June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
Intravitreal Ranibizumab for Acute Central Serous Chorioretinopathy
Author Affiliations & Notes
  • SEUNG JUN LEE
    Ophthalmology, Kangwon National University Hospital, Chuncheon, Republic of Korea
  • Footnotes
    Commercial Relationships SEUNG JUN LEE, None
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Investigative Ophthalmology & Visual Science June 2013, Vol.54, 2811. doi:
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      SEUNG JUN LEE; Intravitreal Ranibizumab for Acute Central Serous Chorioretinopathy. Invest. Ophthalmol. Vis. Sci. 2013;54(15):2811.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: To evaluate the effectiveness of intravitreal ranibizumab injection (IVRI) for acute central serous chorioretinopathy (CSC).

Methods: Patients with symptomatic CSC of less than 3 months were prospectively recruited. Patients (n = 20/group) were randomly assigned to IVRI (0.5 mg/0.05 ml) or observation and followed for 6 months. LogMAR best-corrected visual acuity (BCVA), fluorescein angiography, indocyanine angiography, and central foveal thickness (CFT) were assessed at baseline and at regular follow-ups.

Results: All patients had increased BCVA, decreased CFT, and resolution of the neurosensory detachment. Complete resolution of neurosensory retinal detachment required more time in the observation group (13.0 ± 3.1 vs. 4.2 ± 0.9 weeks; p < 0.001). Mean BCVA and mean CFT improved significantly in both groups, but the changes were not significantly different between groups at 6 months.

Conclusions: IVRI for acute CSC might hasten resolution of neurosensory detachment compared to observation alone. At 6 months, BCVA and CFT did not differ between IVRI and observation groups. Further studies are required to determine the long-term benefits of IVRI.

Keywords: 688 retina • 585 macula/fovea • 452 choroid  
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