Transferability of AI Methods for Diabetes Modelling in Health Technology Assessment

By Melike Belenli Gümüş

July 8, 2024

Introduction

Diabetes, a prevalent global health concern, impacts millions worldwide, with projections indicating a significant rise in cases by 2045. The financial strain of diabetes has surged, prompting the need for advanced treatment approaches. Real-world data (RWD) has emerged as a valuable tool for predicting diabetes complications, offering insights into disease progression. Health technology assessment (HTA) methods based on RWD are evolving, presenting new opportunities and challenges for clinical research. Transferability of these methods across jurisdictions and disease areas remains a critical consideration. Leveraging artificial intelligence (AI), researchers aim to enhance diabetes prediction models and broaden their applicability. The transferability of AI methods for diabetes modelling in HTA is a critical topic. This study investigates how these methods can be applied across different countries, particularly between early and late adopters of emerging health technologies.

Understanding AI in Diabetes Modelling

AI has transformed diabetes care by predicting short- and long-term complications. The International Diabetes Federation reports that 537 million adults live with diabetes, a number expected to rise to 783 million by 2045. AI methods can enhance our understanding of diabetes, improve cost-effectiveness modelling, and refine patient stratification. These advancements can significantly impact clinical and reimbursement decisions across various jurisdictions.

Benefits of AI in Health Technology Assessment

AI methods offer several benefits for HTA. They enable the prediction of short- and long-term diabetes outcomes on both general and individual levels, aiding clinicians in making informed decisions for therapy maintenance. This can lead to better treatment recommendations and improved patient outcomes. For instance, the Clinical Practice Research Datalink (CPRD) in the UK covers over 11.3 million patients, providing valuable data for AI models. Similarly, the Type 1 Diabetes Exchange Registry in the US includes data from over 34,000 participants, offering a rich resource for research.

AI-based methods also allow HTA agencies to combine predictions with results from randomised clinical trials (RCTs) during the evaluation of new medicines, enhancing the overall assessment process. The systematic curation of RWD helps address issues with missing data and improves the quality of datasets. Furthermore, the advancement of AI methodologies is expected to enhance diagnosis and therapy, ultimately benefiting the healthcare system.

Challenges in Transferability

Despite the benefits, transferring AI methods between countries poses challenges. Differences in healthcare systems, patient demographics, and data quality can affect the applicability of AI models. Experts from Central and Eastern European (CEE) countries highlighted the need to clarify how RCT data can be integrated with RWD. This integration is crucial for making AI methods usable in a pragmatic HTA world.

Figure 1: Voting results on ‘challenges in transferring prediction model for diabetes in different countries’.

Recommendations for Successful Implementation

Several steps are necessary in order to successfully implement AI methods in HTA. Access to comprehensive databases, technical and programming expertise, and clear guidelines on RWD usage are essential aspects. Moreover, addressing the variability in patient demographics and co-treatments between countries can improve the transferability of AI models. Experts recommend developing a list of core transferable components and country-specific variables to enhance collaboration and transparency.

Conclusion

The transferability of AI methods for diabetes modelling holds great promise for improving healthcare outcomes. AI-driven methods leveraging RWD hold promise in enhancing diabetes care and facilitating HTA processes. Access to databases, technical proficiency, and clear guidelines are essential for their successful integration into healthcare practices. By addressing the challenges and leveraging the benefits, we can enhance the effectiveness of health technology assessments. This will ultimately lead to better decision-making processes and improved patient care.

Reference url

Recent Posts

semaglutide NAION risk
    

Semaglutide NAION Risk: EMA Review Initiated Amid Conflicting Evidence

🔍 Is semaglutide linked to vision loss?

The European Medicines Agency’s PRAC is currently reviewing the potential risk of non-arteritic anterior ischemic optic neuropathy (NAION) associated with semaglutide-containing medicines, including popular treatments like Ozempic and Wegovy. With recent studies yielding conflicting evidence, this review is crucial for patient safety and the future of these therapies.

Read the full article to understand the implications and what this could mean for healthcare providers and patients alike!

#SyenzaNews #Pharmaceuticals #HealthcarePolicy

cervical cancer screening
        

Cost-Effective Cervical Cancer Screening Strategies for Women with HIV in KwaZulu-Natal

💡 *Are single-visit cervical cancer screenings the key to better health outcomes in high HIV prevalence areas?*
A recent study from KwaZulu-Natal, South Africa reveals that repeat single-visit cervical cancer screening using HPV DNA testing is not only the most effective but also the most cost-effective approach for women living with HIV. This aligns with WHO recommendations for comprehensive cervical cancer elimination strategies.

Explore the insights and implications of this vital research that could transform cervical cancer prevention in resource-limited settings.

#SyenzaNews #HealthEconomics #oncology #GlobalHealth

EU Health Technology Assessment
          

Advancing EU Health Technology Assessment: Insights from the HAG Meeting

💡 How can the EU Health Technology Assessment reshape healthcare delivery?

The recent meeting of the Heads of HTA Agencies Group heralds a new era with the operationalization of the EU’s Health Technology Assessment Regulation, aiming to streamline processes and enhance collaboration across member states.

This initiative promises to improve data transparency, foster innovative health technologies, and ultimately, drive better patient outcomes.

Curious to learn more about these significant updates and what they mean for the future of health assessments in the EU? Jump into the full article!

#SyenzaNews #HealthTech #HealthEconomics #DigitalTransformation

When you partner with Syenza, it’s like a Nuclear Fusion.

Our expertise are combined with yours, and we contribute clinical expertise and advanced degrees in health policy, health economics, systems analysis, public finance, business, and project management. You’ll also feel our high-impact global and local perspectives with cultural intelligence.

SPEAK WITH US

CORRESPONDENCE ADDRESS

1950 W. Corporate Way, Suite 95478
Anaheim, CA 92801, USA

© 2025 Syenza™. All rights reserved.