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Thalassemia, Iron deficiency anemia, chronic disease anemia, sideroblastic anemia
What does TICS stand for?
blood, GI, dietary, absorption, increased
Iron Deficiency Anemia Etiology
_____ loss (chronic)
The major cause of iron deficiency in resource-rich countries
Ex: __ bleed
________ deficiency
Impaired __________
_________ requirement
Iron Deficiency Anemia
What is the most common nutritional disorder and anemia worldwide?
blood, pregnancy
In developed countries, iron deficiency anemia is most commonly from continuous _____ loss and __________
erythropoiesis, immune, cytokine
Iron Deficiency Anemia Pathophys
Iron is needed for proper ____________ and Hgb synthesis
______ function - regulates immune effector mechanisms
________ activities (IFN-y, nitric oxide formation, & T cell proliferation)
pica, cheilitis, fingernails, beeturia, glossitis
IDA Symptoms
Hallmark sign is ____
craving for ice, clay, or starch
Angular ________
___________: brittle, thin, coarsely ridged
“spoon-shaped” or concave (koilonychia)
_______
urine turns red following ingestion of beets
Seen in 49-80% of IDA patients
atrophic _________ with loss of tongue papillae
± tongue pain or dry mouth
serum, transferrin, binding, saturation
Iron Studies/Iron Profile
_____ Iron
___________ / Total iron _______ capacity (TIBC)
% Transferrin _________
Ferritin
Serum Iron
How is circulating iron measured?
transferrin, BM, fluctuates, not
Serum Iron
Circulating Iron
Iron bound to ___________ (transport protein)
Dependent on iron recycling by __ and reticuloendothelial macrophages
_________ with dietary intake and normal diurnal variation
By itself, low serum iron is ___ diagnostic of any condition
Transferrin
a circulating transport protein for iron
TIBC, increased
Serum Transferrin
Transferrin is a circulating transport protein for iron
Can be expressed as ____
It is _______ in iron deficiency
total iron
indirect, available, increased
Total Iron Binding Capacity (TIBC)
Amount of transferrin available to bind iron
________ measure of transferrin and ________ binding sites for iron
As iron is depleted, TIBC is ________
TSAT, serum, TIBC, increased, low
Transferrin Saturation (____)
The ratio of _____ iron to ____
In iron deficiency
Iron is reduced
TIBC is _______
Transferrin saturation is ___
ferritin
a circulating iron storage protein
increased, acute, increased, diagnostic
Serum Ferritin
Ferritin is a circulating iron storage protein
________ in proportion to body iron stores
It is an _____ phase reactant
_______ with inflammation, infection, liver disease, heart failure, malignancy
Very low
low, high, high, low, low
Iron deficiency anemia
Serum iron = ____
Transferrin = ____
TIBC = ____
Transferrin Saturation = ____
Ferritin = ____
serum ferritin
What is the most helpful and reliable test to diagnose iron deficiency anemia if using iron studies?
I
bleeding, leafy, ferrous sulfate, oral
IDA Treatment
Treat the CAUSE
Investigate _______
Diet
Encourage _____ green veggies rich in iron
Treat the anemia
IV Iron (_______ ______)
____ iron
iron overload
What do you have to watch out for when prescribing iron supplements?
normo, normo, micro, hypo, pallor
Anemia of Chronic Disease/Inflammation
Begins as _____cytic-_____chromic
Ends up _____cytic-____chromic
Symptoms: fatigue, _____
ferrokinetic, hepcidin, absorption, macrophages, trapping, synthesis
Anemia of Chronic Disease
___________ Impairment
Chronic inflammation/disease cause a rise in _______
Hepcidin prevents the ________ of iron in the intestines and its release from _________
Abnormal iron metabolism with _______ of iron in macrophages
Iron is not available for new hemoglobin/RBC ________
normo, micro, infectious, malignant
Making the Diagnosis of Anemia of Chronic Disease
Suspect in patients with ____cytosis or ____cytosis and:
Chronic _______
Inflammatory
_________ condition
normal, decreased, acute, creatinine
Diagnosing Anemia of Chronic Disease
CBC
serum iron studies
Ferritin is ______ and TIBC is _______ in ACD
Measurement of _____ phase reactants
sedimentation rate, C-reactive protein
Serum _________ and estimated glomerular filtration rate
BM Stains
What test can be used to differentiate anemia of chronic disease from iron deficiency if iron studies are unclear?
asymptomatic, underlying, erythropoiesis, IV, RBC, avoid
Anemia of Chronic Disease Treatment
Sometimes none (if ___________)
First-line therapy: treat the _________ cause
Hemoglobin <10g/dL: use and _____________-stimulating agent (ESA)
± __ iron (in some symptomatic patients)
If EPO fails and patient is symptomatic
Consider ___ transfusion
____ unless it is necessary d/t adverse reactions
heme, decreased, accumulates, mitochondria, ringed
Sideroblastic Anemia
A group of disorders characterized by:
Defect in incorporation of iron into the ____ molecule
Hemoglobin synthesis is _______
Iron ___________
Particularly in ___________
Erythroblasts w/ perinuclear iron engorged mitochondria (______ sideroblasts)
myelodysplastic, lead, alcoholism, copper
Sideroblastic Anemia Etiology
Most often a subtype of a ______________ syndrome (MDS)
____ poisoning
Chronic _________
______ deficiency
Chronic infection/inflammation
Medications (isoniazid, chloramphenicol)
low, overload, elevated, dimorphic
Sideroblastic Anemia
Retic count is ___
Iron _______
Serum iron, transferrin sat, and ferritin are ________
Smear - _______, small and normal cells + poikilocytosis
Basophilic stippling
What specific finding can be seen on slides of sideroblastic anemia caused by lead poisoning, as well as in thalassemia and other disorders?
erythroid, ineffective
Sideroblastic Anemia
BM (Diagnostic)
________ hyperplasia
Sign of ________ erythropoiesis
Sideroblastic Anemia
What do you have to consider if an elderly patient presents with hypochromic anemia in the absence of iron deficiency or inflammation?
micro, hypo, high, target, tear drop, stippling, nucleated
Thalassemia
_____cytic - ____chromic anemia
Retic count is ____
Abnormal RBC morphology
_____ cells
____ ____ cells
May see basophilic ________
_________ RBCs on smear
Globin, recessive, synthesis
Thalassemia
______ biosynthesis problem
Inherited autosomal _______
Cause an impaired ________ of one of the two chains (alpha or beta) of adult hemoglobin
production, precipitate, destruction
Thalassemias
The normal ratio of alpha globin to beta globin ________ is disrupted
The unpaired chains _________
________ of RBC precursors in the BM
increased
Thalassemia can have normal to _______ RBC counts (unique feature of microcytic anemias)