Effects of treatment interruption on anatomical and functional status of eyes with neovascular age-related macular degeneration receiving anti-VEGF therapy

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AIM: To study anatomical and functional changes in eyes with neovascular age-related macular degeneration (AMD) receiving anti-VEGF therapy and experienced treatment interruption during COVID pandemic.

MATERIAL AND METHODS: This retrospective study included 58 eyes (49 patients, 34 males and 15 females with a mean age of 73.2 ± 9.4 years) with nAMD. Eyes in the first-year treatment group (18 eyes) received up to 7 intravitreal aflibercept injections, eyes in the second-year treatment group (21 eyes) were treated with pro re nata regimen. The treatment interruption period in the first and second-year treatment group was 5.5 ± 0.7 and 5.5 ± 1.0 months, respectively.

RESULTS: Over the treatment interruption period, the first-year treatment group showed no statistically significant differences in best-corrected visual acuity (BCVA) and central retinal thickness (CRT), p = 0.25 and p = 0.09, respectively. At the same time, the second-year treatment group showed a statistically significant decrease in BCVA (p = 0.0004) and an increase in CRT (p = 0.002). Baseline BCVA was positively associated with BCVA at the end of treatment interruption (r = 0.82; p < 0.0001). Presence of sub- and intraretinal fluid (p = 0.015 and p = 0.007, respectively), low BCVA (p < 0.0001), high CRT (p = 0.019), alteration of the ellipsoid zone (p < 0.001) were negatively associated with BCVA at the end of treatment interruption. Age (p = 0.8), gender (p = 0.41), and the number of intravitreal injections (p = 0.5) showed no association with changes in BCVA.

CONCLUSIONS: NAMD patients of the second year of anti-VEGF therapy appear to have a higher risk of functional loss during treatment interruption. Higher CRT and lower BCVA, as well as sub- and intraretinal fluid before treatment interruption, are associated with poorer functional status at the end of the interruption period.

作者简介

Alexandr Kharakozov

S.M. Kirov Military Medical Academy

编辑信件的主要联系方式.
Email: kharakozoff@mail.ru
ORCID iD: 0000-0003-4598-0826
SPIN 代码: 1208-5237

graduated

俄罗斯联邦, 6 Aсademiс Lebedev str., Saint Petersburg, 194044

Alexey Kulikov

S.M. Kirov Military Medical Academy

Email: alexey.kulikov@mail.ru
ORCID iD: 0000-0002-5274-6993
SPIN 代码: 6440-7706
Scopus 作者 ID: 57001225300
Researcher ID: M-2094-2016

MD, PhD, Dr. Sci. (Med.)

俄罗斯联邦, 6 Aсademiс Lebedev str., Saint Petersburg, 194044

Dmitrii Maltsev

S.M. Kirov Military Medical Academy

Email: glaz.med@yandex.ru
ORCID iD: 0000-0001-6598-3982

MD, PhD

俄罗斯联邦, 6 Aсademiс Lebedev str., Saint Petersburg, 194044

参考

  1. Regillo CD, Busbee BG, Ho AC, et al. Baseline predictors of 12-Month treatment response to ranibizumab in patients with wet age-related macular degeneration. Am J Ophthalmol. 2015;160(5):1014–1023. doi: 10.1016/j.ajo.2015.07.034
  2. Hayashi H, Yamashiro K, Tsujikawa A, et al. Association between foveal photoreceptor integrity and visual outcome in neovascular age-related macular degeneration. Am J Ophthalmol. 2009;148(1):83–89. doi: 10.1016/j.ajo.2009.01.017
  3. Kharakozov AS, Kulikov AN, Maltsev DS. Predictors of functional outcome of antiangiogenic therapy in neovascular age-related macular degeneration. Ophthalmology Journal. 2020;13(4):7-13. (In Russ.)] doi: 10.17816/OV46198
  4. Ou WC, Brown DM, Payne JF, et al. Relationship between visual acuity and retinal thickness during anti-vascular endothelial growth factor therapy for retinal diseases. Am J Ophthalmol. 2017;180:8–17. doi: 10.1016/j.ajo.2017.05.014
  5. Boiko EV, Maltsev DS. Quantitative optical coherence tomography analysis of retinal degenerative changes in diabetic macular edema and neovascular age-related macular degeneration. Retina. 2018;38(7):1324–1330. doi: 10.1097/IAE.0000000000001696
  6. Kulikov AN, Sosnovskii SV, Berezin RD, et al. Vitreoretinal interface abnormalities in diabetic macular edema and effectiveness of anti-VEGF therapy: an optical coherence tomography study. Clin Ophthalmol. 2017;11:1995–2002. doi: 10.2147/OPTH.S146019
  7. American Academy of Ophthalmology. Alert: Important coronavirus updates for ophthalmologists. March 23, 2020. Available at: https://www.aao.org/headline/alert-important-coronavirus-context. Accessed: 25.03.2021.
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  9. Wong DHT, Mak ST, Yip NKF, et al. Protective shields for ophthalmic equipment to minimise droplet transmission of COVID-19. Graefes Arch Clin Exp Ophthalmol. 2020;258(7):1571–1573. doi: 10.1007/s00417-020-04683-y
  10. Sacconi R, Borrelli E, Vella G, et al. TriPla regimen: A new treatment approach for patients with neovascular age-related macular degeneration in the COVID-19 “era”. Eur J Ophthalmol. 2020;7:1120672120963448. doi: 10.1177/1120672120963448
  11. The Royal College of Ophthalmologists (2020) Medical retinal management plans during COVID-19. Available at: https://www.rcophth.ac.uk/wp-content/uploads/2020/03/Medical-Retinal-Management-Planduring-COVID-19-UPDATED-300320-1-2.pdf. Accessed 25.03.2021.

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2. Fig. 1. Box-and-whiskers plots showing the changes in best-corrected visual acuity in the first-year treatment (a) and the second-year treatment group (b)

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3. Fig. 2. Optical coherence tomography in eyes with and without subretinal fluid experienced treatment interruption: a – subretinal fluid is presented before treatment interruption; b – subretinal fluid is absent before treatment interruption

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4. Fig. 3. Scattering plot showing correlation of baseline and final best-corrected visual acuity

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版权所有 © Kharakozov A., Kulikov A., Maltsev D., 2021

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