lp 7- immune / hemtology Flashcards
what is blood made up from
plasma,
solutes,
RBCs,
WBCs,
platelets
Hematopoietic
bone marrow function
originate
bone marrow tissues (where blood cells are formed)
-all cells originate in bone marrow
lymphoid tissues
what does
white blood cells mature & circulate)
Red blood cells
aka
shape
what does shape do
AKA erythrocytes- most common
biconcave disks
- allows cells to pass through small capillaries without disrupting cell membrane
Duty of RBCs & Hemoglobin
transport
excretion
Transport O2 to body tissues
Carbon dioxide excretion
normal levels of RBC/hemoglobin
in women/men
Normal levels are Hemoglobin-
(12-16 Women)
(13.5-18-men)
Anemia
low Blood cell count
Polycythemia
–High blood cell count
Erythropoiesis
production starts/end where
how long does it take
RBC production
Production starts in bone marrow
ends in blood/spleen
takes 3-5 days
What stimulates RBC production
when that occurs…
___ stimulates
tissue hypoxia
When this occurs, Kidneys release erythropoietin
erythropoietin stimulates bone marrow to produce RBC’
lifespan of rbc
Lifespan of 120 days
hemolysis-what is it
converted/ what is it/ where goes
Old damaged RBCs are lysed (damaged) by phagocytes
Lysed RBCs are converted into bilirubin
bilirubin( orange/yellow pigment that bilirubin is removed by liver
which is then excreted out
If someone has impaired liver function/disease process
causes
means
causes
, this causes increases hemolysis,
which means bilirubin will be accumulated into serum
causes jaundice
WBC
AKA
where come from
what is duty
leukocytes
Come from stem cells in bone marrow
Duty?- Defense against microorganisms
normal levels of WBC
(4000-11,000
Leukopenia
lower WBc count
Leukocytosis
higher WBc count
Granular Leukocytes
what are they
3 types
Mature fully in bone marrow, then release into blood stream
neutrophils
eosinophils
basophils
Neutrophils
active
first
increases
immature
lifespan
active phagocyte-
first cell to arrive to site of injury-
increases during inflammation-
immature forms will be released during inflammation/infection-
10 hr lifespan
Eosinophils
found
increase
found in large numbers of mucosa of intestines and lungs-
increase during allergic reaction or parasitic infestations
Basophils
contain
which do what
contain inflammatory mediators
which increase during allergic or inflammatory reactions.
Non-Granular Leukocytes
enter
active part
2 types
Enter bloodstream before fully mature
Active part in: inflammatory & Immune responses
2 types-monocytes, lymphocytes
platelets
aka
formed
live for how long
AKA Thrombocytes
Formed in bone marrow-
live for 10 days
duty of platelets
release
produce
Release mediators required for CLOTTING
Produce ATP
normal levels of platelets
Normal levels are 150,000-400,000
Thrombocytosis
excessive amountof platelets
Thrombocytopenia
risk
deficient amount
risk for injury dt bleeding, petechiae, ecchymosis
Anemia
abnormally low RBC count/ low hemoglobin concentration
Duty of RBCs & Hemoglobin
anemia –leads to
Transport O2 to body tissues & Carbon dioxide excretion
Anemia- reduces the oxygen carrying capacity of the blood-leads to hypoxia
Body can compensate and be asymptomatic; if not and symptoms do arise
symtoms
anemia
Pallor; skin, mucous membranes, nail beds
Heart and resp rate increases
Tissue hypoxia; angina, fatigue, dyspnea on exertion
Bone pain
Blood Loss Anemia
caused from
circulating bv->
Anemia caused from acute/chronic blood loss
Circulating blood volume decrease cardiac output falls
Compensatory mechanisms for blood loss anemia
heart rate increases,
blood vessels constricts,
fluid shift from interstical space to vascular space to help maintain fluid volume
Acute blood loss-when return to normal
Return to normal 3-4 weeks
Chronic blood loss-
iron store
microcytic
hypochromic
- iron store eventually depleted; RBCs ->
microcytic(small rbc)
& hypochromic ( pale RBC)
what are nutritional keys to RBC development
Iron
Protein, vitamins, minerals
B 12 and folate specifically
Vit C & Vit E
what are Nutrient Deficits causes
inadequate diet,
malabsorption,
increase need for nutrients
Iron- Deficiency Anemia
most
increases
cause by
Most common type of anemia
Risk factors increase with age,
Cause developed when supply of iron is inadequate for optimal rbc formation
iron deficiency anemia
may result from
defiecneies
decreased
increased
loss/excessive
chronic
Dietary deficiencies
Decreased absorption
Increased metabolic requirements
Blood loss /excessive bleeding
Chronic hemoglobinuria
manifestations for iron defunct anemia
Brittle spoon shaped nails,
sore tongue,
cheilosis-cracked mouth
pica-unusual taste
Treatment: iron deficiency anemia
High iron diet-chicken, beef, egg yolk, brown rice
dietary supplements causes an increase in H&H
Vitamin B 12 Deficiency Anemia
occurs
failure
lack of
Occurs when B 12 is not consumed or absorbed
Failure to absorb is called Pernicious anemia
Lack of intrinsic factor needed for absorption
Who is at risk for vitamin b12 anemia
pts who have had stomach resection.
, chronic gastritis
manifestations of vitamin b 12 Deficiency anemia
Pallor,
smooth sore beefy red tongue,
neurologic symptoms- paresthesia; numbness & tingling/pain of extremities
Treatment -Vitamin B 12 Deficiency Anemia
dietary sources
treatment
b12 found where
Dietary sources of B-12- Eggs, liver, milk, shrimp, cheese
Treatment B-12 injection
B12 is almost exclusively found in food derived from animals
Folic Acid Deficiency Anemia
folicacid is needed for
found in
Needed for normal maturation of RBCs
found in Inadequate dietary intake, increased metabolic needs, malabsorption, impaired metabolism
who is at risk Folic acid deficiency anemia
__older adults,
drug/alcohol issues,
pregnancy,
children dt increased metabolic needs/meds
Folic Acid Deficiency Anemia
Manifestations
similar
difference
Similar to anemia, and B 12- (pallor SOB, heart palpations) -
> difference though? Is folic acid does not have neurologic symptoms
Folic Acid Deficiency Anemia
Strongly associated with
Neural Tube Defects;
spina bifida- Prenatal vitamin
Folic acid anemia
treatment
nutrition
supplemental folic acid
nutrition- broccoli, Brussel sprouts, citrus, ceralacche, peas, beans, green veggies
Hemolytic Anemias
characterized by
Characterized by premature destruction of RBCs
Hemolytic Anemias
causes
causes can be
Causes:
RBC cell membrane defect
, HgB structure defects (Thalassemia, sickle cell),
Mechanical damage,
drugs/chemicals,
bacteria and other infections
Causes can be
intrinsic(disorder within rbc) or
extrinsic(disorder outside of rbc
Thalassemia
inherited
leads to
causing
Inherited disorder hemoglobin synthesis is incomplete meaning it is missing a molecule
Leads to deficient HgB production,->
causing fragile, microcytic, hypochromic characteristics to rbc
Hemolytic Anemias
can be
can cause
manifestations
Can be asymptomatic
Can cause Mild to moderate anemia
Manifestations->splenomegaly, brown skin color, bone marrow hypoplasia
Hemolytic Anemias
Accumulation of iron, following repeated transfusions…
leads to failure of major failure such as heart/liver
Hemolytic Anemias treatment
: Blood transfusions,
folic acid supplements,
splenectomy,
genetic counseling
Sickle cell anemia
what is
characterized by
can be
Hereditary
Characterized by episodes of sickling where rBC become crescent shaped
can be acute or chronic
sickle cell anemia patho
These will clump together and obstruct capillary blood flow, causing ischemia and possible infarction to surrounding tissue.
Symptoms of sickle cell
-pallor,
fatigue,
jaundice,
irritability,
and pain(when RBC clump together)
Aplastic Anemia-
bone marrow
leading to
replaced
will see
develops
Bone marrow fails to produce all three types of blood cells
leading to pancytopenia
Normal bone marrow is replaced by fat
Will see low count of RBC,WBC and platelets.
Anemia develops as bone marrows fails to replace
Manifestations aplastic anemia
Vary with severity of pancytopenia
Pallor, weakness, exertional dyspnea, headache…tachycardia, heart failure
anemia
goal
interventions
treatment
Goal- Ensure adequate tissue oxygenation
interventions- pace activités, encourage rest
TDB- withdrawal of causative agent, blood transfusions, bone marrow transplant
CBC- what looking for
Anemia- Diagnosis
blood cell count,
H&H,
severity of anemia,
shape,
volume,
and can help determine cause of anemia
iron-why
Anemia- Diagnosis
performed to detect iron deficiency anemia