Dispensing Patterns of Ranibizumab and Aflibercept for the Treatment of Neovascular Age-Related Macular Degeneration: A Retrospective Cohort Study in Australia

被引:4
作者
Skelly, Adrian [1 ]
Carius, Hans-Joachim [2 ]
Bezlyak, Vladimir [1 ]
Chen, Fred K. [3 ,4 ]
机构
[1] Novartis Pharma AG, Basel, Switzerland
[2] QuintilesIMS, Frankfurt, Germany
[3] Univ Western Australia, Ctr Ophthalmol & Visual Sci, Incorporating Lions Eye Inst, Perth, WA, Australia
[4] Royal Perth Hosp, Dept Ophthalmol, Perth, WA, Australia
关键词
Aflibercept; Anti-vascular endothelial growth factor; Dispensing pattern; Neovascular age-related macular degeneration; Ophthalmology; Ranibizumab; Vascular endothelial growth factor; ROUTINE CLINICAL-PRACTICE; VISUAL IMPAIRMENT;
D O I
10.1007/s12325-017-0624-6
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Introduction: Anti-vascular endothelial growth factor therapy is the standard of care for neovascular age-related macular degeneration (nAMD). The dosage of two licensed agents, ranibizumab and aflibercept, was established through clinical trials; however, it is unclear if either agent is administered as recommended in routine clinical practice. Using pharmacy claims data, we investigated if the dispensing patterns of ranibizumab differ from those of aflibercept 6 and 12 months after treatment initiation. Methods: Prescription data retrieved from the Australian IMSA (R) AUS LRx database were used to identify nAMD patients with one or more claims for ranibizumab or aflibercept between December 1, 2012, and March 31, 2015, with follow-up of at least 6 months. The number of ranibizumab and aflibercept units dispensed was adjusted for baseline patient Medication-Based Disease Burden Index (MBDBI) scores. No difference in the number of ranibizumab versus aflibercept units dispensed was concluded if the 95% confidence interval (CI) limits of the adjusted mean difference between the study cohorts were 1.00 unit or less. Results: Baseline patient MBDBI scores were similar for the ranibizumab (N = 1235) and aflibercept (N = 959) cohorts. The adjusted mean (standard deviation) number of units dispensed was 5.3 (1.3) versus 5.1 (1.4) at month 6 and 8.9 (2.2) versus 8.9 (2.3) at month 12. The 95% CI limits of the adjusted mean difference did not exceed 1.00 unit dispensed at either time point: 95% CI of 0.09 to 0.32 for an adjusted mean difference of 0.20 at month 6 and -0.23 to 0.30 for an adjusted mean difference of 0.04 at month 12. Mean (standard deviation) dispensing intervals were comparable for both cohorts: 35.3 (19.2) days versus 36.8 (20.0) days at month 6 (adjusted mean difference -1.59 days; 95% CI -2.51 to -0.67 days) and 41.2 (20.9) days versus 41.6 (20.4) days at month 12 (adjusted mean difference -0.40 days; 95% CI -1.70 to 0.91 days). Conclusions: Ranibizumab and aflibercept are dispensed in a similar manner by Australian pharmacies during the first year of treatment.
引用
收藏
页码:2585 / 2600
页数:16
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