Indian Journal of Ophthalmology (Jan 2018)

Polypoidal choroidal vasculopathy: Pearls in diagnosis and management

  • Giridhar Anantharaman,
  • Jay Sheth,
  • Muna Bhende,
  • Raja Narayanan,
  • Sundaram Natarajan,
  • Anand Rajendran,
  • George Manayath,
  • Parveen Sen,
  • Rupak Biswas,
  • Alay Banker,
  • Charu Gupta

DOI
https://doi.org/10.4103/ijo.IJO_1136_17
Journal volume & issue
Vol. 66, no. 7
pp. 896 – 908

Abstract

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Polypoidal choroidal vasculopathy (PCV) is increasingly recognized as an important cause of exudative maculopathy in Asians as against Wet age-related macular degeneration in Caucasians. A panel of retinal experts methodically evaluated pertinent updated literature on PCV with thorough PubMed/MEDLINE search. Based on this, the panel agreed upon and proposed the current consensus recommendations in the diagnosis (clinical and imaging), management and follow-up schedule of PCV. Diagnosis of PCV should be based on the gold standard indocyanine green angiography which demonstrates early nodular hyperfluorescence signifying the polyp with additional features such as abnormal vascular network (AVN). Optical coherence tomography is an excellent adjuvant for diagnosing PCV, monitoring disease activity, and decision-making regarding the treatment. Current treatment modalities for PCV include photodynamic therapy, anti-vascular endothelial growth factor agents, and thermal laser. Choice of specific treatment modality and prognosis depends on multiple factors such as the location and size of PCV lesion, presence or absence of polyp with residual AVN, amount of submacular hemorrhage, presence or absence of leakage on fundus fluorescein angiography, visual acuity, and so on. Current recommendations would be invaluable for the treating physician in diagnosing PCV and in formulating the best possible individualized treatment strategy for optimal outcomes in PCV management.

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