Anatomical and Functional Outcomes with Prompt versus Delayed Initiation of Anti-VEGF in Exudative Age-Related Macular Degeneration
- PMID: 38202118
- PMCID: PMC10779608
- DOI: 10.3390/jcm13010111
Anatomical and Functional Outcomes with Prompt versus Delayed Initiation of Anti-VEGF in Exudative Age-Related Macular Degeneration
Abstract
Purpose: To investigate the correlation between time from diagnosis of treatment-naïve exudative age-related macular degeneration (AMD) to the introduction of anti-VEGF treatment and anatomical and functional outcomes.
Design: Retrospective cohort study.
Methods: Included were treatment-naïve exudative AMD patients who presented to a single tertiary medical center between 2012 and 2018. All patients were treated within the first 30 days of their diagnosis with three monthly intravitreal injections of bevacizumab. Patients were divided into three groups: group 1 (prompt anti-VEGF) were injected with bevacizumab within ten days, group 2 (intermediate anti-VEGF) within 11-20 days, and group 3 (delayed anti-VEGF) within 21-30 days from diagnosis. Baseline characteristics and clinical outcomes were compared up to two years from treatment.
Results: 146 eyes of 146 patients were included. Sixty-eight patients were in the prompt anti-VEGF group, 31 in the intermediate anti-VEGF group, and 47 in the delayed anti-VEGF group. Following the induction phase of three intravitreal bevacizumab injections, the mean central subfield macular thickness (328.0 ± 115.4 µm vs. 364.6 ± 127.2 µm vs. 337.7 ± 150.1 µm, p = 0.432) and the best-corrected visual acuity (0.47 ± 0.38 vs. 0.59 ± 0.48 vs. 0.47 ± 0.44 logMAR units, p = 0.458) were comparable between the prompt, intermediate and delayed anti-VEGF groups. Anatomical and functional outcomes, treatment burden, number of relapses and eyes with second-line anti-VEGF therapy were comparable between the groups at both 1-year and 2-year timepoints.
Conclusions: Our real-world evidence data emphasize that even if anti-VEGF induction cannot be initiated promptly within ten days from diagnosis of naïve exudative AMD, the visual and anatomical prognosis of the patients may not worsen if the treatment is started within one month of diagnosis.
Keywords: anti-VEGF; bevacizumab; central subfield macular thickness; exudative age-related macular degeneration; intravitreal treatment; treatment-naïve.
Conflict of interest statement
The authors declare no conflict of interest.
Figures

Similar articles
-
[Neovascular recurrences in 42 treatment-naive eyes with neovascular age-related macular degeneration (AMD) followed for over 2 years].J Fr Ophtalmol. 2021 May;44(5):626-631. doi: 10.1016/j.jfo.2020.08.030. Epub 2021 Apr 8. J Fr Ophtalmol. 2021. PMID: 33840491 French.
-
Real-World Treatment Outcomes of Age-Related Macular Degeneration and Polypoidal Choroidal Vasculopathy in Asians.Ophthalmol Retina. 2020 Apr;4(4):403-414. doi: 10.1016/j.oret.2019.10.019. Epub 2019 Nov 9. Ophthalmol Retina. 2020. PMID: 31953109
-
VITREOMACULAR TRACTION AFFECTS ANTI-VASCULAR ENDOTHELIAL GROWTH FACTOR TREATMENT OUTCOMES FOR EXUDATIVE AGE-RELATED MACULAR DEGENERATION.Retina. 2015 Sep;35(9):1750-6. doi: 10.1097/IAE.0000000000000714. Retina. 2015. PMID: 26237240
-
Aflibercept administration in neovascular age-related macular degeneration refractory to previous anti-vascular endothelial growth factor drugs: a critical review and new possible approaches to move forward.Angiogenesis. 2015 Oct;18(4):397-432. doi: 10.1007/s10456-015-9483-4. Epub 2015 Sep 7. Angiogenesis. 2015. PMID: 26346237 Review.
-
Radiotherapy for neovascular age-related macular degeneration.Cochrane Database Syst Rev. 2020 Aug 26;8(8):CD004004. doi: 10.1002/14651858.CD004004.pub4. Cochrane Database Syst Rev. 2020. PMID: 32844399 Free PMC article.
References
-
- Burgess D.B., Hawkins B.S., Jefferys J.L., Bressler N.M., Bressler S.B., Hiner C.J., Javornik N.B., Orth D.H., Wilkinson C.P. MPSG Five-Year Follow-up of Fellow Eyes of Patients with Age-Related Macular Degeneration and Unilateral Extrafoveal Choroidal Neovascularization. Arch. Ophthalmol. 1993;111:1189–1199. doi: 10.1001/ARCHOPHT.1993.01090090041018. - DOI - PubMed
LinkOut - more resources
Full Text Sources