Anemia Theraputics Flashcards

0
Q

Oral Iron: types, MOA, Sx, enhancers, inhibitors

A
  • ferrous sulfate, ferrous gluconate, ferrous fumarate
  • MOA: conversion to Fe2+ for absorption; reticulocytes in days, normalizes in 2 Mo
  • Fe def anemia
  • Sx: GI upset, dark stools, constipation, NVD,
    ~ OD is dangerous and can be lethal in kids: NV, CV collapse
    E-lyte imbalance
  • absorption enhanced by: vitamin C
  • absorption inhibited by: Ca, Mg, Al, tetracyclines, PPIs, cholestyramine, food (Fe inhibits absorption of aformentioned)
  • separate interacting drugs by ~ 2 hrs
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1
Q

Blood transfusion (Indications, risks, benefits)

A
  • avoid if possible
  • indicated in rapid Hb decline
  • benefits: rapid correction, works
  • risks: iron overload, hyperkalemia, caogulopathies, immune rxns, infxns, allosensitization
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2
Q

Parenteral Fe: iron Dextrans (enfed better one, dexferim)

A
  • biggest molecular particle
  • colloidal Fe nanoparticle
  • Hb restored much more quickly
  • indicated: intolerance to oral supp. Poor absorption, non-adherence, decreases need for transfusion, hemodialysis PTs
  • Sx: BLACK BOX: anaphylaxis; can worsen active infxn, hypersensitivity, Fe overload, infusion site rxn, other normal rxns
  • cheaper than other forms, slowest release, long 1/2life
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3
Q

Parenteral Fe: Na-Fe gluconate complex

A
  • colloidal Fe nanoparticle
  • Hb restored much more quickly
  • indicated: intolerance to oral supp. Poor absorption, non-adherence, decreases need for transfusion, hemodialysis PTs
  • less risk of anaphylaxis, shortest 1/2life
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4
Q

Parenteral Fe: Iron sucrose

A
  • colloidal Fe nanoparticle (middle weight colloid particle)
  • Hb restored much more quickly
  • indicated: intolerance to oral supp. Poor absorption, non-adherence, decreases need for transfusion, hemodialysis PTs
  • best SE profile, least risk of anaphylaxis
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5
Q

Parenteral Fe: Fermoxytol

A
  • colloidal Fe nanoparticle
  • Hb restored much more quickly
  • indicated: intolerance to oral supp. Poor absorption, non-adherence, decreases need for transfusion, hemodialysis PTs
  • highest risk if anaphylaxis, MRI contraindicated w/in 3 mo.
  • don’t use
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6
Q

Cyanocolobamin

A
  • Megaloblastic B12 deficiency anemia
  • MOA: Cofactor for reactions forming THF methionine metabolization of L-methylmalonyl-CoA
  • IM in neuro Sx are present: oral/intranasal maintenance
  • rapid RBC correction may cause fluid overload, hypokalemia
  • BM in 3 day, strength recovered in 7, neuro Sx diminish in 30, life long Tx
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7
Q

Hydrocolobamin

A
  • Megaloblasticanemia
  • MOA: Cofactor for reactions forming THF methionine metabolization of L-methylmalonyl-CoA
  • not for B12
  • IM in neuro Sx are present: oral/intranasal maintenance
  • rapid RBC correction may cause fluid overload, hypokalemia
  • BM
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8
Q

Folic acid

A
  • inactive THF precursor
  • MOA: essential donor of methyl group for AAs, purines, DNA
  • Folate anemia
  • prevention of chronic methotrexate toxicity, NTDs
  • No Sx at replacement doses
  • reticulocytes -> 7 days, HCT -> 1 mo, Tx usually 4 mo
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9
Q

Leucovorin

A
  • active THF derivative
  • for severe folate antagonism of methotrexate
  • 5FU antineoplastic synergy
  • No Sx at replacement doses
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10
Q

EPO, Alfa and darbopoetin

A
  • MOA: binds EPO receptor -> increase RBC prolif/diff
  • used in anemia 2^ to chronic kidney disease
  • BLACK BOX: increase risk of MI, stroke, VTE, Tumor,
  • Sx: HTN, pure red cell aplasia due to anti-EPO Abs; trt with peginsatide
  • not started until Hb < 10g/dl, retic recovery in days, full effect in 4 weeks
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11
Q

Pegintaside

A
  • MOA: EPO memetic, supports EPO production
  • prevents transfusion
  • BLACK BOX: increase risk of MI, stroke, VTE, Tumor,
  • tx lifelong
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12
Q

Itrogenic Aplastic anemia causes

A
  • chemo
  • chloramphenicol
  • carbamazepine
  • phenytoin
  • HSNs
  • trt: immunosuppressants, anti thymocyte globulin, HPSC transplant
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13
Q

Itrogenic G6PDH Deficiency causes

A
  • sulfa drugs
  • nitrofurantoin
  • phenazopyridine
  • dapsone
  • trt by removing oxidative stress
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14
Q

Itrogenic immune hemolytic anemia trt and causes

A
  • rare; support, discontinue offending agent, symptomatic
  • PCN
  • anti-inflammatoriesopa
  • anti-neoplastics
  • methyl dopa
  • cefotelan
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15
Q

Deferoxamine

A
  • iron chelators: iron overload
  • MOA: hexidentate structure: 1-1 binding
  • indicated when ferritin > 1000 ng/mL
  • Cind: renal failure
  • Sx: red/orange urine, murcomycosis, growth problems, skeletal dysplasia
  • advantages: increases long term survival, redux iron induced heart disease
  • disadvantages: poor bioavailability and short 1/2 life, compliance issues
16
Q

Deferiserox

A
  • tridentate structure
  • MOA: 2:1 iron binding
  • advantages: good oral availability, longer 1/2life, well tolerated
  • disadvantages: no long term efficacy data, req higher doses
  • Cind: renal failure, tcytopenia and neoplasia
  • Sx: NV, rash, renal hepatic dysfunction, sensory toxicity
17
Q

Iron chelator considerations; monitoring, maintenance dose

A
  • monitor liver iron content via MRI
  • ## maintain less than 1000 ng/dL
18
Q

Itrogenic Pure red cell aplasia trt

A

EPO stimulators induce anti EPO Ab

19
Q

Megaloblastic anemia with neuro symptoms

A
  • cyanocolobamin (1st line)

- hydroxycolobamin IM

20
Q

Prevention of chronic methotrexate toxicity

A
  • folate
21
Q

Itrogenic hyperkalemia

A
  • May be a result of blood transfusions
22
Q

Itrogenic Hypokalemia

A
  • cyanocolobamin, rapid b12 correction -> fluid accumulation