Abstract

BackgroundUnderstanding the risk factors for hearing loss is essential for designing the Belgian newborn hearing screening programme. Accordingly, they needed to be updated in accordance with current scientific knowledge. This study aimed to update the recommendations for the clinical management and follow-up of newborns with neonatal risk factors of hearing loss for the newborn screening programme in Belgium.MethodsA literature review was performed, and the Grading of Recommendations, Assessment, Development and Evaluation (GRADE) system assessment method was used to determine the level of evidence quality and strength of the recommendation for each risk factor. The state of scientific knowledge, levels of evidence quality, and graded recommendations were subsequently assessed using a three-round Delphi consensus process (two online questionnaires and one face-to-face meeting).ResultsCongenital infections (i.e., cytomegalovirus, toxoplasmosis, and syphilis), a family history of hearing loss, consanguinity in (grand)parents, malformation syndromes, and foetal alcohol syndrome presented a ‘high’ level of evidence quality as neonatal risk factors for hearing loss. Because of the sensitivity of auditory function to bilirubin toxicity, hyperbilirubinaemia was assessed at a ‘moderate’ level of evidence quality. In contrast, a very low birth weight, low Apgar score, and hospitalisation in the neonatal intensive care unit ranged from ‘very low’ to ‘low’ levels, and ototoxic drugs were evidenced as ‘very low’. Possible explanations for these ‘very low’ and ‘low’ levels include the improved management of these health conditions or treatments, and methodological weaknesses such as confounding effects, which make it difficult to conclude on individual risk factors. In the recommendation statements, the experts emphasised avoiding unidentified neonatal hearing loss and opted to include risk factors for hearing loss even in cases with weak evidence. The panel also highlighted the cumulative effect of risk factors for hearing loss.ConclusionsWe revised the recommendations for the clinical management and follow-up of newborns exhibiting neonatal risk factors for hearing loss on the basis of the aforementioned evidence-based approach and clinical experience from experts. The next step is the implementation of these findings in the Belgian screening programme.Electronic supplementary materialThe online version of this article (doi:10.1186/s12887-015-0479-4) contains supplementary material, which is available to authorized users.

Highlights

  • Understanding the risk factors for hearing loss is essential for designing the Belgian newborn hearing screening programme

  • The prevalence of bilateral hearing loss is substantial, in neonates admitted to the neonatal intensive care unit (NICU) who frequently present with risk factors for hearing loss

  • Literature review Between September 2014 and December 2014, we reviewed the literature from the last 15 years for each risk factor on the original list, and aimed to answer two specific questions for each risk factor: (1) is it scientifically pertinent to consider it as a risk factor for hearing loss in the newborn hearing screening programme? and (2) how is the risk factor defined?

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Summary

Introduction

Understanding the risk factors for hearing loss is essential for designing the Belgian newborn hearing screening programme. They needed to be updated in accordance with current scientific knowledge. This study aimed to update the recommendations for the clinical management and follow-up of newborns with neonatal risk factors of hearing loss for the newborn screening programme in Belgium. In 2007, the Joint Committee on Infant Hearing (JCIH) released a unique list of risk indicators associated with congenital/neonatal hearing loss and delayed-onset/acquired or progressive hearing loss [6]. The JCIH recommends monitoring hearing, and speech and language skills of all infants as well as performing an audiological assessment at least once by 24–30 months of age in infants presenting with one or more risk indicators from this list. Some authors have recently highlighted that the literature does not corroborate some risk indicators listed by the JCIH, especially with respect to their relationship with postnatal hearing loss [8, 9]

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