UAMS MLT-MLS Comprehensive Exam

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Last updated 12:04 AM on 7/24/26
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479 Terms

1
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Which antibody is most associated with delayed hemolytic transfusion reactions?

Anti-Jka

2
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What is most associated with Anti-I?

Mycoplasma pneumonia

3
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IgG antibodies cause ______ hemolysis from sequestration by spleen.

Extravascular

4
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T/F: Enzyme panels will react with Duffy Antibodies (Fya or Fyb).

False

<p>False</p>
5
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T/F: RhIG at 28 weeks can cause a mom to have a low titer anti-D.

True

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What type of blood should be given if from mom to child?

Irradiated

7
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Room temp crossmatch detects _____ errors.

ABO

8
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Why do premature infants typically need transfusions?

Blood loss from lab tests

9
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When phenotyping, use a positive control that is _______ positive.

Heterozygously

10
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Why is cryoprecipitate normally used?

To replace fibrinogen

11
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What can make an auto control positive? (Distinguish by warming, looking under scope or saline replacement)

Rouleaux and Cold auto

12
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Cold auto will react with _____ AHG and ___ Monospecific AHG.

Polyspecific; C3

13
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What kind of plasma can an AB= patient be transfused with?

AB (+ or =)

14
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_____ transfusion must be fresh, CMV =, radiated and collected with CPDA

Intrauterine

15
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How should intrauterine transfusions be handled?

Radiated and collected with CPDA

16
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When is FFP used?

When PT and PTT are prolonged

Fresh frozen plasma (FFP) is used for patients with a coagulopathy who are bleeding or at risk of bleeding, and where a specific therapy or factor concentrate is not appropriate or unavailable.

17
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At what temperature do Lewis antibodies react?

RT and sometimes 37

18
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What type of hemolysis do Lewis antibodies cause?

In Vitro

19
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How long are sexual partners of IV drug users differed from donating?

1 year

20
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+DAT can make the Rh control ___ when doing weak D test

Positive

21
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Storage: Whole Blood

1-6 C; 35 days

22
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Storage: RBCs (Red cells, Packed RBCs, RBCs)

1-6 C (CPDA- 35 days; ADSOL- 42 days)

23
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Storage: Leukocyte- Reduced RBCs

1-6 C (CPDA- 35 days; ADSOL- 42 days)

24
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Storage: Washed Red Cells

1-6 C; 24 hours

25
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Storage: Irradiated Blood to prevent GVHD

1-6 C; 28 days

26
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Storage: Frozen/ Deglycerolized RBCs

-70 C for 10 years; 1-6 C for 24 hours after prepared

27
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Storage: Random Platelets

20-24 C; 5 days with agitation and temp check every 4 hours (4 hours after pooling)

28
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Storage: Platelets, Apheresis (single-donor)

20-24 C with agitation; 5 days

29
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Storage: Granulocytes, Apheresis

20-24 C; 24 hours

30
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Storage: FFP, frozen

-18 C; 1 year

31
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Storage: FFP, thawed

1-6 C; 24 hours

32
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Storage: Frozen Cryoprecipitated AHF

-18 C; 1 year

33
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Storage: Thawed Cryoprecipitated AHF

RT if used for Factor VIII; 1-6 if used for fibrinogen

34
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Storage: Pooled Cryoprecipitated AHF

20-24 C; 4 hours

35
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What are whole blood transfusions used for?

Cells and volume

36
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What are packed RBC transfusions used for?

Anemia

37
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What are Washed RBC transfusions used for?

Allergy to plasma proteins in IgA deficiencies

38
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What are Leuko-depleted RBC transfusions used for?

Febrile from HLA or CMV risk

39
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What are Frozen, deglycerolized RBC transfusions used for?

Rare or autologous

40
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What must be done to issue red cell products?

ABO, Rh and screening compatible

41
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How are PLTs and WBCs stored?

RT (20-25 C)

42
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What are Leuko-reduced PLT or WBC transfusions used for?

Prevent febrile from HLA and prevent CMV

43
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What are granulocyte transfusions used for?

Severe neutropenia

44
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What are FFP transfusions used for?

Coag disorders (type compatible)

45
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What are cryo transfusions used for?

Factor VIII and IX concentrate- Virus inactivated and lyophilized

46
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What does PT monitor?

Coumadin

47
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What will a cold agglutinin not affect on the cell counter?

Hemoglobin

48
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What does Protein C deficiency cause?

Thrombosis (Thrombosis occurs when blood clots block your blood vessels.)

49
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What does Factor XII deficiency cause?

Thrombosis instead of bleeding

50
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How does old blood affect the RBCs and WBCs?

Crenate RBCs and cause vacuoles in WBCs.

51
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What happens when you mix patient plasma (with a high PTT) with normal plasma?

Corrects Factor Deficiency (Not correct lupus anticoagulant)

52
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Sickle cells and spherocytes will ____ a sed rate.

Lower

53
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Patient with polycythemia needs to have anticoagulant adjusted for ___ or ____

PT or PTT

54
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90% of the hemoglobin is Hgb C and the rest A2 and F on electrophoresis.

Hgb C disease

<p>Hgb C disease</p>
55
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Associated with hyper-segmented neutrophils, pancytopenia and macrocytes.

Megaloblastic anemia

<p>Megaloblastic anemia</p>
56
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What are Howell-jolly bodies made up of?

DNA fragments

<p>DNA fragments</p>
57
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When are Howell-Jolly Bodies seen?

Non-function spleen & accelerated or abnormal erythropoiesis

58
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What is basophilic stippling made up of?

Denatured RNA

<p>Denatured RNA</p>
59
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When is basophilic stippling seen?

Lead poisoning & thalassemia

60
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What are pappenheimer bodies (Siderocytes) made up of?

mitochondria and ribosomes that contain iron

<p>mitochondria and ribosomes that contain iron</p>
61
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When are pappenheimer bodies (Siderocytes) seen?

Sideroblastic anemia, thalassemia, splenectomy

62
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When are Heinz bodies seen?

G6PD deficiency, unstable hemoglobin causing iron to be unprotected, oxidizing drugs, alpha thalassemia

<p>G6PD deficiency, unstable hemoglobin causing iron to be unprotected, oxidizing drugs, alpha thalassemia</p>
63
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What are Heinz bodies made up of?

Denatured hemoglobin

64
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When are Cabot rings seen?

Severe anemias, pernicious anemia, dyserythropoiesis

<p>Severe anemias, pernicious anemia, dyserythropoiesis</p>
65
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What are Cabot rings made up of?

arginine-rich histone and non-hemoglobin iron (remnants of spindle fibers)

66
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When are hemoglobin c crystals seen?

Hemoglobin C disease

<p>Hemoglobin C disease</p>
67
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What are hemoglobin C crystals made up of?

Abnormal hemoglobin crystallizes

68
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When are Dohle Bodies seen?

May Hegglin Anomaly

<p>May Hegglin Anomaly</p>
69
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DIC lab tests

^PT, PTT, TT, FSP; low Fibrinogen & PLT count; + D-dimer; schistocytes

<p>^PT, PTT, TT, FSP; low Fibrinogen &amp; PLT count; + D-dimer; schistocytes</p>
70
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What are Dohle Bodies made of?

Strands of endoplasmic reticulum RNA

<p>Strands of endoplasmic reticulum RNA</p>
71
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Lab tests for Multiple Myeloma

Protein electrophoresis (M-spike), N/N anemia, pancytopenia (low PLT, RBC & WBC); rouleaux; BM biopsy >30% plasma cells

<p>Protein electrophoresis (M-spike), N/N anemia, pancytopenia (low PLT, RBC &amp; WBC); rouleaux; BM biopsy &gt;30% plasma cells</p>
72
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How do you distinguish Hemophilia A from VWD?

Normal BT

73
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How does lipemia affect the results of the automated CBC?

Falsely elevated Hgb. Correct by replacing lipemic plasma with saline.

74
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Osmotic fragility results with hereditary spherocytosis

Increased; cells are Hyperchromic and easily lyse

75
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Lysed RBC- hypotonic; diluted; can cause false neg

Ghost cell

<p>Ghost cell</p>
76
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WBC in a hypotonic urine

Glitter cell

<p>Glitter cell</p>
77
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Hypertonic; can cause false negative

Crenated RBC

<p>Crenated RBC</p>
78
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Composed of Tamm-Horsfall protein; made in the distal convoluted tubules (nephrons)

Casts

79
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Cystine crystals; smell like sulfur

Cystinuria

<p>Cystinuria</p>
80
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Tyrosin crystals; liver disease

Tyrosyluria

<p>Tyrosyluria</p>
81
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Mouse odor

PKU

82
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Diabetes mellitus

Micro-albumin

83
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Gout; Horizontal = blue

MSU

Gout is a common crystal-induced arthritis, in which monosodium urate (MSU) crystals precipitate within joints and soft tissues and elicit an inflammatory response.

84
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Pseudogout; Horiz = yellow

CPPD

Pseudogout (SOO-doe-gout) is a form of arthritis characterized by sudden, painful swelling in one or more of the joints. Episodes can last for days or weeks.

85
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Syrup odor, leucine crystals

MSUD

<p>MSUD</p>
86
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+ Clinitest

Clinitest (reagent tablet) is a semi-quantitative test used for the determination of total reducing substances in urine, which include glucose, galactose, lactose, and pentose.

Galactosemia

Galactosemia is a rare, hereditary disorder of carbohydrate metabolism that affects the body's ability to convert galactose to glucose.

87
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Effects of prolonged storage of urine

Alkaline

A solution of a soluble base has a pH greater than 7.0.

88
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+ WBC, Bacteria

Cystitis

Cystitis is inflammation of the bladder, usually caused by a bladder infection. It's a common type of urinary tract infection (UTI),

89
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+ WBC, bacteria, WBC cast

Pyelonephritis

A kidney infection is also called pyelonephritis. A kidney infection needs prompt medical treatment.

<p>Pyelonephritis</p><p>A kidney infection is also called pyelonephritis. A kidney infection needs prompt medical treatment.</p>
90
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RBC, RBC casts

AGN

Acute glomerulonephritis (AGN) comprises a specific set of kidney diseases in which an immunologic mechanism triggers inflammation and proliferation of glomerular tissue that can result in damage to the basement membrane, mesangium, or capillary endothelium.

<p>AGN</p><p>Acute glomerulonephritis (AGN) comprises a specific set of kidney diseases in which an immunologic mechanism triggers inflammation and proliferation of glomerular tissue that can result in damage to the basement membrane, mesangium, or capillary endothelium.</p>
91
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Fatty casts, OFB, cholesterol

Nephrotic syndromeephrotic syndrome

A kidney disorder that causes the body to excrete too much protein in the urine.

<p>Nephrotic syndromeephrotic syndrome</p><p>A kidney disorder that causes the body to excrete too much protein in the urine.</p>
92
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RTE/ RTE casts, Waxy/ broad

Renal failure

<p>Renal failure</p>
93
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Urine color: amber/ brown-orange

Bilirubin; yellow foam

94
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Urine color: orange

Pyridium

Pyridium is a prescription and over the counter medicine used to prevent treat the symptoms of the lower urinary tract. Pyridium

95
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Urine color: red, cloudy

Intact RBCs (hematuria)

96
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Urine color: red, clear

Hemoglobin; myoglobin

97
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Urine color: red-purple/ burgundy

Porphyrins

98
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Urine color: black

Melanin or homogentistic acid

99
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Urine color: cloud

WBCs, crystals

100
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Urine color: milky

Fats, nephrotic Syndrome