1. CHRONIC CENTRAL SEROUS CHORIORETINOPATHY
- Author
-
Mariacristina Parravano, Barbara Boccassini, Adele Chiaravalloti, Pierluigi Iacono, Massimiliano Tedeschi, and Monica Varano
- Subjects
Adult ,Male ,0301 basic medicine ,Fovea Centralis ,medicine.medical_specialty ,Time Factors ,Visual acuity ,endocrine system diseases ,Fundus Oculi ,medicine.medical_treatment ,Visual Acuity ,Photodynamic therapy ,Chronic central serous chorioretinopathy ,03 medical and health sciences ,0302 clinical medicine ,Ophthalmology ,Humans ,Medicine ,Prospective Studies ,Fluorescein Angiography ,Prospective cohort study ,Photosensitizing Agents ,medicine.diagnostic_test ,Choroid ,business.industry ,Follow up studies ,Verteporfin ,General Medicine ,Fluorescein angiography ,eye diseases ,Serous fluid ,030104 developmental biology ,Central Serous Chorioretinopathy ,Photochemotherapy ,Chronic Disease ,030221 ophthalmology & optometry ,Female ,medicine.symptom ,business ,Tomography, Optical Coherence ,Follow-Up Studies ,medicine.drug - Abstract
To describe early and late morphological and functional changes in subjects receiving photodynamic therapy (PDT) for chronic central serous chorioretinopathy.Patients with chronic central serous chorioretinopathy were prospectively enrolled and received standard PDT. At the baseline examination, each subject underwent complete ophthalmological examination, including best-corrected visual acuity (BCVA) assessment, fluorescein angiography and indocyanine green angiography, spectral domain optical coherence tomography, and microperimetry. Spectral domain optical coherence tomography, microperimetry, and BCVA assessment were repeated in multiple sections over 7 days after PDT and at 1-, 3-, and 12-month intervals. Main outcome measures were: identification of early changes (1-week examination) in BCVA, retinal sensitivity, and spectral domain optical coherence tomography parameters and their influence on outcomes at the 1-year follow-up.Three main patterns of early response to PDT were identified during the 1-week examination. The neurosensory retinal detachment most frequently decreased rapidly (12/19 pts), with complete resolution in 50% of cases. An increase in neurosensory retinal detachment height was registered in 16% (3/19) of cases, whereas in 21% (4/19), a large fluctuation in neurosensory retinal detachment was encountered. Best-corrected visual acuity declined significantly in 5/12 patients in the first group and was stable or improved in the remaining cases. Overall, retinal sensitivity diminished in 16/19 subjects, with a mean worsening of 2.56 dB (P = 0.0002). At the 12-month examination, final mean BCVA improved by 14.4 letters (P = 0.001) and a similar progressive recovery in the retinal sensitivity was observed (+2.69 dB, P = 0.0039). The neurosensory retinal detachment completely resolved in 18/19 (95%) cases, with a parallel significant reduction in central foveal choroidal thickness (P0.0001).Three patterns of early response to standard PDT can be identified. Although an early and abrupt reduction in BCVA and retinal sensitivity after treatment is possible, this does not compromise a final improvement in visual functions.
- Published
- 2019
- Full Text
- View/download PDF