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Referrals for Elevated Thyroid Stimulating Hormone to Pediatric Endocrinologists
Sarah Gammons1, Brent K Presley1, Perrin C White1
1Division of Pediatric Endocrinology, UT Southwestern Medical Center, Dallas, Texas.
Insights
Thyroid-stimulating hormone (TSH) levels alone are not sufficient to diagnose pediatric hypothyroidism. Referral to pediatric endocrinologists should be based on clinical concern, not just mildly elevated TSH levels.
Area of Science:
- Pediatric Endocrinology
- Thyroid Function Testing
- Clinical Diagnostics
Background:
- Thyroid-stimulating hormone (TSH) testing is crucial for diagnosing hypothyroidism in children.
- Reproducibility of TSH levels and prediction of treatment decisions require further investigation.
Purpose of the Study:
- To assess the reproducibility of TSH testing in pediatric patients.
- To identify TSH thresholds predicting autoantibodies and levothyroxine treatment initiation/continuation.
Main Methods:
- Retrospective analysis of 325 children (1-18 years) with suspected hypothyroidism.
- Used receiver operating characteristic (ROC) analysis to evaluate TSH predictive ability for treatment decisions, autoantibodies, and TSH reproducibility.
Main Results:
- An initial TSH of 11 mIU/L predicted a repeat TSH ≥11 with 90% sensitivity and specificity.
- TSH predicted autoantibodies (AUC 0.711) and treatment decisions (AUC 0.878) with optimal cutoffs at 8.8 and 8.2 mIU/L, respectively.
- Combined TSH, antibody status, and examination findings best predicted treatment (AUC 0.930).
Conclusions:
- Mildly elevated TSH levels alone do not warrant referral to pediatric endocrinologists.
- Clinical suspicion and other factors are essential for guiding referral and treatment decisions in pediatric hypothyroidism.
Objective:
We aimed to determine the reproducibility of TSH testing in pediatric patients referred to pediatric endocrinologists and to identify the threshold TSH levels that would predict the presence of antithyroid autoantibodies and inform decisions by pediatric endocrinologists to initiate or continue treatment with levothyroxine.
Study Design:
We analyzed a retrospective case series of 325 children aged 1 to 18 years referred for hypothyroidism to the endocrinology clinic at a tertiary care children's hospital. The receiver operating characteristic area under curve (AUC) determined the ability of the initial TSH level to predict pediatric endocrinologists' treatment decisions, presence of thyroid autoantibodies, and reproducibility of elevated TSH on repeat testing.
Results:
Of 325 patients, 191 were treated. The treated patients were more likely to have had a higher referral TSH, positive autoantibodies, and abnormal thyroid gland examination findings. An initial TSH of 5 had a specificity of only 14% for a repeat TSH of ≥5. An initial TSH level of 11 had a specificity of 90% for a repeat TSH of ≥11, with sensitivity of 90%. TSH was a relatively poor predictor (AUC, 0.711) of the presence of autoantibodies with optimal classification at TSH >8.8 mIU/L. It was better (AUC, 0.878) at predicting whether endocrinologists started or continued treatment with levothyroxine, with optimal classification at 8.2 mIU/L. TSH levels combined with antibody status and thyroid examination findings had the best ability to predict treatment (AUC, 0.930).
Conclusions:
TSH levels slightly above the reference range should not prompt referral to pediatric endocrinologists unless another basis for clinical concern is present.
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