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Outcome of congenitally hypothyroid screening program in isfahan: iran from prevention to treatment
Mahin Hashemipour1, Elham Hashemi Dehkordi, Silva Hovsepian
1Professor of Pediatric Endocrinology, Department of Pediatrics, Isfahan Endocrine & Metabolism Research Center (IEMRC), Isfahan University of Medical Sciences (IUMS), Isfahan, Iran.
Insights
Early treatment for congenital hypothyroidism (CH) is vital. This study in Isfahan found that while treatment initiation was timely, optimal outcomes for CH patients require early, high-dose interventions, especially for severe cases.
Area of Science:
- Pediatrics
- Endocrinology
- Neonatal Screening
Background:
- Congenital hypothyroidism (CH) requires prompt treatment to prevent neurodevelopmental issues.
- Isfahan has a notable prevalence of CH, necessitating local treatment outcome evaluations.
Purpose of the Study:
- To assess the treatment outcomes of CH patients identified through a screening program in Isfahan.
- To evaluate the timeliness and effectiveness of CH treatment based on key biochemical markers.
Main Methods:
- A cohort of CH neonates diagnosed via screening in Isfahan (May 2002-September 2009) was studied.
- Treatment quality was assessed by monitoring age at treatment initiation and thyroid-stimulating hormone (TSH) and thyroxine (T4) levels.
- Biochemical markers were evaluated pre-treatment, post-treatment, and during the first two years of life.
Main Results:
- The prevalence of CH was identified as 1 in 420 live births.
- The mean age for initiating treatment was 22.9 ± 13.2 days, with 93.7% starting before day 45.
- Initial post-treatment T4 and TSH levels were outside the acceptable range in 3.9% and 9.8% of patients, respectively, though they normalized over time, with T4 normalizing faster than TSH.
Conclusions:
- Treatment initiation age was within acceptable limits.
- Optimal CH management, particularly for severe cases, necessitates both early and high-dose therapeutic interventions.
- Further research is required to elucidate treatment outcomes across diverse etiologies of CH.
Objectives:
Early and proper treatment is crucial to prevent neuropsychologic deficits in congenital hypothyroidism (CH). Considering the high prevalence of CH in Isfahan, the aim of this study was to evaluate the outcome of treatment in CH patients.
Methods:
In this study CH neonates diagnosed during screening program in Isfahan from May 2002 to September 2009 were studied. Frequent visits were performed to CH patients to monitor and follow their treatments. Quality of treatment was assessed by evaluating mean age of treatment initiation and mean TSH and T4 levels before and after treatment and during the first and second years according to their normal reference ranges.
Results:
Of 225,224 screened neonates, 536 were diagnosed as CH patients. The prevalence of CH was 1/420 live births. Mean age at starting treatment was 22.9 ± 13.2 days. In 93.7% of patients, treatment was begun before the 45th day of life. In the first measurement after initiating the treatment, T4 and TSH were not in their acceptable range in 3.9% and 9.8% of CH patients, respectively. Mean T4 and TSH reached to normal range during the treatment period. T4 reached the normal range earlier than TSH.
Conclusions:
The mean age of treatment initiation was in acceptable range but the findings suggest that both early and high-dose treatments are crucial for optimal treatment, especially in patients with severe CH. Further studies are needed to determine the outcome of treatment specially regarding to different etiologies of CH.
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