anemia Flashcards

1
Q

what is anemia

A

-anemia is defined as a reduction in the number of circulating red blood cells, as measured by hemoglobin (Hb) or hematocrit (Hct)

(hematocrit is the percentage of red blood cells in your blood. Hemoglobin is part of your red blood cell. Hemoglobin helps your red blood cells carry oxygen throughout your body so Hb is amount of oxygen-carrying protein in the blood)

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2
Q

what does anemia maily affect that lead to organ damage

A

• Anemia affects tissue oxygenation; oxygen is needed by all vital tissues for normal function bcz Hb
deliver o2 from the lungs to tissues and get rid of co2 so anemia may lead to organ dysfunc.on.
• Anemia-> low Hb-> low o2 delivery to body

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3
Q

Causes of anemia(general):

A
  1. Blood loss anemia
  2. Decreased production
    -Nutritional deficiency anemias-iron
    -B12, folate
    -Marrow disease, since the BM is the factory (e.g., infiltration with cancer, leukemia, myeloma), malignancy, radiation
  3. Increased destruction: hemolytic anemia
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4
Q

as general rule blood transfusion is not recommended unless either of the following is true:

A
  1. The HB concentration <7 g/dL OR
  2. the patient requires increased oxygen-carrying capacity (e.g.,patient with coronary artery disease or some other cardiopulmonary disease)
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5
Q

clinical features of anemia

A
  1. fatigue
  2. dyspnea
  3. headache
  4. palpitation
  5. tachycardia
  6. pallor (most noted in the conjunc.va)
  7. signs and symptoms of the underlying cause:
    a. orthostatic lightheadedness, syncope or hypertension if acute bleeding
    b. jaundice if hemolytic anemia
    c. blood in stool if GI bleeding
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6
Q

what do you look for in diagnosing the cause of anemia

A

reticulocyte index
-if < 2% not gd bone marrow , check if microcytic, macrocytic , or normocytic anemia

-if the reticulocyte index is >2% indicating an adequate bone marrow response, and differential diagnoses include:
a. acute blood loss
b. hemolysis

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7
Q

If microcytic anemia (MCV<80), the differential diagnosis includes:

A

TAILS - thalassmia, anemia of chronic disease , IDA, lead poisoning , syderoblastic anemia

I. Iron deficiency anemia- most common cause

II. anemia of chronic disease -iron is present in the body but is not available for hemoglobin synthesis due to iron trapping in macrophages

III. thalassemia -defective synthesis of globin chain

IV. sideroblastic anemia (include a lead poisoning, pyridoxine deficiency, toxic effects of alcohol)- defective synthesis of protoporphyrin leading to iron accumulation in mitochondria

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8
Q

If macrocytic anemia (MCV >100), the differential diagnosis includes:

A

VITAMINS

• V → Vitamin B12 deficiency
• I → Inherited disorders (congenital anemia, metabolic disorders)
• T → Toxins (alcohol, lead, drugs like methotrexate or zidovudine)
• A → Alcohol & liver disease
• M → Myelodysplastic syndromes (MDS), marrow failure syndromes
• I → Increased reticulocytes (hemolysis, bleeding recovery)
• N → Non-thyroid endocrine disorders (hypothyroidism, adrenal insufficiency)
• S → Sideroblastic anemia

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9
Q

If normocytic anemia ( MCV 80 to 100), differential diagnosis include:

A

I. Aplastic anemia – bone marrow failure
II. Bone marrow fibrosis
III. bone marrow infiltration
IV. anemia of chronic disease
V. renal failure -decreesed erythropoietin production result in decreased erythropoiesis

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10
Q

what is a conditon in which the hemoglobin content of blood is lower than normal as a result of
deficiency of one or more essential nutrients.

A

nutritional anemia

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11
Q

why is iron important

A

Iron is important for heme synthesis in hemoglobin molecules in red cells ( heme = protoporphyrin + iron ) so if no or less iron = no or less heme

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12
Q

what is the diff btwn ferrous (FE2+) and ferric (FE3+)

A

• Heme Iron = ferrous (Fe2+), from meat, better absorbed (iron content in red meats is higher than in vegetables)

• Non-Heme Iron = ferric (Fe3+), from vegetables & cereal, reduced to Fe2+ by brush border ferrireductase enzyme

• Transported in plasma bound to transferrin.

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13
Q

Most of the iron is found in our RBC but where is iron absorbed?

A

duodenum upper part of small
intes.ne.

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14
Q

someone had an upper intestine removal and then he was fatigued what is the reason?

A

IDA

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15
Q

There are two types of iron:

A
  1. Ferritin: is the iron that is found in ALL types of cell
  2. Hemosiderin: is the excess iron that is stored in case of diseases
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16
Q

what is the role of transferrin

A
  1. If serum iron has increased ->the protein will be reduced because my cells have enough iron and I don’t need more iron so this protein “transferrin” will be reduced
  2. If serum iron has reduced -> the protein will be increased because I need more iron to enter the cell so this protein “transferrin” will be increased.
  3. Serum iron reduced->transferrin increased
    Serum iron increased-> transferrin reduced
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17
Q

in elderly patients with irons deficiency anemia, we must rule out

A

colon cancer ( colon cancer is a common cause of GI bleeding in the elderly)

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18
Q

someone had a gastric bypass surgery, soon after the surgery he is feeling dizzy and fatigue, what is the reason?

A

iron deficiency anemia, why? simply because he was bleeding after the surgery (blood loss = iron loss, remember the main cause of iron deficiency anemia is bleeding )

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19
Q

causes of IDA

A

Mnemonic: “LID” (Loss, Intake, Demand/Absorption Issues)

  1. Blood loss (most common cause) -> from GI or menses ( menstrual blood loss is the most common source, in the absence of menstrual bleeding, GI blood loss is most likely), hookworm (feeds on the blood of the host tissue leading to the loss of iron and protein resulting in anemia, bleeding in the intestine )
  2. Increased demand (growth or pregnancy) or poor intake
    • Dietary deficiency/increased iron requirements, which are primarily seen in the following three age groups:
    –>Infants and toddlers: occurs especially if the diet is predominantly human milk , which is low in iron :children in this age group also have an increased requirement for iron due to accelerated growth
    –>Adolescents: increased requirements for iron due to rapid growth, adolescent women are particularly at risk due to loss of menstrual blood
    –>Pregnant women: pregnancy increased iron requirements
  3. Decreased absorption -> gastrectomy/small bowel disease (celiac, tropical sprue)
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20
Q

why do symptoms occur in IDA

A

Due to low Hb > low O2

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21
Q

symptoms of IDA

A
  1. Anemia > fatigue, pallor ( the most common sign, by looking at the mucus membrane like conjunctiva and buccal ) , SOB ( dyspnea on exertion) , tachycardia ( to compensate the low Hb and low O2)
  2. Brittle hair and nails
  3. Atrophic glossitis, angular stomatitis
  4. Koilonychia ( spooning, flaRened, concave nails)
  5. Pica (crush ice or scratch the paint on the wall and eat it)
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22
Q

investigations for diagnosis of IDA

A

• Low hemoglobin (Hb) → Confirms anemia
• Low hematocrit (Hct)
• Low mean corpuscular volume (MCV) → Microcytic anemia (MCV < 80 fL)
• Low mean corpuscular hemoglobin (MCH) → Hypochromic anemia
• High red cell distribution width (RDW) → Suggests iron deficiency

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23
Q

blood film for diagnosis

A

a. small hypochromic RBCs
b. anisocytosis (size) (RBC unequal in size )
c. poikilocytosis (shape)

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24
Q

tx of IDA

A

Oral iron supplements (ferrous sulphate/gluconate):

o must be treated for 3 to 6 months before determining response

o Monitor response by increase in re.culocyte followed by increase in Hb 10g/L per week until normal.

o Lack of response could be due to: noncompliance, malabsorption, or ongoing loss ex: menorrhagia)

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25
iron studies in IDA
a. Decreased Iron b. Decreased ferritin ( storage iron , the most imp.test) c. Decreased transferrin saturation- how much iron bound to transferrin d. Increased TIBC ( total iron binding capacity , it is an indirect measure of transferrin ) e. increased Transferrin receptor # (levels)
26
what is sideroblastic anemia
Sideroblastic anemia is a type of anemia where the body has enough iron, but it can’t use it properly to make hemoglobin. This leads to the formation of ringed sideroblasts, which are abnormal red blood cell precursors with iron trapped inside their mitochondria.
27
what is the defect in sideroblastic anemia
protoporphyrin synthesis
28
what does sideroblastic anemia cause
refractory anemia (dont have enogh rbc) , abnormality in rbc iron metabolism
29
aquired causes of sideroblastic anemia
1. Myelodysplasia or myelodysplastic syndrome (neoplastic disease , group of cancers in which immature blood cells in the bone marrow do not mature or become healthy blood cells. In a healthy person, the bone marrow makes blood stem cells (immature cells) that become mature blood cells over time.) 2. Alcohol 3. lead toxicity 4. drugs: isoniazid, chloramphenicol 5. Vitamin B6 (pyridoxine) deficiency
30
blood film in sideroblastic anemia
hypochromic cells
31
bone marrow in sideroblasts
ringed sideroblasts (erythroblasts with iron deposited in mitochondria) [Prussian blue stain]
32
megaloblastic anemia characterized by what
by impairment of DNA synthesis This causes cell growth without division, leading to large, immature red blood cells (megaloblasts) that don’t function properly.
33
vitamin b12 Serves as a cofactor in two important reactions required for normal erythropoiesis and CNS functioning ( It is an important vitamin for DNA synthesis in RBCs and myelin sheath synthesis and CNS)
1. the conversion of homocysteine to methionine 2. the conversion of methyl Al only-CoA to succinylcholine-CoA
34
transport of vit b12 steps
✅ Stomach: Acid & pepsin release B12 → binds to R-binder. ✅ Duodenum: Pancreatic enzymes break R-binder → B12 binds to Intrinsic Factor (IF). ✅ Ileum: B12-IF absorbed into the blood. ✅ Blood: B12 binds to transcobalamin II for transport.
35
causes of vit b12 defeciency
1. Poor diet (vegan) 2. Malabsorption ex: celiac, tropical sprue 3. Pernicious anemia
36
what is pernicious anemia
is an autoimmune condition that leads to Vitamin B12 deficiency due to the destruction of parietal cells in the stomach, which results in a lack of Intrinsic Factor (IF)—a protein required for B12 absorption in the small intestine.
37
vit b12 symptoms
• Patients with B12 deficiency have both with UMN signs & LMN signs (mixed picture; ex: absent ankle reflexes with exaggerated knee reflexes) • Dementia, optic atrophy -> visual disturbances
38
causes of folate defeciency
1. Poor intake (most common cause) , alcoholism 2. Excess utilization (pregnancy, ICU, chronic hemolysis) 3. Malabsorption (celiac, tropical sprue) 4. Drugs (methotrexate, phenytoin, trimethoprim, sulfasalazine)
39
in pernicious anemia what antibodies would u see
antiparietal cell antibodies, anti.-IF antibodies
40
what is a complication of b12 and folate replacement
hypokalemia
41
what is macrocytic anemia w normoblastic bone marrow
Macrocytosis without hypersegmented neutrophils
42
what is anemia of chronic disease
-Anemia of chronic disease is a hypoproliferative anemia that develops in response to systemic illness or inflammation. - It is the commonest cause of anemia among patients with chronic illness.
43
pathophysiology of ACD
1) IL1 , IL6 , TNF alpha are produced and enhance the production of hepcidin in the liver 2) & reduce erythropoietin in the kidney & reduce erythropoiesis in BM (suppress BM) 3) also it affects reticuloendothelial system by preventing macrophages from delivering iron for erythropoiesis even though there is iron.
44
lab findings in ACD
⬆ hepcidin, ⬇ Serum iron, ⬇ TIBC, ⬆ /N ferritin, ⬇ Hb, Hct, ⬇ transferrin, transferrin saturation
45
what is aplastic anemia
bone marrow stops making enough blood cells (red blood cells, white blood cells, and platelets). This happens because the bone marrow stem cells are damaged or destroyed.
46
symptoms of apalastic anemia
• Symptoms of anemia ( fatigue, dyspnea, headache, palpitations,pallor ) • Increased susceptibility to infection (mouth infections common) due to neutropenia • Bleeding (bruising, bleeding gums, epistaxis, petechiae) •Can transform into acute leukemia
47
diagnosis of aplastic anemia
pancytopenia decreased or absent retics normocytic anemia w decreased neutrophils and platelets
48
tx of aplastic anemia
BM transplantation
49
what is hemolytic anemia
inc destruction of RBC
50
what is hemolysis
destructions of red blood cells before their normal 120 day life span.
51
bone marrow has the capacity to inc erythropoises 6-8 times normal if needed
1- Compensated hemolysis: increase erythropoiesis in bone marrow compensates for increased destruction ( hemolysis without anemia ) 2- Uncompensated hemolysis: where increased erythropoiesis can’t compensate for excessive hemolysis, a hemolytic anemia will develop if BM activity can’t compensate anymore for erythrocyte loss ➡ drop in hemoglobin and red cell count.
52
what does schistocytes indicate
intravascular hemolysis
53
spherocytes indicate in blood film helmet cells
extravascular hemolysis
54
sickled RBC
sickle cell anemia
55
heinz bodies indicate
G6PD defeciency
56
thalasemia abdnormal production
57
what is intravascular hemolysis
1. Intravascular Hemolysis (Inside Blood Vessels) • Where? RBCs break inside blood vessels. • What happens? Free hemoglobin (Hb) is released into the blood and then leaks into urine. • Signs: • Hemoglobinemia (Hb in blood) • Hemoglobinuria (Hb in urine → red/brown urine) • Low haptoglobin (used up binding free Hb) • High LDH (enzyme released from destroyed RBCs) • Schistocytes (RBC fragments on blood smear)
58
causes of intravascular hemolysis
• G6PD deficiency • Mechanical damage (TTP, HUS, DIC, heart valves) • Mismatched blood transfusion • Paroxysmal nocturnal hemoglobinuria (PNH) • Cold autoimmune hemolytic anemia (IgM) • Malaria
59
extravascular hemolysis
Extravascular Hemolysis (Outside Blood Vessels, in Spleen/Liver) • Where? RBCs are eaten by macrophages in the spleen and liver. • What happens? RBCs are broken down slowly → Hb converted to bilirubin. • Signs: • Jaundice (yellow skin from increased bilirubin) • Splenomegaly (big spleen from overwork) • No hemoglobinuria (since Hb is broken down inside macrophages) • Normal or slightly low haptoglobin • Spherocytes (small, round RBCs on blood smear)
60
causes of extravascular hemolysis
Causes: • Sickle cell disease, thalassemia • Hereditary spherocytosis • Warm autoimmune hemolytic anemia (IgG) • Hemolytic disease of the newborn