# Birth weight, ototoxic medication, and surgical history predict individual hearing loss risks: a systematic review and meta-analysis

**Authors:** Hanwen Luo, Jianghua He, Dapeng Chen, Xiaoming Xu, Jing Zhao, Xiaoyan Yang, Jing Shi

PMC · DOI: 10.3389/fped.2026.1729458 · Frontiers in Pediatrics · 2026-02-06

## TL;DR

This study identifies key risk factors for hearing loss in neonates admitted to the NICU, including very low birth weight and exposure to certain medications.

## Contribution

The study provides a systematic review and meta-analysis of neonatal hearing loss risk factors in NICU settings.

## Key findings

- Very low birth weight (<1,500 g) is significantly associated with hearing loss in NICU neonates.
- Exposure to ototoxic drugs and surgical ligation of PDA are linked to increased hearing loss risk.
- Low Apgar score, prematurity, and sepsis were not significantly correlated with hearing loss.

## Abstract

Hearing loss (HL) impairs sound perception and includes sensorineural, conductive, and mixed subtypes. Compared with healthy newborns, infants admitted to the neonatal intensive care unit (NICU) are at substantially increased risk of congenital anomalies and exposure to HL-related risk factors. However, the specific determinants of neonatal HL remain controversial.

This systematic review and meta-analysis seeks to identify risk factors linked to HL in neonates admitted to the NICU.

PubMed, the Cochrane Library, Embase, and Web of Science were systematically searched from March 26, 1996, to February 25, 2025. Eligible studies were English-language retrospective studies employing multivariate logistic regression to evaluate potential risk factors for HL in NICU neonates. Meta-analyses were conducted using STATA, and pooled estimates were reported as odds ratios or relative risks (OR/RR) with 95% confidence intervals (CI).

This study included 21 retrospective studies with a total of 21,143 participants. Meta-analysis indicated that very low birth weight (<1,500 g), exposure to ototoxic drugs (aminoglycosides, loop diuretics), history of the surgical ligation of patent ductus arteriosus (PDA), craniofacial anomalies, family history of HL, and TORCH infections were significantly associated with HL in NICU neonates (all P ≤ 0.05). In contrast, low Apgar score, prematurity, low birth weight (1,500–2,500 g), duration of vancomycin exposure, sex, and sepsis were not significantly correlated. The findings were robust, and no evident publication bias was detected.

Statistically significant risk factors for HL included craniofacial anomalies, family history of HL, TORCH infections, and surgical ligation of PDA, as well as hyperbilirubinemia, exposure to loop diuretics and other ototoxic drugs, mechanical ventilation, and very low birth weight (<1,500 g) (all P ≤ 0.05). In contrast, low Apgar score, preterm birth, and sepsis were not significantly linked to HL.

https://www.crd.york.ac.uk/PROSPERO/search, PROSPERO CRD420250653476.

## Linked entities

- **Chemicals:** vancomycin (PubChem CID 14969)
- **Diseases:** hearing loss (MONDO:0005365)

## Full-text entities

- **Genes:** GJB2 (gap junction protein beta 2) [NCBI Gene 2706] {aka BAPS, CX26, DFNA3, DFNA3A, DFNB1, DFNB1A}
- **Diseases:** respiratory distress syndrome (MESH:D012128), HL (MESH:D034381), SNHL (MESH:D006319), hypoxia (MESH:D000860), otitis media (MESH:D010033), congenital structural anomalies (MESH:D020914), hypoxic injury (MESH:D002534), Intracranial hemorrhage (MESH:D020300), auditory neuropathy (MESH:C538268), cochlear injury (MESH:D015834), CHL (MESH:D006314), neurotoxic (MESH:D020258), Meningitis (MESH:D008580), congenital head and neck deformities (MESH:D006258), congenital anomalies (MESH:D000013), injuries (MESH:D014947), inflammatory (MESH:D007249), hyperoxia (MESH:D018496), Hyperbilirubinemia (MESH:D006932), Sepsis (MESH:D018805), acoustic trauma (MESH:D006317), congenital organ malformations (MESH:D000092124), ototoxic drug (MESH:D000081015), inner ear injury (MESH:D007759), prematurity (MESH:C536271), PDA (MESH:D004374), preterm birth (MESH:D047928), infections (MESH:D007239), birth asphyxia (MESH:D001237), Ototoxicity (MESH:D006311), MHL (MESH:D046089), Craniofacial anomalies (MESH:D019465), toxicity (MESH:D064420), TORCH (MESH:C535607)
- **Chemicals:** netilmicin (MESH:D009428), Vancomycin (MESH:D014640), bilirubin (MESH:D001663), oxygen (MESH:D010100), Aminoglycosides (MESH:D000617), amikacin (MESH:D000583), loop (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** m.1555A>G

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## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12920535/full.md

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Source: https://tomesphere.com/paper/PMC12920535