Month: April 2021

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[av_heading heading=’VALUE-Dx investigates HTA, Reimbursement and Pricing of Diagnostic Tests for CA-ARTI’ tag=’h3′ link_apply=” link=’manually,http://’ link_target=” style=’blockquote modern-quote modern-centered’ size=” subheading_active=’subheading_below’ subheading_size=’15’ margin=” margin_sync=’true’ padding=’10’ color=” custom_font=” av-medium-font-size-title=” av-small-font-size-title=” av-mini-font-size-title=” av-medium-font-size=” av-small-font-size=” av-mini-font-size=” av_uid=’av-knr9eayp’ custom_class=” admin_preview_bg=”][/av_heading]

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In January 2021, the VALUE-Dx project produced a report that aims to map policies related to Health Technology Assessment (HTA), pricing and reimbursement of diagnostics for CA-ARTI in Europe.

The study indicates that the overall level of policy implementation in pricing and reimbursement for diagnostics is rather low. In addition, it is shown that HTA as a supportive tool to inform pricing and reimbursement decisions at national levels is rarely used in the study countries. Diagnostics for CA-ARTI constitute a valuable instrument to ensure rational antibiotic prescribing and thus to tackle antimicrobial resistance (AMR). Pricing and reimbursement policies, supported by HTA, can contribute to patient access and uptake of health products, such as diagnostics for CA-ARTI. Further research will be conducted in the course of the VALUE-Dx project.

In its fight against AMR, VALUE-Dx seeks to investigate the economic value, policies and innovative funding models. One of the goals of Work Package 5 is to review and analyze the current policy environment in Europe and identify good practices for the assessment of diagnostics.

The successful implementation and long-term viability of rapid diagnostic testing does not solely depend on developing, selling, and marketing these kind of medical devices. It is also important to demonstrate the economic value – especially from a long-term societal perspective – and to incentivize the uptake of rapid diagnostic tests through appropriate policies with regards to pricing, reimbursement (funding), and HTA.

Read the report
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[av_heading heading=’Funding models and health economics of diagnostics’ tag=’h3′ link_apply=” link=’manually,http://’ link_target=” style=’blockquote modern-quote modern-centered’ size=” subheading_active=’subheading_below’ subheading_size=’15’ margin=” margin_sync=’true’ padding=’10’ color=” custom_font=” av-medium-font-size-title=” av-small-font-size-title=” av-mini-font-size-title=” av-medium-font-size=” av-small-font-size=” av-mini-font-size=” av_uid=’av-kmylo7k2′ custom_class=” admin_preview_bg=”][/av_heading]

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WP5 is researching the funding models and health economics of diagnostics. What does exactly make these innovative diagnostics valuable and what are the barriers for healthcare providers and policy makers to start adopting them? These questions can only be answered using an interdisciplinary approach across disciplines such as microbiology, sociology, epidemiology, and economics; but it is also vital to combine the views from governmental organisations, industry, and academics.

WP5 comprises of seven tasks:

The task 5.1 team continues to work on preparing for the second Expert Advisory Panel meeting scheduled on 11 March 2021. This will provide expert input into the ongoing work on developing the economic models as well as other tasks in VALUE-Dx.

In task 5.2, we are focussing on updating the literature review on the economic modelling of diagnostics and therapies for infectious diseases, and on three scientific articles derived from the literature review (respiratory tract infections, gastro-intestinal infections, and sepsis).

Task 5.3 is collecting cost data from different sources to populate the economic evaluation models, which will be elaborated from the Prudence and Adequate trials.

Task 5.4’s focus is on the long-term value of diagnostics to prescribe antibiotics more appropriately and we are now working on antimicrobial resistance forecasts, which will allow the model to incorporate future trends and costs related to resistance.

Task 5.5 has reached deliverable 5.2 and we finalised the corresponding report on “HTA, Reimbursement and Pricing of Diagnostic Tests for CA-ARTI: An international overview of policies”. The next step will be the analysis of key facilitators and barriers for the adequate reimbursement of diagnostic tests for community-acquired respiratory infections.

Task 5.6 is continuing model development and validation. Task 5.7 will explore stakeholders’ views and experiences of supporting the adoption of new diagnostic tests in European community care to manage community acquired respiratory tract infections. We have identified stakeholders  from different health care organisations, policy departments and diagnostic companies. Interviews will start in March 2021 and we aim to finish data collection by autumn 2021.
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