Hypothyroidism
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Transcript of Hypothyroidism
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THYROID DISORDERS:
HYPOTHYROIDISM
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REFERENCES
1. Practice Guidelines for Thyroid DisordersThe Malaysian Consensus 2000Ministry of Health Malaysia
2. Oxford Handbook of Endocrinology & DiabetesHelen E. Turner, and John A.H. Wass1st edition, 2003
3. Update on the management of hyperthyroidism and hypothyroidism, Kenneth A. Woeber,, Arch Fam Med (2000) 9; 743-747
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INTRODUCTION
• Hypometabolic state due to deficiency of thyroid hormones
• Accumulation of GAGs (mucopolysaccharides) in the SC tissue
• Incidence : mid-50s : male:female ratio → 1:10
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ETIOLOGY
1. PRIMARY : THYROID FAILURE (95%)
2. SECONDARY : PITUITARY TSH DEFICIT
3. TERTIARY : HYPOTHALAMIC DEFICIENCY
OF TSH
4. PERIPHERAL RESISTANCE TO THE ACTIONS
OF THYROID HORMONES
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• Autoimmune hypothyroidism:-Hashimoto’s thyroiditis- Atrophic thyroiditis
• Iatrogenic:-Radio-iodine therapy- Thyroidectomy- External radiation to the neck (lymphoma/CA)
• Drugs : -Antithyroid drugs, amiodarone, lithium, interferon
• Congenital hypothyroidism:-Thyroid agenesis- Dyshormogenesis- TSH-R mutation
PRIMARY CAUSES
• Iodine deficiency
• Infiltrative disorder
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2°, 3° AND OTHER CAUSES
• Hypopituitarism (2°):– Tumour– Surgery– Radiation – Postpartum: Sheehan’s
syndrome
• Hypothalamic causes (3°):– Tumour– Trauma
• Peripheral resistance (rare)
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LABORATORY INVX• Diagnosis : serum TSH
: serum T4 total or free?
: thyroid autoantibodies• In outpatient setting → serum TSH !!!
SUBCLINICAL HYPOTHYROIDISM:
• patient is not overtly
hyperthyroid
• serum free T4 is normal, but TSH is
↑
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MANAGEMENT• Aim: to make patient euthyroid, clinically &
biochemically.
• Treatment with L-thyroxine is life-long → ensure compliance!!
• Monitoring:– Clinically & biochemically– Measure TSH and free T4 2-3 month after initiation of therapy →
determine maintenance dose
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1) OVERT HYPOTHYROIDISM– Starting dose : 50-100 ug/d →→ 100-200ug/d
within 2 weeks
– IHD / grossly hypothyroid / elderly:• Start at 25 ug/d• ↑ slowly within 2-4/52 according to pt response• Angina: withhold / ↓ dose. Proper mx of IHD
– Hypopituitarism:• Cortisol: to avoid adrenal crisis
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2) SUBCLINICAL HYPOTHYROIDISM:– L-thyroxine to ↓ risk of CAD– 50-100 ug/d →→ adjust to maintain TSH at
normal level
3) PREGNANCY:– ↑ dose, especially in 2nd / 3rd trimester
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EMERGENCY:MYXEDEMA COMA
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• Severe, uncompensated form of prolonged hypoTH
• Precipitated by stress / infection / drug
• Complication:– Hypoventilation– Cardiac failure– Fluid & electrolyte imbalance– coma
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PLAN OF MANAGEMENT
1. Treat precipitating cause2. Gradual rewarming → blanket3. Accurate core T° → rectal thermometer
– Aim for slow ↑ in core T° : 0.5 °C/hr4. Cardiac monitoring5. Correction of electrolyte abnormalities6. Adequate hydration & nutrition (dextrose)7. L-thyroxine (300-400 ug oral/iv) &
tri-iodothyronine 10 ug 8 hrly8. Hydrocortisone : blood cortisol
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CONGENITALHYPOTHYROIDISM
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• Incidence : 1 in 4000-5000 live births
• Importance of TH hormones:• Normal development of nervous system !!
• Features: – Prolonged jaundice– Poor feeding– Constipation– Unusually quite baby
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• Signs (if left untreated, appear at 3-6 months):– Coarse facies– Dry skin– Hoarse cry– Umbilical hernia – macroglossia– Delayed developmental milestones
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MANAGEMENT• Newborn screening• Diagnosis confirmed → treat ASAP • Dose: start at 10-12 ug/kg/day• Aim : maintain TSH at normal level
: maintain free T4 at upper limit of normal range
• Life-long treatment: if transient hypoTH is suspected, re-evaluate at 2 years old.
• Monitoring: antropometry/milestones/bone age progression
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THANKYOU
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