Digoxin Flashcards

1
Q

What are some symptoms associated with digoxin toxicity?

A
  • Confusion
  • Nausea, vomiting, poor appetite
  • Changes in rate or rhytm of heartbeat (slow or irregular)
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2
Q

What is an antidote for digoxin?

A

Digibind

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3
Q

What is the mechanism of action for digoxin?

A

Slowing heart rate:
It inhibits the Na+/K+/ATPase pumps (highly expressed in cardiac and skeletal cells)

These pumps regulate K+ and Na+ transport in these cells

In Na+ influx into cell, Ca2+ is effluxed out by antiporter

If inhibited, Ca2+ starts to build up in cell. In muscle cells this causes contraction, slows heart beat by not relaxing as quickly for another cycle (therefore it is a positive inotrope)

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4
Q

What are some oral absorption PK characteristics for digoxin?

A

F:
- Tablets (70-80%)
- Pediatric solutions (70-85%)
- Capsule (90-100%)

Food has minimal effect

No significant first-pass effects in 90% of patients

In 10% of patients, GI metabolism by hydrolysis or reduction

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5
Q

What are some drug interactions associated with digoxin?

A
  • Kaolin-pectin (diarrhea treatment) decreases F by 62% (separate dose by 2h)
  • Antacids decrease F by 25-35%
  • Cholestyramine decreases F by 20-35% (separate doses by 8h)
  • High fibre decreases F
  • Metoclopramide increases GI motility and decreases F
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6
Q

What compartment model is digoxin most similar to?

A

two-compartment model

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7
Q

What are the Vd values of digoxin for adults, children, and neonates?

A

Vd (adults): 7.3L/kg (large due to Na+/K+/ATPase distribution)

Obese: use IBW

Vd (children): 16L/kg

Vd (neonates): 7.5 to 10L/kg

Distribution phase lasts 6 to 8 hours

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8
Q

What are some plasma protein binding characteristics of digoxin?

A

Binds to albumin

fu(b)=0.7-0.8 in adults

Changes in fu(b) is not clinically significant (changes in Css total, but not Css free)

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9
Q

What are some tissue distribution characteristics of digoxin?

A

Significant distribution to skeletal and cardiac muscle because high concentration of Na+/K+/ATPase pumps

Vd not influenced by obesity

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10
Q

Review slide 12 for all of the factors that can impact digoxin Vd

A
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11
Q

What are some hepatic clearance characteristics of digoxin?

A

1/3 of dose is hepatically cleared

  • BIliary excretion by P-gp
  • GI breakdown in 10% of patients
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12
Q

What are some renal clearance characteristics of digoxin?

A

2/3 of dose is renally excreted

Pushed out of the body by glomerular filtration and tubular secretion

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13
Q

What are some types of digoxin toxicities?

A
  1. Cardiac (major toxicity): 70-90%
    - Sinus bradycardia, AV block, SA block
    - Premature ventricular contractions can occur too
  2. GI: 50-70%
    - N, V, D, feeding intolerance, abdominal pain
  3. Ocular (classic symptoms of digoxin toxicity)
    - Blurred vision (yellow or green halos)
  4. CNS
    - Drowsiness, fatigue, lethargy
    - Confusion and dizziness
  5. Misc.
    - Hyperkalemia with acute toxicity
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14
Q

What are some factors that impact digoxin response?

A

Mineral status
- Hypokalemia, Hypomagnesaemia and hypercalcemia (enhance digoxin effects and even toxicity)

Age
- Higher dose in young due to higher Cls
- Lower dose in elderly due to increased sensitivity

Thyroid
- HypoT4 (decrease Cls)
- HyperT4 (increase Cls)

Cor Pulmonale
- Increased toxicity due to arterial hypoxia

Nature and Severity of Heart Disease
- Increased sensitivity with CAD
- Decreased sensitivity with tolerance (Afib)

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15
Q

What are some factors that influence digoxin systemic clearance?

A

Renal dysfunction (decreases Clh and Clr)
Not significantly eliminated by dialysis

Thyroid disease
- HypoT4 (decrease Cls)
- HyperT4 (increase Cls)

Obesity (decreases Clh and Clr)

Congestice Heart Failure (Decreases Clh and Clr)

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16
Q

Review slide 19 for the degree to which certain drugs can influence Cls of digoxin

A
17
Q

What are the three types of digoxin analyses?

A
  1. Radioimmunoassay
  2. Enzyme-immunoassay (EMIT)
  3. Fluorescence polarization immunoassay

An issue with all three is low specificities as they pick up DLIS as digoxin

18
Q

What are DLIS?

A

Digoxin-like Immunoreactive Substances (DLIS)

They are endogenous substances that are present at detectable levels in digoxin-free patients

ex. Renal failure, hepatic failure, low renin HTN, pregnant women (3rd trimester), neonates, infants

19
Q

What are some indications for TDM in digoxin therapy?

A
  1. Confirmation of toxicity
  2. Assessing effect of facttos altering PK
  3. Therapeutic failure
  4. Medication compliance
20
Q

What are some issues with TDM of digoxin therapy?

A
  • Correlation between Cp and response is not great (due to issues in assay specificity)
  • Variation in respinse due to alterations in serum electrolytes
  • Assay not specific
  • Dosage adjustment difficult because of fixed tablet strength (not a lot of choices)
21
Q

What is the therapeutic range for digoxin?

A

CHF: 1.0-2.5 nmol/L (0.5-1.0 ng/mL)
- At higher therapeutic dose, 50% of patients exhibit toxicity

Afib: 1.5-2.0 or 2.5ng/mL (rely on patient response)

22
Q

What are the population PK parameters of digoxin?

A

Vd: (7.3L/kg)

t1/2: 36 +/- 8 hours

Cls: 1.303 * ClCr + Clnr

F(elixir or capsule) = 0.8-0.85
F(tab)= 0.62 to 0.7

23
Q
A