4.6 Article

Half-Dose Photodynamic Therapy Versus Eplerenone in Chronic Central Serous Chorioretinopathy (SPECTRA): A Randomized Controlled Trial

Journal

AMERICAN JOURNAL OF OPHTHALMOLOGY
Volume 233, Issue -, Pages 101-110

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ajo.2021.06.020

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Funding

  1. Stichting Macula Fonds
  2. Retina Nederland Onderzoek Fonds
  3. Stichting Blinden-Penning
  4. Algemene Nederlandse Vereniging ter Voorkoming van Blindheid
  5. Landelijke Stichting voor Blinden en Slechtzienden
  6. Oogfonds
  7. Rotterdamse Stichting Blindenbelangen (Rotterdam, the Netherlands)
  8. Stichting Leids Oogheelkundig Ondersteuningsfonds (Leiden, the Netherlands)
  9. Haagse Stichting Blindenhulp (The Hague, the Netherlands)
  10. Stichting Ooglijders (Rotterdam, the Netherlands)
  11. Gisela Thier Fellowship of Leiden University, Leiden
  12. Netherlands Organization for Scientific Research (VENI)

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This study compared the efficacy and safety of half-dose photodynamic therapy and eplerenone therapy for treating chronic central serous chorioretinopathy. The results showed that half-dose PDT was superior to eplerenone treatment in terms of short-term safety and efficacy outcomes.
PURPOSE: To compare the efficacy and safety between half-dose photodynamic therapy (PDT) and eplerenone therapy for treating chronic central serous chorioretinopathy (cCSC). DESIGN: This was a multicenter, open-label, randomized controlled trial. METHODS: This investigator-initiated trial was conducted in 3 academic medical centers in the Netherlands. Eligible patients were randomized at a 1:1 ratio to receive either indocyanine green angiography-guided half dose PDT or oral eplerenone for 12 weeks. Both anatomical and functional outcomes were evaluated at 3 months after the start of treatment. RESULTS: A total of 107 patients were randomly assigned to receive either half-dose PDT (n = 53) or eplerenone treatment (n = 54). Thirteen patients (3 in the PDT group and 10 in the eplerenone group) did not adhere to the study protocol. At the 3-month evaluation visit, 78% of patients in the PDT group had complete resolution of subretinal fluid accumulation compared to only 17% of patients in the eplerenone group (P < .001). Mean best-corrected visual acuity in Early Treatment of Diabetic Retinopathy Study letters at the 3-month evaluation visit was 83.7 +/- 10.8 and 82.8 +/- 9.0 in the PDT and eplerenone groups, respectively (P = .555). In addition, mean retinal sensitivity on microperimetry was 25.4 +/- 3.4 dB and 23.9 +/- 4.0 dB in the PDT and eplerenone groups, respectively (P = .041). Finally, mean vision related quality of life scores were 87.2 +/- 8.5 and 83.8 +/- 12.1 in the PDT and eplerenone groups, respectively (P = .094). Three patients (6%) in the PDT group experienced adverse events during the study compared to 18 patients (33%) in the eplerenone group. CONCLUSIONS: Half-dose PDT is superior to oral eplerenone for cCSC with respect to both short-term safety and efficacy outcomes. (C) 2021 Published by Elsevier Inc.

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