Our Newborn Hearing Screening Results of Infants with Congenital Hypothyroidism
Öz
Objective: We aimed to reveal newborn hearing screening test results and risk factors of babies diagnosed with congenital hypothyroidism (CH) in our hospital.
Material and Methods: The files of the newborns who were evaluated within the scope of the national newborn screening program between January and December 2019 were retrospectively reviewed. Risk factors were evaluated by comparing newborn hearing screening test results of babies with CH and euthyroid control groups.
Results: There was no significant difference between the two groups in terms of demographic and pregnancy datas. There was no significant difference between the CH and control groups in terms of the rate of failed/passed patients from the hearing screening tests. Patients with thyroid hypoplasia at CH group failed at a higher rate from the first hearing screening test.
Conclusion: In this study, there was no significant difference between CH and control groups in terms of hearing screening results.
Anahtar Kelimeler
Destekleyen Kurum
Proje Numarası
Teşekkür
Kaynakça
- 1. American Academy of Pediatrics (AAP); American Thyroid Association (ATA); Lawson Wilkins Pediatric Endocrine Society (LWPES). Update of newborn screening and therapy for congenital hypothyroidism. Pediatrics. 2006;117:2290-303.
- 2. Maciel LM, Kimura ET, Nogueira CR, Mazeto GM, Magalhães PK, Nascimento PL, et al., Congenital hypothyroidism: recommendations of the thyroid department of the Brazilian society of endocrinology and metabolism, Arq. Bras. Endocrinol. Metabol. 2013; 57: 184–92.
- 3. Özon A, Tekin N, Şıklar Z, Gülcan H, Kara C, Taştekin A et al., Gebelikte tiroid hastalıklarının neonatal etkileri ve TSH yüksekliği olan bebeğe yaklaşım: Türk Neonatoloji ve Çocuk Endokrinoloji ve Diyabet Dernekleri uzlaşı raporu. Turk Pediatri Ars 2018; 53: 209-23.
- 4. Jain V, Argawal R, Deorari AK, Paul VK. Congenital hypothyroidism. Indian J Pediatr. 2008;75:363-7.
- 5. De Andrade CLO, Machado GC, Magalhães LPF, Cerqueira TLO, Fernandes LC, Ramos HE et al., Cochlear dysfunction evidenced by reduction of amplitude of otoacustic responses in patients with congenital hypothyroidism. Int J Pediatr Otorhinolaryngol. 2019; 122: 12-7.
- 6. Ovalı P. Yenidoğan Taramaları. Klinik Tıp Pediatri Dergisi. 2019; 11: 193-9. 7. Arıcıgil M, Ulutaş RA, Yücel A, Arbağ H. Yenidoğan İşitme Tarama Sonuçlarımız. Selçuk Med J 2015;31: 121-3.
- 8. Li D, Henley CM, O'Malley Junior BW. Distortion product otoacoustic emissions and outer hair cell defects in the hyt/hyt mutant Mouse. Hear Res. 1999; 138: 65–72.
- 9. Mustapha M, Frang Q, Gong TW, Dolan DF, Raphael Y , Camper SA, et al., Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit 1dw mutants, J. Neurosci. 2009; 29: 1212–23.
Ayrıntılar
Birincil Dil
İngilizce
Konular
İç Hastalıkları
Bölüm
Klinik Araştırma
Yayımlanma Tarihi
25 Mayıs 2021
Gönderilme Tarihi
25 Temmuz 2020
Kabul Tarihi
22 Aralık 2020
Yayımlandığı Sayı
Yıl 2021 Cilt: 15 Sayı: 3