Tag: registry

Most “Big Data” research has “very low” academic impact

The use of large registry-based datasets in spinal research has exploded in recent years. Often criticised for potentially limited clinical relevance, little research has...

Two-year Scoli-Risk-1 data offer revealing adult spinal deformity results

A number of studies presented at the Scoliosis Research Society Annual Meeting (SRS; 21–24 September, Prague, Czech Republic) and at Eurospine (5–7 October, Berlin,...

Depressed adult spinal deformity patients improve at same magnitude as non-depressed...

The first prospective study analysing the impact of depressive symptoms in surgically-treated severe adult spinal deformity patients on health-related quality of life outcomes has...