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Health economic modeling for medical technologies in Europe

Early and comprehensive economic models to determine economic value proposition and inform healthcare decision-makers

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Reimbursement summary for angioplasty of arteries of lower extremities

This post presents an extract from our reimbursement analysis for angioplasty of arteries lower extremities using plain and drug-coated balloons (DCBs) for peripheral artery disease in England, France and Germany. Plain balloon angioplasty is reimbursement via DRG solely and DCBs are reimbursement via combination of DRG and add-on reimbursement.
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Med Tech-related technology assessments and clinical guidelines from NICE in April 2023

In April 2023, NICE published seven new Interventional Procedures Guidance (IPG). IPG is developed for most of the novel interventional procedures entering the English market. The program focuses solely on clinical evidence. Recommendations may vary from "for research only" to "for use with standard arrangements for clinical governance, consent, and audit." Recommendations are not binding, although they are followed by providers and commissioners.

NICE recommended the following procedures to be used with standard arrangements for clinical governance, consent, and audit, as evidence of their safety and efficacy is adequate:

Recommendations for endoscopic ultrasound-guided biliary drainage (EUS-BD) for biliary obstruction differ depending on the clinical condition leading to obstruction:

  • EUS-BD for biliary obstruction caused by distal malignant disease is recommended for use with standard arrangements for clinical governance, consent, and audit, as evidence on the safety and efficacy is adequate;
  • EUS-BD for biliary obstruction caused by the malignant hilar or benign disease should be used only in research, as evidence on the safety and efficacy is inadequate in quality and quantity.

NICE recommended the following procedures to be used with special arrangements for clinical governance, consent, and audit or research:

One procedure, Daytime intraoral neuromuscular electrical tongue stimulation using a removable device for obstructive sleep apnoea, is recommended to be used only in research, as evidence of the safety and efficacy is inadequate in quantity and quality.

Medical Technologies Guidance (MTG) evaluates new, innovative medical devices and diagnostics. It looks at medical technologies that deliver treatment, like those implanted during surgical procedures, gives greater independence to patients, or detect or monitor medical conditions.

In April 2023, NICE issued one new MTG on AposHealth for knee osteoarthritis. NICE recommended it as a cost-saving option to manage knee osteoarthritis in adults if non-surgical standard care has not worked well enough and their condition meets the referral criteria for total knee replacement surgery, but they do not want surgery, and data is collected (on quality of life, health resource use and knee replacement surgery in the long term). Further research is recommended.

The MedTech Innovation Briefings (MIBs) is the advice program of NICE for innovative technologies. It provides an overview of clinical effectiveness, safety, and cost. It does not offer formal guidance, and it, therefore, does not provide any recommendations.

One new MIB published in April 2023 concerned Fasciotens for abdominal wall closure. It uses controlled traction and allows the closure of complex hernias and the open abdomen, reducing the need for mesh bridging or component separation.

Three clinical guidelines were updated in April 2023:

See the full details for guidance here and for MIBs here.

This news is just one of about 300 market access news collected by our team in the subscription services "HTA Alerts" and "Reimbursement Alerts" every two weeks from more than 80 organizations. Access our paid subscription services to stay on top of all developments specifically for your products in Europe (reimbursement news) and globally (HTA news). Contact us to get a free, three-month, no-obligation trial.