Digital Technology Applications in the Management of Adverse Drug Reactions: Bibliometric Analysis

Author:

Litvinova Olena12ORCID,Yeung Andy Wai Kan23ORCID,Hammerle Fabian Peter24ORCID,Mickael Michel-Edwar5ORCID,Matin Maima5,Kletecka-Pulker Maria26,Atanasov Atanas G.25ORCID,Willschke Harald24

Affiliation:

1. Department of Management and Quality Assurance in Pharmacy, National University of Pharmacy of the Ministry of Health of Ukraine, 61002 Kharkiv, Ukraine

2. Ludwig Boltzmann Institute Digital Health and Patient Safety, Medical University of Vienna, 1090 Vienna, Austria

3. Oral and Maxillofacial Radiology, Applied Oral Sciences and Community Dental Care, Faculty of Dentistry, University of Hong Kong, Hong Kong, China

4. Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, 1090 Vienna, Austria

5. Institute of Genetics and Animal Biotechnology of the Polish Academy of Sciences, 05-552 Magdalenka, Poland

6. Institute for Ethics and Law in Medicine, University of Vienna, 1010 Vienna, Austria

Abstract

Adverse drug reactions continue to be not only one of the most urgent problems in clinical medicine, but also a social problem. The aim of this study was a bibliometric analysis of the use of digital technologies to prevent adverse drug reactions and an overview of their main applications to improve the safety of pharmacotherapy. The search was conducted using the Web of Science database for the period 1991–2023. A positive trend in publications in the field of using digital technologies in the management of adverse drug reactions was revealed. A total of 72% of all relevant publications come from the following countries: the USA, China, England, India, and Germany. Among the organizations most active in the field of drug side effect management using digital technologies, American and Chinese universities dominate. Visualization of publication keywords using VOSviewer software 1.6.18 revealed four clusters: “preclinical studies”, “clinical trials”, “pharmacovigilance”, and “reduction of adverse drug reactions in order to improve the patient’s quality of life”. Molecular design technologies, virtual models for toxicity modeling, data integration, and drug repurposing are among the key digital tools used in the preclinical research phase. Integrating the application of machine learning algorithms for data analysis, monitoring of electronic databases of spontaneous messages, electronic medical records, scientific databases, social networks, and analysis of digital device data into clinical trials and pharmacovigilance systems, can significantly improve the efficiency and safety of drug development, implementation, and monitoring processes. The result of combining all these technologies is a huge synergistic provision of up-to-date and valuable information to healthcare professionals, patients, and health authorities.

Publisher

MDPI AG

Reference63 articles.

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2. (2024, February 01). Patient Safety. Available online: https://www.fip.org/file/4757.

3. (2024, February 01). Safety of Medicines—Adverse Drug Reactions. Available online: https://www.who.int/docs/default-source/medicines/safety-of-medicines--adverse-drug-reactions-jun18.pdf?sfvrsn=4fcaf40_2.

4. Hodkinson, A., Tyler, N., Ashcroft, D.M., Keers, R.N., Khan, K., Phipps, D., Abuzour, A., Bower, P., Avery, A., and Campbell, S. (2020). Preventable Medication Harm across Health Care Settings: A Systematic Review and Meta-Analysis. BMC Med., 18.

5. Adverse Drug Reactions in Hospitalized Patients: Results of the FORWARD (Facilitation of Reporting in Hospital Ward) Study;Giardina;Front. Pharmacol.,2018

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