Article Text
Abstract
Objective In a national study of Australian children aged 11–12 years old, we examined the (1) prevalence and characteristics of hearing loss, (2) its demographic risk factors and (3) evidence for secular increases since 1990.
Methods This is a cross-sectional CheckPoint wave within the Longitudinal Study of Australian Children. 1485 children (49.8% retention; 49.7% boys) underwent air-conduction audiometry. Aim 1: hearing loss (≥16 decibels hearing level (dB HL)) was defined in four ways to enable prior/future comparisons: high Fletcher Index (mean of 1, 2 and 4 kHz; primary outcome relevant to speech perception), four-frequency (1, 2, 4 and 8 kHz), lower frequency (1 and 2 kHz) and higher frequency (4 and 8 kHz); aim 2: logistic regression of hearing loss by age, gender and disadvantage index; and aim 3: P for trend examining CheckPoint and reported prevalence in studies arranged by date since 1990.
Results For high Fletcher Index, the prevalence of bilateral and unilateral hearing loss ≥16 dB HL was 9.3% and 13.3%, respectively. Slight losses (16–25 dB HL) were more prevalent than mild or greater (≥26 dB HL) losses (bilateral 8.5% vs 0.8%; unilateral 12.5% vs 0.9%), and lower frequency more prevalent than higher frequency losses (bilateral 11.0% vs 6.9%; unilateral 15.4% vs 11.5%). Demographic characteristics did not convincingly predict hearing loss. Prevalence of bilateral/unilateral lower and higher frequency losses ≥16 dB HL has risen since 1990 (all P for trend <0.001).
Conclusions and relevance Childhood hearing loss is prevalent and has risen since 1990. Future research should investigate the causes, course and impact of these changes.
- hearing loss
- prevalence
- risk factors
- secular trend
- children
Statistics from Altmetric.com
Footnotes
Contributors MW conceived the CheckPoint study with the CheckPoint team. MW was the primary student supervisor, along with RAB and VS, and oversaw all aspects of the study and the manuscript preparation. RSL contributed to hearing data collection and, under the guidance of PC, designed the hearing protocols. JW and CMPC conducted data extraction, cleaning and handling. JW performed data analysis and wrote the main paper. MW, PC, FKM and LG advised on statistical issues and interpretation. All authors critically reviewed the manuscript and had final approval of the submitted and published version of this paper. MW and JW had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.
Funding This work was supported by the National Health and Medical Research Council (NHMRC) of Australia (1041352, 1109355), The Royal Children’s Hospital Foundation (2014-241), the Murdoch Children’s Research Institute, The University of Melbourne, the National Heart Foundation of Australia (100660) and Financial Markets Foundation for Children (2014-055, 2016-310). The funding bodies did not play any role in the study. The following authors were supported by the NHMRC: VS (Early Career Fellowship 1125687), PC (Centre of Research Excellence in Child Language 1023493), RSL (Postgraduate Scholarship 1114567), FKM (Career Development Fellowship 1111160), LG (Early Career Fellowship 1035100) and MW (Senior Research Fellowship 1046518). VS was additionally supported by a Cottrell Research Fellowship from the Royal Australasian College of Physicians; CMPC by a Ter Meulen Grant from the Royal Netherlands Academy of Arts and Sciences; RAB by the HEARing Cooperative Research Centre, established and supported under the Cooperative Research Centres Program, an Australian Government Initiative; and MW by Cure Kids New Zealand.
Competing interests None declared.
Patient consent Obtained.
Ethics approval The Royal Children’s Hospital Human Research Ethics Committee (HREC33225) and The Australian Institute of Family Studies Ethics Committee (AIFS14-26) approved the study.
Provenance and peer review Not commissioned; externally peer reviewed.