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liothyronine (Cytomel, Triostat, Liothyronine T3, Thyroid Hormone)

 

Classes: Thyroid Products

Dosing and uses of Cytomel, Triostat (liothyronine)

 

Adult dosage forms and strengths

injectable solution

  • 10mcg/mL

tablet

  • 5mcg
  • 25mcg
  • 50mcg

 

Hypothyroidism

Initial: 25 mcg PO qDay; may increase by 25 mcg q1-2Weeks; not to exceed 100 mcg/day

Maintenance: 25-75 mcg PO qDay

May use 10-12.5 mcg T3 in combo with T4 (decrease T4 dose by 50 mcg)

 

Nontoxic Goiter

Initial: 5 mcg PO qDay; may increase by 5-10 mcg q1-2Weeks (5 mcg in elderly)

When reach 25 mcg PO qDay, may increase by 12.5 mcg or 25 mcg q1-2Weeks

Maintenance: 75 mcg PO qDay

 

Myxedema

Initial: 5 mcg PO qDay; may increase by 5-10 mcg/day q1-2Weeks

When reach 25 mcg PO qDay, may increase by 5-25 mcg q1-2Weeks

Maintenance: 50-100 mcg PO qDay

 

Myxedema Coma

Initial: 25-50 mcg IV

Patients with CVD: 10-20 mcg IV

Doses of at least 65 mcg/day IV associated with lower mortality

Allow 4-12 hr between doses; not to exceed 12 hours

 

Pediatric dosage forms and strengths

injectable solution

  • 10mcg/mL

tablet

  • 5mcg
  • 25mcg
  • 50mcg

 

Congenital Hypothyroidism

Initial: 5 mcg PO qDay; may increase by 5 mcg q3-4Days

Maintenance

  • <1 year: 20 mcg PO qDay
  • 1-3 years: 50 mcg PO qDay
  • >3 years: 25-75 mcg PO qDay

 

Nontoxic Goiter

Initial: 5 mcg PO qDay; may increase by 5-10 mcg q1-2Weeks

When reach 25 mcg PO qDay, may increase by 12.5 mcg or 25 mcg q1-2Weeks

Maintenance: 75 mcg PO qDay

 

Geriatric dosage forms and strengths

5 mcg/day PO; may increase by 5 mcg/day q2Weeks

 

Cytomel, Triostat (liothyronine) adverse (side) effects

1-10%

Tachycardia (3%)

Hypotension (2%)

Myocardial infarction (2%)

Cardiopulmonary arrest (2%)

 

<1%

Congestive heart failure

Hypertension

Twitching

Phlebitis

Angina

Fever

 

Warnings

Black box warnings

Thyroid hormones, either alone or with other therapeutic agents, should not be used for the treatment of obesity or for weight loss

In euthyroid patients, doses within the range of daily hormonal requirements are ineffective for weight reduction; larger doses may produce serious or even life-threatening manifestations of toxicity, particularly when given in association with sympathomimetic amines, such as those used for their anorectic effects.

 

Contraindications

Hypersensitivity to thyroid hormone

Acute MI uncomplicated by hypothyroidism, thyrotoxicosis, untreated adrenal insufficiency

Treatment of obesity or infertility

 

Cautions

Caution in angina, cardiovascular disease, hypopituitarism, Dm

May use judiciously in acute MI caused/complicated by hypothyroidism

Perform periodic assessment of thyroid status when using as thyroid replacement

Myxedematous patients are very sensitive to thyroid hormone; start at very low dose

 

Pregnancy and lactation

Pregnancy category: A

Lactation: Excreted into breast milk; use caution

 

Pregnancy categories

A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.

NA: Information not available.

 

Pharmacology of Cytomel, Triostat (liothyronine)

Mechanism of action

A synthetic form of natural T3 hormone with same actions as natural product; thyroid hormone raises basal metabolic rate, increases utilization and mobilization of glycogen store, and promotes gluconeogenesis

 

Absorption

95% absorption

Onset: 2-4 hr

Duration: Several days (hypothyroidism)

Peak plasma time: PO: 1-2 hr

Max response: 2-3 days

 

Distribution

Protein bound: 99.7%, but not firmly

 

Metabolism

Hepatic, to deiodinated and conjugated metabolites

 

Elimination

Half-life: 2.5 days

Excretion: Urine, feces

 

Administration

IV Administration

Administer q4hr; no more than 12 hr apart