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Predicting pathological fracture in femoral metastases using a clinical CT scan based algorithm: A case–control study

  • Stein J. Janssen*
  • , Nuno Rui Paulino Pereira
  • , Timion A. Meijs
  • , Miriam A. Bredella
  • , Marco L. Ferrone
  • , C. Niek van Dijk
  • , Jos A.M. Bramer
  • , Santiago A. Lozano-Calderón
  • , Joseph H. Schwab
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Background: We assessed whether there was a difference in attenuation measurements (in Hounsfield units – HU) and geometric distribution of HU between femora with metastatic lesions that fracture, and metastatic lesions that did not fracture nor underwent prophylactic fixation. Methods: Nine patients with femoral metastases who underwent CT and developed a pathological fracture were matched to controls. All femora were delineated in axial CT slices using a region of interest (ROI) tool; the HU within these ROIs were used to calculate: (1) the cumulative HU of the affected over the nonaffected side per slice and presented as a percentage, and (2) the cumulative HU accounting for geometric distribution (polar moment of HU). We repeated the analyses including cortical bone only (HU of 600 and above). Results: CT-based calculations did not differ between patients with a lesion that fractured and those that did not fracture nor underwent prophylactic fixation when analyzing all tissue. However, when including cortical bone only, the pathological fracture group had a lower cumulative HU value compared to the no fracture and no fixation group for the weakest cross-sectional CT image (pathological fracture group, mean: 71, SD: 23 and no fracture and no prophylactic fixation group, mean: 85, SD: 18, p = 0.042) and the complete lesion analysis (pathological fracture group, mean: 78, SD: 21 and no fracture and no prophylactic fixation group, mean: 92, SD: 15, p = 0.032). Conclusion: The demonstrated CT-based algorithms can be useful for predicting pathological fractures in metastatic lesions.

Original languageEnglish
Pages (from-to)394-402
Number of pages9
JournalJournal of Orthopaedic Science
Volume23
Issue number2
DOIs
Publication statusPublished - 1 Mar 2018
Externally publishedYes

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