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Predictive value of pre-plus disease in retinopathy of prematurity
David K Wallace1, Sharon F Freedman, M E Hartnett
1Duke University Eye Center, DUMC 3802, Durham, NC 27710, USA. david.wallace@duke.edu
Insights
Early detection of pre-plus disease in premature infants strongly predicts the need for laser treatment for severe retinopathy of prematurity (ROP). This finding aids in timely intervention for ROP progression.
Area of Science:
- Ophthalmology
- Neonatology
- Medical Imaging
Background:
- Retinopathy of prematurity (ROP) is a significant cause of visual impairment in premature infants.
- Early identification of infants at risk for severe ROP is crucial for timely intervention.
- Pre-plus disease is an early indicator of potential ROP progression.
Purpose of the Study:
- To prospectively evaluate if pre-plus disease predicts the progression to severe ROP requiring laser treatment.
- To determine the prognostic value of pre-plus disease in ROP management.
Main Methods:
- Prospective study involving 214 premature infants over 5 years.
- Posterior retinal video recordings analyzed by masked experts for plus disease, pre-plus disease, or neither.
- Primary analysis focused on eyes at 33-34 weeks' postmenstrual age.
Main Results:
- Eyes with pre-plus disease at 33-34 weeks' postmenstrual age had a 70% rate of requiring laser treatment, compared to 9% for eyes without pre-plus or plus disease.
- Pre-plus disease independently predicted the need for laser treatment (adjusted odds ratio, 7.6).
- Laser treatment was typically administered 1.6 weeks after pre-plus disease diagnosis.
Conclusions:
- Early detection of pre-plus disease is a strong predictor of severe ROP requiring laser treatment.
- Pre-plus disease offers prognostic value beyond traditional ROP staging factors (birth weight, gestational age, zone, stage).
- Close observation of infants with pre-plus disease is recommended for optimal intervention timing.
Objectives:
To investigate prospectively whether the presence of pre-plus disease predicts progression to severe retinopathy of prematurity (ROP) requiring laser treatment.
Methods:
Posterior retinal video recordings were obtained during 710 indirect ophthalmoscopy examinations of 214 premature infants over a period of 5 years. Two masked experts reviewed short video recordings and determined whether there was plus disease, pre-plus disease, or neither. The primary analysis included results of one examination of the right eye at 33 to 34 weeks' postmenstrual age. The primary outcome was a comparison of the proportion of eyes subsequently requiring laser treatment between the group graded as having pre-plus disease vs the group graded as having neither plus disease nor pre-plus disease.
Results:
Of 10 eyes with pre-plus disease at 33 to 34 weeks' postmenstrual age, 7 (70%) subsequently required laser treatment; of 154 eyes without pre-plus disease or plus disease at 33 to 34 weeks' postmenstrual age, 14 (9%) subsequently required laser treatment (risk ratio, 7.7; 95% confidence interval, 4.1-14.8; P < .001). The mean time between the examination diagnosing pre-plus disease and laser treatment was 1.6 weeks (range, 1.0-2.4 weeks). When adjusting for birth weight, gestational age, ROP location (zone), and ROP severity (stage), the presence of pre-plus disease at 33 to 34 weeks' postmenstrual age independently predicted the need for laser treatment (adjusted odds ratio, 7.6; 95% confidence interval, 1.4-42.3; P = .02).
Conclusions:
Pre-plus disease observed early during the course of ROP is strongly associated with the development of severe ROP requiring laser treatment. The diagnosis of pre-plus disease has prognostic value beyond that already provided by birth weight, gestational age, ROP zone, and ROP stage. Eyes with pre-plus disease should be closely observed to allow optimal timing of intervention.
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