Information letter on the introduction of ANQ quality measurement for SIRIS shoulder prostheses

We would like to take this opportunity to inform you about the upcoming introduction of the new ANQ quality measurement for the SIRIS shoulder register, which will become mandatory from 1 January 2025. This measurement is part of the continuous efforts to improve the quality of treatment in shoulder arthroplasty and was developed by the ANQ together with the SIRIS Foundation and the SIRIS Scientific Advisory Board (SSAB).
 

Key points:

• Obligation to participate: Registration in the SIRIS Shoulder Register will start on 1 January 2025 with a transition period during which clinics and hospitals will have the opportunity to adapt to the new requirements. From 1 July 2025, the registration of all primary shoulder prostheses and follow-up operations will then be mandatory.
• Patient consent: Written consent from the patient for data registration is mandatory. In the case of emergencies, this can also be obtained retrospectively during the hospitalisation. However, it must be obtained separately from the consent for surgery.
• Data integration: Data is recorded on the same platform as for SIRIS Hip and Knee, with the addition of a specific shoulder module. In addition to manual data entry, there are options for integration into existing hospital information systems via web service interfaces.
• Training: From January 2025, various training courses will be available to ensure the smooth implementation and use of the registry.

Detailed information on the introduction and the corresponding training courses can be found on the SIRIS website under ANQ SharingToo