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Thyroid Emergencies. Jim Holliman, M.D., F.A.C.E.P. Professor of Military and Emergency Medicine Uniformed Services University of the Health Sciences Clinical Professor of Emergency Medicine George Washington University Bethesda, Maryland, U.S.A. Thyroid Emergencies Lecture Goals.
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Thyroid Emergencies Jim Holliman, M.D., F.A.C.E.P. Professor of Military and Emergency Medicine Uniformed Services University of the Health Sciences Clinical Professor of Emergency Medicine George Washington University Bethesda, Maryland, U.S.A.
Thyroid Emergencies Lecture Goals • Review pathophysiology of thyroid related illnesses • Present information on recognition and management of medical emergencies related to thyroid diseases
The Thyroid Emergencies • Previously undiagnosed hyperthyroidism • "Apathetic thyrotoxicosis" • Thyroid Storm • Myxedema coma • Airway compression or superior vena cava syndrome from goiter or tumor
Maria de Medici, wife of King Henry IV of France in 1625, with a goiter
Thyroid Physiology • Thyroid gland secretes 2 hormones : • Thyroxine (tetraiodothyronine or T4) • Triiodothyronine (T3) • Secretion ratio T4 to T3 is 15:1 • Iodine is attached to tyrosine amino acid residues of thyroglobulin in the gland (organification) • Coupling of these residues then produces T4 & T3
Thyroid Physiology (cont.) • T4 & T3 released by the gland are bound & transported by serum proteins : • Thyroxine-Binding Globulin (TBG) : 75 % • Thyroxine-Binding Prealbumin (TBPA) • Albumin • The free (or unbound) hormone levels are the levels which are maintained constant by feedback & regulate thyroid function • Total measured serum T4 includes bound & unbound
Variations in Thyroxine Binding Proteins • Causes of increased TBG levels : • Pregnancy, estrogens, cirrhosis, hepatitis, porphyrias • Causes of decreased TBG levels : • Protein malnutrition, nephrotic syndrome, hepatic failure, androgenic steroids, high dose glucocorticoids • Free T4 (FT4) usually constant in the above conditions
Thyroid Hormone Action in the Tissues • T4 deiodonated in periphery to T3 • This is 80 % of T3 produced • Other metabolite of T4 is reverse T3 (rT3) which is metabolically inactive • T3 enters cells & binds to group of nuclear receptors, then affects wide range of cellular metabolic functions • Thyroid hormone required for normal cell metabolism
Feedback Regulation of Thyroid Hormone Levels • Normal regulation requires intact hypothalamic-pituitary system • Hypothalamus secretes Thyrotropin-Releasing Hormone (TRH) • TRH then stimulates synthesis & release of thyrotropin (Thyroid Stimulating Hormone or TSH) by the anterior pituitary • TSH then stimulates the thyroid gland to uptake iodine, synthesize & release T4 & T3 • T4 & T3 levels feedback to both hypothalamus & pituitary affecting TRH & TSH release
Thyroid Function Tests • Radioimmunoassay for T4 (T4RIA) is most useful single test of thyroid function • Normal levels 4 to 12 mcg / dl • Free thyroid homone difficult to measure directly, so "indirect" tests developed • T3 Resin Uptake (T3RU) measures amount of radioactive T3 unbound when added to patient's serum • Reflects # of sites available for binding T4 &T3 • Is indirect measure of level of circulating T4 • Normal is 25 to 35 %
Other Thyroid Function Tests • Free T4 Index (FT4I) • Correlates with level of Free T4 • Is the product of T4RIA & T3RU • T3 radioimmunoassay (less useful) • Normal 75 to 195 ng / dl • Serum TSH • Normal is 0.3 to 5.0 mcU / ml • TRH Stimulation Test • Measures TSH response to TRH IV injection • Normal is increase in TSH to 30 mcU / ml
Clinical Interpretation of Thyroid Function Tests • T3RU : • Low in hypothyroidism & high TBG states • High in hyperthyroidism & low TBG states • T4RIA & the T3RU go in same direction with thyroid disease & in opposite directions with TBG level abnormalities • TSH • Elevated in primary hypothyroidism • If patient hypothyroid & TSH is low, then lesion is in hypothalamic-pituitary axis, and TRH Stimulation Test should be done
Directional Changes in Thyroid Function Tests Clinical State Total T4 T3RU FT4I Free T4 TSH Euthyroid N N N N N Hyper- thyroid Hypothyroid High TBG N N N Low TBG N N N Nonthyroid Illness N or N or N or N or (N = Normal)
Medications Which May Cause "Euthyroid Hyperthyroxinemia" • Oral contraceptives • Narcotics (methadone, heroin) • Perphenazine • Clofibrate • 5-flurouracil • Heparin • Amiodarone • Iodine contrast agents
Disorders of Thyroid Hormone Excess • "Thyrotoxicosis" is the term for all disorders with increased levels of circulating thyroid hormones • "Hyperthyroidism" refers to disorders in which the thyroid gland secretes too much hormone • Radioactive iodine uptake test (RAUI) distinguishes hyperthyroidism from other forms of thyrotoxicosis
The Radioactive Iodine Uptake Test (RAIU) • Quantitates the fraction of a dose of radioiodine I-123 taken up by the thyroid gland within 24 hours • Normal is 5 to 30 % • Elevated when thyroid gland is overstimulated • Decreased when thyroid gland is suppressed (as by ectopic production of T4 or T3) • Is decreased falsely by recent iodine load (as from contrast computed tomography scan)
Thyroid scans Graves Disease Toxic multinodular goiter with hot nodule
Causes of Thyrotoxicosis with Elevated RAUI • Graves' Disease • Pituitary tumor secreting excess TSH • Pituitary insensitivity to feedback • Hydatidiform mole • Choriocarcinoma • Testis embryonal carcinoma • Toxic multinodular goiter • Toxic uninodular goiter
Causes of Thyrotoxicosis with Decreased RAUI • Acute autoimmune thyroiditis (may later lead to hypothyroidism) • Infectious thyroiditis • Postpartum thyroiditis • Factitious (taking PO excess thyroid hormone) • Metastatic thyroid cancer • Struma ovarii (dermoid tumors or teratomas of the ovary)
Medications Which Can Induce Hyperthyroidism • Iodine • Amiodarone • Lithium Also rarely due to ground beef contaminated with bovine thyroid glands
Features of Graves' Disease (Toxic Diffuse Goiter) • Most common cause of hyperthyroidism (70 to 85 % of all cases) • Caused by thyroid stimulating immunoglobulins • Mainly in young adults ages 20 to 50 • 5 times more frequent in women • Half of cases have infiltrative ophthalmopathy with exopthalmos (not seen with other causes of hyperthyroidism) • 5 % have pretibial myxedema
51 year old male who presented with urinary retention and proved to have Graves Disease
Pretibial myxedema and “square toes” in the same patient on the prior slide
Asymmetric ophthalmo- pathy with lag ophthalmos in Graves Disease
Features of Toxic Multinodular Goiter • Second most common cause of hyperthyroidism • Most cases in women in 5th to 7th decades • Often have long standing goiter • Symptoms usually develop slowly
Symptoms Suggestive of Thyrotoxicosis • Nervousness, restlessness,shortened attention span, emotional lability, difficulty sleeping • Increased appetite • Weight loss • Heat intolerance, perhaps low fever • Diaphoresis • Weakness • Menstrual irregularities
Signs Suggestive of Thyrotoxicosis • Sinus tachycardia, PVC's, PAC's, atrial fibrillation • Tremor, hyperreflexia, muscle wasting • Warm, erythematous, moist skin • Alopecia, nail friability & separation from bed • Hyperventilation • Eyelid retraction, lid lag, persistent stare • Hyperactive bowel sounds • With Graves' : may have exopthalmos, tender enlarged thyroid, & pretibial myxedema
Onycholysis (irregular separation of nail plate from nail bed near distal end) in the same patient on the prior slide
Possible Complications of Thyrotoxicosis at Presentation • High output congestive heart failure • Dehydration • Electrolyte imbalance (from diarrhea) • Corneal lesions from exopthalmos • Worsening of preexistent angina
Syndrome of "Apathetic" or "Nonactivated" Thyrotoxicosis • Represents potentially dangerous degree of hyperthyroidism masked by other preexistent chronic conditions or illnesses • High mortality if not recognized & patient has surgery or another new illness • Most cases in elderly or patients with compromised communication ability
Clinical Features of Apathetic Thyrotoxicosis • May present with any of these seemingly isolated symptoms : • Congestive heart failure • Atrial fibrillation • Recent weight loss > 20 kg • Somnolence, apathy • Irritability and uncooperative behavior • If not recognized and treated, patients may slip into coma and die
Thyroid Storm, A True Medical Emergency • Exact pathogenesis not understood • No clear cut clinical feature separation from thyrotoxicosis • Represents diffuse life-threatening decompensated dysfunction of the body's metabolism • Cases now very rare and sporadic
Thyroid Storm Definitions • "Exaggerated or florid state of thyrotoxicosis" • "Life threatening, sudden onset of thyroid hyperactivity" • May represent end stage of a continuum : • Thyroid hyperactivity to thyrotoxicosis to thyrotoxic crisis to thyroid storm • "Probably reflects the addition of adrenergic hyperactivity, induced by a nonspecific stress, into the setting of untreated or undertreated hyperthyroidism"
Thyroid Storm Background Etiology • Most cases secondary to Graves' disease • Some due to toxic multinodular goiter • Rare causes : • Acute thyroiditis • Factitious • Malignancies (most do not efficiently produce thyroid hormones) • Very rare in children
Thyroid Storm Prognosis • Old references quote almost 100 % mortality untreated, and 20 % treated (but these reports were before use of beta blockers) • Current mortality ? should be < 5% (although not well studied or reported due to rarity of cases)
Thyroid Storm Clinical Presentation • 2 most important defining features : • High fever (usually over 40 degrees C) • Significantly abnormal mental status • Agitation, confusion, psychosis, coma • May also exhibit : • Marked tachycardia • Vomiting, diarrhea • Jaundice (in 20 %) • Associated signs of Graves' disease
Thyroid Storm Precipitating Factors • Infection, especially pneumonia • Cerebrovascular accident • Acute coronary syndrome, Congestive heart failure • Pulmonary embolus • Diabetic ketoacidosis • Parturition / toxemia • Major trauma • Surgery • Iodine 131 Rx or iodine contrast agents • Rapid withdrawl of antithyroid medications
Thyroid Storm Differential Diagnosis • Environmental heatstroke • Cocaine, amphetamine, or phencyclidine toxicity • Neuroleptic malignant syndrome • Meningitis or encephalitis • Intracranial hemorrhage • Malignant hyperthermia • Falciparum cerebral malaria
Progression of Neurologic Findings in Thyroid Storm • Emotional lability • Restlessness • Hyperkinesis • Confusion • Psychosis • Lethargy • Somnolence • Obtundation • Coma
Cardiovascular Findings in Thyroid Storm • Marked tachycardia • Sinus tach or atrial fibrillation • Increased myocardial irritability • PVC's, PAC's, first degree AV block • Wide pulse pressure • Apical systolic murmur • Loud S1 and S2 valve sounds • Some have high output CHF
Case Reports of Unusual Presentations of Thyroid Storm • Coma without prominent cardiovascular findings • Status epilepticus • Nonembolic cerebral infarction • Abdominal pain and fever • Acute renal failure / rhabdomyolysis
Usual Indicated Initial Lab Studies for Thyroid Storm • Glucose (stat fingerstick because of altered mental status) • Pulse oximetry (+/- ABG) • CBC, electrolytes, BUN, creatinine • T4RIA, T3RU, TSH, +/- T3RIA • Urinalysis • Liver function tests • Serum cortisol
Thyroid Storm Usual Lab Results • Lab studies do NOT distinguish thyrotoxicosis from thyroid storm • Usually T4 and T3 are elevated, but may only be elevated T3 • Usually plasma cortisol is low for degree of stress present • Hyperglycemia common
Thyroid Storm Emergent Rx • High flow O2 • Rapid cooling if markedly hyperthermic • Ice packs, cooling blanket, mist / fans, nasogastric tube lavage, acetominophen (Salicylates contraindicated because cause peripheral deiodination to T3) • IV fluid bolus if dehydrated • May need inotropes instead if in CHF • Propranolol 1 mg doses or labetolol 10 to 20 mg doses IV & repeat doses as needed
Thyroid Storm Further Rx • IV diltiazem +/- digoxin for rate control for atrial fib • IV diuretics if in CHF • IV hydrocortisone (or equivalent) 100 mg • Propylthiouracil (PTU) 600 to 1200 mg PO or by NG • Sodium iodide 1 gram IV one hour after the PTU • Find and treat the precipitating cause