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Aflibercept in clinical practice; visual acuity, injection numbers and adherence to treatment, for diabetic macular oedema in 21 UK hospitals over 3 years

Aflibercept in clinical practice; visual acuity, injection numbers and adherence to treatment, for diabetic macular oedema in 21 UK hospitals over 3 years
Aflibercept in clinical practice; visual acuity, injection numbers and adherence to treatment, for diabetic macular oedema in 21 UK hospitals over 3 years

Introduction: randomised controlled trials provide evidence that a treatment works. Real world evidence is required to assess if proven treatments are effective in practice. 

Method: retrospective data collection on patients given aflibercept for diabetic macular oedema over 3 years from 21 UK hospitals: visual acuity (VA); Index of multiple deprivation score (IMD); injection numbers; protocols used, compared as a cohort and between sites. 

Results: complete data: 1742 patients (from 2196 eligible) at 1 year, 860 (from 1270) at 2, 305 (from 506) at 3 years. The median VA improved from 65 to 71, 70, 70 (ETDRS letters) at 1, 2 and 3 years with 6, 9 and 12 injections, respectively. Loss to follow-up: 10% 1 year, 28.8% at 3. Centres varied: baseline: mean age 61–71 years (p < 0.0001); mean IMD score 15–37 (p < 0.0001); mean VA 49–68 (p < 0.0001). Only four centres provided a loading course of five injections at monthly intervals and one 6. This did not alter VA outcome at 1 year. Higher IMD was associated with younger age (p = 0.0023) and worse VA at baseline (p < 0.0001) not total number of injections or change in VA. Lower starting VA, higher IMD and older age were associated with lower adherence (p = 0.0010). 

Conclusions: the data showed significant variation between treatment centres for starting age, VA and IMD which influenced adherence and chances of good VA. Once treatment was started IMD did not alter likelihood of improvement. Loading dose intensity did not alter outcome at one year.

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Talks, S.J.
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Stratton, I.
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Peto, T.
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Lotery, A.
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Chakravarthy, U.
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Eleftheriadis, H.
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Izadi, S.
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Dhingra, N.
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Scanlon, P.
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Kashani, Sharam
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Georgas, Nasos
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Jones, Colin
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Gashut, Abdisattar
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Santiago, Cynthia
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Antcliff, Richard
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the UK Aflibercept Users’ Group
Talks, S.J.
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Stratton, I.
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Peto, T.
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Lotery, A.
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Scanlon, P.
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Kashani, Sharam
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Georgas, Nasos
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Jones, Colin
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Gashut, Abdisattar
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Santiago, Cynthia
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Chhabra, Romi
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Antcliff, Richard
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Bailey, Clare
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Ghanchi, Faruque
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Tahir, Irfan
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Talks, S.J., Stratton, I., Peto, T., Lotery, A., Chakravarthy, U., Eleftheriadis, H., Izadi, S. and Scanlon, P. , the UK Aflibercept Users’ Group (2022) Aflibercept in clinical practice; visual acuity, injection numbers and adherence to treatment, for diabetic macular oedema in 21 UK hospitals over 3 years. Eye (Basingstoke), 36 (1), 72-77. (doi:10.1038/s41433-021-01625-8).

Record type: Article

Abstract

Introduction: randomised controlled trials provide evidence that a treatment works. Real world evidence is required to assess if proven treatments are effective in practice. 

Method: retrospective data collection on patients given aflibercept for diabetic macular oedema over 3 years from 21 UK hospitals: visual acuity (VA); Index of multiple deprivation score (IMD); injection numbers; protocols used, compared as a cohort and between sites. 

Results: complete data: 1742 patients (from 2196 eligible) at 1 year, 860 (from 1270) at 2, 305 (from 506) at 3 years. The median VA improved from 65 to 71, 70, 70 (ETDRS letters) at 1, 2 and 3 years with 6, 9 and 12 injections, respectively. Loss to follow-up: 10% 1 year, 28.8% at 3. Centres varied: baseline: mean age 61–71 years (p < 0.0001); mean IMD score 15–37 (p < 0.0001); mean VA 49–68 (p < 0.0001). Only four centres provided a loading course of five injections at monthly intervals and one 6. This did not alter VA outcome at 1 year. Higher IMD was associated with younger age (p = 0.0023) and worse VA at baseline (p < 0.0001) not total number of injections or change in VA. Lower starting VA, higher IMD and older age were associated with lower adherence (p = 0.0010). 

Conclusions: the data showed significant variation between treatment centres for starting age, VA and IMD which influenced adherence and chances of good VA. Once treatment was started IMD did not alter likelihood of improvement. Loading dose intensity did not alter outcome at one year.

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Accepted/In Press date: 2 June 2021
e-pub ahead of print date: 9 July 2021
Published date: January 2022
Additional Information: Funding Information: SJT: Research and Advisory boards for Bayer; Novartis; Roche; Allergan; Alimera; IS: Consultant for Novo Nordisk; TP: Speaker and advisory board Bayer, Novartis, Roche; AL: None; UC: Chair of International trials sponsored by Bayer; HE: Research and Travel Bayer; SI: Research Bayer; travel Bayer and Novartis; ND: Research Novartis; Travel Novartis; Allergan; Bayer; Speaker Novartis; Advisory Board Novartis; PS: Research and audit grants from Allergan, Boehringer, Novartis, Bayer; Advisory Boards for Pfizer; Allergan; Roche; Boehringer and Bayer.

Identifiers

Local EPrints ID: 486994
URI: http://eprints.soton.ac.uk/id/eprint/486994
ISSN: 0950-222X
PURE UUID: c97e91d7-b0ca-4c33-8506-8c653083e03d
ORCID for I. Stratton: ORCID iD orcid.org/0000-0003-1172-7865
ORCID for A. Lotery: ORCID iD orcid.org/0000-0001-5541-4305

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Date deposited: 09 Feb 2024 17:36
Last modified: 18 Mar 2024 04:01

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Contributors

Author: S.J. Talks
Author: I. Stratton ORCID iD
Author: T. Peto
Author: A. Lotery ORCID iD
Author: U. Chakravarthy
Author: H. Eleftheriadis
Author: S. Izadi
Author: N. Dhingra
Author: P. Scanlon
Author: Quresh Mohamed
Author: Sharam Kashani
Author: Nasos Georgas
Author: Colin Jones
Author: Abdisattar Gashut
Author: Cynthia Santiago
Author: Romi Chhabra
Author: Richard Antcliff
Author: Clare Bailey
Author: Faruque Ghanchi
Author: Linda Mcinerney
Author: Salim Natha
Author: Rehna Khan
Author: Indra Dias
Author: Raj Mukhrejee
Author: Irfan Tahir
Corporate Author: the UK Aflibercept Users’ Group

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