Visual prognosis of posterior and combined persistent fetal vasculature

Veronique Promelle1,2, Sophie Bryselbout1, Solange Milazzo1,2

  • 1Ophthalmology Department, Amiens Picardie University Hospital Center, Amiens, France.

Insights

Persistent fetal vasculature (PFV) posterior and combined forms have poor visual outcomes. Surgery may be needed for severe cases to achieve results comparable to patching for moderate PFV.

Area of Science:

  • Ophthalmology
  • Pediatric Ophthalmology
  • Congenital Eye Anomalies

Background:

  • Persistent fetal vasculature (PFV) involves congenital anomalies from abnormal hyaloid vascular system persistence.
  • PFV can manifest as anterior, posterior, or combined forms, impacting visual development.
  • Understanding visual outcomes in posterior and combined PFV is crucial for timely intervention.

Purpose of the Study:

  • To evaluate and report the visual outcomes for patients with posterior and combined forms of persistent fetal vasculature.
  • To compare the effectiveness of different treatment modalities on visual acuity in PFV patients.

Main Methods:

  • A retrospective, single-center study analyzed patients with posterior or combined PFV.
  • Visual acuity was the primary endpoint, assessed at the study's conclusion.
  • Data included patient demographics, PFV form, and treatment received (surgery, patching, or none).

Main Results:

  • 18 eyes from 14 patients (10 male) were included; 12/18 had the combined form, and 4/14 had bilateral PFV.
  • Visual acuity ranged from 20/2000 to 20/25.
  • Surgical intervention (cataract extraction, phacovitrectomy) yielded a best visual acuity of 20/63, while patching for amblyopia resulted in 20/100. One untreated patient achieved 20/25.

Conclusions:

  • Posterior and combined PFV forms are associated with a generally poor visual prognosis.
  • Severe or occulting PFV presentations necessitate surgical intervention for optimal visual outcomes.
  • Surgical results can be comparable to those achieved with patching therapy in moderate PFV cases.
Abstract

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