Osseointegrated Amputation Prosthesis for Patients

Osseo-integrated prostheses involve direct contact between the titanium implant and the bone. They provide an alternative for patients who cannot use conventional socket prostheses, because of recurrent skin infections, ulceration in the socket contact area, a short residual limb or extensive skin grafting.

For a well-defined group of patients, this type of prostheses has proven to be efficient and safe. Hence, the commission de remboursement des implants et des dispositifs medicaux invasifs (CRIDMI) of the RIZIV-INAMI recently decided to reimburse osseo-integrated prostheses under the conditions mentioned in annex 2.

Registration of additional information via healthdata is part of the reimbursement conditions. 3 years after the start of the reimbursement, the implanting and rehabilitation centres will have to draft a report to the CRIDMI based on the registered data.

Data and Resources

Osseointegrated Amputation Prosthesis for Patientsjson
Machine-readable representation of this dataset.

Download
Case Report Form Reimbursement Of Implants That Allow The Fixation Of An External Prosthesis (Amputation) v1.0html
Go to resource

Field	Value
Modified	2019-10-25
Release Date	2018-08-14
Identifier	3e6af9bd-57a2-41d7-82ce-1bf91db569b0
License	Creative Commons Attribution
Public Access Level	Public

Protocol

Protocol
Full title of the project	Osseointegrated Amputation Prosthesis for Patients
Title of the project for lay people, in easily understood, i.e. non-technical, language	AMPUTATION
Name or abbreviated title of the project where available	AMPUTATION
Source type	Administrative sources Patient registries

Sponsor(s)

Primary organization that oversees implementation of study and is responsible for data analysis.
Name of organisation	Rijksinstituut voor Ziekte- en Invaliditeitsverzekering – Institut National d’Assurance Maladie Invalidité (RIZIV-INAMI)

Commissioner(s)

Organisation that commissioned this project
Name of organisation	National Institute for Health and Disability Insurance
Website(s) of organisation	Website

Source(s) of Monetary or Material Support

Organisation providing support
Name of organisation	National Institute for Health and Disability Insurance
Website(s) of organisation	Website

Governance

Governance
Is there a Steering / Accompanying committee?	No

General information

General information
Project description	Osseo-integrated prostheses involve direct contact between the titanium implant and the bone. They provide an alternative for patients who cannot use conventional socket prostheses, because of recurrent skin infections, ulceration in the socket contact area, a short residual limb or extensive skin grafting. For a well-defined group of patients, this type of prostheses has proven to be efficient and safe. Hence, the commission de remboursement des implants et des dispositifs medicaux invasifs (CRIDMI) of the RIZIV-INAMI recently decided to reimburse osseo-integrated prostheses under the conditions mentioned in annex 2. Registration of additional information via healthdata is part of the reimbursement conditions. 3 years after the start of the reimbursement, the implanting and rehabilitation centres will have to draft a report to the CRIDMI based on the registered data.
Links	Data Collection overview for project Amputation

Therapeutic area
Disease	Musculoskeletal Diseases

Objective of the project
Main objective of the project	The objectives of the registration are to assess the quality of life after implantation, the re-education process, the lifespan of the implant as well as the revisions that are required.
Additional information	No additional information available

Scope
Scope	Public Administration Quality of care research Therapy

Legal basis

Type of legal basis
Type of legal basis	Unknown

Legal documents
Full reference of legal document	Het K.B. van 25 juni 20141

Design of the project

Principal inclusion and exclusion criteria
Principal inclusion criteria	Patients who comply to the inclusion criteria as determined in CRIDMI note n° 2016/323 – see annex 2: Patients with a major amputation of at least 2/3rd of the femoral length or ½ of the humeral length, and for whom the use of a socket prosthesis is technically impossible. OR Patients who had a transfemoral or transhumeral amputation and for whom a normal and sustainable use of the socket prosthesis is impossible as a result of recurring dermatological problems which can not be treated by a prosthesist, by dermatological treatment or via surgery. AND The patient’s general condition must allow implanting the implant according to the instructions and must allow to attend a rehabilitation program. The patient is less than 70 years of age, and in case of a femoral implant has a weight (prosthesis included) of less than 100kg. The patient engages to strictly follow the rehabilitation program The number of patients that are eligible for reimbursement is estimated at around 10 per year.

Data transfer frequency
Data transfer frequency	Ad hoc (event based)

Method of data transfer
Data transfer method(s)	eHealthbox of eHealth Platform

Sites involved in the project

Type of site(s)
Care Provider	University hospitals

Health professionals involved (encoding) in the project

Health professionals involved (encoding) in the project
Care Giver	Physicians
Specialty of physicians involved (encoding) in the project	Unknown
Type of paramedical professionals involved (encoding) in the project	Unknown

Informed consent

Informed consent
Are subjects informed?	Yes
How are subjects informed?	No information available
Do subjects have to give their consent?	No information available
How do subjects give their consent?	No information available
Is there a procedure to provide subjects the ability to consult their registered information?	No information available
Is there a procedure to provide subjects the ability to correct their registered information?	No information available
Additional information	No additional information available

Review

Ethics Committee
Authorization by an Ethics Committee?	Not applicable

Sectoral Committee National Registry (Privacy Commission)
Authorization by the sectorial committee Health / Social affairs of the Privacy Commission	No

Sectoral Committee Health / Social affairs (Privacy Commission)
Authorization by the sectorial committee Health / Social affairs of the Privacy Commission	Yes
Full name committee	Sectoraal Comité van de Sociale Zekerheid en van de Gezondheid
Date of decision	2017-05-16
Title decision	BERAADSLAGING NR. 17/043 VAN 16 MEI 2017 BETREFFENDE DE MEDEDELING VAN GECODEERDE PERSOONSGEGEVENS DIE DE GEZONDHEID BETREFFEN DOOR ZORGVERLENERS VIA HET HEALTHDATA-PLATFORM IN HET KADER VAN HET PROJECT “OSSEO-INTEGRATED PROSTHESES FOR AMPUTATION PATIENTS”
Nr. Decision	SCSZG/17/088

Sectoral Committee Crossroads Bank of Enterprises (Privacy Commission)
Authorization by the sectorial committee Crossroads Bank of Enterprises of the Privacy Commission (Y/N)	Not applicable

Data dictionary

Classifications and Terminology
Name	Unknown

Data quality

Data quality
First year for which data is available	No information available
Procedures for checking and validating the source data	Validation levels are incorporated in the data collection process: Validation rules: validation rules are the set of predefined and functional definitions that are defined by the responsible researcher of organization. Every new registration entered in the application needs to comply to these validation rules before they can be transferred. Revision: a revision of the data is done by the responsible researcher after receiving the data to exclude any anomaly that was not detected by the validation rules.
Data compilation process	No information available
Punctuality for the most recent completed data collection: the data collection was completed	No information available
Participation rate of the health institutions	No information available
Participation rate of the health professionals	No information available
Extent of unit non-response	No information available
Extent of the item non-response	The rate of item non-response is not known or unacceptably high (>50%)
Extend to which the collected data are comparable across the Belgian regions	Comparability across the Belgian areas is unknown
Comparable or reconcilable over time	Comparability over time is unknown
Additional information	No additional information available
Extent of problems with the misclassification of statistical units for their key variables	No information available
Can records belonging to same entity be matched?	No information available
Additional information	No additional information available

Data storage

Data storage
The organisation in charge of storage of the collected data, is certified as being compliant with the international standards on information security management system (eg. ISO27001)?	No
Additional information	No additional information available

Data access

Data access
Written Data sharing policy?	No information available

Request data

Primary tabs

License

Other Access