Nursing Pharmacology: Chapter 30: Thyroid and Antithyroid Drugs
Hypothyroidism is characterized by inadequate thyroid hormone synthesis.
Cretinism occurs when hypothyroidism is present from birth and accompanied by developmental abnormalities.
Myxedema represents severe hypothyroidism that is associated with:
Deposition of hydrophilic mucopolysaccharides in the dermis (ground substance) and other tissues which causes:
Facial feature thickening
Doughy skin induration
Pretibia myxedema
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Hypothyroidism: Causes/Classification
Thyroprivic* |
Goitrous |
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Pituitary |
Hypothalamic |
Panhypopituitarism |
Congenital defect |
Isolated low TSH levels |
Infection (e.g. encephalitis) |
Neoplasm; Infiltrative (sarcoidosis) |
Inadequate thyroid hormone synthesis causes TSH hypersecretion which results in goiter.
If compensatory physiological response is insufficient, goitrous hypothyroidism occurs
Causes of goitrous hypothyroidism inNorth America
Most common cause: Hashimoto's disease
Mechanism:
Defective binding of iodide
Abnormal secretion of iodoproteins
Iodide-induced goiter with or without hypothyroidism reflects intrinsic defective inorganic binding mechanism.
Euthyroid patients with Graves' disease, particularly following surgery or radioiodine therapy, patients with Hashimoto's disease, and normal fetuses are particularly susceptible to iodide-induced goiter.
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Hypothyroidism: Clinical presentation
Cretinism may be present at birth, but usually is apparent within the first few months after birth as a function of the extent of thyroid failure.
Manifestations
Physiologic jaundice
Constipation
Somnolence
Feeding problems
Since early clinical diagnosis may be difficult and early treatment is necessary to ensure normal intellectual development, neonates should be screened for hypothyroidism by measuring serum T4 or TSH.
Young ehildren clinical presentations
Coarse features, protruding tongue, broad, flat nose, widely set eyes, dry skin, coarse hair. impaired mental development, retarded bone age, epiphyseal dysgenesis, delayed dentition.
Retardation of linear growth, delayed puberty
Poor school performance
Fatigue, lethargy, constipation, cold intolerance,
Slowing of intellectual and motor activity
Lessened appetite; increased weight
Dry skin; dry hair (may fall out)
Deeper, hoarser voice
With Advanced Disease: (florid myxedema)
Dull, expressionless facies, sparse hair, periorbital puffiness , large tongue, rough and doughy skin (cool, pale)
Enlarged heart (dilation, pericardial effusion)
Adynamic ileus
Without treatment: myxedema coma possible with respiratory depression and increased PCO2 .
Single most useful: serum TSH
Increased levels in thyroprivic and goitrous
Normal or undetectable in pituitary or hypothalamic hypothyroidism
In hypothalamic hypothyroidism: TSH hypersecretion is associated with hypersecretion of other pituitary hormones
All hypothyroidism:
Decreased serum T4 and free T4I
Serum T3 may be decreased less than serum serum T4
Some other abnormal laboratory results:
Increase serum cholesterol (hypothyroidism of thyroid origin)
Increased creatinine phosphokinase
Increased aspartate transaminase
Indications of pernicious anemia
Levothyroxine
Liothyronine
Liotrix (combination of new L-thyroxine and liothyronine)
Neonatal, infantile, and juvenile hypothyroidism: early full replacement therapy vital to improve likelihood of:
Normal intellectual development
Normal growth
If neonatal, infantile, and juvenile presentations result from pituitary and hypothalamic hypothyroidism, treatment with hydrocortisone should precede thyroid replacement therapy:
Rationale:acute adrenocortical insufficiency may because by the increase in metabolic rate with increase glucocorticoid clearance following thyroid hormonal treatment
Rapid treatment desirable especially in patients with:
Myxedema coma
hypothyroid patients needing to undergo emergency surgery (these patients have extreme sensitivity to CNS depressants);
IV levothyroxine with hydrocortisone may be appropriate
To patients with myxedema coma and systemic illness may have reduced ability to convert T4 to T3. In these cases supplemental liothyronine may be added to levothyroxine.
*- Thyroprivic: refering to lack of thyroidhormone (e.g. removal of the gland or suppression of glandular function)
Greenspan, F.S., and Dong, B. J.. Histamine, Thyroid and Antithyroid Drugs, in Basic and Clinical Pharmacology, (Katzung, B. G., ed) Appleton-Lange, 1998, pp 619-633.
Wartofsky, L., Diseases of the Thyroid, In Harrison's Principles of Internal Medicine 14th edition, (Isselbacher, K.J., Braunwald, E., Wilson, J.D., Martin, J.B., Fauci, A.S. and Kasper, D.L., eds) McGraw-Hill, Inc (Health Professions Division), 1998, pp 2012-2034