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Evaluation of raised intraocular pressure post EyeCee One preloaded intraocular lenses implantation

Eye (2023)Cite this article

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Medicine and Healthcare products Regulatory Agency (MHRA) issued a Device Safety Information (DSI) notification (DSI/2023/001) on 26 January 2023 regarding reported cases of increased intraocular pressure (IOP) in patients who received implantation of EyeCee One preloaded intraocular lenses (IOLs) (manufactured by Nidek, Japan and distributed by Bausch & Lomb UK Ltd) and instructed all eye centres in the UK to stop using and to quarantine these products [1]. Reportedly, a rate of 2–4% of high IOP (value unspecified) was found in some patients, who apparently experienced minimal symptoms [2].

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Authors and Affiliations

  1. Ophthalmology Department, Sheffield Teaching Hospital NHS Trust, Sheffield, UK

    Haoyu Wang, Stephanie J. Chiu, William L. Kay & Jennifer H. Y. Tan

  2. Academic Unit of Medical Education, University of Sheffield, Sheffield, UK

    Haoyu Wang, Joel L. Z. Jong, Stephanie J. Chiu & Jennifer H. Y. Tan

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  1. Haoyu Wang
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  2. Joel L. Z. Jong
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  3. Stephanie J. Chiu
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  4. William L. Kay
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  5. Jennifer H. Y. Tan
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Contributions

Concept and Design of the work: HW and JHT. Acquisition, analysis or interpretation of data: HW, JLJ, SJC, WLK, and JHT. Drafting the manuscript or revising it critically: HW, SJC, and JHT. Final approval of the version to be published: HW, JLJ, SJC, WLK, and JHT.

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Correspondence to Haoyu Wang or Jennifer H. Y. Tan.

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Wang, H., Jong, J.L.Z., Chiu, S.J. et al. Evaluation of raised intraocular pressure post EyeCee One preloaded intraocular lenses implantation. Eye (2023). https://doi.org/10.1038/s41433-023-02487-y

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  • DOI: https://doi.org/10.1038/s41433-023-02487-y

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