Real-world Evaluation of Prevalence of Ocular Adverse Events in Patients With Neovascular (Wet) Age-related Macular Degeneration (AMD) Who Received Anti-vascular Endothelial Growth Factor (VEGF) Agents (Komodo Health)
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This was the cross-sectional study to assess the period prevalence of IOI in patients with wet AMD who were treated with anti- VEGF agents (excluding brolucizumab) over a one-year period in 2019.
Full description
In this cross-sectional study of patients with wet AMD who received ≥1 anti-VEGF injection (excluding brolucizumab), evidence was generated to describe the period prevalence of specific ocular AEs. The study was conducted using the Komodo Healthcare Map, and all results were based on the study period from 01/01/2018 to 12/31/2019.
Komodo Healthcare Map data from 01/01/2018 to 12/31/2019 for patients with a diagnosis of wet AMD who were treated with ≥1 anti-VEGF agent (excluding brolucizumab) were included.
- Identification period: Patients fulfilling the selection criteria during the period from 01/01/2019 to 12/31/2019 were identified
- Index date: 01/01/2019
- Study Period: 01/01/2018 to 12/31/2019
- Pre-index period: 01/01/2018 to 12/31/2018
- Post-index period: 01/01/2019 to 12/31/2019
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Inclusion criteria
- ≥1 International Classification of Diseases, Clinical Modification-9/10 (ICD-9/10) code for wet AMD in 2019
- ≥1 Healthcare Common Procedure Coding System (HCPCS) code (J code) or National Drug Code (NDC) code for treatment with an anti-VEGF agent (excluding brolucizumab) in 2019
- ≥18 years old in 2019
- ≥2 wet AMD-related office visits in 2019
Exclusion criteria
- ≥1 HCPCS code (J code) or NDC code for treatment with brolucizumab in 2019
Trial design
369,600 participants in 4 patient groups
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Data sourced from clinicaltrials.gov
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