Assessment of Hematologic Function Flashcards

1
Q

Hematologic System

  • Blood
  • Lymph nodes/nodules
  • Thymus
  • Accessory organs (liver, spleen)
  • Bone marrow
A
  • Lymph nodes are interconnected in our bodies by lymph vessels. Most are found in the thoracic and abdominal cavities, the neck, axilla, inguinal, and superficial areas
    > Look to see if there are changes to the lymph shape or size
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2
Q

Lymph nodes produce Ig and IgA (immunoglobulins)

Nodules are smaller than lymph nodes but equally important

A
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3
Q

?

Is an endocrine organ responsible for producing T cells

The accessory organs are the liver and spleen

A

Thymus

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4
Q

?

Is the primary producer of most clotting factors; is the storage site for most blood cells

A

Liver

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5
Q

?

This organ balances blood cell production and destruction; assists with immune function; iron metabolism; and restores platelets and blood cells

A

Spleen

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6
Q

?

Is the major site of blood cell and stem cell formation

Produces most of the cells of the blood (RBC’s, WBC’s, platelets) and is involved in the immune response

A

Bone marrow

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7
Q

Blood Function

  • Carry oxygen to cells
  • Assist with acid-base balance
  • Transport carbon dioxide back to the lungs
  • Coagulation
  • Defense against infection
A
  • Blood volume is higher in males (5-6L) opposed to females (4-5L) [can vary based on factors]
  • Blood is more viscous than water; made in the bone marrow, spleen, and liver
  • Affected by age, body composition, nutrition, hydration, medications
    > NSAIDs impair the hematologic system
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8
Q

Blood Composition

  • Plasma (55%)
    > Proteins (8%) [albumin, globulin, fibrinogen]
    > Water (90%)
    > Other solutes (2%) [nutrients, electrolytes, waste products, hormones, gases]
A
  • Buffy coat: WBC’s and platelets (<1%)
  • RBC’s (45%)
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9
Q

?

Is the component of plasma involved in blood clotting

A

Fibrinogen

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10
Q

?

Is the component of plasma that maintains osmotic pressure of the blood which prevents plasma from leaking into tissues

A

Albumin

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11
Q

?

Is the component of plasma that is involved in the transportation of substances and antibiotic function

A

Globulin

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12
Q

Erythrocytes (RBC’s)

  • Erythrocyte - mature RBC
  • Reticulocyte - immature RBC
  • Needs Vitamin B12 and folic acid for RBC maturation
A
  • Lifespan is 120 days
  • Normal: 4-6 million
  • Responsible for producing hemoglobin
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13
Q

Hemoglobin’s main function is to carry oxygen; carry iron to tissues, lungs, and other organs
> Needs iron in order to produce hemoglobin (Hgb)

A
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14
Q

?

Normal Hgb in females ?

A

12-16

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15
Q

?

Normal Hgb in males ?

A

13-18

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16
Q

?

Is a growth factor that stimulates RBC production in the bone marrow
> Is released by the kidneys and the bone marrow produces it

A

Erythropoietin

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17
Q

Leukocytes (WBC’s)

  • Function = inflammation/immunity
  • Most are formed in the bone marrow
  • What is a normal count?
  • What are the 2 categories?
A

5000 - 10,000 μL

Granulocytes, agranulocytes

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18
Q

What are the 3 types of granulocytes?

A
  • Neutrophils
  • Eosinophils
  • Basophils
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19
Q

?

Are responsible for allergic reactions/responses

A

Eosinophils

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20
Q

?

Are involved in the allergic response; release histamine and also heparin to correct tissue damage

A

Basophils

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21
Q

?

Are the primary responders to inflammation; comprise 55-70% of WBC’s

A

Neutrophils

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22
Q
  • Chemotherapy patients may need an ANC level done daily
    > What is their neutrophil count?
  • ANC determines the risk for bacterial infection; looks at immune status helps determine the need for reverse precautions
    > The higher the ANC, the higher the chance to being resistant to infection; a lower # indicates being more susceptible to infection
A

<1000 = risk for bacterial infection

<500 - high risk

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23
Q

What are the 2 types of agranulocytes?

A
  • Monocytes
  • Lymphocytes
24
Q

?

These cells destroy bacteria

25
? These cells enhance the immune response
Lymphocytes
26
Leukopenia - a reduction in WBC's
Someone with a very low ANC ⥰ Neupogen
27
Rx's that affect WBC's Might these lower or increase the WBC count? * Beta adrenergic agonists (i.e., albuterol) * Corticosteroids * Epinephrine * Granulocyte colony stimulating factor * Heparin * Lithium
may INCREASE
28
Might these lower or increase the WBC count? * Antibiotics, anticonvulsants * Anti-thyroid, arsenicals * Captopril * Chemotherapy drugs, Chlorpromazine * Clozapine, diuretics * Histamine-2 blockers * Sulfonamides * Quinidine, terbinafine, ticlopidine
may LOWER
29
Thrombocytes (Platelets) * Smallest cell ! Controls bleeding Normal count is ? Lifespan of 1-2 weeks ! Thrombocytopenia is a deficiency in platelets
150,000 - 400,000 μL
30
Thrombocytes (Platelets) * Formed in the bone marrow; stored in the spleen; and released as needed. Used to control bleeding * Stick to an injured vessel wall and form platelet plugs; helps to repair damage to small cells to control bleed <50,000 μL = huge risk for bleeding
Bleeding & Coagulation Measurements * PT * INR * PTT or aPTT * Platelet agglutination/aggregation
31
What is a normal PT?
10-13
32
What is a normal INR?
0.8-1.2
33
What is a normal PTT/aPTT?
20-36
34
* INR can be used with PT for those on warfarin * Therapeutic INR for coumadin is 2.0-3.0 * PTT - looks at how long it takes the blood to clot and evaluates clotting factors II, V, VII, and IX
* PTT usually drawn on patients receiving heparin therapy; ranges can differ based on patient complication (cardiac issue vs DVT)
35
Which hematological measurement is looked at for warfarin?
PT/INR
36
Which hematological measurement is looked at for heparin?
PTT
37
Age-Related Changes to the Hematological System > As the body ages, the # of cells are gradually reduced > Lean body mass decreases > Fat tissue increases until around 60 > Bone mass and intracellular fluids also tend to decrease > Normal aging causes a decrease in total body water
* Blood volume decreases with age; bone marrow activity production to make RBCs and WBCs may be decreased * Circulating Hgb and Hct levels may be lower, leading to fatigue in the older individual * Reduction in lymphocyte count leads to decreased ability to fight infection
38
? * An insufficient supply of healthy RBCs * Common causes = nutritional, hereditary, bone marrow disease, or bleeding
Anemia ! Is a clinical sign; NOT a specific disease; can be referred to as a disease These patients have an insufficient amount of RBCs; decreased Hgb, Hct ! Hgb (g/dL) will determine how severe the anemia is
39
Mild anemia: 10-14 g/dL Moderate: 6-10 g/dL Severe: <6 g/dL
40
Hematocrit - the % of RBCs Normal % in males is __-__%; is slightly higher than females __-__% ! Hct is 3x the Hgb
Males: 42-52% Females: 37-47%
41
Clinical Manifestations of Anemia * Pallor, fatigue * Intolerance to cold, cold to touch * Nails brittle/ridged "spoon shaped" * Tachycardia * Weakness, palpitations * Orthostatic hypotension, headache
Types of Anemia > Iron deficiency > Vitamin B12 deficiency > Folic acid deficiency > Aplastic * Iron deficiency anemia **lacking iron** as opposed to aplastic anemia **where the bone marrow doesn't make enough new blood cells**
42
Iron Deficiency Anemia * Most common * Causes - insufficient dietary intake, blood loss, impaired absorption - Common in women, menstruating women, childbearing or pregnant women, older adults, and people with poor dietary habits - Type tends to be chronic and dietary intake is a big factor
* Another source is from blood loss (i.e., from the GI tract [coffee-ground emesis, black tarry stools] or menstruation) > Also, the patient with impaired intestinal absorption or someone who's had gastric bypass surgery * Increase dietary intake - red meat, organ meat, egg yolks, leafy green vegetables > May need iron supplements [! Constipation = offset with fiber or increased water intake] or IM injections
43
Vitamin B12 Deficiency * Lack of B12 in the diet * Poor absorption * Diagnosed: CBC, MMA (methylmalonic acid), or Schilling Test * Treatment = dietary, B12 injections, nasal inhalation
* Increase intake through animal protein, meat, seafood, eggs, and dairy * Psychiatric and neurological dysfunction; *glossitis* and paresthesia * Someone who is unable to absorb vitamin B12 may be lacking the intrinsic factor needed to absorb B12; known as **pernicious anemia** (**glossitis**) * Identifying the cause and whether the patient is able to absorb it or not will help determine treatment
44
Folic Acid Deficiency Causes (Water-Soluble B9) * Dietary * Malabsorption * Medications * Affects the elderly, chronic illness, chronic ETOH abuse
* Occurs in those who don't eat vegetables or go on extreme diets * Also, malabsorption due to Crohn's or gastric bypass; chronic illness; chronic alcohol abuse * Rx's - oral contraceptives, metformin, anticonvulsants, chemotherapeutic agents (methotrexate) ! Increase intake of fortified cereals, grains, green vegetables, yeast extracts, nuts, and folic acid supplements
45
? ! Rare - Deficiency in circulating RBCs - Chronic exposure to toxic agents, congenital - Accompanied by decreased leukocytes, platelets
Aplastic anemia
46
- Can cause heart arrythmias - Can be caused by chronic exposure to toxic agents like pesticides or insecticides, radiation, autoimmune disease, chemotherapy, and other medications. Can also be idiopathic
* Treatment with blood transfusions or immunosuppressive therapy
47
Anemia Management * Early identification of those at risk * Dietary modification * Supplements/rx's * Blood transfusion
Transfusion Therapy * Verify prescription * Test donor's and recipient's blood for compatibility (type and screen/cross-match) * Examine blood bag for identification * Check expiration date * Inspect blood for discoloration, gas bubbles, or cloudiness
48
Transfusion Responsibilities * Provide patient education > Obtain informed consent * Assess VS > May need to pre-medicate with Tylenol or Benadryl * Begin transfusion slowly and stay with the patient for the first 15-30 minutes
* Ask patient to report unusual sensations such as chills, SOB, hives, or itching * Administer blood products per protocol * Assess for hyperkalemia ! Occurs due to cellular damage and release of potassium into the blood; can occur from units of blood that are too old or too cold [a blood warmer may be used]
49
Transfusion Reactions * Febrile transfusion reaction > Chills, fever, tachycardia, HTN, tachypnea * Hemolytic transfusion reactions > When the blood type or blood antigens are incompatible > Fever, chills, headache, tachycardia, tachypnea, chest pain, HTN
* Allergic transfusion reaction > Itching, bronchospasm, anaphylaxis
50
* Bacterial transfusion reaction > Can be caused by contaminated blood > Tachycardia, HTN, fever, chills, and in severe cases, shock
* Circulatory overload > Happens when blood is infused too quickly > HTN, bounding pulse, distended neck veins, dyspnea, restlessness, confusion
51
Autologous Blood Transfusion * Collection and infusion of patient's own blood * Eliminates compatibility problems; reduces risk for transmission of bloodborne disease
- Also a way to minimize transfusion reactions - Useful for a surgery; need to be infection-free; Hgb >11 g/dL; and by a provider's prescription
52
Sickle Cell Disease (Anemia) * Increased RBC destruction * Genetic disorder * Sickle-shaped RBCs * Painful
- RBCs cannot effectively transport oxygen and deliver oxygen to tissues, organs, etc. - Those with the disease go into times of crisis > Crisis can be caused by hypoxia, dehydration, infection, pregnancy, high altitudes, stress, alcohol, and strenuous activities
53
* Pain is the first and most severe symptom - Blood is not getting to the tissue and there is poor oxygenation from the obstructed blood flow * We give these patients more oxygen, analgesics to help with the pain, rehydration, and blood transfusions > Typically need opiate rx's to ease their pain
54
? * A greater than normal RBC count * Temporary or permanent * Treatment = phlebotomy, hydration, anticoagulants
Polycythemia vera
55
Hgb >18 g/dL Hct >48-52 in men Massive production of RBCs, WBCs, and platelets ! A dark, flushed appearance, intense itching, HTN, poor tissue oxygenation (the greater viscosity of blood slows down oxygen exchange to the tissues) > Are at a high risk for clotting
* 2-3x/week for phlebotomy isn't unusual * Give radiation or Interferon ! Complications of this disorder are thrombosis, or blood clotting, and hemorrhage; bone marrow scarring; development of AML; HF from the heart being overtaxed; PE concern - May get hypoxic