EFFECT OF RANIBIZUMAB AND AFLIBERCEPT ON RETINAL PIGMENT EPITHELIAL DETACHEMENT, SUBRETINAL AND INTRARETINAL FLUID IN AGE-RELATED MACULAR DEGENERATION
Language English Country Czech Republic Media print
Document type Journal Article
PubMed
35922146
DOI
10.31348/2022/20
PII: 131365
Knihovny.cz E-resources
- Keywords
- aflibercept, age related macular degeneration, age-related macular degeneration, intraretinal fluid, pigment epithelium detachment, ranibizumab, subretinal fluid,
- MeSH
- Angiogenesis Inhibitors pharmacology therapeutic use MeSH
- Intravitreal Injections MeSH
- Humans MeSH
- Retinal Detachment * diagnosis MeSH
- Tomography, Optical Coherence MeSH
- Ranibizumab therapeutic use MeSH
- Receptors, Vascular Endothelial Growth Factor MeSH
- Recombinant Fusion Proteins therapeutic use MeSH
- Retinal Pigments therapeutic use MeSH
- Retrospective Studies MeSH
- Vascular Endothelial Growth Factor A MeSH
- Wet Macular Degeneration * diagnosis drug therapy MeSH
- Visual Acuity MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- aflibercept MeSH Browser
- Angiogenesis Inhibitors MeSH
- Ranibizumab MeSH
- Receptors, Vascular Endothelial Growth Factor MeSH
- Recombinant Fusion Proteins MeSH
- Retinal Pigments MeSH
- Vascular Endothelial Growth Factor A MeSH
PURPOSE: The aim of the study was to compare the effect of three initial doses of the anti-VEGF ranibizumab and aflibercept medication on serous pigment epithelial detachment (PED), subretinal fluid (SRF) and intraretinal fluid (IRF) in the macula of treatment naive neovascular AMD (nvAMD) patients. MATERIAL AND METHODS: The cohort consists of 148 patients, of which 74 patients were treated with ranibizumab (51 females and 23 males) and 74 with aflibercept (46 females and 28 males). The data was recorded prospectively from the moment of diagnosis and start of treatment for a period of 3 months. At the moment of diagnosis and 3 months later, an OCT examination (Spectralis OCT, Heidelberg Engineering, Heidelberg, Germany) was performed. The OCT examination included a macular scan with 25 scans. Using the OCT instrument software, we measured the maximum anterior-posterior elevation of serous PED, the highest thickness of SRF and the largest diameter of the intraretinal cystic space. The statistical significance of differences between groups was evaluated using the t-test for continuous data and the Fisher exact test for categorical data. Changes in values of continuous variables over time were evaluated using the Wilcoxon paired test. Paired comparisons of binary parameters were determined by the McNemar test. RESULTS: Full regression of PED, SRF and IRF occurred in 3 (4.1%), 25 (39%) and 20 (51%) patients treated with ranibizumab, and in 5 (7.9%, p = 0.470), 28 (47%, p = 0.470) and 25 (57%, p = 0.827) patients treated with aflibercept, respectively. The average regression of PED, SRF and IRF was -60.4 μm (median -37.5 μm), -84.3 μm (median -85 μm) and -109.3 μm (median -81 μm) in patients treated with ranibizumab, and -46.3 μm (median -30 μm, p = 0.389), -127.7 μm (median -104 μm, p = 0.096) and -204.4 μm (median -163 μm, p = 0.005) in patients treated with aflibercept, respectively. We did not show a statistically significant difference in the regression rates of PED, SRF and IRF between the ranibizumab and aflibercept groups. (in patients with IRF after adjustment of the higher baseline IRF volumes in patients treated with aflibercept, p = 0.891). CONCLUSION: We are convinced that ranibizumab and aflibercept have the same effect on serous PED, SRF and IRF in the macula in patients with treatment naive nvAMD during the initial loading phase.
References provided by Crossref.org