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Associations between retinopathy of prematurity and the risks of hearing loss: A propensity matched analysis
Hejin Jeong1, Chelsea Cleveland2, Todd Otteson3
1Case Western Reserve University School of Medicine, 9501 Euclid Ave, Cleveland, OH, 44106, United States.
Insights
Children with retinopathy of prematurity (ROP) have a higher risk of hearing loss (HL). This study suggests increased hearing screening for ROP patients to detect potential hearing impairments early.
Area of Science:
- Ophthalmology
- Pediatrics
- Audiology
Background:
- Retinopathy of prematurity (ROP) and hearing loss (HL) share common risk factors.
- The relationship between ROP and the subsequent risk of developing HL is not well-established.
Purpose of the Study:
- To investigate the association between retinopathy of prematurity (ROP) and the risk of hearing loss (HL) in children.
- To determine if ROP diagnosis increases the likelihood of HL.
Main Methods:
- Retrospective review of a US national database of electronic medical records.
- Comparison of hearing loss (HL) odds between a cohort of patients with ROP and a control cohort without ROP.
- Propensity score matching was used to control for confounding variables.
- Secondary analyses stratified ROP patients by disease severity and treatment status.
Main Results:
- Patients with ROP demonstrated significantly higher odds of having hearing loss (HL) compared to controls (OR = 1.42).
- No significant difference in HL odds was observed between mild and severe ROP cases.
- Treatment status for ROP did not significantly alter the odds of developing HL.
Conclusions:
- Hearing loss (HL) is more prevalent in children diagnosed with retinopathy of prematurity (ROP), even after accounting for other risk factors.
- Findings support the need for enhanced hearing screening protocols for pediatric ROP patients.
- Further research is warranted to confirm this association in controlled settings.
Purpose:
While retinopathy of prematurity (ROP) and hearing loss (HL) share many risk factors, whether patients with ROP have a higher risk of HL remains largely unknown. Therefore, this study aimed to explore the association between ROP and the risk of having HL.
Methods:
The electronic medical records contained in a United States national database were retrospectively reviewed. Patients younger than 18 years old with a record of receiving hearing screening were included. Eligible patients with a history of ROP were assigned to the ROP cohort, while those without ROP diagnosis after vision screening served as controls. After adjusting for covariates via propensity score matching, the two cohorts were compared to evaluate the odds ratios (OR) of having hearing loss. To assess the impact of ROP severity and treatment on the OR, secondary analyses were additionally performed by further stratifying the ROP cohort based on the severity and treatment status.
Results:
The primary analysis revealed that, compared to controls (n = 2,978, mean age: 2.34 ± 2.77 years; 51.1 % female) the ROP cohort (n = 2,978, mean age: 2.40 ± 3.13 years; 50.9 % female) had higher odds of having HL (OR = 1.42, CI = 1.25-1.61). However, among patients with ROP, the odds of HL did not differ between the mild and severe cohorts (OR = 0.99, CI = 0.73-1.34) or between the treated and untreated cohorts (OR = 0.79, CI = 0.50-1.24).
Conclusion:
HL was more common among children with ROP after adjusting for other risk factors of HL. Confirmation of this association in future controlled research settings could provide a rationale for increasing the frequency of hearing screening in children with ROP.
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