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Polypoidal choroidal vasculopathy: Pearls in diagnosis and management
Giridhar Anantharaman1, Jay Sheth1, Muna Bhende2
1Department of Vitreoretina, Giridhar Eye Institute, Kochi, Kerala, India.
Insights
Polypoidal choroidal vasculopathy (PCV) is a key cause of exudative maculopathy in Asians. Expert consensus provides updated guidelines for diagnosing and managing PCV, improving patient outcomes.
Area of Science:
- Ophthalmology
- Retinal Diseases
- Medical Imaging
Background:
- Polypoidal choroidal vasculopathy (PCV) is a significant cause of exudative maculopathy, particularly in Asian populations.
- It is often distinguished from wet age-related macular degeneration, more common in Caucasians.
Purpose of the Study:
- To establish consensus recommendations for the diagnosis, management, and follow-up of PCV.
- To provide guidance for retinal specialists based on a systematic literature review.
Main Methods:
- A panel of retinal experts conducted a methodical evaluation of updated literature on PCV.
- A comprehensive PubMed/MEDLINE search was performed to identify relevant studies.
- Consensus was reached on diagnostic criteria, imaging interpretation, and treatment strategies.
Main Results:
- Indocyanine green angiography (ICGA) is the gold standard for PCV diagnosis, showing characteristic polypoid lesions and abnormal vascular networks (AVN).
- Optical coherence tomography (OCT) serves as an essential adjuvant for diagnosis, monitoring disease activity, and guiding treatment decisions.
- Treatment options include photodynamic therapy, anti-VEGF agents, and thermal laser, with choices influenced by lesion characteristics and disease severity.
Conclusions:
- The consensus recommendations offer a framework for accurate PCV diagnosis using ICGA and OCT.
- Individualized treatment strategies considering various clinical factors are crucial for optimal PCV management.
- These guidelines aim to enhance physician decision-making and improve patient outcomes in PCV.
Abstract:
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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