Diffusion-Weighted Imaging Distinguishes Between Osteomyelitis, Bone Marrow Edema, and Healthy Bone on Forefoot Magnetic Resonance Imaging.


Journal

Journal of magnetic resonance imaging : JMRI
ISSN: 1522-2586
Titre abrégé: J Magn Reson Imaging
Pays: United States
ID NLM: 9105850

Informations de publication

Date de publication:
11 2022
Historique:
revised: 16 01 2022
received: 20 11 2021
accepted: 19 01 2022
pubmed: 3 2 2022
medline: 15 10 2022
entrez: 2 2 2022
Statut: ppublish

Résumé

Diagnosis of osteomyelitis by imaging can be challenging. The feasibility of diffusion-weighted imaging (DWI) as ancillary sequence was evaluated in this study. To evaluate DWI for differentiation between osteomyelitis, bone marrow edema, and healthy bone on forefoot magnetic resonance imaging (MRI). Prospective. A total of 60 consecutive patients undergoing forefoot MRI divided into three study groups (20 subjects each): osteomyelitis, bone marrow edema, and healthy bone. A 1.5T and 3T MRI scanners; readout-segmented multishot echo planar DWI. Two independent radiologists measured apparent diffusion coefficient (ADC) values within abnormal or healthy bone. ADC values were compared between groups (pairwise t-test with Bonferroni-Holm correction for multiple testing). Intraclass correlation coefficient (ICC) was calculated to assess inter-reader agreement. Threshold ADC values were determined as the cutoffs that maximized the sum of sensitivity and specificity. Receiver operating characteristic (ROC) analysis was performed with statistical threshold of P < 0.05. Inter-reader agreement was 0.92 in the healthy bone group and 0.78 in both the edema and osteomyelitis groups. Average ADC values were significantly different between groups: 1432 ± 222 × 10 DWI with ADC maps distinguishes between healthy and abnormal bone on forefoot MRI. Calculated cutoff values allow confirmation or exclusion of osteomyelitis in a high proportion of subjects. 2 TECHNICAL EFFICACY: Stage 2.

Sections du résumé

BACKGROUND
Diagnosis of osteomyelitis by imaging can be challenging. The feasibility of diffusion-weighted imaging (DWI) as ancillary sequence was evaluated in this study.
PURPOSE
To evaluate DWI for differentiation between osteomyelitis, bone marrow edema, and healthy bone on forefoot magnetic resonance imaging (MRI).
STUDY TYPE
Prospective.
SUBJECTS
A total of 60 consecutive patients undergoing forefoot MRI divided into three study groups (20 subjects each): osteomyelitis, bone marrow edema, and healthy bone.
FIELD STRENGTH/SEQUENCE
A 1.5T and 3T MRI scanners; readout-segmented multishot echo planar DWI.
ASSESSMENT
Two independent radiologists measured apparent diffusion coefficient (ADC) values within abnormal or healthy bone.
STATISTICAL TESTS
ADC values were compared between groups (pairwise t-test with Bonferroni-Holm correction for multiple testing). Intraclass correlation coefficient (ICC) was calculated to assess inter-reader agreement. Threshold ADC values were determined as the cutoffs that maximized the sum of sensitivity and specificity. Receiver operating characteristic (ROC) analysis was performed with statistical threshold of P < 0.05.
RESULTS
Inter-reader agreement was 0.92 in the healthy bone group and 0.78 in both the edema and osteomyelitis groups. Average ADC values were significantly different between groups: 1432 ± 222 × 10
DATA CONCLUSION
DWI with ADC maps distinguishes between healthy and abnormal bone on forefoot MRI. Calculated cutoff values allow confirmation or exclusion of osteomyelitis in a high proportion of subjects.
EVIDENCE LEVEL
2 TECHNICAL EFFICACY: Stage 2.

Identifiants

pubmed: 35106870
doi: 10.1002/jmri.28091
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1571-1579

Informations de copyright

© 2022 International Society for Magnetic Resonance in Medicine.

Références

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Auteurs

Konrad A Kruk (KA)

Division of Radiology and Nuclear Medicine, Kantonsspital St. Gallen, St. Gallen, CH-9007, Switzerland.
Faculty of Medicine, University of Zurich, Zurich, CH-8091, Switzerland.

Tobias J Dietrich (TJ)

Division of Radiology and Nuclear Medicine, Kantonsspital St. Gallen, St. Gallen, CH-9007, Switzerland.
Faculty of Medicine, University of Zurich, Zurich, CH-8091, Switzerland.

Simon Wildermuth (S)

Division of Radiology and Nuclear Medicine, Kantonsspital St. Gallen, St. Gallen, CH-9007, Switzerland.
Faculty of Medicine, University of Zurich, Zurich, CH-8091, Switzerland.

Sebastian Leschka (S)

Division of Radiology and Nuclear Medicine, Kantonsspital St. Gallen, St. Gallen, CH-9007, Switzerland.
Faculty of Medicine, University of Zurich, Zurich, CH-8091, Switzerland.

Andreas Toepfer (A)

Department of Orthopaedics and Traumatology, Kantonsspital St. Gallen, St. Gallen, Switzerland.

Stephan Waelti (S)

Division of Radiology and Nuclear Medicine, Kantonsspital St. Gallen, St. Gallen, CH-9007, Switzerland.
Faculty of Medicine, University of Zurich, Zurich, CH-8091, Switzerland.

Chan-Hi Olaf Kim (CO)

Division of Radiology and Nuclear Medicine, Kantonsspital St. Gallen, St. Gallen, CH-9007, Switzerland.

Sabine Güsewell (S)

Clinical Trials Unit, Kantonsspital St. Gallen, St. Gallen, Switzerland.

Tim Fischer (T)

Division of Radiology and Nuclear Medicine, Kantonsspital St. Gallen, St. Gallen, CH-9007, Switzerland.
Faculty of Medicine, University of Zurich, Zurich, CH-8091, Switzerland.

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