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. 2024 Feb 27;10(1):21.
doi: 10.1186/s40942-024-00536-6.

Comparative analysis of risk factors for retinopathy of prematurity in single and multiple birth neonates

Affiliations

Comparative analysis of risk factors for retinopathy of prematurity in single and multiple birth neonates

Mohammadkarim Johari et al. Int J Retina Vitreous. .

Abstract

Aim: To conduct a comparative analysis of risk factors for retinopathy of prematurity (ROP) in single- and multiple-born neonates.

Methods: In a retrospective evaluation of 521 premature neonates, encompassing singletons, twins, and triplets born at or before 34 weeks of gestational age with a birthweight of less than 2000 g and who completed the ROP screening program, between 2020 and 2023, in outpatient referral ROP screening clinic affiliated by Shiraz University of Medical Sciences, were included. Neonates with the eligibility criteria were enrolled in the screening program from 28 days old age and followed up to discharge or treatment based on national ROP screening guideline. Data on ROP severity, outcome, treatment modality, and risk factors, including gestational age (GA), birth weight (BW), sex, duration of neonatal intensive care unit (NICU) admission, oxygen supplementation, mechanical ventilation, blood transfusion, method of delivery, and maternal and neonatal comorbidities, were extracted and compared between premature neonates from singleton and multiple births.

Results: The analysis of the ROP severity distribution revealed 238 neonates (45.7%) with low-risk (type 2 prethreshold ROP or less severe) ROP and 16 (3.1%) with high-risk (type I prethreshold ROP or more severe) ROP who underwent treatment. According to the comparative analysis of risk factors in neonates with ROP requiring treatment, multiple birth neonates exhibited significantly greater GA (27.50 ± 3.27 vs. 30.00 ± 2.00 vs. 31.14 ± 0.38 weeks, p = 0.032 for singletons, twins and triplets, respectively); greater BW (861.67 ± 274.62 vs. 1233.33 ± 347.75 vs. 1537.14 ± 208.86 g, p = 0.002); and shorter duration of NICU admission (60.17 ± 21.36 vs. 34.00 ± 12.17 vs. 12.00 ± 6.32 days, p = 0.001) and oxygen supplementation (47.33 ± 16.57 vs. 36.00 ± 8.49 vs. 4.60 ± 2.41 days, p = 0.001). There was no significant difference between single-born neonates and multiple-born neonates regarding the prevalence of other risk factors. Multiple-born neonates with no ROP and low risk ROP showed significantly lower GA and BW compared to singletons (p < 0.001).

Conclusion: Multiple gestation neonates may develop high-risk ROP requiring treatment at a greater gestational age and birth weight and at a lower duration of oxygen supplementation and NICU admission compared to the single birth neonates. This pattern prompts a reevaluation of screening criteria, suggesting a potential need to consider multiple birth neonates with lower traditional risk factors in screening programs. This pattern should be further evaluated in larger populations of multiple born premature neonates.

Keywords: Multiple birth; Multiple gestation; ROP; Retinopathy of prematurity; Risk factor; Triplet; Twin.

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Conflict of interest statement

No conflicts of interest to declare.

Figures

Fig. 1
Fig. 1
The included singletons, twins and triplets premature neonates in the analysis
Fig. 2
Fig. 2
Comparative analysis of risk factors in neonates with severe ROP. The graphs show a consistent pattern of higher gestational age and birth weight as well as shorter durations of NICU admission and oxygen support in patients needing treatment for severe ROP (type I ROP or more severe) among multiple birth neonates compared to singletons

References

    1. Senjam SS, Chandra P. Retinopathy of prematurity: addressing the emerging burden in developing countries. J Family Med Prim care. 2020;9(6):2600. doi: 10.4103/jfmpc.jfmpc_110_20. - DOI - PMC - PubMed
    1. Blencowe H, Lawn JE, Vazquez T, Fielder A, Gilbert C. Preterm-associated visual impairment and estimates of retinopathy of prematurity at regional and global levels for 2010. Pediatr Res. 2013;74(1):35–49. doi: 10.1038/pr.2013.205. - DOI - PMC - PubMed
    1. Tan Z, Chong C, Darlow B, Dai S. Visual impairment due to retinopathy of prematurity (ROP) in New Zealand: a 22-year review. Br J Ophthalmol. 2015;99(6):801–6. doi: 10.1136/bjophthalmol-2014-305913. - DOI - PubMed
    1. Kim SJ, Port AD, Swan R, Campbell JP, Chan RP, Chiang MF. Retinopathy of prematurity: a review of risk factors and their clinical significance. Surv Ophthalmol. 2018;63(5):618–37. doi: 10.1016/j.survophthal.2018.04.002. - DOI - PMC - PubMed
    1. Owen LA, Morrison MA, Hoffman RO, Yoder BA, DeAngelis MM. Retinopathy of prematurity: a comprehensive risk analysis for prevention and prediction of disease. PLoS ONE. 2017;12(2):e0171467. doi: 10.1371/journal.pone.0171467. - DOI - PMC - PubMed

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