Positive appraisal for add-on reimbursement of Philips Volcano’s coronary fractional flow reserve (FFR) pressure wires in France

09

May 2017

National Commission for the Evaluation of Medical Devices and Health Technologies (CNEDiMTS) positively appraised Verrata and Verrate Plus guidewires for add-on reimbursement via LPPR title V. Level of added clinical value was considered moderate (ASA III) in comparison with management strategy, based solely on angiography data. 

Fractional flow reserve was firstly introduced into French payment system in 2016 following the creation of procedure (CCAM) code DDQF202 “Mesure du flux de réserve coronarien [FFR] au cours d’une artériographie coronaire” in October 2015.

Conditions for reimbursement were established in the report of National Authority of Health (HAS) in 2015. The estimated target population for FFR is about 26,000 – 31,000 patients annually.

In order to create specific and sufficient reimbursement for guidewire device, Philips Volcano applied for add-on reimbursement via LPPR title V, which is dedicated for invasive non-implantable devices. MTRC has reported recently that Medtronic’s IN.PACT Admiral was among first invasive non-implantable devices to get add-on reimbursement in France.

No specific clinical data were available for guidewires in scope. The applicant claimed equivalence to the PRESSUREWIRE device (St. Jude Medical, now Abbott), which was used in the landmark FAME I and FAME II trials. Verrata guidewire was partly used in the French FUTURE study, which was stopped preliminary. Decision of the Committee was mainly based on the results of FAME I and FAME II trials.

The inscription is expected after negotiation about price, which will be determined nationally for technology. It can take about a year until reimbursement will be established. Once established, inscription will be valid for 3 years.

Decision of CNEDiMTS is available in French here.

Positive decision of CNEDiMTS in relation to products of Philips Volcano just 2 months after positive decision in relation to Abbott’s (previously – St. Jude Medical) PressureWire (Certus, Aeris and X) devices indicates that two companies will have more or less simultaneous start with add-on reimbursement on the French market.

Subscribe to our biweekly newsletter not to miss important reimbursement information.

The latest related news

24

Mar 2022

The HTA body of the Tuscany Regional Healthcare issues two types of documents: HTA forms and motivational forms. With a regional decree 2472 of February 10, 2022, Tuscany Regional Healthcare has published assessments of five medical devices of various therapeutic areas, such as cardiovascular and peripheral vascular areas.

Read more

18

Mar 2022

On February 22, 2022, a repository of innovative acts outside the nomenclature of biology and anatomopathology (RIHN) and a Supplementary list of IVD tests were published. Minor changes were introduced in the 2022 RIHN list.

Read more

15

Mar 2022

The Belgian Health Care Knowledge Center (KCE) initiated a study aimed at defining a clear and transparent procedure for the evaluation of digital health technologies in Belgium.

Read more

14

Mar 2022

In February 2021, the Clinical Coding and Schedule Development (CCSD) working group, which develops and maintains procedural and diagnostics nomenclature for private payers in England, published Bulletins 0182 and 0079 with changes to be implemented no later than April 10, 2022. Three new procedure codes concerned robotic surgery in orthopaedic area, spinal procedures, and ophthalmology, and five new diagnostic codes were introduced.

Read more

11

Mar 2022

On February 07, 2022, the Dental and Pharmaceutical Benefits Agency has announced the withdrawal of the assessments of the PhysioMem PM 100 and CardioMem CM 100 XT and the finalization of the assessments of the Zenicor ECG, Coala Heart Monitor Pro, and KardiaMobile. For the conducted assessments, it was outlined that the portable devices provide more limited information than standard ECG measurements; therefore, it was mainly estimated for atrial fibrillation.

Read more