Artificial intelligence for optimizing benefits and minimizing risks of pharmacological therapies: challenges and opportunities
- PMID: 40979393
- PMCID: PMC12443109
- DOI: 10.3389/fdsfr.2024.1356405
Artificial intelligence for optimizing benefits and minimizing risks of pharmacological therapies: challenges and opportunities
Abstract
In recent years, there has been an exponential increase in the generation and accessibility of electronic healthcare data, often referred to as "real-world data". The landscape of data sources has significantly expanded to encompass traditional databases and newer sources such as the social media, wearables, and mobile devices. Advances in information technology, along with the growth in computational power and the evolution of analytical methods relying on bioinformatic tools and/or artificial intelligence techniques, have enhanced the potential for utilizing this data to generate real-world evidence and improve clinical practice. Indeed, these innovative analytical approaches enable the screening and analysis of large amounts of data to rapidly generate evidence. As such numerous practical uses of artificial intelligence in medicine have been successfully investigated for image processing, disease diagnosis and prediction, as well as the management of pharmacological treatments, thus highlighting the need to educate health professionals on these emerging approaches. This narrative review provides an overview of the foremost opportunities and challenges presented by artificial intelligence in pharmacology, and specifically concerning the drug post-marketing safety evaluation.
Keywords: artificial intelligence; machine learning; pharmacoepidemiology; pharmacological therapies; pharmacovigilance; real-world evidence.
Copyright © 2024 Crisafulli, Ciccimarra, Bellitto, Carollo, Carrara, Stagi, Triola, Capuano, Chiamulera, Moretti, Santoro, Tozzi, Recchia and Trifirò.
Conflict of interest statement
Author GR was employed by daVi DigitalMedicine Srl. Author LS was employed by Roche Spa. GT has served, over the last 3 years, on advisory boards/seminars funded by Sanofi, MSD, Eli Lilly, Sobi, Celgene, Daichii Sankyo, Novo Nordisk, Gilead, and Amgen; he is also a scientific coordinator of the academic spin-off “INSPIRE srl,” which has received funding from several pharmaceutical companies (i.e., PTC Pharmaceuticals, Kiowa Kirin, Shonogi, Shire, Novo Nordisk, and Daichii Sankyo) for conducting observational studies. Additionally, he is currently a consultant for Viatris in a legal case concerning an adverse reaction to sertraline. None of these listed activities are related to the topic of the article. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Figures
References
-
- Anderson J. P., Icten Z., Alas V., Benson C., Joshi K. (2017). Comparison and predictors of treatment adherence and remission among patients with schizophrenia treated with paliperidone palmitate or atypical oral antipsychotics in community behavioral health organizations. BMC Psychiatry 17, 346. 10.1186/s12888-017-1507-8 - DOI - PMC - PubMed
-
- Ben Abacha A., Chowdhury M. F. M., Karanasiou A., Mrabet Y., Lavelli A., Zweigenbaum P. (2015). Text mining for pharmacovigilance: using machine learning for drug name recognition and drug-drug interaction extraction and classification. J. Biomed. Inf. 58, 122–132. 10.1016/j.jbi.2015.09.015 - DOI - PubMed
Publication types
LinkOut - more resources
Full Text Sources
Research Materials
