Please use this identifier to cite or link to this item: http://hdl.handle.net/11434/933
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dc.contributor.authorFeller, Julian-
dc.contributor.authorWhitehead, Timothy-
dc.contributor.otherCicuttini, Flavia-
dc.contributor.otherLloyd, David-
dc.contributor.otherBryant, A. L.-
dc.contributor.otherWang, Xinyang-
dc.contributor.otherWang, Yuanyuan-
dc.contributor.otherBennell, Kim-
dc.contributor.otherWrigley, Tim-
dc.contributor.otherFortin, K.-
dc.contributor.otherSaxby, David-
dc.contributor.otherVan Ginckel, Ans-
dc.contributor.otherDempsey, A. R.-
dc.contributor.otherGrigg, N.-
dc.contributor.otherVertullo, C.-
dc.contributor.otherBryant, A. L.-
dc.date.accessioned2016-11-29T03:29:31Z-
dc.date.available2016-11-29T03:29:31Z-
dc.date.issued2015-10-
dc.identifier.citation2015 Oct. 27en_US
dc.identifier.issn0942-2056 (Print); 1433-7347 (Online)en_US
dc.identifier.urihttp://hdl.handle.net/11434/933-
dc.description.abstractPURPOSE: To examine differences in cartilage morphology between young adults 2-3 years post-anterior cruciate ligament reconstruction (ACLR), with or without meniscal pathology, and control participants. METHODS: Knee MRI was performed on 130 participants aged 18-40 years (62 with isolated ACLR, 38 with combined ACLR and meniscal pathology, and 30 healthy controls). Cartilage defects, cartilage volume and bone marrow lesions (BMLs) were assessed from MRI using validated methods. RESULTS: Cartilage defects were more prevalent in the isolated ACLR (69 %) and combined group (84 %) than in controls (10 %, P < 0.001). Furthermore, the combined group showed higher prevalence of cartilage defects on medial femoral condyle (OR 4.7, 95 % CI 1.3-16.6) and patella (OR 7.8, 95 % CI 1.5-40.7) than the isolated ACLR group. Cartilage volume was lower in both ACLR groups compared with controls (medial tibia, lateral tibia and patella, P < 0.05), whilst prevalence of BMLs was higher on lateral tibia (P < 0.001), with no significant differences between the two ACLR groups for either measure. CONCLUSIONS: Cartilage morphology was worse in ACLR patients compared with healthy controls. ACLR patients with associated meniscal pathology have a higher prevalence of cartilage defects than ACLR patients without meniscal pathology. The findings suggest that concomitant meniscal pathology may lead to a greater risk of future OA than isolated ACLR.en_US
dc.publisherSpringeren_US
dc.subjectAnterior Cruciate Ligament Reconstructionen_US
dc.subjectOsteoarthritisen_US
dc.subjectMeniscal Injuryen_US
dc.subjectMagnetic Resonance Imagingen_US
dc.subjectCartilageen_US
dc.subjectACLRen_US
dc.subjectMRIen_US
dc.subjectCartilage Morphologyen_US
dc.subjectLligament Reconstructionen_US
dc.subjectMedial Tibiaen_US
dc.subjectLateral Tibiaen_US
dc.subjectPatellaen_US
dc.subjectMedial Femoral Condyleen_US
dc.subjectBone Marrow Lesionsen_US
dc.subjectBMLsen_US
dc.subjectConcomitant Meniscal Pathologyen_US
dc.subjectOAen_US
dc.subjectOsteoarthritisen_US
dc.subjectMusculoskeletal Clinical Institute, Epworth HealthCare, Victoria, Australiaen_US
dc.titleCartilage morphology at 2-3 years following anterior cruciate ligament reconstruction with or without concomitant meniscal pathology.en_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1007/s00167-015-3831-1en_US
dc.identifier.journaltitleKnee Surgery, Sports Traumatology, Arthroscopyen_US
dc.description.pubmedurihttps://www.ncbi.nlm.nih.gov/pubmed/26506844en_US
dc.description.affiliatesCentre for Health, Exercise and Sports Medicine, Department of Physiotherapy, School of Health Sciences, The University of Melbourne, Melbourne, VIC, Australia. xinyangw@student.unimelb.edu.au.en_US
dc.description.affiliatesSchool of Public Health and Preventive Medicine, Alfred Hospital, Monash University, Melbourne, VIC, Australia. yuanyuan.wang@monash.edu.en_US
dc.description.affiliatesCentre for Health, Exercise and Sports Medicine, Department of Physiotherapy, School of Health Sciences, The University of Melbourne, Melbourne, VIC, Australia. k.bennell@unimelb.edu.au.en_US
dc.description.affiliatesCentre for Health, Exercise and Sports Medicine, Department of Physiotherapy, School of Health Sciences, The University of Melbourne, Melbourne, VIC, Australia. timw@unimelb.edu.au.en_US
dc.description.affiliatesSchool of Public Health and Preventive Medicine, Alfred Hospital, Monash University, Melbourne, VIC, Australia. flavia.cicuttini@monash.edu.en_US
dc.description.affiliatesCentre for Health, Exercise and Sports Medicine, Department of Physiotherapy, School of Health Sciences, The University of Melbourne, Melbourne, VIC, Australia. kfortin@unimelb.edu.au.en_US
dc.description.affiliatesCentre for Musculoskeletal Research, Griffith University, The Gold Coast, QLD, Australia. davidsaxby@gmail.com.en_US
dc.description.affiliatesCentre for Health, Exercise and Sports Medicine, Department of Physiotherapy, School of Health Sciences, The University of Melbourne, Melbourne, VIC, Australia. ans.van@unimelb.edu.au.en_US
dc.description.affiliatesCentre for Musculoskeletal Research, Griffith University, The Gold Coast, QLD, Australia. a.dempsey@murdoch.edu.au.en_US
dc.description.affiliatesSchool of Psychology and Exercise Science, Murdoch University, Perth, WA, Australia. a.dempsey@murdoch.edu.au.en_US
dc.description.affiliatesCentre for Musculoskeletal Research, Griffith University, The Gold Coast, QLD, Australia. ngrigg.phd@gmail.com.en_US
dc.description.affiliatesOrthopaedic Surgery and Sports Medicine Centre, The Gold Coast, QLD, Australia. vertullo@me.comen_US
dc.description.affiliatesLa Trobe University Medical Centre, Melbourne, VIC, Australia. feller.admin@osv.com.au.en_US
dc.description.affiliatesCentre for Musculoskeletal Research, Griffith University, The Gold Coast, QLD, Australia. david.lloyd@griffith.edu.au.en_US
dc.description.affiliatesCentre for Health, Exercise and Sports Medicine, Department of Physiotherapy, School of Health Sciences, The University of Melbourne, Melbourne, VIC, Australia. albryant@unimelb.edu.au.en_US
dc.type.studyortrialCohort Studyen_US
dc.type.contenttypeTexten_US
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