Amaç: Çalışmamızın amacı, hastanemiz odyoloji bilim dalına başvuran Down sendromlu hastaların odyolojik test bulgularını incelemek ve bu hastaların, normal işitme ve işitme kaybı oranını belirlemektir. Gereç ve Yöntemler: Ocak 2012 ve Aralık 2020 tarihleri arasında Marmara Üniversitesi Tıp Fakültesi Odyoloji Bilim Dalına başvuran Down sendromlu hastaların, odyolojik değerlendirme sonuçları retrospektif olarak incelenmiştir. Çalışmaya, 0-18 yaş (yaş ortalaması: 3,67±3,46) arasında 45 kız, 70 erkek olmak üzere toplam 115 Down sendromlu hasta dâhil edilmiştir. Çalışmaya dâhil edilen hastalarda yenidoğan işitme taraması, timpanometri, otoakustik emisyon, işitsel beyin sapı yanıtları ve davranım odyometrisi sonuçları değerlendirilmiştir. Bulgular: Çalışmaya dâhil edilen hastalar, yenidoğan işitme taraması bakımından incelendiğinde, 97 hastaya yenidoğan işitme taraması yapılmıştır. Yenidoğan işitme taraması uygulanan 194 kulaktan, 52'si taramadan geçmiş ve 142 kulak taramadan kalmıştır. Toplam 125 kulakta Tip B, 60 kulakta Tip A, 29 kulakta Tip As, 14 kulakta Tip C ve 2 kulakta Tip Ad timpanogram gözlenmiştir. Toplam 52 kulakta otoakustik emisyon elde edilip; 178 kulakta otoakustik emisyon elde edilmemiştir. Hastaların 18'inde işitme eşikleri, bilateral normal sınırlarda gözlenmiştir. Hastaların 72'sinde bilateral ve 25'inde unilateral olmak üzere toplam 97 hastada işitme kaybı olduğu belirlenmiştir. Sonuç: Sonuç olarak Down sendromu, işitme kaybı için bir risk faktörüdür. Hastalarda, iletim tip işitme kaybı görülebileceği gibi sensörinöral ve mikst işitme kaybı da görülebilmektedir. Uzun süreli kalıcı iletim tip işitme kaybı olan hastalara; işitsel girdi sağlanabilmesi, konuşma ve dil gelişiminin etkilenmemesi açısından işitsel amplifikasyon önerilmelidir. Ek olarak bu hastalarda, konuşma ve dil gelişiminin sağlanabilmesi için işitsel rehabilitasyon önerilmelidir.
Anahtar Kelimeler: Down sendromu; işitme kaybı; akustik direnç testleri; saf ses odyometrisi; uyarılmış potansiyeller, işitsel, beyin sapı
Objective: The aim of our study are to examine the audiological test results of patients with Down syndrome who applied to the audiology department and to determine the normal hearing and hearing loss rate of these patients. Material and Methods: A retrospective review of the results of audiological examinations was conducted for patients with Down syndrome between the years 2012 and 2020 at the Department of Audiology, Marmara University Faculty of Medicine. The subjects consisted of 115 Down syndrome (45 female and 70 male) patients between the ages of 0-18 years (mean age: 3.67±3.46). Patients included in the study had their newborn hearing screening, tympanometry, otoacoustic emission, auditory brainstem responses, and behavioural audiometry results evaluated. Results: Newborn hearing screening was examined on the patients included in the study; 97 of them patients were performed newborn hearing screening. Of the 194 ears that were performed newborn hearing screening, 52 ears passed and 142 ears failed. Type B tympanograms were detected in 125 ears, Type A in 60 ears, Type As in 29 ears, Type C in 14 ears, and Type Ad in 2 ears. While otoacoustic emission was obtained in 52 ears, it was not obtained in 178 ears in total. Hearing thresholds were within the normal range bilaterally in 18 patients. Hearing loss was noted in 97 patients, of whom 72 were bilateral and 25 were unilateral. Conclusion: In summary, Down syndrome is a risk factor for hearing loss. Patients may have conductive hearing loss as well as sensorineural and mixed hearing loss. Patients with permanent conductive hearing loss should be offered auditory amplification to provide auditory input. In these patients, auditory rehabilitation should be recommended to ensure speech and language development.
Keywords: Down syndrome; hearing loss; acoustic impedance tests; pure-tone audiometry; evoked potentials, auditory, brain stem
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