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Minimal Invasive Resection of Large Retrosternal Thyroid Goiter
Published on: September 20, 2024
[Low initial dose of levothyroxine for treatment of congenital hypothyroidism]
Zheng-yan Zhao1, Rong-wang Yang, Li Liang
1The Affiliated Children's Hospital, College of Medicine, Zhejiang University, Hangzhou 310003, China. zchzzy@mail.hz.zj.cn
Insights
This study found that an initial levothyroxine dose of 4.3 mcg/(kg.d) effectively treats congenital hypothyroidism in infants. Individualizing dosage ensures optimal outcomes for all infants with this condition.
Area of Science:
- Pediatric Endocrinology
- Neonatal Screening
- Thyroid Disorders
Context:
- Congenital hypothyroidism (CH) requires timely treatment to prevent developmental issues.
- Neonatal screening identifies newborns with primary CH.
- Levothyroxine is the standard treatment for CH.
Purpose:
- To evaluate the efficacy of a low initial dosage of levothyroxine in treating infants with congenital hypothyroidism.
- To determine the optimal initial levothyroxine dosage based on CH severity.
- To assess the normalization time of thyroid hormone levels and clinical symptoms.
Summary:
- 138 infants with CH received initial levothyroxine doses ranging from 3.5 to 4.7 mcg/(kg.d) based on severity.
- Thyroid hormone levels (TT3, TT4, TSH) normalized within 1-3 months.
- Clinical symptoms resolved within 2 months, and developmental quotients (DQ) averaged 116.7.
Impact:
- A mean initial levothyroxine dose of 4.3 mcg/(kg.d) is appropriate for most infants with CH.
- Individualized dosing is recommended for optimal treatment outcomes.
- Early and effective treatment of CH supports normal neurodevelopment.
Objective:
To evaluate the results of treatment of infants with congenital hypothyroidism (CH) with a low initial dosage of levothyroxine.
Methods:
138 newborns with primary CH detected by neonatal screening were divided into 3 groups according to levels of serum TSH, TT(3) and TT(4): sub-clinical CH (TSH >50 mU/L), mild CH (TT(4) <54 nmol/L), severe CH (TT(4)<54 nmol/L and TT(3)<1.2 nmol/L). The initial dose of levothyroxine was (3.5 +/-1.0) microg/(kg.d) for sub-clinical CH group, (4.3 +/-0.7)microg/(kg.d) for mild CH group and (4.7 +/- 0.6)microg/(kg.d) for severe CH group. Follow-up evaluation was carried out at 1, 2 and 3 months of age by measuring serum levels of TT(3), TT(4) and TSH. The time, when clinical signs and symptoms were eliminated and serum levels of TT(3), TT(4) and TSH normalized, was recorded. Development Quotient (DQ) testing was performed when CH cases were about 2 years old.
Results:
The mean initial dose of levothyroxine in 138 cases was (4.3 +/-0.9)microg/(kg.d). In one month the serum TT(3) and TT(4) levels returned to normal, while for TSH levels 67.4 % cases reached normal range in 2 months and 84.1 % in 3 months. Two months after therapy, the levels of TT(3) and TT(4) reached to the upper half of normal range and there were no signs or symptoms of hypothyroidism. The time for all cases in 3 groups to reach the normal clinical and biochemical indicators was similar (P=0.925). The dosage for cases with low circulating thyroxine before treatment was higher than that of the other groups (P<0.01). The average DQ score of 18 cases after treatment was 116.7 +/- 17.0.
Conclusion:
he levothyroxine dosage of (4.3 +/- 0.9)microg/(kg.d) is appropriate for the initial treatment of the majority of infants with CH. However it is better to individualize the dosage for each case.
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