Abstract | BACKGROUND: METHODS: Fifteen patients were included in a prospective interventional case series. Verteporfin PDT as a bolus infusion of 6 mg/m body surface area and a light dose of 100 J/cm at 689 nm applied over 166 seconds were administered. Standardized evaluation was performed every 3 months within the first year and at 12-month intervals during follow-up. RESULTS: At baseline, all patients presented with significant vision loss ranging from 20/26 to 20/500. During a mean follow-up of 36.6 months (range, 12-66 months), no patient had evidence of recurrence. Mean final visual acuity ranged from 20/20 to 20/400. In all patients, complete and permanent regression with no signs of tumor regrowth or recurring subretinal fluid was found. Of 15 patients, 13 had a substantial increase in visual acuity (range, 2-9 lines), and 2 patients' visual acuity remained stable. Chorioretinal atrophy at the previous tumor site did not enlarge over time. Retreatments after completion of the primary treatment were not necessary. CONCLUSION: Persistent and complete absence of choroidal hemangioma associated with persistent improvement in visual acuity and central visual fields can be obtained with verteporfin PDT.
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Authors | Stephan Michels, Rike Michels, Christian Simader, Ursula Schmidt-Erfurth |
Journal | Retina (Philadelphia, Pa.)
(Retina)
Vol. 25
Issue 6
Pg. 697-703
(Sep 2005)
ISSN: 0275-004X [Print] United States |
PMID | 16141856
(Publication Type: Journal Article)
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Chemical References |
- Photosensitizing Agents
- Porphyrins
- Verteporfin
- Indocyanine Green
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Topics |
- Choroid Neoplasms
(diagnostic imaging, drug therapy, pathology)
- Fluorescein Angiography
- Follow-Up Studies
- Hemangioma
(diagnostic imaging, drug therapy, pathology)
- Humans
- Indocyanine Green
- Photochemotherapy
- Photosensitizing Agents
(therapeutic use)
- Porphyrins
(therapeutic use)
- Prospective Studies
- Treatment Outcome
- Ultrasonography
- Verteporfin
- Visual Acuity
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