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Review
. 2024 Nov;41(11):897-906.
doi: 10.1007/s40266-024-01155-4. Epub 2024 Oct 26.

Pilocarpine in the Treatment of Presbyopia: Progress, Issues, and Future Prospects

Affiliations
Review

Pilocarpine in the Treatment of Presbyopia: Progress, Issues, and Future Prospects

Xiuwen Zhang et al. Drugs Aging. 2024 Nov.

Abstract

Presbyopia is a common age-related visual impairment. With the aging of the population, the incidence of presbyopia is increasing globally, becoming a worldwide public health concern. Treatment options for presbyopia include optical lens correction, surgical intervention, and pharmacological therapy. Pharmacological treatments for presbyopia are non-invasive, reversible, and have emerged over the past decade. Following the US Food and Drug Administration's approval of 1.25% pilocarpine for presbyopia, the use of pilocarpine and its compound formulations has gained increased attention, with some drugs entering clinical phase II/III trials ( www.clinicaltrials.gov ). Therefore, this article primarily describes and analyzes the progress of research on the use of pilocarpine and its compound formulations for presbyopia, as well as the challenges that remain to be addressed. The optimal dosage form, the optimal concentration, the long-term safety, and patient compliance should be further explored, and there is a lack of multi-center evidence-based medicine research to support it. The aim of this article is to provide a reference for researchers to conduct further in-depth investigations in this area.

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Conflict of interest statement

Declarations Funding This study was supported by the Shanghai Municipal Health Commission (202140069) and the Young Clinical Scientist Training Program at Shanghai Medical College of Fudan University, Science and Technology Commission of Shanghai Municipality (No. 23ZR1409100). Conflicts of Interest Xiuwen Zhang, Xiaomei Xiong, Haixin Zhang, Taomin Huang, and Xingtao Zhou have no conflicts of interest that are directly relevant to the content of this article. Ethics Approval Not applicable. Consent to Participate Not applicable. Consent for Publication Not applicable. Availability of Data and Material Not applicable. Code Availability Not applicable. Authors’ Contributions All authors contributed to the study conception and design. Material preparation, data collection, and analysis were performed by XZ, XX, HZ, TH, and XZ. The first draft of the manuscript was written by XZ and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.

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