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Title: [Systematic hearing screening for newborns in the Champagne-Ardennes region: 32,500 births in 2 years of experience]. Author: Schmidt P, Leveque M, Danvin JB, Leroux B, Chays A. Journal: Ann Otolaryngol Chir Cervicofac; 2007 Sep; 124(4):157-65. PubMed ID: 17669353. Abstract: OBJECTIVES: To report a Universal Newborn Hearing Screening (UNHS) program developed in the Champagne-Ardennes region in 2004-2005. METHODS: A team of ENT specialists and pediatricians set up a UNHS program designed to reduce the age of diagnosis and care of bilateral congenital deafness. The program was mainly based on automated acoustic otoacoustic emissions and a strict follow-up by the Regional Neonatal Screening Center. RESULTS: In 2004 and 2005, 29,944 neonates from 30,518 births were screened (98.11%). Of the neonates screened, 409 (1.38%) failed the test and were referred. The average retest delay was 2 weeks. Eleven were lost to follow-up, 371 (94%) had a successful second test on one or both ears, 27 (7%) failed the test a second time and had a diagnosis of ABR. Twenty-four cases of bilateral deafness were identified early, 14 of which had no risk factors. One of the children lost to follow-up was actually deaf, which was diagnosed at 18 months of age. Since the beginning of the UNHS program, the average age of diagnosis was lowered to less than 3 months. CONCLUSION: Our experience tends to demonstrate that UNHS is possible and the program allows an early diagnosis of bilateral congenital hearing loss.[Abstract] [Full Text] [Related] [New Search]