Treatment of Congenital Iodine-Deficiency in Confirmed Primary Hypothyroidism

This protocol covers the management of congenital iodine-deficiency in neonates in whom primary hypothyroidism has been biochemically confirmed — whether on routine neonatal screening or on subsequent thyroid function testing.

Clinical scenario

Serum fT4 below the age-specific reference interval with serum TSH clearly above the age-specific reference interval; or serum TSH >20 mU/L at confirmatory testing; or, where thyroid function tests are unavailable, filter paper TSH >40 mU/L at neonatal screening.

Treatment approach

Oral thyroid hormone replacement, initiated as soon as possible after confirmed diagnosis, is the recommended intervention. The dosing approach is calibrated to the severity of biochemical findings at presentation — the complete starting-dose algorithm, adjustment criteria, and monitoring schedule are detailed in the full regimen.

Treatment goals

Rapid normalization of serum TSH within the age-specific reference interval — with serum fT4 maintained in the upper half of the age-specific reference interval — to optimise neurodevelopmental outcomes.

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References

DOI: 10.1089/thy.2020.0333

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