Strategic insights into pharmacogenomics coverage: a theory-informed SWOT analysis of UAE insurance stakeholders’ perspectives
Maram O. Abbas, Azhar T. Rahma, Iffat Elbarazi, Bassam R. Ali, George P. Patrinos, Hana Ghadibah, Fatma Al-Maskari

TL;DR
This study explores UAE insurance stakeholders' views on expanding pharmacogenomics, highlighting barriers like costs and awareness, and suggesting strategies for better adoption.
Contribution
The novel contribution is a theory-informed SWOT analysis of UAE insurance stakeholders' perspectives on pharmacogenomics implementation.
Findings
Insurers identified economic constraints and lack of physician/public awareness as major barriers to PGx adoption.
Executives emphasized strategic policies and ROI, while middle management focused on operational challenges.
Collaborative efforts and advanced health information systems are seen as critical for successful PGx integration.
Abstract
Pharmacogenomic (PGx) testing improves treatment outcomes by tailoring therapy to a patient’s genetic profile. However, PGx implementation faces global challenges, including costs, reimbursement, and regulations. Initial PGx guidelines exist in the United Arab Emirates (UAE), but insurers’ perspectives remain understudied. This study explores insurers’ views on policies and strategies to expand PGx adoption and overcome implementation barriers. This qualitative study used a semi-structured interview design to explore the perspectives of twelve executive and middle management insurance representatives selected through purposive convenience and snowball sampling. Thematic analysis was conducted inductively, supported by comparative analysis, the Institutional Theory, the TAM, and SWOT analysis to interpret the findings. Analysis revealed variable awareness of PGx, highlighting both…
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsPharmacogenetics and Drug Metabolism · Genomics and Rare Diseases · BRCA gene mutations in cancer
