-freeze plasma once it has been thawed.