Health technology assessment of medical devices: a survey of non-European union agencies

Ciani, Oriana; Wilcher, Britni; Blankart, Carl Rudolf Berchtold; Hatz, Maximilian; Rupel, Valentina Prevolnik; Erker, Renata Slabe; Varabyova, Yauheniya; Taylor, Rod S (2015). Health technology assessment of medical devices: a survey of non-European union agencies. International journal of technology assessment in health care, 31(3), pp. 154-165. Cambridge University Press 10.1017/S0266462315000185

Full text not available from this repository. (Request a copy)

OBJECTIVES The aim of this study was to review and compare current health technology assessment (HTA) activities for medical devices across non-European Union HTA agencies. METHODS HTA activities for medical devices were evaluated from three perspectives: organizational structure, processes, and methods. Agencies were primarily selected upon membership of existing HTA networks. The data collection was performed in two stages: stage 1-agency Web-site assessment using a standardized questionnaire, followed by review and validation of the collected data by a representative of the agency; and stage 2-semi-structured telephone interviews with key informants of a sub-sample of agencies. RESULTS In total, thirty-six HTA agencies across twenty non-EU countries assessing medical devices were included. Twenty-seven of thirty-six (75 percent) agencies were judged at stage 1 to have adopted HTA-specific approaches for medical devices (MD-specific agencies) that were largely organizational or procedural. There appeared to be few differences in the organization, process and methods between MD-specific and non-MD-specific agencies. Although the majority (69 percent) of both categories of agency had specific methods guidance or policy for evidence submission, only one MD-specific agency had developed methodological guidelines specific to medical devices. In stage 2, many MD-specific agencies cited insufficient resources (budget, skilled employees), lack of coordination (between regulator and reimbursement bodies), and the inability to generalize findings from evidence synthesis to be key challenges in the HTA of medical devices. CONCLUSIONS The lack of evidence for differentiation in scientific methods for HTA of devices raises the question of whether HTA needs to develop new methods for medical devices but rather adapt existing methodological approaches. In contrast, organizational and/or procedural adaptation of existing HTA agency frameworks to accommodate medical devices appear relatively commonplace.

Item Type:

Journal Article (Original Article)

Division/Institute:

11 Centers of Competence > Center of Comptetence for Public Management (KPM)

UniBE Contributor:

Blankart, Carl Rudolf Berchtold

Subjects:

300 Social sciences, sociology & anthropology > 350 Public administration & military science
300 Social sciences, sociology & anthropology > 330 Economics

ISSN:

1471-6348

Publisher:

Cambridge University Press

Language:

English

Submitter:

Carl Rudolf Berchtold Blankart

Date Deposited:

05 Apr 2018 17:24

Last Modified:

05 Apr 2018 17:24

Publisher DOI:

10.1017/S0266462315000185

Related URLs:

PubMed ID:

26044729

Uncontrolled Keywords:

Health technology assessment Medical devices Reimbursement

URI:

https://boris.unibe.ch/id/eprint/112005

Actions (login required)

Edit item Edit item
Provide Feedback