Hemtaologic System (transfusion reactions, sickle cell, DIC)

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87 Terms

1
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what does a CBC include?

RBCs, WBCs, and platelets

2
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what is the normal range of RBCs for males and females

males: 4.7-6.1

female: 4.2-5.4

3
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what is a normal WBC count?

5,000-10,000

4
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what is a normal platelet count?

150,000-400,000

5
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what is pancytopenia?

suppression of all blood cells (RBCs, WBCs, and platelets)

6
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what does RBC suppression cause?

anemia

7
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what does WBC suppression cause?

neutropenia

8
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what does platelet suppression cause?

thrombocytopenia

9
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what does a peripheral smear show?

morphology (shape, size, color) of blood cellswhat

10
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what disorders can peripheral smear help diagnose?

sickle cell, leukemia

11
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what does thrombocytopenia increase the risk for?

spontaneous hemorrhage

12
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what does thrombocytosis increase the risk for?

excessive clotting

13
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what blood type is a universal donor?

O-

14
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what blood type is the universal recipient?

AB+

15
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what test determines Rh status?

Coombs test

16
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when are PRBCs used?

for anemia ONLY (NOT actively bleeding)

17
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when are platelets given?

for thrombocytopenia (deficiency of platelets)

18
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when is FFP given?

active bleeding, DIC, coat factor depletion

19
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when is albumin used?

(relative) hypovolemia, hypoalbuminemia

20
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when is cryoprecipitate used?

fibrinogen and clotting factor replacement

21
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what fluid can run with blood products?

ONLY NS 0.9%

22
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why can’t dextrose or LR run with blood products?

it causes hemolysis

23
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how long do you have to start a blood infusion after getting the blood?

30 minutes

24
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what is the maximum infusion time for blood?

4 hours

25
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how fast is blood initially run over the first 15 minutes?

60-120 mL/hr (max 2L/min)

26
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who must check the blood at bedside?

2 RNs

27
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when are vitals taken for a transfusion?

before starting, 15 minutes after, and after completion 

28
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who can do vitals after the first 15 minutes of a transfusion?

UAP- but the RN must do vitals at the 15 minute mark

29
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when do acute transfusion reactions occur?

within the first 15 minutes

30
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what are key signs of a hemolytic reaction?

  • fever

  • chills

  • low back (flank pain)

  • tachycardia

  • hypotension

  • dark urine (hemoglobinuria)

31
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what is the first action after nothing a hemolytic reaction?

STOP the transfusion

32
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what are key signs of a febrile reaction?

  • fever

  • chills

  • headache

  • tachycardia

  • tachypnea

33
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what are the key signs of a mild allergic transfusion reaction?

hives, rash, flushing

34
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what are they key severe signs of a severe allergic transfusion reaction?

anxiety, wheezing, decreased BP

35
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what is a TACO ?

transfusion associated circulatory overload

36
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what are causes of a TACO?

fluid overload (cardiogenic)

37
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what are s/s of a TACO?

  • HTN

  • JVD

  • crackles in the lungs

  • NO FEVER

  • increased BNP

38
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what is a TRALI?

transfusion related acute lung injury

39
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what is the cause of a TRALI?

donor antibodies that contain neutrophils which attack and damage the alveoli in the lungs

40
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what are s/s of a TRALI?

  • SOB

  • hypoxia

  • crackles

  • FEVER

  • HYPOtension

    • occurs within 6 hours

41
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when do delayed transfusion reactions occur?

days to months later

42
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what are s/s of a delayed transfusion reaction?

  • fever

  • jaunidce

  • low Hct & low Hgb

43
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what is the treatment for a TACO?

STOP the transfusion

raise HOB

medications

44
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Are we going to give a TACO diuretics and why?

Yes b/c it helps to get off the extra fluid causing the circulatory overload

45
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are we going to give a TACO fluids and why?

No b/c they are already in circulatory overload and it would worsen their condition

46
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what is the treatment for a TRALI?

STOP transfusion

give O2

intubation/mechanical ventilation if needed

47
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What medications are given to a TRALI?

fluids b/c they may be hypotensive

they need leukocyte reduced blood FOR LIFE

48
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who can recieve cell-salvaged blood?

trauma/surgical patients, Jehovah’s Witnesses

49
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what CANNOT receive stored autologous blood?

Jehovah’s witnesses

50
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what causes sickle cell disease?

genetic disorder where RBCs become sickle-shaped, stiff, and sticky—> block blood flow

51
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which populations are commonly affected with sickle cell?

African American, Sub-Saharan African, Mediterranean

52
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what can trigger a sickling crisis?

  • infection (MOST COMMON)

  • dehydration

  • stress

  • high altitude

  • low oxygen tension

  • pneumonia

53
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what is the number one complication of pneumonia?

infection (PNEUMONIA)

54
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why does infection risk increase?

increased spleen damage —> autosplenectomy —> reduced immune function

55
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what organ problems occur due to repeated infections?

  • splenomegaly

  • avascular necrosis (bones)

  • stroke

  • renal failure

  • liver damage

  • HF

  • acute chest syndrome

56
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what occurs during a sickle cell crisis?

sickled cells block vessels —> severe pain, tissue hypoxia, capillary leak, hypovolemia, SHOCK

57
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what are some common locations of infarcts/pain with sickle cell?

  • arms

  • back

  • abdomen

  • femurs

58
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what are some key clinical manifestations of sickle cell?

  • acute and chronic pain

  • fever, sweating

  • tachypnea

  • HTN

  • N/V

  • anemia (pallor/jaundice)

  • organ dysfunction (splenomegaly, hepatomegaly)

59
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what is a peripheral smear going to show with sickle cell?

sickled cells and hemolysis

60
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why does jaundice occur with sickle cell?

increased bilirubin from a large breakdown of RBCs

61
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what are some expected lab changes with sickle cell?

  • decreased H&H

  • decreased folate

  • decreased reticulocytes

  • increased bilirubin

62
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what is the first priority in a sickle cell crisis?

oxygen (“O'“ in HOP)

63
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what does hydration do in sickle cell?

reduces blood viscosity making it easier for the cells to move through the blood vessels and decreases sickling

64
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why is DVT prophylaxis needed with sickle cell?

sickle cell increases risk for clotting

65
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what are the treatments for acute chest syndrome?

  • O2

  • fluids

  • antibiotics

  • exchange transfusion

66
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what are the first-line medications for sickle cell pain?

IV opioids (morphine, hydromorphone)

67
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what are the adjunct pain therapies for sickle cell?

NSAIDs, neuropathic meds, nerve blocks, heat, PT/OT

68
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what vaccines are essential with sickle cell?

Pneumococcal, H. influenzane, influenza, hepatitis

69
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what is hydroxyurea used for?

prevents a sickle cell crisis by increasing fetal hemoglobin. NOT for a CRISIS

70
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when is hydroxyurea used?

only preventative NOT a crisis

71
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what is the risk with frequent transfusion in sickle cell?

iron overload

72
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how is iron overload treated in sickle cell?

chelation therapy

73
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what is the only cure for sickle cell disease?

hematopoietic stem cell transplant

74
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what is DIC?

a bleeding a clotting disorder where clotting factors and platelets are consumed —> simultaneous hemorrhage + thrombosis

75
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what is the biggest danger in DIC?

bleeding (because the clotting factors become depleted)

76
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what are some acute causes of DIC?

  • shock

  • hemolytic processess

  • obstetric complications

  • malignancies

  • tissue damage (trauma, burns, crash injury)

77
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what are chronic causes of DIC?

  • liver disease

  • SLE

  • malignancy

78
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what are some clinical manifestations of DIC?

  • pallor, cyanosis, necrosis

  • tachypnea, orthopnea, PE, ARDS

  • tachycardia, hypotension, EKG changes

  • distension, bloody stools, ileus

  • oliguria, renal failure

  • visual changes, HA, ALOC, irritability

    • bone/joint pain

79
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what labs are increased with DIC?

  • PT

  • PTT

  • aPTT

  • D-dimer

80
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what labs are decreased with DIC?

  • fibrinogen

  • platelets

  • antithrombin

  • plasminogen

81
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what is a normal PTT?

11-12.5 seconds

82
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what is a normal INR?

0.5-1.1

83
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what is the first priority in treating DIC?

stabilize ABCs and treat the underlying cause

84
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what blood product is used for significant bleeding in DIC?

Fresh frozen plasma (FFP)— to replace clotting factors

85
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why is FFP given with DIC?

they have no clotting factors which is why they are hemorrhaging (it treats the underlying cause)

86
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when might anticoagulants be used with DIC?

in selected chronic DIC cases where clotting is the predominant issue

87
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what are key nursing priorities with DIC?

  • continuous VS monitoring

  • assess for bleeding

  • manage fluids/blood products

  • monitor tissue perfusion

  • reduce anxiety of the client

  • monitor coags (PT, PTT, INR, platelets, Hbg/Hct)