Evidence map›Paper›PMID 40625064›Full record

ArticleInternational journal of technology assessment in health care2025

Institutionalization of Health Technology Assessment of medical devices: a cluster analysis of EU, EEA, and EFTA countries.

Mario Cesare Nurchis, Gian Marco Raspolini, Pietro Derrico, Carlo Favaretti, Matteo Ritrovato, Giandomenico Nollo, Gianfranco Damiani

Abstract read
In one paragraph

Article in International journal of technology assessment in health care, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Mario Cesare NurchisDepartment of Life Science, Health, and Health Professions, https://ror.org/035mh1293Università degli Studi Link, Rome, Italy.ORCID https://orcid.org/0000-0002-9345-4292
Gian Marco RaspoliniDepartment of Health Science and Public Health, Section of Hygiene, https://ror.org/03h7r5v07Università Cattolica del Sacro Cuore, Rome, Italy.ORCID https://orcid.org/0000-0002-7983-5814
Pietro DerricoSocietà Italiana di Health Technology Assessment (SIHTA), Rome, Italy.
Carlo FavarettiLeadership in Medicine Research Center, https://ror.org/03h7r5v07Università Cattolica del Sacro Cuore, Rome, Italy.
Matteo RitrovatoSocietà Italiana di Health Technology Assessment (SIHTA), Rome, Italy.
Giandomenico NolloSocietà Italiana di Health Technology Assessment (SIHTA), Rome, Italy.
Gianfranco DamianiDepartment of Health Science and Public Health, Section of Hygiene, https://ror.org/03h7r5v07Università Cattolica del Sacro Cuore, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesHealth technology assessment of medical devices (HTA-MDs) presents unique challenges compared to pharmaceuticals. Total MD expenditure continues to grow in Europe, and countries typically conduct their own HTA-MDs evaluations, with varying institutionalization arrangements. European Union's (EU's) HTA Regulation aims to establish collaborative clinical assessments across Member States, potentially expediting the path from EU safety certification of MDs to pricing and reimbursement decisions. This study aims to identify emergent configurations among institutionalizations of HTA-MDs in the EU, European Economic Area (EEA), and European Free Trade Association (EFTA) countries.

methodsPublicly available data were cross-sectionally collected for EU, EEA, and EFTA countries until August 2024 to allow a cross-country analysis of HTA-MDs institutionalizations. Countries were included if they had at least one publicly mandated body for HTA-MDs. Data sources were scientific databases, institutional websites, and HTA bodies' documentation. A framework of 16 elements, qualitatively describing the institutionalization of HTA-MDs, was developed based on a document review and used as a dataset for agglomerative hierarchical cluster analysis to identify patterns of HTA-MDs institutionalization.

resultsThe 21 included countries formed three clusters: Cluster 1 featured regulatory-focused, legally bound HTA-MDs systems with mandatory assessments determining reimbursement decisions; Cluster 2 was characterized by regulatory functions, external expert collaboration, formal prioritization processes, and organized Horizon Scanning; Cluster 3 showed recommendatory functions, nonmandatory assessments, and limited impact on reimbursement decisions.

conclusionsHTA-MDs institutionalizations could benefit from implementing prioritization processes of evaluations, establishing networks of collaborative assessment centers, and ensuring links between evaluations and reimbursement decisions.

Indexed as

Equipment and SuppliesTechnology Assessment, BiomedicalCluster AnalysisCross-Sectional StudiesEuropeEuropean UnionHumansbiomedicalcluster analysisequipment and suppliesEuropepolicy makingtechnology assessment

Identifiers

PMID40625064
PMCPMC12303692

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.