2014
DOI: 10.1016/j.bjps.2014.05.037
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Characteristic features and natural evolution of Kienböck's disease: Five years' results of a prospective case series and retrospective case series of 106 patients

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Cited by 13 publications
(6 citation statements)
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“…This situation is rarely described in the literature, and emphasizes the need to evaluate the vascularity of the proximal scaphoid pole better, because most of the cases were intermediate grade, rather than complete necrosis or fully viable bone. Other pathologies that involve avascular necrosis have been studied in more detail, such as Kienböck's disease or avascular necrosis of the maxilla [35,36]. Therefore, our data provide prognostic information regarding this difficult condition, and further experimental and clinical studies are required to determine the successful surgical outcome, depending on the histological pattern.…”
Section: Discussionmentioning
confidence: 89%
“…This situation is rarely described in the literature, and emphasizes the need to evaluate the vascularity of the proximal scaphoid pole better, because most of the cases were intermediate grade, rather than complete necrosis or fully viable bone. Other pathologies that involve avascular necrosis have been studied in more detail, such as Kienböck's disease or avascular necrosis of the maxilla [35,36]. Therefore, our data provide prognostic information regarding this difficult condition, and further experimental and clinical studies are required to determine the successful surgical outcome, depending on the histological pattern.…”
Section: Discussionmentioning
confidence: 89%
“…Demographic parameters and stage distributions were comparable among all treatment groups except when comparing the pre-operative stages in the RSO group and in the RSO and VBG groups. However, group classification according to the initial stage of KD was not performed for the following reasons: (1) it has been previously suggested that initial KD stage, according to Lichtman, has no influence on treatment outcome [ 25 , 26 ]; (2) the validity of current classifications has been questioned because arthritis of the lunate can be observed in the absence of lunate fracture or carpal collapse [ 1 ]; (3) the reliability and comparability of KD stages in literature is limited because no distinction is generally made regarding the localization of arthritis (lunate cartilage, lunate facet, or the entire radiocarpal joint) and because there is no consensus regarding the diagnostic requirements for KD and associated arthritis (X-ray, MRI, CT scan, or arthroscopy) [ 1 ]; (4) because KD may progress from a preserved lunate shape to fragmentation within 6 months [ 1 ], staging may not be accurate if more than 4 weeks have elapsed between diagnosis and surgery; (5) a correlation between radiological parameters of KD classifications and the clinical course has not been established, while many authors have observed a poor correlation with clinical findings [ 27 , 28 ].…”
Section: Discussionmentioning
confidence: 99%
“…If no response was received in the following 6 weeks, the patients were contacted by telephone, and an appointment for the clinical examination was arranged during which the self-assessment questionnaire was given to the patient. The questionnaire was developed by a multidisciplinary team consisting of one occupational physician, two hand surgeons, one psychiatrist, and one epidemiologist, as previously described [ 1 ].…”
Section: Methodsmentioning
confidence: 99%
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“…• Previous wrist injuries • Genetic predisposition 38,39 • Kienböck's disease 40 • Preiser's disease 41 • Rheumatoid arthritis • Postinfectious arthritis…”
Section: Cartilage Injuries and Carpal Bone Fracturesmentioning
confidence: 99%