Pathophysiology 1 - Chapter 13

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66 Terms

1
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Total blood volume in men

75.5 mL/kg

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Total blood volume in women

66.5 mL/kg

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Plasma makes up what percent of the blood volume?

~55-60%

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Blood cells make up what percent of blood volume?

~40-45%

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Plasma is composed of what?

92% water, 7% plasma proteins, and 1% hormones, vitamins, enzymes, lipids

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True or False: Red blood cells have a nucleus

False, red blood cells lack a nucleus.

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Blood is what % of body weight?

7-8%, around 5-6 Liters total

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What is erythropoietin?

Hormone from kidney that stimulates erythrocyte production

9
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Per 1 hemoglobin molecule, how many oxygen molecules can bind to it?

4 oxygen molecules

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What do hemoglobin carry?

oxygen molecules in the blood

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Where does the production of hemoglobin take place?

In immature RBCs

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What is required for hemoglobin synthesis

Iron

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What nutritional requirements are needed for normal RBC development?

Protein and Vitamins B12, Folate, B6, Riboflavin, Niacin, E, & C

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RBC + Bone marrow precursors =

Erythron

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A decrease in hemoglobin decreases what in kidneys?

Decreases the tissue oxygen tension in kidneys

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What do RBCs need energy for?

To survive ~120 days and to operate membrane pumps for maintaining

  • high intracellular potassium ion

  • low intracellular sodium ion

  • very low intracellular calcium ion

17
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Where do RBCs get digested by macrophages?

In the spleen and liver

18
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True or False: The 3% that is dissolved in plasma is measured as PO2

True

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True or False: Globin and iron portions are conserved and reused

True

20
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What does the oxygen-hemoglobin dissociation curve describe?

The relationship between PO2 (pressure) and SO2 (saturation)

21
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What process does RBC rely on to produce energy, due to no organelles?

Glycolysis

  • produces 2 pyruvates and 2 ATP molecules

22
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What three forms is CO2 transported as?

  • dissolved gas (5%)

  • bicarbonate ion (75%)

  • in association with hemoglobin forming carbaminohemoglobin (20%)

23
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PaO2 =

PO2 in arterial blood = 80-100 mmHg

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PvO2 =

PO2 in venous blood = 35-40 mmHg

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True or False: Carbaminohemoglobin releases CO2 in the lungs which we exhale out

True

26
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Decreased oxygen reaching the tissues results in secretion of ____ and increase in the production of ___

erythropoietin (EPO); RBCs

27
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What are the RBC disorders?

Anemia and Polycythemia

28
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General Anemia Definition

Deficit of RBC

  • Patient has tissue hypoxia due to low-oxygen-carrying capacity of blood

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General Polycythemia Definition

Excess of RBC

  • Patient has increased blood viscosity and volume due to the increase in RBC numbers

30
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Relative anemia

  • “dilutional anemia”

  • normal total red cell mass with disturbances in regulation of plasma volume

  • too much plasma = proportion of RBC to plasma is small

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Relative anemia example

in pregnancy plasma volume increases ~40%

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Absolute Anemia

  • actual decrease in numbers of red cells

    • decreased production

    • increased destruction

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General effects of anemia

  • reduction in oxygen-carrying capacity

    • tissue hypoxia (low oxygen)

  • compensatory mechanism to restore tissue oxygenation

    • increased heart rate

    • increased cardiac output

    • preferential increased flow to vital organs (limits blood flow to extremeties = paler skin)

    • increase in erythropoietin

34
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Describe mild anemia

  • usually no clinical symptoms

  • elderly with cardiovascular, pulmonary disease may have symptoms

35
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Describe mild to moderate anemia

  • fatigue

  • generalized weakness

  • loss of stamina, followed w/ tachycardia and exertional dyspnea

36
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Describe moderate to severe anemia

  • decrease in blood pressure (orthostatic)

  • vasoconstriction

  • pallor

  • tachypnea, dyspnea

  • tachycardia

  • intermittent claudication (muscle cramping)

  • headache, lightheadedness, and faintness

  • tinnitus (roaring in ears)

37
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Aplastic anemia etiology and pathogenesis

  • stem cell disorder characterized by reduction of hematopoietic tissue, fatty marrow replacement

  • caused by toxic, radiant, or immunologic injury to the bone marrow stem cells

38
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Aplastic anemia laboratory features

  • pancytopenia (low RBC, WBC, and platelets)

    • low WBC important for prognosis: low leukocytes = susceptibility to infections

  • diagnosed with bone marrow biopsy

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Aplastic anemia clinical manifestation

  • insidious onset of symptoms

  • late symptoms

  • thrombocytopenia (prone to bleeding)

  • neutropenia (prone to infections)

  • disease of the young

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Aplastic anemia treatment and prognosis

  • determine efficacy of bone marrow transplantation

  • administer immunosuppressive therapy or stimulate hetopoiesis and bone marrow regeneration

  • will be fatal unless bone marrow transplant successful

  • bone marrow highly successful and curative for majority of untransfused patients, and 55% of patients with multiple transfusions

41
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Anemia of chronic renal failure etiology and pathogenesis

  • primarily from failure of the renal endocrine function, which causes impaired erythopoietin (EPO) production

  • secondarily from failure of renal excretory function

    • leading to hemolysis, bone marrow cell depression and blood loss

42
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Anemia of chronic renal failure laboratory features and clinical manifestations

  • low RBC, hematocrit, hemoglobin count

  • grossly deformed RBC

  • general signs and symptoms of anemia usually manifest when hematocrit decreases <20%

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Anemia of chronic renal failure treatment and prognosis

  • dialysis

  • administration of erythropoietin

    • EPO is only used until hemoglobn is 12 g/dL

  • replacement of iron, folate, and B12 due to dietary restrictions and anorexia

  • 95% respond to erythropoietin therapy

44
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Anemia in relation to vitamin B12 or folate deficiency causes a disruption in what

DNA synthesis of blast cells produces megaloblasts (macrocytic)

45
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Pernicious anemia is caused by lack of what which causes what

intrinsic factor which leads to vitamin B12 deficiency

  • problem is with B12 absorption NOT deficiency

46
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Anemia related to Vitamin B12 or folate deficiency laboratory features

  • low RBC, WBC, and platelet counts = megaloblastic dysplasia

  • microcytic and hyper-segmented neutrophils

47
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Clinical features of vitamin B12 deficiency

  • paranoia, dementia, cognitive dysfunction, delusions, hallucinations

  • peripheral nerve degeneration and memory impairment

48
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Clinical features of both B12 and folate deficiency

  • Edema in feet

  • tachypnea

  • weight loss

49
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Vitamin B12 or folate deficiency anemia treatment and prognosis

  • administer B12 and folate parenterally or orally

  • majority respond well to treatment

  • reversibility of the neurologic damage is low though

50
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Most common cause of anemia

Iron deficiency anemia

51
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Iron deficiency anemia cause

unavailability of iron for hemoglobin synthesis

52
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Iron deficiency anemia laboratory features

  • smaller and paler RBC

  • low red cell indices

  • decreased serum ferritin

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Iron deficiency anemia treatment and prognosis

  • oral administration of ferrous sulfate

  • treat underlying cause

  • prognosis is very good usually

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possible causes of iron deficiency anemia

  • low iron intake

  • diminished absorption

  • increased requirement for iron (ex. pregnancy)

  • excessive iron loss (ex. hemorrhage)

  • renal failure

  • hemodialysis

  • GI bleed

  • menorrhagia

55
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True or False: Thalassemia has increased RBC destruction referred to as hemolysis

True

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Thalassemia etiology and pathogenesis

  • associated with mutant genes that suppress rate of globin chain synthesis

  • classified by the polypeptide chain(s) with deficient synthesis

    • a-thalassemia or b-thalassemia

    • most clinically severe form: thalassemia major (homozygous)

57
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Sickle cell anemia etiology and pathogenesis

  • genetically determined defect of hemoglobin synthesis resulting in hemoglobin instability and insolubility

  • in Hemoglobin S, a single amino acid substitution causes the structural abnormality

  • sickled cells cause vascular occlusion

    • cant carry enough O2

    • sickled shape RBC stacks on each other = blockage

58
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For hemolytic newborns, what is clinically relevant?

Rh incompatibility

  • fetal RBCs cross placenta and stimulate production of maternal antibodies against antigen on fetal RBC - not from mother

  • maternal antibodies cross into fetal circulation causing destruction of fetal cells in subsequent pregnancies

59
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Hemolytic disease of the newborn treatment and prognosis

  • standard dose of anti-Rh immune globulin (RhoGAM) is given to mother before or after delivery

  • severe cases in utero blood transfusion and early delivery

  • prognosis: death, possible retardation, or barely perceptible hemolytic process

60
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antibody-mediated drug reactions cause

exposure to a drug causes destruction and lysis of sensitized person’s own RBCs

61
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antibody-mediated drug reactions treatment and prognosis

  • recognition and discontinuation of responsible drug

  • steroid therapy i cases of severe hemolysis

62
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acute blood loss treatment and prognosis

  • blood volume replacement therapy with crystalloids, colloids, and fresh whole blood

  • prognosis is excellent with treatment unless blood loss is severe

63
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Polycythemia definition

excess RBC results in increased blood viscosity, leading to clinical symptoms such as hypertension

64
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Polycythemia Vera

neoplastic transformation of bone marrow stem cells

  • “true polycythemia”

  • absolute increase in RBC mass, leukocytosis, thrombocytosis - increased uric acid because of excess proliferation, oxygen saturation is normal

65
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Secondary Polycythemia

caused by chronic hypoxemia with resultant increase in erythropoietin production

  • increased RBC production without increase in WBCs or platelets

66
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Relative Polycythemia

caused by dehydration with spurious increase in RBC production

  • elevated hematocrit, hemoglobin, and RBC count

  • two groups: disturbed fluid balance and stress polycythemia