Class 9 - Alterations in Cardiovascular Function Flashcards

1
Q

Red Blood Cells

A

Purpose: To carry oxygen and CO2
Building Blocks: Iron B12, folic acid, others
Lab Values
- Hemoglobin: 120-180 g/L
- Hematocrit: % of blood that is RBC’s
- If saline is given hematocrit decreases

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2
Q

Anemia

A
  • Reduction in the number of RBC’s in the blood or a decrease in the level of hemoglobin
  • Less RBC = lower oxygen carrying capacity
  • Manifestations - Tiredness

Etiology: Impaired production of

  1. Iron, B12, folate, causes chronic disease
  2. Blood loss or destruction (hemolysis) of RBC’s
  3. Or a combination of both

Size
- Identified by terms that end in cytic “microcytic, macrocytic, normocytic,

Colour

  • Hemoglobin content
  • Identified by terms that end in cytic
  • Hypochromic (paler), normochromic
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3
Q

Iron Deficiency Anemia

A
  • Cells will be smaller than normal (microcytic)
  • Cells will be paler, hypochromic
  • Related to nutritional iron intake, increased need (from pregnancy), or continuous blood loss

Clinical Manifestations

  • Fatigue, weakness, dyspnea, pallor
  • Spoon-shaped nails
  • Glossitis (red, sore, painful tongue)

Treatment

  • Treat the cause
  • Iron supplements
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4
Q

Pernicious Anemia

A

Caused by an inability to absorb vitamin B12

  • Malabsorption
  • Lack of intrinsic factor from the gastric parietal cells. Required for vitamin B12
  • Cells are large, macrocytic

Clinical Manifestations

  • Fatigue, weakness, dyspnea, pallor
  • Nerve demyelination: paresthesia of feet (numbness, burning, tingling), loss of position sense, dementia

Treatment
- Lifelong B12 supplementation

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5
Q

Folate Deficiency Anemia

A
  • Folate deficiency: green leafy vegetables, fruits, cereals, meats
  • Poor absorption of folate
  • Increased requirements of folate (pregnancy)

Similar to pernicious anemia

  • Macrocytic cells
  • So large they have trouble getting out of the bone marrow, and spleen gets rid of abnormal blood cells

Clinical Manifestations

  • Fatigue, weakness, dyspnea, pallor
  • Lack of folate is also linked to cardiovascular disease and neural tube defects in children

Treatments

  • Dietary adjustments
  • Supplemens

Linked to Spina Bifida

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6
Q

Anemia due to Chronic Disease

A

Pathologic mechanisms

  • Inadequate production of erythropoietin
  • Ineffective bone marrow response to erythropoietin
  • Decreased erythrocyte life span
  • Depletion of iron stores

Associated with systemic lupus erythematous (SLE), rheumatoid arthritis, and chronic renal failure

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7
Q

Blood Loss Anemia

A
  • Can be acute or chronic
  • Acute symptoms are usually related to blood loss (tachycardia, hypotension)
  • Chronic use of iron stores
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8
Q

Hemolytic Anemia

A
  • Premature destruction
  • Hemolytic disease of the newborn
  • Sickle Cell disease
  • Venoms, infections, snake bites, E Coli, malaria
  • Transfusion reaction
  • Mechanical heart valve
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9
Q

Sickle Cell Anemia

A
  • Abnormal production hemoglobin
  • An autosomal recessive disorder
  • More common in those living near the equator, increased malaria resistance
  • Triggered by dehydration and hypoxemia
  • HbS can revert back to normal, or can become irreversibly sickled

Major consequences

  1. Chronic hemolytic anemia
    - Premature destruction by spleen
  2. Blood vessel occlusion
    - Hypoxia
    - Pain
    - Organ failure
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10
Q

Leukocytosis

A

Increased white blood cells
May be normal protective physiologic response physiologic stressors
- Neutrophils

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11
Q

Leukopenia

A

Decreased white blood cells

  • Never normal
  • Radiation, chemotherapy, immune deficiencies
  • Predisposes a patient to infection
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12
Q

Neoplasia

A
  • Both leukaemia and lymphoma are caused by malignancies of blast cells
  • Leukaemia starts in the bone marrow
  • Lymphoma starts in the lymph nodes
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13
Q

Leukemia

A

Malignancy of precursors to WBC, immature white blood cells (leukaemia blasts)

Types:

  1. Acute lymphocytic leukemia - Children
  2. Acute myelogenous leukemia - Worst
  3. Chronic lymphocytic leukemia - Best
  4. Chronic myelogenous luekemia

Incidence

  • Rates are rising
  • Leading cause of death in young children
  • Most common in caucasian children

Risk Factors

  • Genetics: down syndrome for acute leukemia, Philadelphia chromosome (CML)
  • Ionizing radiation
  • Chemotherapy
  • Chemical exposure
  • Smoking
  • Leukemia blasts crowd out bone marrow and causes pancytopenia (decreased cellular proliferation of all types of blood cells)
  • Infiltrate spleen, liver etc

Manifestations

  • Pancytopenia (decreased cellular proliferation)
  • Infiltration into the liver, spleen, lymph
  • Fatigue, weakness, dyspnea, pallor
  • Bone pain
  • Hepatomegaly
  • Splenomegaly
  • Weight loss and night sweats

Diagnosis
- Blood and bone marrow studies

Treatment

  • Chemotherapy
  • Bone marrow or stem cell transplant
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14
Q

Lymphatic System

A

Links immune and hematological systems
- Site where various WBC;s mature and function

Primary structures

  • Thymus
  • Spleen

Secondary Structures
- Lymph nodes

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15
Q

Lymphadenopathy

A

Enlarged lymph nodes that become palpable and tender
Local: can be normal (strep throat)
Generalized: related to some type of cancer

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16
Q

Hodgkin Lymphoma

A
  • Proliferation of malignant lymphocytes in the lymphatic system
  • 5 year survival is 83%
  • Tends to start locally
  • Spreads along the chain of nodes and then is more widespread

Causes

  • Unknown
  • Genetic, immune mechanisms
  • Linked to epstein-barr virus

Bimodal

  • 15-40 years
  • > 55 years

Manifestations

  • Lymphadenopathy, single node or chain
  • Fever
  • Night sweats
  • Fatigue
  • Weight loss

Diagnosis
- Lymph node biopsy, reed-Sternberg (RS) cells in lymph tissue

Treatment
- Chemotherapy and radiation

17
Q

Non-Hodgkin Lymphoma

A
  • Generic term for neoplasms of B-cell, T-cell, NK-cell
  • Impairment of immune system and infectious agents
  • Incidence has almost doubled since the 1970’s
  • Usually in people > 50 years
  • 5 year survival is 55-60%
  • Multiple lymph nodes are affcted at once
  • Spread less predictably than Hodgkin lymphoma

Manifestations

  • Lymphadenopathy, single node or chain
  • Fever
  • Night sweats
  • Fatigue
  • Weight loss

Diagnosis
- Lymph node biopsy

Treatment
- Chemotherapy and radiation

18
Q

Thrombocytopenia

A
  • Too few
  • Decreased production
  • Increased breakdown or consumption

Thrombocytosis
- Too many

19
Q

Immune Thrombocytopenic Purpura (ITP)

A
  • Also known as idiopathic thrombocytopenia purpura
  • Occurs in flares

Pathophysiology

  • Acute or chronic
  • Autoimmune destruction of platelets
  • IgG antibody coats platelets, later removed the spleen
  • Immune response type 2, attack on the surface of the cells

Signs and Symptoms

  • Bleeding: gums, shaving, intracranial hemorrhaging, iv sites
  • Excessive bruising
  • Purpura: larger splotches, not uniform like a bruise
  • Petechiae: smal spots of bleeding

Diagnosis: blood test to measure platelets and measure IgG levels

Treatment
- Corticosteroids to decrease immune response or spleen removal

20
Q

Heparin-Induced Thrombocytopenia (HIT)

A
  • Adverse drug reaction to unfractionated heparin (old)