WINROP Algorithm Validation for Retinopathy Screening in a Cohort of Premature Infants

Central Hospital, Nancy, France

Status: Completed

Conditions: Retinopathy of Prematurity

Study type: Observational

Funder types: Other

Identifiers

NCT03347799

PSS2016/WINROP-HASCOET/VS

Details and patient eligibility

About

When a child was born too early, it is more likely to develop an alteration of its visual function than in the case of term birth. Significant visual disturbances are found in 3% of children born prematurely, but visual impairment can be very severe, up to the loss of vision in case of retinopathy of prematurity (ROP) in the most immature infants. The introduction of screening surveillance systems, such as WINROP software, might reduce the need for stressful eye examination in low risk neonates. This retrospective study aimed at validating the WINROP algorithm in a cohort of premature infants, born below 32 weeks of gestation, who had systematic eye examination for ROP screening over 4 year period.

Enrollment: 570 patients

Sex: All

Ages: 24 to 40 weeks old

Volunteers: No Healthy Volunteers

Inclusion criteria

• All infants born below 32 weeks gestation within the study period
• At least one eye examination recorded by Retcam

Exclusion criteria

• Any ophthalmic abnormality
• Any genetic abnormality