Clinical survey of current practice regarding treatment of children with borderline thyroid abnormalities

Samantha Lain1, Natasha Nassar1, Michelle Jack2

  • 1Children's Hospital at Westmead Clinical School, University of Sydney, Sydney, New South Wales, Australia.

Insights

Clinical practice for treating mild thyroid deficiency in newborns varies significantly among Australian and New Zealand pediatric endocrinologists. Updated guidelines are needed to ensure consistent treatment for congenital hypothyroidism.

Area of Science:

  • Pediatric Endocrinology
  • Neonatal Screening
  • Thyroid Disorders

Background:

  • Debate exists on lowering newborn screening (NBS) thyroid-stimulating hormone (TSH) cut-offs for mild thyroid deficiency.
  • Identifying infants with mild thyroid deficiency via NBS necessitates further clinical evaluation and potential treatment.
  • Current clinical practices for managing mild thyroid deficiency identified through NBS are not well-documented.

Purpose of the Study:

  • To survey pediatric endocrinologists in Australia and New Zealand.
  • To understand current clinical practices for treating mild thyroid deficiency in infants.
  • To identify variations in investigations, treatment, and follow-up based on serum TSH levels.

Main Methods:

  • A piloted questionnaire was distributed to members of the Australasian Paediatric Endocrinologist Group.
  • The survey collected data on clinical approaches for infants with varying confirmatory serum TSH levels.
  • 42 completed surveys were analyzed, yielding a 34% response rate.

Main Results:

  • Significant variation in treatment decisions was observed among clinicians.
  • For a TSH of 8.7 mU/L, only 7% of clinicians would initiate thyroxine treatment.
  • Treatment initiation increased with higher TSH levels: 69% for 21.4 mU/L, 76% for 24.3 mU/L, and 95% for 44.7 mU/L.

Conclusions:

  • Clinical practice for treating mild thyroid deficiency in children shows extensive variation.
  • Existing international and national guidelines for congenital hypothyroidism require updating.
  • Updated guidelines should incorporate new evidence to promote consistency in clinical practice.
Abstract

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