Impact of Routinely Performed Optical Coherence Tomography Examinations on Quality of Life in Patients with Retinal Diseases—Results from the ALBATROS Data Collection

Author:

Schuster Alexander K.1,Wolfram Christian2,Hudde Tobias3,Klatt Alexander4,Schnegelsberg Birthe5,Midani-Oezkan Heven5,Ross Mike5,Ziemssen Focke67ORCID,Pfeiffer Norbert1

Affiliation:

1. Department of Ophthalmology, University Medical Center, Johannes Gutenberg-University Mainz, Langenbeckstr. 1, 55131 Mainz, Germany

2. Department of Ophthalmology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, 20246 Hamburg, Germany

3. Eye Hospital Wolfsburg-Fallersleben, Am Spieker 10, 38440 Wolfsburg, Germany

4. Eye Center Klatt, Henry-Wetjen-Platz 3, 28844 Weyhe, Germany

5. Novartis Pharma GmbH, Roonstr. 25, 90429 Nuremberg, Germany

6. Department of Ophthalmology, Leipzig University Hospital, University of Leipzig, Liebigstraße 12, Haus 1, 04109 Leipzig, Germany

7. Center for Ophthalmology, Eberhard-Karls-Universität Tübingen, Elfriede-Aulhorn-Str. 7, 72076 Tübingen, Germany

Abstract

The use of OCT to monitor intravitreal treatment varies in clinical practice and is not always mandatory. The ALBATROS data collection aimed to clarify the impact of routinely implemented OCT on clinical outcomes and its impact on vision-related quality of life (VRQoL). Methods: An observational cohort study included patients with retinal diseases starting an intravitreal anti-vascular endothelial growth factor treatment in Germany. Treatment followed clinical practice except mandatory OCT examination during the 12-month observation period. VRQoL was assessed by NEI VFQ-25 and compared with respect to OCT examinations and number of intravitreal injections in the different diseases (nAMD, DME, BRVO, CRVO). Results: 1478 patients (74.5 ± 10.9 years, 54.9% female) were included in the analysis. Patients had neovascular AMD (65.2%), DME (18.4%), BRVO (9.5%), or CRVO (6.9%). 8.8 ± 2.6 OCT examinations and 6.1 ± 3.2 intravitreal injections were performed within 12 months. VRQoL differed between indications at baseline, with substantially lower values for neovascular AMD and CRVO. After twelve months, an increase in visual acuity and visual functional scale was observed for nAMD, DME, and BRVO, while in DME only, there was an association between number of OCT examinations and VRQoL. Conclusion: Intravitreal treatment was able to maintain VRQoL over twelve months in a real-world setting. Regular OCT examinations were associated with higher gain in VRQoL in DME patients after 12 months.

Funder

Novartis Pharma GmbH, Nuremberg, Germany

Publisher

MDPI AG

Subject

General Medicine

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