13 Alterations in Oxygen Transport Flashcards

(41 cards)

1
Q

Erythrocyte/RBC

A

count: 4.2-6.2 million cells/mm3

- buffers blood pH: carbonic anhydrase

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2
Q

hematopoiesis

A

stem cells> reticulocytes/erythroblast> mature RBC/erythrocytes

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3
Q

erythropoietin/EPO

A

made in kidney (adult)

  • fetus + newborn made in liver + kidney
  • renal disease causes anemia
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4
Q

nutritional requirements for erythropoiesis

A

-requires adequate amounts of iron, protein, vitamins, + minerals

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5
Q

folate + B12 deficiencies lead to…

A

impaired DNA synth in erythroid cells bs vitamins are coenzymes of key rxns in cell metab

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6
Q

absorption of B12 in sm intestines require…

A

intrinsic factor

-produced by parietal cells of stomach

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7
Q

Bilirubin

A
  • rbc destruction
  • porphyn is reduced to bilirubin in liver + excreted in bile
  • intestinal bacteria convert bilirubin into URObilirubin which is excreted mostly in stool but also in urine
  • too much bilirubin=jaundice
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8
Q

Anemia

A

deficit of RBC

-lox O-carrying capacity leads to hypoxia

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9
Q

Polycythemia

A

excess of RBC

  • primary or acquired
  • incr in blood viscosity + volume
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10
Q

general effects anemia

A
  • reduction in O-carrying capacity (tissue hypoxia)
  • compensatory mechanism to restore tissue oxygenation
  • –SNS: incr heart rate, CO, circ rate, flow to vital organs
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11
Q

aplastic anemia

A
  • stem cell disorder characterized by reductin of hematopoietic tissue, fatty marrow transplant, + pancytopenia
  • disease of young or old (15-25; 60+)
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12
Q

pancytopenia

A

low RBC, WBC, + platelets

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13
Q

aplastic anemia

cause + diagnosis

A
  • caused by toxic, radiant, immunologic injury to the bone marrow stem cells
  • diagnosed w bone marrow biopsy
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14
Q

aplastic anemia

treatment

A
  • bone marrow transplantation

- administer immunosuppressive therapy or stim hematopoiesis + bone marrow regeneration

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15
Q

anemia of chronic renal failure

A

failure of renal endocrine function impairs ERYTHROPOIETIN PRODUCTION + bone marrow compensation

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16
Q

anemia of chronic renal failure

treatment

A

-dialysis
-administer erythropoietin
(only used until Hgb is 12g/dl)
-replacement of iron, folate, + B12

95% respond to erythropoietin therapy

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17
Q

cobalamin

18
Q

anemia related to B12 or folate deficiency

A

-disrupt DNA synth of blast cells produces megaloblast

19
Q

macrocytic

A

type of anemia related to B12 deficiency

-more overly large RBC (megaloblasts) than normal RBC

20
Q

pernicious anemia

A

type of anemia related to B12 deficiency

-due to lack of intrinsic factor

21
Q

folate deficiencies are usually from…

A

dietary deficiencies, alcoholism, cirrhosis, pregnancy, or infancy

22
Q

pernicious anemia

clinical manifestations

A
  • decreased RBC, WBC, + platelet counts
  • increased MCV, megaloblastic dysplasia
  • peripheral nerve degeneration
  • shillings test indicates low B12
  • gastric analysis reveals achlordydria
  • megoblastic madness
23
Q

achlordydria

A

absence of hydrochloric acid in gastric secretions

- a manifestation of pernicious anemia

24
Q

Iron Deficiency Anemia

A
  • insufficient iron for hemoglobin synth
  • hypochromic, microcytic RBC, low MCV, MCH, + MCHC
  • dec in serum ferritin level, serum iron level
  • incr in total iron binding capacity
25
most common nutritional deficiency in the world
iron deficiency anemia
26
microcytic
smaller than normal RBC
27
MCV, MCH, MCHC
MCV: mean corpuscular vol MCH: mean corpuscular hemoglobin MCHC: mean corpuscular hemoglobin concentration
28
Iron Deficiency Anemia manifestations
- PICA - koilonychias (spoon-shaped nails) - blue sclerae
29
Pica
cravings for nonfood substances like dirt, clay, ice, cardboard, hair
30
Iron Deficiency Anemia treatment + prognosis
- oral administration of FERROUS SULFATE or IV FERRIC GLUCONATE (only in severe cases) - -cont for 4-6 months - treat underlying cause -prognosis is excellent
31
Thalassemia
- incr hemolysis - hypochromic, microcytic RBC - autosomal recessive - classifies by polypeptide chains w deficient synth (a or b-thalassemia - low MCV, MHC, MCHC - erythroblastic hyperplasia
32
hemolysis
RBC destruction
33
autosomal recessive
assoc. w mutant genes that suppress the rate of globin chain synth
34
most clinically severe form of thalassemia
thalassemia MAJOR
35
Sickle Cell Anemia
- genetically determined defect of hemoglobin synth - results w hemoglobin instability + insolubility - sickled cell causes vascular occlusion
36
sickle cell anemia is found exclusively in which population
black race
37
Sickle Cell Anemia treatment + prognosis
- crisis: major medical event - treatment of choice is stem cell transplant prognosis is death if no/unsuccessful transplant
38
hemolytic disease of newborn
- fetal RBCs cross placenta, stim production of MATERNAL ANTIBODIES AGAINST Rh+ antigen on fetal RBC - --not inherited fr mother; mother is Rh- - maternal antibodies cross into fetal circulation causing destruction of fetal cells - --ABO compatibility is most common - ---Rh incompatibility more clinically relevant
39
hemolytic disease of newborn treatment + prognosis
- standard dose of anti Rh- immune globulin [RhoGAM] is given to mother before or after delivery - severe cases, in utero blood transfusion + early delivery prognosis: death, possible retardation, barely perceptible hemolytic process
40
RhoGAM
anti-Rh immune globulin | -given to mother before or after delivery when Rh incompatible
41
vocab checklist: ``` 1 polycythemia 2 pancytopenia 3 macrocytic 4 megaloblast 5 pernicious A. 6 aplastic A. 7 achlordydria 8 pica 9 thalassemia 10 hemolysis ```
``` 1 excess RBC (opp of "anemia") 2 low RBC, WBC, platelet 3 B12 related anemia 4 large RBC 5 B12 related anemia due to lack of intrinsic factor 6 stem cell disorder 7 absence of HCl acid in gastric secretion (due to pernicious A) 8 craving of nonfood 9 incr hemolysis 10 destruction of RBC ```