Results of Ranibizumab Treatment of the Myopic Choroidal Neovascular Membrane according to the Axial Length of the Eye
Status PubMed-not-MEDLINE Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
32454987
PubMed Central
PMC7243022
DOI
10.1155/2020/3076596
Knihovny.cz E-zdroje
- Publikační typ
- časopisecké články MeSH
AIM: A retrospective evaluation of the results of treatment of myopic choroidal neovascularization (mCNV) with intravitreal injections of ranibizumab in a pro re nata (PRN) regimen in three groups of patients distributed according to axial length. METHODS: The paper presents a retrospective multicenter study carried out with the cooperation of several Departments of Ophthalmology in the Czech Republic. The study included 60 eyes of 60 patients suffering from mCNV, divided according to axial length into three groups. The first group consisted of 20 patients with an axial length of the eyes shorter than 28 mm (Group 1), the second group included 27 patients with axial lengths ranging from 28 mm to 29.81 mm (Group 2), and 13 patients had axial lengths longer than 30 mm (Group 3). All patients were first administered 3 initial intravitreal ranibizumab injections at monthly intervals (loading phase), and other injections were administered according to a PRN treatment regimen. Patients were evaluated before treatment and then at intervals of 3, 6, 9, and 12 months. The effect of ranibizumab treatment on the functional and morphological parameters of the affected eye was evaluated. RESULTS: The average baseline BCVA ± SD in Group 1 was 52.6 ± 12.5 letters of ETDRS optotypes, and at the end of the one-year follow-up, it was 63.3 ± 11.8 letters. The average baseline of CRT ± SD in this group was 377.4 ± 80.0 μm, and in the 12th month, it was 311.1 ± 63.7 μm. The average baseline BCVA ± SD in Group 2 was 50.2 ± 9.0 ETDRS letters, and at the end of the follow-up, it was 60 ± 12.4 letters. The average baseline of CRT ± SD in Group 2 was 391.2 ± 85.2 μm, and in the 12th month, it was 323.9 ± 91.2 μm. In Group 3, the average baseline of BCVA was 48.5 ± 14.5 ETDRS letters, and at the end of the one-year follow-up, it was 55.7 ± 16.1 letters. The average baseline CRT ± SD for Group 3 was 342.1 ± 94.9 μm, and after 12 months, it was 287.8 ± 88.4 μm. An improvement of BCVA by ≥15 letters of ETDRS optotypes was achieved by 3 patients of 20 (15%) in Group 1, by 5 patients of 27 (18.5%) in Group 2, and by 3 patients of 13 (23.1%) in Group 3. All these changes were statistically significant in comparison with the input values (p < 0.05). CONCLUSION: Ranibizumab treatment in patients with mCNV in our study resulted in statistically significant improvement in BCVA and a decrease in CRT in all groups of patients. Our results from a routine clinical practice correspond with the results of large clinical studies; we confirm a particularly good effect of treatment in patients with axial lengths of the eye smaller than 28 mm.
Zobrazit více v PubMed
Wong T. Y., Foster P. J., Hee J., et al. Prevalence and risk factors for refractive errors in adult Chinese in Singapore. Investigative Ophthalmology & Visual Science. 2000;41(41):2486–2494. PubMed
Fredrick D. R. Myopia. BMJ. 2002;324(7347):1195–1199. PubMed PMC
Miller D. G., Singerman L. J. Natural history of choroidal neovascularization in high myopia. Current Opinion in Ophthalmology. 2001;12(3):222–224. doi: 10.1097/00055735-200106000-00014. PubMed DOI
Neelam K., Cheung C. M. G., Ohno-Matsui K., Lai T. Y. Y., Wong T. Y. Choroidal neovascularization in pathological myopia. Progress in Retinal and Eye Research. 2012;31(5):495–525. doi: 10.1016/j.preteyeres.2012.04.001. PubMed DOI
Curtin B. J. The Myopias: Basic Science and Clinical Management. Philadelphia, PA, USA: Harper & Row; 1985. The prevalence of myopia.
Grossniklaus H. E., Green W. R. Pathologic findings in pathologic myopia. Retina. 1992;12(2):127–133. doi: 10.1097/00006982-199212020-00009. PubMed DOI
Vongphanit J., Mitchell P., Wang J. J. Prevalence and progression of myopic retinopathy in an older population. Ophthalmology. 2002;109(4):704–711. doi: 10.1016/s0161-6420(01)01024-7. PubMed DOI
Liu H. H., Xu L., Wang Y. X., Wang S., You Q. S., Jonas J. B. Prevalence and progression of myopic retinopathy in Chinese adults: the Beijing Eye Study. Ophthalmology. 2010;117(9):1763–1768. doi: 10.1016/j.ophtha.2010.01.020. PubMed DOI
Curtin B. J., Karlin D. B. Axial length measurements and fundus changes of the myopic eye. I. The posterior fundus. Transactions of the American Ophthalmological Society. 1970;68(68):312–334. PubMed PMC
Hayashi K., Ohno-Matsui K., Shimada N., et al. Long-term pattern of progression of myopic maculopathy. Ophthalmology. 2010;117(8):1595–1611. doi: 10.1016/j.ophtha.2009.11.003. PubMed DOI
Wong T. Y., Ferreira A., Hughes R., Carter G., Mitchell P. Epidemiology and disease burden of pathologic myopia and myopic choroidal neovascularization: an evidence-based systematic review. American Journal of Ophthalmology. 2014;157(1):9–25. doi: 10.1016/j.ajo.2013.08.010. PubMed DOI
Narayanan R., Kuppermann B. D., Jones C., Kirkpatrick P. Ranibizumab. Nature Reviews Drug Discovery. 2006;5(10):815–816. doi: 10.1038/nrd2157. PubMed DOI
Lai T. Y. Y., Chan W.-M., Liu D. T. L., Lam D. S. C. Intravitreal ranibizumab for the primary treatment of choroidal neovascularization secondary to pathologic myopia. Retina. 2009;29(6):750–756. doi: 10.1097/iae.0b013e31819ed6bd. PubMed DOI
Monés J. M., Amselem L., Serrano A., Garcia M., Hijano M. Intravitreal ranibizumab for choroidal neovascularization secondary to pathologic myopia: 12-month results. Eye. 2009;23(6):1275–1281. doi: 10.1038/eye.2009.88. PubMed DOI
Lalloum F., Souied E. H., Bastuji-Garin S., et al. Intravitreal ranibizumab for choroidal neovascularization complicating pathologic myopia. Retina. 2010;30(3):399–406. doi: 10.1097/iae.0b013e3181bcef24. PubMed DOI
Calvo-Gonzalez C., Reche-Frutos J., Donate J., Fernandez-Perez C., Garcia-Feijoo J. Intravitreal ranibizumab for myopic choroidal neovascularization: factors predictive of visual outcome and need for retreatment. American Journal of Ophthalmology. 2011;151(3):529–534. doi: 10.1016/j.ajo.2010.09.021. PubMed DOI
Lorenzo D., Arias L., Alcubierre R., et al. Intravitreal ranibizumab for choroidal neovascularization secondary to pathological myopia: 12-month follow-up. Ophthalmologica. 2011;226(3):103–109. doi: 10.1159/000328980. PubMed DOI
Wu T.-T., Kung Y.-H. The 12-month outcome of three consecutive monthly intravitreal injections of ranibizumab for myopic choroidal neovascularization. Journal of Ocular Pharmacology and Therapeutics. 2012;28(2):129–133. doi: 10.1089/jop.2011.0106. PubMed DOI PMC
Wolf S., Balciuniene V. J., Laganovska G., et al. RADIANCE: a randomized controlled study of ranibizumab in patients with choroidal neovascularization secondary to pathologic myopia. Ophthalmology. 2014;121(3):682–692. doi: 10.1016/j.ophtha.2013.10.023. PubMed DOI
Wong T. Y., Ohno-Matsui K., Leveziel N., et al. Myopic choroidal neovascularisation: current concepts and update on clinical management. British Journal of Ophthalmology. 2015;99(3):289–296. doi: 10.1136/bjophthalmol-2014-305131. PubMed DOI PMC
Cohen S. Y. Anti-VEGF drugs as the 2009 first-line therapy for choroidal neovascularization in pathologic myopia. Retina. 2009;29(8):1062–1066. doi: 10.1097/iae.0b013e3181b1bb1a. PubMed DOI
Yoon J. U., Byun Y. J., Koh H. J. Intravitreal anti-VEGF versus photodynamic therapy with verteporfin for treatment of myopic choroidal neovascularization. Retina. 2010;30(3):418–424. doi: 10.1097/iae.0b013e3181bd2fe4. PubMed DOI
Holz F. G., Tufail A., Leveziel N., et al. Ranibizumab in myopic choroidal neovascularization: a subgroup Analysis by ethnicity, age, and ocular characteristics in radiance. Ophthalmologica. 2016;236(1):19–28. doi: 10.1159/000446027. PubMed DOI
Seasonal Variations in Ocular Axial Length Increase among Children in the Czech Republic