Anemia Flashcards

1
Q

MCV < 80 fL

A

microcytic
-due to iron deficiency

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2
Q

MCV 80-100 fL

A

normocytic
-cause: acute blood loss, malignancy, CKD, bone marrow, hemolysis

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3
Q

MCV > 100 fL

A

macrocytic
-likely due to vitamin B12 or folate deficiency

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4
Q

dx of iron deficiency anemia

A
  • decrease Hgb, low MCV, RBC production
    -decrease serum iron, ferritin and TSAT
  • increase TIBC
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5
Q

iron deficiency anemia tx

A

-100-200 mg elemental iron/day
-take on empty stomach
-avoid H2RAs and PPI - separate from antacids

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6
Q

ferrous sulfate

A

20% elemental iron
-325 mg (65 mg of elemental iron) PO TID

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7
Q

ferrous sulfate dried

A

30% elemental iron
-160 mg (50 mg elemental iron)

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8
Q

safety of oral iron

A

-accidental overdose of iron-containing products in children that can cause fatal poisoning under 6
-constipation, dark and tarry stools

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9
Q

iron overdose antidote

A

deferoxamine (desferal)

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10
Q

antacids, H2RAs and PPIs

A

decrease iron absorption by increasing gastric PH
-take 2 hours before or 4 hours after taking antacids

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11
Q

quinolone and tetracycline abx & iron

A

take iron two hours before or 4-8 hrs after these agents due to chelation

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12
Q

bisphosphonates & iron

A

take iron 60 min after oral ibandronate or 30 minutes after alendronate/risedronate

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13
Q

levothyroxine and iron

A

separate from iron by 2-4 hours

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14
Q

vitamin C

A

increases the absorption of iron

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15
Q

when to use IV iron

A

CKD on HD
CKD on ESAs
unable to tolerate oral iron or failure of oral therapy

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16
Q

iron sucrose (venofer) and ferumoxytol (feraheme)

A

-serious and sometimes fatal anaphylactic reactions iron dextran or ferumoxytol; all patients receiving iron dextran should be given a test dose
-all parenteral iron products carry a risk for hypersensitivity reactions

17
Q

causes of macrocytic anemia

A

vitamin B12, folate deficiency, alcoholism, poor nutrition, GI disorders, and pregnancy

18
Q

dx of macrocytic anemia

A

-low hgb and high MCV
-low B12 or folate

19
Q

tx of macrocytic anemia

A

-vitamin B12 injections (cyanocobalmin) are first line - IM or deep SC 100-1000 mcg daily/weekly/monthly
-Folic acid, folate

20
Q

Anemia of chronic kidney disease

A

deficiency in EPO

21
Q

tx of anemia of CKD

A

IV iron is first line for HD patients (non-HD can have oral iron

22
Q

ESAs

A

Epoetin Alfa (Epogen, Procrit)
Darbepoetin (Aranesp)

*help maintain Hgb levels and reduce the need for blood transfusions but are ineffective if iron stores are low

23
Q

Epogen, Procrit

A

CKD:
-3x/week
-initiate when Hgb < 10 g/dL
-decrease or interrupt dose when Hgb approaches or exceeds 11 g/dL
Cancer:
-initiate when Hgb < 10 g/dL

24
Q

Aranesp

A

CKD:
-IV or SC weekly
-half-life is 3 fold longer than epogen

25
all ESAs
-increase risk of death, MI, stroke, VTE, thrombosis -use lowest effective dose -CKD: increase risk of death when hgb > 11 g/dL -cancer: no indicated when the anticipated outcome is cure -HTN, arhtralgias -monitor: H/H TSAT, serum ferritin, BP -do not shake
26
hemolytic anemia
drug induced, sickle cell, or G6PD deficiency
27
drugs that cause hemolytic anemia
cephalosporins, dapsone, isoniazid, levodopa, methyldopa, methylene blue, nitrofurantoin, pegloticase, penicillins, primaquine, quinidine, quinine, rasburicase, rifampin, sulfonamides
28
immunizations in sickle cell disease: routine childhood series
Hib and PCV13
29
immunizations in sickle cell disease: additional vaccines for functional asplenia
meningococcal conjugate series + booster meningococcal serogroup B pneumococcal vaccines: PCV20 x1 or PCV15 x1 followed by PPSV23 > 8 weeks later
30
Infections: sepsis and meningitis
S.pneumoniae, H. influenza, N. menigitidis -utilize prophylactic penicillin
31
disease-modifying drug in sickle cell disease
hydroxyurea
32
Hydroxyurea (Draxia, Hydrea, Siklos)
-myelosuppression, fetal toxicity, avoid live vaccinations -CBC w/diff every 2-4 weeks during initiation and titration -contraception required -folic acid supplementation -hazardous (wear gloves and wash hands)
33
L-glutamine (Endari)
reduce complications of SCD
34
Voxelotor (Oxbryta)
inhibiting HgbS polymerization
35
Crizanlizumab (Adakveo)
reduce frequency VOC in SCD