Clinical Chemistry
Blood Bank
Micro
Heme II
Random
100

A CMP is a combination of which other panels?

Combination of a BMP and a hepatic function panel

100

Name 2 high incidence antigens.

e, k, Kpb, Jsb, Lub

100

What type of media is MAC?

(Moderately) selective and differential

100

What would we expect to see in the peripheral blood of an individual with lead poisoning?

Basophilic stippling

100

What erroneous results would we expect to see in the instance of EDTA contamination?

Falsely elevated K+ and falsely decreased Ca2+
200

What blood gas results would you expect to see in a patient with metabolic acidosis with respiratory compensation?

A decreased pH, decreased HCO3-, as well as a decreased pCO2

200

Antibodies to which antigen group are most commonly associated with a delayed hemolytic transfusion reaction?

Kidd

200

What organism causes folliculitis, furuncles and carbuncles?

Staph aureus

200

A 27-year-old patient just had a bone marrow exam. What is the expected percent cellularity of their BM?

73 +/- 10%

(100 - Age) +/- 10%

200

What two species does MALDI-ToF struggle to differentiate between?

E. coli and Shigella

300

What is the difference between turbidimetry and nephelometry and which one is more sensitive?

Both detect immune complex formation

Turbidimetry: decrease in light transmitted due to Ag-Ab formation

Nephelometry: detection of scattered or reflected light from a Ag-Ab complex 

Nephelometry is more sensitive

300

What is the required time interval between RBC apheresis donations?

16 weeks

300

How do we distinguish Bacillus anthracis from other Bacillus sp.?

Non-motile, non-hemolytic, ground glass/Medusa head morphology

300

A 25-year-old African American woman applies to donate blood. She is asymptomatic and has no known medical conditions. Routine screening includes a hemoglobin electrophoresis test, which reveals:

  • HbA: 60%

  • HbS: 38%

  • HbA2: 2%

  • HbF: <1%


What is the most likely diagnosis, and explain why these electrophoresis results appear this way.

  • Diagnosis: Sickle cell trait (HbAS)

  • Explanation: In sickle cell trait, the patient has one normal β-globin gene (HbA) and one sickle β-globin gene (HbS). This results in the presence of both HbA and HbS on electrophoresis, with HbA typically being higher than HbS (~60:40 ratio), and no symptoms under normal conditions.

300

what does CMV stand for, how does one become infected, and what methods reduce the risk of infection?

1. Cytomegalovirus--> Often asymptomatic in healthy people, but dangerous in immunocompromised patients and newborns

2. CMV is carried in donor white blood cells

3. Leukoreduction (CMV-negative donor also acceptable)

400

There are two major ways to assess renal function. Which one is the older more problematic way- what is it and why is it problematic? Which new method is recommended by the NKF and why?

1. eGFR--> estimates based off of muscle mass, historically has used race and gender in the calculation

2. Cystatin C--> not affected by diet, race, or gender (CKD-EPI 2021 equation also acceptable answer)

400

An 82-year-old woman with a history of congestive heart failure receives 2 units of packed red blood cells for symptomatic anemia. One hour into the second unit, she develops acute dyspnea, hypertension, jugular venous distension, and bilateral crackles on lung exam. Chest X-ray shows pulmonary edema. BNP is elevated.


What is the most likely transfusion reaction, and what steps should be taken to manage and prevent it in future transfusions?

  • Most likely reaction: TACO (Transfusion-Associated Circulatory Overload)

  • Management: Stop transfusion, give diuretics, provide oxygen support

  • Prevention: In future transfusions, use slower infusion rates, and transfuse smaller volumes 

400

Which one would be positive for Group A strep AND Enteroccocus?

a.       Bacitracin

b.       Bile esculin

c.       PYR

d.       Beta-lactamase

c.       PYR

400

What is the most common cause of acquired thrombophilia?

Anti-Phospholipid Antibody Syndrome

400

What disorder of primary hemostasis mainly affects kids and ften follows bacterial infection with E. coli O157:H7 or Shigella?

Hemolytic Uremia Syndrome (HUS)

500

Name 4 immunosuppressant drugs.

Cyclosporine, tacrolimus, sirolimus, mycophenolate, everolimus

500

Following a FMH a positive rosette test is obtained. Flow cytometry results indicate that 3.2% fetal cells were present in the mother. How many vials of Rhogam will be given to this mother?

(3.2*50/30) = 5.3 -> 6 + 1 = 7

(%fetal cells*50)/30 --> always round up and add one

500

What are the XV reactions and hemolysis patterns for: 

a.       H. parainfluenzae

b.       H. influenzae

c.       H. haemolyticus

d.       H. aegyptius

X (-), V(+), XV (+); beta-hemolysis (-)
= Haemophilus parainfluenzae

X (-), V(-), XV (+); beta-hemolysis (-)
= Haemophilus influenzae

X (-), V(-), XV (+); beta-hemolysis (+)
= Haemophilus haemolyticus

X (-), V(-), XV (+); beta-hemolysis (-)

= Haemophilus aegyptius

500

What is the gold standard for HIT diagnosis?

Serotonin release assay

500

What are the following media pairs are used for?

a.       Thayer Martin and Martin Lewis

b.       BCYE and Regan Lowe

c.       Todd Hewitt and Lim Broth

d.       TCBS and HE

a. Neisseria gonorrhoeae

b. Legionella/Bordetella

c. Group B Strep

d. Enterics, specificially Vibrio spp. and Salmonella/Shigella

M
e
n
u