Modified early intensive and treat-and-extend regimen of anti-vascular endothelial growth factor for diabetic macular edema in Taiwan.
Humans
Ranibizumab
Macular Edema
/ drug therapy
Diabetic Retinopathy
/ drug therapy
Angiogenesis Inhibitors
Taiwan
Visual Acuity
Receptors, Vascular Endothelial Growth Factor
/ therapeutic use
Vascular Endothelial Growth Factors
Intravitreal Injections
Recombinant Fusion Proteins
/ therapeutic use
Diabetes Mellitus
/ drug therapy
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
07 11 2023
07 11 2023
Historique:
received:
14
06
2023
accepted:
30
09
2023
medline:
9
11
2023
pubmed:
8
11
2023
entrez:
7
11
2023
Statut:
epublish
Résumé
Given the rising prevalence of patients with diabetes and increasing treatment burden for patients with vision-threatening diabetic macular edema (DME), we aimed to explore the efficacy of modified early intensive and treat-and-extend regimen of anti-vascular endothelial growth factor (VEGF) therapy under the Taiwan National Insurance Bureau reimbursement policy. We obtained data on 69 eyes treated with initial 4-monthly intravitreal injections of aflibercept or ranibizumab, plus individualized treat-and-extend regimen. At 12 months, the mean (SD) change in LogMAR best corrected visual acuity from baseline was - 0.28 (0.31) in all eyes, while that in the aflibercept and ranibizumab groups were - 0.30 (0.34) and - 0.25 (0.28), respectively. Central retinal thickness decreased by 137.2 (122.4) in all eyes, 138.1 (134.2) in the aflibercept group, and 136.2 (110.9) in the ranibizumab group. Additionally, the aflibercept group had a lower mean number of injections than the ranibizumab group (8.5 vs. 8.7). The last extended dosing interval of > 12 weeks was 31.0% and 16.7% of the eyes in the aflibercept and ranibizumab groups, respectively. The modified anti-VEGF regimens effectively managed DME in terms of functional and anatomical outcomes, and efficiently reduced the healthcare burden by reducing the number of injections and extending treatment intervals within 12 months.
Identifiants
pubmed: 37935742
doi: 10.1038/s41598-023-43931-z
pii: 10.1038/s41598-023-43931-z
pmc: PMC10630418
doi:
Substances chimiques
Ranibizumab
ZL1R02VT79
Angiogenesis Inhibitors
0
Receptors, Vascular Endothelial Growth Factor
EC 2.7.10.1
Vascular Endothelial Growth Factors
0
Recombinant Fusion Proteins
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
19349Informations de copyright
© 2023. The Author(s).
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