High prevalence of congenital hypothyroidism in Isfahan, Iran
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M Hashemipour , M Amini , R Iranpour , A Javadi , GH Sadri , N Javaheri , G Sattari , S Haghighi , S Hovsepian  |
, emrc@mui.ac.ir |
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Abstract: (29420 Views) |
Introduction: Hypothyroidism is one of the preventable causes of mental retardation, which according to its clinical manifestations within the neonatal period, can be diagnosed in only fewer than 10% of cases. Delayed diagnosis results in irreversible cerebro-auditory complications unless the problem is diagnosed by screening programs. Materials and Methods: From May to December 2002, T4 and TSH concentrations of 20,000 serum samples obtained from newborns on 3rd-7th day of birth, born in seventeen hospitals throughout Isfahan were measured by RIA and IRMA, respectively. The newborns with abnormal screening results (TSH> 20 mIU/L, T4<6.5 μg/dL and based on the weight) were re-examined. Newborns with TSH >10mIU/L and T4<6.5 μg/dL on the second measurement were considered to be hypothyroid so treatment was begun. After performing complementary tests, the hypothyroid patients received replacement therapy with levothyroxine. Results: From 20,000 neonates that were examined, 531 were recalled (Recall rate = 2.65%) and 54 newborns were diagnosed as hypothyroid. The prevalence of neonatal hypothyroidism was estimated to be 1/370. Conclusion: Considering the high prevalence of the disease in the population, the necessity of routine neonatal screening programs is underscored. |
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Keywords: Congenital hypothyroidism, Screening, T4, TSH |
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Full-Text [PDF 289 kb]
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Type of Study: Original |
Subject:
Endocrinology Received: 2006/11/20 | Published: 2004/03/15
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