ROP is a condition caused by abnormal development of retinal blood vessels, occurring as a complication of preterm birth and/or low birth weight. ROP may lead to partial or complete vision loss if the condition is severe and the retina detaches. Effective screening, timely treatment, and ongoing eye care are essential for preventing ROP- associated vision loss. ROP is a leading cause of lifelong visual impairment.
ROP resources from Prevent Blindness include fact sheets, web pages, social media graphics in English and Spanish, and medical expert and patient testimonial videos. The ROP Education and Support Initiative and ROP Awareness Week are supported by funding from Regeneron Pharmaceuticals, Inc.
In addition to family and patient assistance, the ROP Education and Support Initiative provides expert-approved materials for healthcare professionals about creating a holistic support system for families and children with ROP after they leave the neonatal intensive care unit (NICU). Materials are specifically tailored for neonatologists, nurses, professionals who serve babies in the NICU, and professionals in the healthcare, early care and education, and school systems. Prevent Blindness collaborates with leading parent and advocacy organizations, including Hand to Hold, National Coalition for Infant Health, and the SPAN Parent Advocacy Network, in this effort.
During ROP Awareness Week, Prevent Blindness will debut a new Focus on Eye Health Series episode featuring NICU parent Tracy P., who will share her experience navigating the ROP diagnosis and care for her child with ROP. Also, as part of the February episode of the Prevent Blindness Focus on Eye Health Podcast, Daria B. discusses her experience as a person living with ROP and how access to education, resources, and support, like the Prevent Blindness ASPECT Patient Engagement Program, have helped her.
Additionally, the National Center for Children’s Vision and Eye Health at Prevent Blindness (NCCVEH) is seeking parents or guardians with a child aged 10 years or younger who has spent time in the NICU and has been diagnosed with ROP. The purpose is to conduct these focus groups to gain a better understanding of:
- Experiences families have had when their child has been in the neonatal intensive care unit (NICU), diagnosed with retinopathy of prematurity (ROP)
- Families’ journeys raising a child with ROP in relation to medical care, social/emotional support, and educational services
- Barriers families experience in accessing and attending eye care appointments for their child’s ROP
- The incidence and prevalence of ROP among Medicaid-enrolled infants, providing a robust estimation of disease burden
- Examine geographic variation, highlighting areas or regions with especially high concentrations of ROP
- Assess demographics and clinical characteristics of ROP patients including gestational age, comorbidities, and other factors relevant to ROP risk and treatment
- Evaluate healthcare utilization patterns, such as screening frequencies, follow-up services, and treatment adoption, to identify potential gaps in care
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