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Congenital hypothyroidism in Indian preterm babies - screening, prevalence, and aetiology
Hemchand Krishna Prasad1, Poornima Pulluru2, Lakshmi Venugopalan2
1Department of Pediatric Endocrinology, Mehta Multispeciality Hospitals India Pvt Ltd, India.
Insights
Congenital hypothyroidism affects 1 in 77 Indian preterm infants, with 50% having permanent thyroid defects. Repeat testing is crucial for accurate diagnosis and timely thyroxine therapy.
Area of Science:
- Neonatology
- Endocrinology
- Pediatrics
Background:
- Limited data exists on hypothyroidism in Indian preterm infants.
- Screening for congenital hypothyroidism is essential for early intervention.
Purpose of the Study:
- To determine the prevalence of primary hypothyroidism in preterm infants in India.
- To investigate the causes and screening experiences for hypothyroidism in this population.
Main Methods:
- A 3-year prospective observational study included preterm infants (<37 weeks gestation) born in a tertiary care unit.
- Heel prick screening for Thyroid Stimulating Hormone (TSH) was performed, with confirmatory venous testing for elevated TSH levels.
- Etiological evaluation and thyroxine therapy were initiated for confirmed cases.
Main Results:
- The prevalence of congenital hypothyroidism was found to be 1 in 77 preterm infants.
- Repeat venous testing at term identified additional cases, highlighting the need for re-evaluation.
- Maternal antibodies and permanent thyroid defects were equally responsible for congenital hypothyroidism (50% each).
Conclusions:
- A high prevalence of congenital hypothyroidism necessitates robust screening protocols in Indian preterm infants.
- Repeat venous testing is crucial, regardless of initial screening results, to ensure accurate diagnosis.
- Half of the confirmed cases had permanent thyroid defects, emphasizing the importance of early detection and management.
Introduction:
Paucity of data on hypothyroidism in Indian preterms. Aim of the study: To describe the prevalence, aetiology, and experience with screening for primary hypothyroidism in preterm babies.
Material And Methods:
A prospective observational study conducted for 3 years in a tertiary care unit, where all babies born < 37 weeks screened by heel prick for Thyroid Stimulating Hormone (TSH) were included. All screen positive cases (TSH ≥ 6 µIU/ml) underwent venous testing immediately; venous TSH ≥ 20 or Free T4 < 0.9 ng/dl was considered as confirmed positive. All babies underwent venous testing at term. Etiological testing was performed where feasible. Confirmed cases were initiated on thyroxine therapy and followed up.
Results:
1167 preterm babies presented during the study period. 1147 (98%) underwent TSH screening and 17 (1.4%) were screen positive; 15 babies underwent confirmatory venous test. Of these 15 babies, 2 were confirmed and started on therapy. The remaining 13 babies underwent retest venous sample at term, and 8 of these were confirmed cases. Of the screen-negative babies, 94% underwent repeat venous testing at term/ prior to discharge. Five were confirmed to have congenital hypothyroidism. Thus, the prevalence of congenital hypothyroidism was 1 in 77 preterm babies. No correlation was observed between screening TSH and venous TSH (p > 0.05). Aetiological evaluation in 8 babies revealed secondary to maternal antibody in 4 cases (50%) and permanent thyroid defects in 4 cases (50%).
Conclusions:
We observed a high prevalence (1 in 77), need for repeat venous testing, irrespective of initial screening, and significant permanent congenital hypothyroidism (50%) in our series.
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