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Stage 5 retinopathy of prematurity: An update
Parveen Sen1, Smriti Jain1, Pramod Bhende1
1Shri Bhagwan Mahavir Vitreoretinal Services, Medical Research Foundation, Sankara Nethralaya, Chennai, Tamil Nadu, India.
Insights
Stage 5 Retinopathy of Prematurity (ROP) is a severe form of preventable childhood blindness requiring complex surgery. Early detection and treatment are crucial, as surgical outcomes for advanced ROP are often limited.
Area of Science:
- Ophthalmology
- Pediatrics
- Genetics
Background:
- Retinopathy of prematurity (ROP) is a leading cause of preventable childhood blindness.
- Many infants present with advanced, blinding Stage 5 ROP due to lack of awareness, particularly in developing nations.
- Stage 5 ROP involves total retinal detachment, necessitating complex surgical management.
Purpose of the Study:
- To provide a comprehensive overview of Stage 5 Retinopathy of Prematurity.
- To discuss the pathogenesis, clinical aspects, surgical interventions, and outcomes of advanced ROP.
- To highlight the need for improved screening, treatment guidelines, and parental education.
Main Methods:
- Review of existing literature on Stage 5 Retinopathy of Prematurity.
- Analysis of surgical techniques and their anatomical and visual outcomes.
- Discussion of potential genetic predispositions and emerging pharmacological adjuncts.
Main Results:
- Surgical success rates for anatomical outcomes in Stage 5 ROP range from 20%-50%.
- Visual outcomes after successful surgery are often slow to develop and remain limited.
- Newer pharmacological treatments show promise in managing ROP.
Conclusions:
- Effective screening and treatment guidelines involving pediatricians and ophthalmologists are essential to prevent ROP-related blindness.
- Surgical management for Stage 5 ROP has limited success rates, and parents must be informed about potential visual benefits and follow-up needs.
- Further research into genetic factors and novel therapies is warranted for improved ROP management.
Abstract:
Retinopathy of prematurity (ROP) is one of the most common causes of preventable blindness in children. In spite of the availability of various treatment options, and favorable results with timely intervention, many infants present to the ophthalmologists in the advanced end stage of the disease due to lack of awareness especially in the developing nations. This blinding or Stage 5 of ROP presents with total retinal detachment and has to be managed surgically. The surgical techniques for Stage 5 ROP are unique and demanding. The successful anatomical results after surgery are only seen in 20%-50% of cases. In spite of a successful anatomical result, the visual outcome may be slow and limited. The use of newer pharmacological adjuncts has shown promising results. Because of heterogeneity of presentation of the disease severity, a genetic predisposition has also been proposed. A concerted effort from the pediatricians, ophthalmologists, and healthcare workers is required to establish effective screening and treatment guidelines to prevent blindness due to ROP. Till then surgical management has to be done. Parents must be educated regarding the limited visual benefits of surgery and the need for prolonged follow-up. This review gives a comprehensive overview of the pathogenesis, clinical aspects, surgical interventions, and their outcomes and future prospects of Stage 5 ROP.
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