Clinical features and follow-up results of pulsating polypoidal choroidal vasculopathy treated with photodynamic therapy
Article first published online: 26 JUN 2009
DOI: 10.1111/j.1755-3768.2009.01517.x
© 2009 The Authors. Journal compilation © 2009 Acta Ophthalmol
Additional Information
How to Cite
Byeon, S. H., Lew, Y. J., Lee, S. C. and Kwon, O. W. (2010), Clinical features and follow-up results of pulsating polypoidal choroidal vasculopathy treated with photodynamic therapy. Acta Ophthalmologica, 88: 660–668. doi: 10.1111/j.1755-3768.2009.01517.x
Publication History
- Issue published online: 27 AUG 2010
- Article first published online: 26 JUN 2009
- Received on April 4th, 2008. Accepted on November 29th, 2008.
- Abstract
- Article
- References
- Cited By
Keywords:
- haemorrhage;
- photodynamic therapy (PDT);
- polypoidal choroidal vasculopathy (PCV);
- pulsatile blood flow;
- pulsation
Acta Ophthalmol. 2010: 88: 660–668
Abstract.
Purpose: To report on the clinical course of pulsating polypoidal choroidal vasculopathy (PCV) treated with photodynamic therapy (PDT).
Methods: A total of 63 eyes of 58 consecutive patients diagnosed with PCV, treated with PDT and followed up for at least 6 months were enrolled. Best-corrected visual acuity (BCVA), fluorescein angiography and high-speed indocyanine green angiography (ICGA) using confocal scanning laser ophthalmoscopy (HRA) were performed.
Results: Of the 63 PCV eyes, 14 eyes (22.2%) of 14 patients were classified as having pulsating PCV. The mean age of pulsating PCV patients was 60.6 ± 7.0 years (48–69 years), which was younger than non-pulsating PCV patients (65.7 years, p = 0.035). The mean follow-up period was 23.9 ± 10.7 months, and PDT was administered 1.6 ± 0.9 times to pulsating PCV patients. The mean logMAR BCVAs were 0.85 ± 0.47 at presentation and 0.71 ± 0.52 at final examination. Extensive haemorrhagic events were more common in pulsating than in non-pulsating PCV patients (57.1% versus 26.5%, p = 0.032). However, the risk of haemorrhage within 3 months of PDT was similar for both pulsating PCV and the remaining patients (14.3% versus 20%, p = 0.723).
Conclusion: Pulsating PCV showed distinctive features including a relatively younger patient age at presentation, and a haemorrhagic tendency (especially extensive). However, the use of PDT did not directly increase the risk of haemorrhage in pulsating PCV patients.

1755-3768/asset/olbannercenter.gif?v=1&s=baf172706d8b0315485b0acf45bb6cfebe7a6ecc)
