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Opportunistically identifiable vertebral fractures on routine radiological imaging predict mortality: observational cohort study.
Skjødt, Michael Kriegbaum; Nicolaes, Joeri; Smith, Christopher Dyer; Olsen, Kim Rose; Libanati, Cesar; Cooper, Cyrus; Abrahamsen, Bo.
Affiliation
  • Skjødt MK; Department of Medicine, Holbæk Hospital, Holbæk, Denmark. miksk@regionsjaelland.dk.
  • Nicolaes J; OPEN - Open Patient data Explorative Network, Department of Clinical Research, University of Southern Denmark and Odense University Hospital, Odense, Denmark. miksk@regionsjaelland.dk.
  • Smith CD; Department of Electrical Engineering (ESAT), Center for Processing Speech and Images, KU Leuven, Leuven, Belgium.
  • Olsen KR; UCB Pharma, Brussels, Belgium.
  • Libanati C; OPEN - Open Patient data Explorative Network, Department of Clinical Research, University of Southern Denmark and Odense University Hospital, Odense, Denmark.
  • Cooper C; DaCHE, Institute of Public Health, University of Southern Denmark, Odense, Denmark.
  • Abrahamsen B; UCB Pharma, Brussels, Belgium.
Osteoporos Int ; 35(4): 691-703, 2024 Apr.
Article in En | MEDLINE | ID: mdl-38236389
ABSTRACT
In men and women with opportunistically identifiable vertebral fractures (VFs) on routine CT scans including the chest and/or abdomen, the risk of death is 51% higher than in those with no VF on the CT scan, and 325% higher than an age- and sex-matched general population cohort.

PURPOSE:

There is little knowledge about the risk of death in patients with VFs present on routine radiological imaging. We evaluated the risk of death in men and women aged 50 years or older with opportunistically identifiable VFs on routine CT scans and not treated with osteoporosis medications.

METHODS:

Thoracic and lumbar VFs were identified through a blinded, two-step approach on CT scans performed as part of normal clinical care in a Danish hospital in 2010 or later. Subjects with VF were matched on age and sex against those with no VF (12-ratio) and a general population cohort (13-ratio), respectively, and followed for up to 7 years through the national Danish registers. Subjects treated with an osteoporosis medication in the year prior to baseline were excluded.

RESULTS:

Subjects with VF had a significantly higher risk of death during follow-up as compared to subjects with no VF on the CT scan (adjusted hazard ratio [HR] 1.51 [95% confidence interval 1.27-1.79; p < 0.001]) and even more so when compared to the general population cohort (HR 4.25 [3.53-5.12; p < 0.001]). In subjects with versus without VF on the CT scan, the risk was higher in those with moderate or severe VF, in those with no malignancy prior to baseline, and in those with a lower Charlson comorbidity index score.

CONCLUSION:

Subjects with VF available for identification on routine CT scans face a substantially increased risk of death. Opportunistic identification and reporting of VF is important to identify these patients to allow intervention if indicated.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteoporosis / Spinal Fractures / Osteoporotic Fractures Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male / Middle aged Language: En Journal: Osteoporos Int Journal subject: METABOLISMO / ORTOPEDIA Year: 2024 Document type: Article Affiliation country: Dinamarca

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteoporosis / Spinal Fractures / Osteoporotic Fractures Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male / Middle aged Language: En Journal: Osteoporos Int Journal subject: METABOLISMO / ORTOPEDIA Year: 2024 Document type: Article Affiliation country: Dinamarca