Ill. Admin. Code tit. 77, § 661.330 - Congenital Hypothyroidism (CH)
a)
Interpretation of Results. Although the majority of infants affected by CH will
be identified by this screening, due to genetic variabilities and variations in
health status, specimen quality, and timing of specimen collection, not all
infants affected by the disorder may be identified. As with any laboratory
test, false positive and false negative results are possible. Newborn screening
test results are insufficient information on which to base diagnosis or
treatment.
1) Neonatal levels for thyroid
stimulating hormone (TSH) vary with gestational age, birth weight, time of
collection and in response to concurrent medical problems. Normal TSH and
normal thyroxine (T4) levels shall be established using accepted statistical
techniques (for example, as described by the Association of Public Health
Laboratories, see Section
660.20).
2) When the TSH level or the T4 level is
deemed to be abnormal, the Department will recommend a repeat newborn blood
spot screening test or referral of the newborn to a designated pediatric
endocrinologist for further evaluation for CH and additional serum testing for
thyroid function.
b)
Designation of Medical Specialist. In addition to the minimum qualifications
set out in Section 661.230, medical specialists
designated by the Department to follow-up on a screen positive for CH shall
possess training in pediatric endocrinology with certification of special
competence in pediatric endocrinology by the American Board of
Pediatrics.
c) Diagnosis and
Treatment. Medical management by a designated pediatric endocrinologist is
highly recommended. Replacement therapy with thyroid hormone is currently the
standard treatment. Long-term follow-up of children with CH is necessary to
adjust medication and to assess growth and development.
Notes
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