Overview
Video: Interview with Everard Munting (EUROSPINE’s President) on Spine Tango
Video: Why the registires matter? by Northgate Public Services, the host of Spine Tango
Since 2002, Spine Tango has been EUROSPINE’s international spine registry for quality assurance and research on surgical and non-surgical treatments and their outcomes.
Our mission is to gather data from international participants to provide performance benchmarking and a collective evidence base of treatment effectiveness, patient safety and best practice.
Our aim is that all registry participants and stakeholders should be able to benefit from access to these data.
The Spine Tango registry has many benefits for users and societies. A summary of the key benefits can be found in this document
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Spine Tango, a web-based application, is hosted by Northgate Public Services Ltd. (NPS) in the UK.
Why document your work? To monitor your performance and adverse events and benchmark them with the pool, providing real-life evidence of your work. Furthermore, the registry is your own research database.
Why a joint approach?
To date, over 750,000 forms from five continents have been collected.
We strongly encourage other national societies, hospitals and individual clinicians to join our internationally-recognised registry. Help gather collective evidence and benefit from feedback services.
Our mission is to gather data from international participants to provide performance benchmarking and a collective evidence base of treatment effectiveness, patient safety and best practice.
Our aim is that all registry participants and stakeholders should be able to benefit from access to these data.
The Spine Tango registry has many benefits for users and societies. A summary of the key benefits can be found in this document
.Spine Tango, a web-based application, is hosted by Northgate Public Services Ltd. (NPS) in the UK.
Why document your work? To monitor your performance and adverse events and benchmark them with the pool, providing real-life evidence of your work. Furthermore, the registry is your own research database.
Why a joint approach?
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To date, over 750,000 forms from five continents have been collected.
We strongly encourage other national societies, hospitals and individual clinicians to join our internationally-recognised registry. Help gather collective evidence and benefit from feedback services.
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