Korean J Ophthalmol.  2017 Jun;31(3):209-216. 10.3341/kjo.2015.0158.

Comparison of Ranibizumab and Bevacizumab for Macular Edema Associated with Branch Retinal Vein Occlusion

Affiliations
  • 1Department of Ophthalmology, Kyung Hee University Medical Center, Kyung Hee University School of Medicine, Seoul, Korea. hwkwak@khu.ac.kr

Abstract

PURPOSE
To assess the effectiveness and safety of intravitreal ranibizumab compared with bevacizumab for the treatment of macular edema associated with branch retinal vein occlusion (BRVO).
METHODS
This was a retrospective study of 80 eyes with macular edema associated with BRVO. Patients received either 0.5 mg of ranibizumab (n = 24) or 1.25 mg of bevacizumab (n = 56) intravitreally. Both groups received three initial monthly injections followed by as-needed injections. The best-corrected visual acuity, central subfield thickness, mean number of injections, and retreatment rate were evaluated monthly for 6 months after the initial injection.
RESULTS
The best-corrected visual acuity significantly improved from logarithm of the minimal angle of resolution (logMAR) 0.55 ± 0.26 at baseline to 0.24 ± 0.26 at 6 months in the ranibizumab group (p < 0.001) and from logMAR 0.58 ± 0.21 at baseline to 0.29 ± 0.25 at 6 months in the bevacizumab group (p < 0.001), which is not a statistically significant difference (p = 0.770). The mean reduction in central subfield thickness at 6 months was 236 ± 164 µm in the ranibizumab group (p < 0.001) and 219 ± 161 µm in the bevacizumab group (p < 0.001), which is not also a statistically significant difference (p = 0.698). The mean numbers of ranibizumab and bevacizumab injections were 3.25 ± 0.53 and 3.30 ± 0.53, respectively (p = 0.602). In addition, after the three initial monthly injections, the retreatment rates for ranibizumab and bevacizumab injections were 20.8% and 26.7%, respectively (p = 0.573).
CONCLUSIONS
Both ranibizumab and bevacizumab were effective for the treatment of BRVO and produced similar visual and anatomic outcomes. In addition, the mean number of injections and the retreatment rates were not significantly different between the groups.

Keyword

Bevacizumab; Branch retinal vein occlusion; Macular edema; Ranibizumab

MeSH Terms

Bevacizumab*
Humans
Macular Edema*
Ranibizumab*
Retinal Vein Occlusion*
Retinal Vein*
Retinaldehyde*
Retreatment
Retrospective Studies
Visual Acuity
Bevacizumab
Ranibizumab
Retinaldehyde

Figure

  • Fig. 1 Change in best-corrected visual acuity (BCVA). Mean logarithm of the minimal angle of resolution (logMAR, visual acuity) significantly improved after treatment with ranibizumab or bevacizumab from baseline to 6 months (*significantly different from baseline, p < 0.05). IVL = ranibizumab; IVA = bevacizumab.

  • Fig. 2 Change in central subfield thickness. Mean central subfield thickness significantly decreased after treatment with ranibizumab or bevacizumab from baseline to 6 months (*significantly different from baseline, p < 0.05). IVL = ranibizumab; IVA = bevacizumab.

  • Fig. 3 Number of injections. In the ranibizumab group, 19 (79%) patients had three injections, four (17%) had four injections, and 1 (4%) received five injections. In the bevacizumab group, 41 (73%) patients had three injections, 13 (23%) had four injections, and two (4%) received five injections. IVL = ranibizumab; IVA = bevacizumab.


Cited by  1 articles

A Comparison of Three Intravitreal Modalities of Branch Retinal Vein Occlusion Macular Edema
Han Song, Hee Jun Song, Ji Ho Yang, Do Gyun Kim
J Korean Ophthalmol Soc. 2018;59(9):834-841.    doi: 10.3341/jkos.2018.59.9.834.


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