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Increased risk of retinopathy of prematurity since increased O2 saturation targets: A multi-centre study
Michael Isaacs1,2, Shaheen P Shah1,2, Shuan Dai1,2
1Department of Ophthalmology, Queensland Children's Hospital, Brisbane, Queensland, Australia.
Insights
Increased oxygen saturation targets for premature infants, while reducing mortality, have led to a higher prevalence of retinopathy of prematurity (ROP). This necessitates individualized neonatal intensive care unit (NICU) approaches to ROP screening and management.
Area of Science:
- Neonatal Medicine
- Ophthalmology
- Public Health
Background:
- Retinopathy of prematurity (ROP) is a primary cause of visual impairment in premature infants.
- Recent oxygen (O2) saturation target increases in neonates, recommended by major trials, aim to reduce mortality but are a known risk factor for ROP.
- The study investigates the impact of these updated O2 guidelines on ROP prevalence.
Purpose of the Study:
- To determine if higher oxygen saturation targets in preterm neonates have increased the prevalence of retinopathy of prematurity (ROP).
- To assess the risk of ROP in higher-risk subgroups of preterm neonates under the new oxygen guidelines.
Main Methods:
- A retrospective cohort study analyzed data from 17,298 neonates born before 32 weeks' gestational age (GA) and/or weighing less than 1500g between 2012-2018.
- Adjusted odds ratios (aORs) were calculated for ROP risk (any ROP, ROP ≥ Stage 2, treated ROP) in the post-2015 period.
- Sub-analyses were performed for neonates with GA <28 weeks, <26 weeks, birth weight <1500g, and <1000g.
Main Results:
- The risk of any ROP significantly increased post-2015 (aOR=1.23) and in preterm infants with GA <28 weeks (aOR=1.31), <26 weeks (aOR=1.57), <1500g (aOR=1.24), and <1000g (aOR=1.34).
- ROP ≥ Stage 2 also showed increased risk in infants with GA <28 weeks (aOR=1.30), <26 weeks (aOR=1.57), <1500g (aOR=1.18), and <1000g (aOR=1.26).
Conclusions:
- Current oxygen therapy guidelines implemented since 2015 have led to reduced mortality but concurrently increased the incidence of ROP.
- Individualized adjustments in ROP screening and follow-up protocols within neonatal intensive care units (NICUs) are crucial to manage the clinical burden of ROP.
Background/Aims:
Retinopathy of prematurity (ROP) is a leading cause of visual impairment in premature neonates. The BOOST II, SUPPORT and COT trials recommended increasing O2 saturation targets for pre-term neonates to reduce mortality; however, this is a risk factor for ROP. We aimed to determine whether these targets increased prevalence of ROP among pre-term neonates and higher risk groups.
Methods:
Retrospective cohort study conducted using data from the Australian and New Zealand Neonatal Network. 17 298 neonate cohort born 2012-2018 at <32 weeks' GA and/or <1500 g BW was analysed. Adjusted odds ratios (aORs) were calculated for post-2015 risk of: any ROP; ROP ≥ Stage 2; and treated ROP. Sub-analysis stratified at <28 GA, < 26 weeks' GA, <1500 g BW and <1000 g BW was performed.
Results:
Risk of any ROP increased in the post-2015 group (aOR = 1.23, 95% confidence interval (CI) = 1.14-1.32), <28 weeks' GA (aOR = 1.31, 95% CI = 1.17-1.46), <26 weeks (aOR = 1.57, 95% CI = 1.28-1.91), <1500 g (aOR = 1.24, 95% CI = 1.14-1.34) and <1000 g (aOR = 1.34, 95% CI = 1.20-1.50). ROP ≥ Stage 2 increased at <28 weeks (aOR = 1.30, 95% CI = 1.16-1.46), <26 weeks (aOR = 1.57, 95% CI = 1.28-1.91), <1500 g (aOR = 1.18, 95% CI = 1.08-1.30), and <1000 g (aOR = 1.26, 95% CI = 1.13-1.42).
Conclusion:
O2 therapy guidelines since 2015 have resulted in decreased mortality but increased risk of ROP. Individualised NICU adjustments of ROP screening/follow-up methods are necessary to address the clinical burden.
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