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Congenital Hypothyroidism among Infants Undergoing Thyroid Function Test in a Tertiary Care Centre: A Descriptive
Bijaya Mishra1, Nisha Keshary Bhatta2, Mohan Chandra Regmi3
1Department of Biochemistry, B.P. Koirala Institute of Health Sciences, Buddha Road, Dharan, Nepal.
JNMA; Journal of the Nepal Medical Association
|June 12, 2022
Summary
Congenital hypothyroidism affects 4.5% of infants in this study. Early newborn screening for congenital hypothyroidism is crucial to prevent mental retardation, as routine screening is not yet standard practice in many regions.
Area of Science:
- Pediatrics
- Endocrinology
- Public Health
Background:
- Congenital hypothyroidism is a leading preventable cause of intellectual disability in infants.
- Routine screening for congenital hypothyroidism is not universally implemented, particularly in certain global regions.
- This study addresses the need for prevalence data in a tertiary care setting.
Purpose of the Study:
- To determine the prevalence of congenital hypothyroidism among infants undergoing thyroid function tests.
- To highlight the importance of newborn screening for congenital hypothyroidism.
- To provide data from a tertiary care center in Nepal.
Main Methods:
- A descriptive, cross-sectional study utilizing laboratory records from April 2013 to April 2020.
- Thyroid function tests from 1243 infants were analyzed.
- Data analysis included calculating point prevalence with 95% Confidence Intervals.
Main Results:
- A prevalence of 4.50% (95% CI: 3.35-5.65) for congenital hypothyroidism was found among 1243 infants.
- The identified prevalence was higher compared to similar studies in comparable settings.
- Treatment-induced hyperthyroidism was an unexpected finding.
Conclusions:
- The study reveals a significant prevalence of congenital hypothyroidism, underscoring the need for systematic newborn screening.
- The observation of treatment-induced hyperthyroidism suggests potential gaps in regular and timely follow-up care for affected infants.
- Findings emphasize the importance of establishing and maintaining robust screening and follow-up protocols for congenital hypothyroidism.
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