Drugs to treat anemia Flashcards

1
Q

Main goal of therapy of Iron Deficiency Anemia

A

Main goal of therapy is to identify and treat the underlying cause

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2
Q

some causes of Iron Deficiency Anemia

A

o Blood loss from tumor, varicosity, or other bleeding lesion
o Iron malabsorption

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3
Q

patient presentation with Iron Deficiency Anemia

A

o Weakness
o Headache
o Irritability
o Varying fatigue and exercise intolerance
o Pica [especially ice craving (pagophagia), but can be other things]
o Restless leg syndrome

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4
Q

Iron Deficiency Anemia General Treatment Issues

A
  • “Secondary” treatment is via iron supplementation
  • Choice of preparation is based on acuity of illness as well as the ability of the patient to tolerate PO formulations
  • PO is first-line in most patients
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5
Q

PO Iron: Products

A

Most appropriate (equally effective) contains ferrous salt such as:
o Ferrous sulfate: 65 mg elemental iron/tablet
o Ferrous fumarate: 106 mg elemental iron/tablet
o Ferrous gluconate: 28-36 mg/ iron/tablet

Dose is 150-200 mg/d of elemental iron
o Ex: single 325 mg ferrous sulfate tablet taken PO tid provides 195 mg of elemental iron per day

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6
Q

PO Iron: Treatment Issues

A

o GI ADRs decrease adherence
o Malabsorptive states (e.g., celiac disease, Whipple’s disease, bacterial overgrowth syndromes)
o PO iron may take 2 months to improve anemia and 6-8 months to restore iron stores
o IBD patients may have worsening of disease
o Heavy blood loss may not be corrected by PO iron supplements
o Dialysis patients do not respond enough to PO iron
o CKD patients may not absorb PO iron (impaired iron transport, concomitant use of Ca-containing salts, H2 blockers, phosphate binders, general malabsorption)

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7
Q

PO iron Frequent GI ADRs

A

metallic taste, constipation, diarrhea, and thick/green/foul-smelling stool

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8
Q

GI-related ADRs seem to be directly related to the amount of______

A

elemental iron

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9
Q

Should PO iron be dosed on empty stomach?

A

yes

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10
Q

what medium is Po iron best absorbed?

A

acidic medium

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11
Q

how is PO iron dosed with antacids/calcium

A
  • Dosed 2 hours before or 4 hours after antacids/calcium
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12
Q

PO Iron: DDIs

A
  • H2 Blockers, PPIs, antacids decrease absorption
  • Tetracyclines & Quinolones decrease absorption
  • Ca salts: decrease absorption
  • Vitamin C: increase absorption
  • decrease absorption of thyroid hormones- Avoid dosing at same time as thyroid hormones
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13
Q

PO Iron Response- how fastvwill Pagophagia and RLS respond?

A
  • Pagophagia and RLS will respond almost immediately
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14
Q

how long will it take for fatigue and energy to be improved after taking PO iron?

A

Fatigue and energy will improved within a few days

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15
Q

what it the PO iron response in regards to hemoglobin and iron stores?

A
  • Hemoglobin will rise slowly after 1-2 weeks and the deficit should be halved within 1 month and return to normal within 6-8 weeks
  • Iron stores may take 3-6 months to return to normal
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16
Q

what Select Indications for Parenteral Iron?

A
  • Excessive continuing blood loss
  • Inflammatory bowel diseases
  • Chronic kidney disease
  • Anemic cancer patients
  • Patients intolerant or unresponsive to PO iron
  • Large doses needed: estimated that only about 25 mg/d of elemental Fe can be absorbed via PO but up to 1000 mg can be given IV
  • Known malabsorption states (e.g., celiac, GI bypass surgery, etc.)
17
Q

Parenteral Iron: Products

A
  • LMW iron dextran (INFeD, Cosmofer): IV/IM
  • Ferric gluconate (Ferrlecit): IV
  • Iron sucrose (Venofer): IV
  • Ferumoxytol (Feraheme): IV
  • Ferric carboxymaltose (Injectafer): IV
18
Q
  • Historically, many clinicians have been reluctant to use due to severe ADRs of older Parental iron formations such as?
A

anaphylaxis, shock, death

19
Q

In parental iron, you often give test dose and pretreat with _____, if there is history of multiple allergies and/or asthma

A

IV steroid

20
Q

Parenteral Iron: ADRs

A

**Anaphylactoid reactions: give test dose prior to infusion
o ~1% of patients
o More common with iron dextran v. ferric gluconate and iron sucrose

Delayed reactions (2-7 days) can occur
o	Fever, urticaria, arthralgias, lymphadenopathy

Others: chest pain, headache, hypotension, n/v/d, abdominal cramping

21
Q

B12/Folate: Clinical Presentation

A

Macrocytic RBCs +/- anemia

Hypersegmented neutrophils

Unexplained neurologic signs and symptoms
o Dementia/delirium, weakness, sensory ataxia, paresthesias

22
Q

B12/Folate: Risk Factors

A
  • Elderly
  • Alcoholics
  • Malnourished
  • Strict vegans
  • Bariatric surgery
23
Q

how to increase Vitamin B12 (Cyanocobalamin)

A

Foods with B12:
o Fortified foods and animal sources

Oral B12 OTC: could use in pt w/o neurologic sxs
o 1 mg cobalamin tablets

SubQ or IM Injection: pt w/ neurologic sxs
o Daily x 1 week, then weekly x 1 month, then monthly

24
Q

How are ADRs of vitamin B12

A

usually well-tolerated

can get HA, N/V/D, hypokalemia

25
Q

How should you monitor b12 levels?

A

Every 1-2 months until stable then every 6-12 months

26
Q

Folic Acid Deficiency- how much for replacing body stores or malabsorption?

A

Replacing body stores: 1 mg daily

If malabsorption: 1-5 mg daily

27
Q

what should the dose be for pregnancy supplementation of folic acid?

A

0.4 to 5 mg daily depending on risk factors

28
Q

Anemia of Chronic Disease- Erythropoietin-stimulating Agents (ESAs) MOA

A
  • Stimulates erythroid progenitor division and differentiation
29
Q

Anemia of Chronic Disease- Erythropoietin-stimulating Agents (ESAs) products

A
  • Epoetin alpha (Procrit)

- Darbepoetin alpha (Aranesp)

30
Q

Procrit & Aranesp

can be administered how?

A
  • Subcutaneous or IV
31
Q

what Is Target Hgb?

A

Target Hgb 10-12gm/dL

32
Q

Procrit & Aranesp BBW?

A

o increased CV risk (death) in CRF pts
o increased risk of death & tumor progression in CA pts
o increased risk of thromboembolic events in surgery pts

33
Q

contraindications of Procrit & Aranesp?

A

uncontrolled HTN, Ab-mediated anemia

34
Q

Procrit & Aranesp ADRs

A

HTN, edema, tachycardia, N/V/D, thrombosis

Serious ADES: tumor progression, ↑mortality, CHF, stroke, MI, seizure, embolism

35
Q

Erythropoietin-stimulating Agents uses?

A
o	CKD
o	Dialysis
o	Malignancy
o	Chronic disease
o	HIV
o	Surgery