Abstract
To investigate disparities in hearing aid use across the life span for borderline/mild hearing loss, a cross-sectional epidemiologic study in the National Health and Nutrition Examination Survey was conducted. Multivariable logistic regressions controlling for hearing level analyzed the association between hearing aid use and age in borderline/mild hearing loss. Age was grouped into quartiles. Of 2470 subjects, 2.0% (n = 50) were <25 years old; 12.0% (n = 297), 25 to 49 years; 65.5% (n = 1618), 50 to 74 years; and 20.5% (n = 505), ≥75 years. When compared with the youngest quartile and while controlling for hearing level, those in the second quartile were 4.6 times less likely to use hearing aids (P < .01); those in the third were 4.2 times less likely (P < .01); and those in the fourth were 4.7 times less likely (P < .001). The dramatically lower hearing aid usage of all older age groups as compared with children/younger adults represents a large unaddressed age-related disparity in the treatment of borderline/mild hearing loss.
Keywords: hearing loss, hearing aids, mild hearing loss, ageism
Children are routinely screened for hearing loss (HL) because of its effect on cognitive, language, and social development.1-3 In contrast, adults are not screened, remaining undiagnosed until HL is more severe. 4 This age-related care gap may stem from the stigma of hearing aids (HAs) and ageism, misperceptions of hearing ability, and hesitancy to treat a “normal” consequence of aging. 5 However, HL in later life, even when minimal, is associated with deleterious conditions, such as cognitive impairment and depression.6-8 Moreover, treatment of mild HL in adults with HAs is effective in decreasing negative psychosocial effects.9,10 Thus, it would seem that minimal HL should be treated with equivalent urgency in older adults as in children. 11 Studies quantitatively investigating this are lacking. We present the most detailed analysis to date assessing HA usage across the life span for borderline/mild HL.
Methods
This was an epidemiologic study in the National Health and Nutrition Examination Survey (NHANES; 1999-2016). NHANES is a national recurrent cross-sectional survey conducted by the National Center for Health Statistics (NCHS) under the Centers for Disease Control and Prevention (CDC) that includes interviews and examinations to determine the prevalence and risks of diseases. It contains a complex survey design to be representative of the US population. It does not suffer from participation bias of convenience samples at medical clinics. Columbia University Institutional Review Board exemption was granted. Only subjects with audiograms and HA data were included.
Age was grouped into quartiles (<25, 25-49, 50-74, ≥75 years). Pediatric HL is relatively rare, making finer categorization impossible. Hearing was defined by 4-freqency pure tone average (PTA) in the better ear (500, 1000, 2000, 4000 Hz). Only subjects with borderline/mild HL (21-40 dB PTA) 12 were included. We included borderline HL (21-25 dB) because children are often identified and treated for HL at this level. When age-related treatment disparities are studied, it is critical to avoid double standards in defining the disorder. 13 In earlier cycles, HA use was assessed in those aged ≥12 years by the question “Ever worn a hearing aid?” and, in later cycles, by “Ever worn a hearing aid/cochlear implant?” with the follow-up “If yes, which one?” HA uptake was calculated as those who had borderline/mild HL and used HAs at a given age, divided by those at that age who had borderline/mild HL or used HAs.
Multivariable logistic regressions controlling for hearing were conducted to analyze the association between HA use and age quartile.
Results
An overall 2470 subjects had borderline/mild HL (21-40 dB PTA) and possessed HA usage data ( Table 1 ): 2.0% (n = 50) were <25 years old; 12.0% (n = 297), 25 to 49 years; 65.5% (n = 1618), 50 to 74 years; and 20.5% (n = 505), ≥75 years. Average hearing was within 4 dB across all quartiles. HA usage plummeted after the first quartile ( Figure 1 ), from 14.0% (n = 7) to 3.7% (n = 11), then slightly increased to 5.1% (n = 82) and 6.7% (n = 34). (The first 2 quartiles had several ages with no HA use due to the rarity of HL in these age groups.) When compared with subjects <25 years old and while controlling for hearing, those 25 to 49 years were 4.6 times less likely to use HAs (95% CI, 1.6-13.2; P < .01); those 50 to 74 years were 4.2 times less likely (95% CI, 1.67-10.2; P < .01); and those ≥75 years were 4.7 times less likely (95% CI, 1.8-12.2; P < .001). A similar drop-off in HA use over quartile is observed solely for mild HL (26-40 dB PTA; Table 2 ).
Table 1.
Demographics of Subjects With Borderline/Mild Hearing Loss (21-40 dB) by Age Quartile.
| Age, No. (%) or mean ± SD | |||||
|---|---|---|---|---|---|
| <25 y | 25-49 y | 50-74 y | ≥75 y | Total | |
| No. | 50 | 297 | 1618 | 505 | 2470 |
| Sex | |||||
| Female | 18 (36.0) | 99 (33.3) | 622 (38.4) | 255 (50.5) | 994 (40.2) |
| Male | 32 (64.0) | 198 (66.7) | 996 (61.6) | 250 (49.5) | 1476 (59.8) |
| Age, y | 18.5 ± 3.71 | 41.5 ± 6.24 | 63.0 ± 6.48 | 79.4 ± 2.77 | 62.8 ± 13.6 |
| PTA in better ear, dB | 26.2 ± 5.40 | 26.1 ± 4.87 | 27.7 ± 5.10 | 30.2 ± 5.64 | 28.0 ± 5.34 |
| Hearing aid use | |||||
| No | 43 (86.0) | 286 (96.3) | 1536 (94.9) | 471 (93.3) | 2336 (94.6) |
| Yes | 7 (14.0) | 11 (3.7) | 82 (5.1) | 34 (6.7) | 134 (5.4) |
Abbreviation: PTA, pure tone average.
Figure 1.

Hearing aid uptake for borderline/mild hearing loss (21-40 dB) declines after childhood/young adulthood. Each point represents summary of all participants for a particular age.
Table 2.
Multivariable Logistic Regression: Hearing Aid Nonuse by Age Quartile, Controlling for Level of Hearing Loss.
| Age, odds ratio (95% CI) | ||||
|---|---|---|---|---|
| <25 y | 25-49 y | 50-74 y | ≥75 y | |
| Hearing loss, dB | ||||
| Borderline/mild: 21-40 | Reference | 4.56 (1.57-13.16) a | 4.15 (1.69-10.21) a | 4.69 (1.82-12.19) b |
| Mild: 26-40 | Reference | 4.23 (1.13-15.38) c | 4.18 (1.36-12.82) c | 5.41 (1.69-17.24) a |
P < .01.
P < .001.
P < .05.
Discussion
HA use for borderline/mild HL dropped precipitously after the first quartile of life (<25 years) and remained low for the life span thereafter. Subjects in the upper 3 age quartiles (25-49, 50-74, ≥75 years) were 4 to 5 times less likely to wear HAs than the youngest quartile, despite equivalent mean levels of hearing. This treatment disparity was nearly the same in mild HL.
Borderline/mild HL is important to study as it is likely the level with the greatest age-related treatment disparity. The disparity cause is likely multifactorial. Medicaid covers HAs for children in some states, whereas Medicare does not and few private insurances routinely cover HAs for adults. However, this difference in coverage is a manifestation of a disparity rather than the explanation of one. Health care disparities are defined as a difference in a health outcome closely linked with disadvantage, which includes age. 14 Disparities often result from societal discrimination against a disadvantaged group. The stigma of appearing old due to HAs is often cited as a reason for low usage. 15 Ageism, our inherent negative bias against older adults,16,17 is likely a factor. To improve equity in HL treatment across the life span, a multifactorial approach is needed, including awareness of ageism and installing measures to combat it. This could include reducing stigmas of HAs through education and marketing, as well as improving access through upcoming over-the-counter HAs.
An argument against needing to treat mild HL in adults is that it is less impactful than HL in children. Children undergo a critical period of education and cognitive development when hearing is essential. However, adults undergo a period of cognitive decline in later life and are susceptible to dementia. Numerous studies have associated even minimal untreated HL with cognitive decline and dementia.18-22 While randomized controlled trials are needed to prove causation, evidence no longer supports the assumption that mild HL is innocuous in adults. Increased awareness across medicine and the public may lead to higher adult HA uptake.
Although prior studies have observed differences in HA use in children vs adults, 23 this is the first to focus on borderline/mild HL and to do so in a national population. Age quartiles were chosen as opposed to a child/adult distinction in part due to low numbers of participants in NHANES aged <18 years with HL. Using the lower quartile (<25 years) allowed additional power. Quartiles also allow comparison across the life span, whereas age <18 vs ≥18 groups all adults as one. Under the Affordable Care Act, US health insurance companies cover dependents under their parents’ plans until age 26 years 24 ; thus, dependents would likely not stop using HAs through ages 18 to 25 due to insurance.
Study limitations include reporting bias, present in any survey-based study. Future studies should include granular usage information (eg, hours/day), although this would still include reporting bias, unless measured objectively. 25 NHANES queried usage frequency differently across cycles, prohibiting inclusion of these data in this analysis. Additionally, analyses with more pediatric participants would allow finer age categorization.
Conclusion
Treatment of borderline/mild HL with HAs is 4 to 5 times lower in all upper age quartiles vs <25 years. This glaring age-related treatment disparity warrants further investigation into possible causes and solutions.
Author Contributions
Maeher Grewal, project design, data analysis, and primary manuscript author; Jacqueline Dragon, data analysis and manuscript editing; Justin S. Golub, project design, data analysis, and manuscript editing.
Disclosures
Competing interests: Justin S. Golub—travel expenses for industry-sponsored meetings (Alcon), consulting fees or honoraria (Alcon), department received unrestricted educational grants (Storz, Stryker, Medtronic, Acclarent, 3NT).
Sponsorships: None.
Funding source: None.
Footnotes
This article was accepted for presentation at the 2022 Triological Society Combined Otolaryngology Spring Meetings; April 27–May 1, 2022; Dallas, Texas.
ORCID iDs: Maeher Grewal
https://orcid.org/0000-0002-3482-9162
Justin S. Golub
https://orcid.org/0000-0003-2432-5291
References
- 1. Moore DR, Zobay O, Ferguson MA. Minimal and mild hearing loss in children: association with auditory perception, cognition, and communication problems. Ear Hear. 2020;41(4):720-732. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2. Tharpe AM. Unilateral and mild bilateral hearing loss in children: past and current perspectives. Trends Amplif. 2008;12(1):7-15. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3. Walker EA. Evidence-based practices and outcomes for children with mild and unilateral hearing loss. Lang Speech Hear Serv Sch. 2020;51(1):1-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4. USPSTF screening for hearing loss in older adults: US Preventative Services Task Force recommendation statement. JAMA. 2021;325(12):1196-1201. [DOI] [PubMed] [Google Scholar]
- 5. Ruusuvuori JE, Aaltonen T, Koskela I, et al. Studies on stigma regarding hearing impairment and hearing aid use among adults of working age: a scoping review. Disabil Rehabil. 2021;43(3):436-446. [DOI] [PubMed] [Google Scholar]
- 6. Chern A, Golub J. Age-related hearing loss and dementia. Alzheimer Dis Assoc Disord. 2019;33(3):285-290. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Golub JS, Brickman AM, Ciarleglio AJ, Schupf N, Luchsinger JA. Association of subclinical hearing loss with cognitive performance. JAMA Otolaryngol Head Neck Surg. 2020;146(1):57-67. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8. Golub JS, Sharma RK, Rippon BQ, Brickman AM, Luchsinger JA. The association between early age-related hearing loss and brain beta-amyloid. Laryngoscope. 2021;131(3):633-638. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9. Johnson CE, Danhauer JL, Ellis BB, Jilla AM. Hearing aid benefit in patients with mild sensorineural loss: a systematic review. J Am Acad Audiol. 2016;27(4);293-310. [DOI] [PubMed] [Google Scholar]
- 10. Cox RM, Johnson JA, Xi J. Impact of advanced hearing aid technology on speech understanding for older listeners with mild to moderate, adult-onset sensorineural hearing loss. Gerontology. 2014;60(6):557-568. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11. Ferguson K. What to do about age-related hearing loss. Real Health. Published August 30, 2021. https://www.realhealthmag.com/article/agerelated-hearing-loss
- 12. Pasha R, Golub JS. Otolaryngology Head and Neck Surgery Clinical Reference Guide. 5th ed. Plural Publishing; 2018. [Google Scholar]
- 13. Alvidrez J, Castille D, Laude-Sharpe M, Rosario A, Tabor D. The National Institute on Minority Health and Health Disparities research framework. Am J Public Health. 2019;109(suppl 1):S16-S20. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14. Secretary’s Advisory Committee on National Health Promotion and Disease Prevention Objectives for 2020. Section IV: Advisory Committee findings and recommendations. In: Phase I Report: Recommendations for the Framework and Format of Healthy People 2020. US Department of Health and Human Services; 2008. [Google Scholar]
- 15. Erler SF, Garstecki DC. Hearing loss– and hearing aid–related stigma: perceptions of women with age-normal hearing. Am J Audiol. 2002;11(2):83-91. [DOI] [PubMed] [Google Scholar]
- 16. São José JM, Amado CA. On studying ageism in long-term care: a systematic review of the literature. Int Psychogeriatr. 2017;29(3):373-387. [DOI] [PubMed] [Google Scholar]
- 17. Butler RN. Age-ism: another form of bigotry. Gerontologist. 1969;9(4):243-246. [DOI] [PubMed] [Google Scholar]
- 18. Irace AL, Armstrong NM, Deal JA, et al. Longitudinal associations of subclinical hearing loss with cognitive decline. J Gerontol A Biol Sci Med Sci. Published September 13, 2021. doi: 10.1093/gerona/glab263 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19. Golub JS, Brickman AM, Ciarleglio AJ, Schupf N, Luchsinger JA. Association of subclinical hearing loss with cognitive performance. JAMA Otolaryngol Head Neck Surg. 2020;146(1):57-67. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20. Brewster KK, Hu MC, Wall MM, et al. Age-related hearing loss, neuropsychological performance, and incident dementia in older adults. J Alzheimers Dis. 2021;80(2):855-864. doi: 10.3233/JAD-200908. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21. Loughrey DG, Kelly ME, Kelley GA, Brennan S, Lawlor BA. Association of age-related hearing loss with cognitive function, cognitive impairment, and dementia: a systematic review and meta-analysis. JAMA Otolaryngol Head Neck Surg. 2018;144(2):115-126. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22. Hubbard HI, Mamo SK, Hopper T. Dementia and hearing loss: interrelationships and treatment considerations. Semin Speech Lang. 2018;39(3):197-210. [DOI] [PubMed] [Google Scholar]
- 23. Dammeyer J, Lehane C, Marschark M. Use of technological aids and interpretation services among children and adults with hearing loss. Int J Audiol. 2017;56(10):740-748. [DOI] [PubMed] [Google Scholar]
- 24. NCSL legal research, 2016; State Health Facts by KFF. Legal review, 2011-2015: Richard Cauchi, NCSL Health Program. [Google Scholar]
- 25. Doyle JB, Raghunathan RR, Cellum I, Li G, Golub JS. Longitudinal tracking of sound exposure and hearing aid usage through objective data logs. Otolaryngol Head Neck Surg. 2018;159(1):110-116. [DOI] [PMC free article] [PubMed] [Google Scholar]
