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Parkinson's disease is overdiagnosed clinically at baseline in diagnostically uncertain cases: A 3‐year European multicenter study with repeat [123I]FP‐CIT SPECT

Identifieur interne : 000A43 ( Main/Corpus ); précédent : 000A42; suivant : 000A44

Parkinson's disease is overdiagnosed clinically at baseline in diagnostically uncertain cases: A 3‐year European multicenter study with repeat [123I]FP‐CIT SPECT

Auteurs : Vicky L. Marshall ; Cornelia B. Reininger ; Moritz Marquardt ; Jim Patterson ; Donald M. Hadley ; Wolfgang H. Oertel ; Hani T. S. Benamer ; Paul Kemp ; David Burn ; Eduardo Tolosa ; Jamie Kulisevsky ; Luis Cunha ; Durval Costa ; Jan Booij ; Klaus Tatsch ; K. Ray Chaudhuri ; Gudrun Ulm ; Oliver Pogarell ; Helmut Höffken ; Anja Gerstner ; Donald G. Grosset

Source :

RBID : ISTEX:82F70FF4E28E22E0A207F3F5207597591906AA0A

English descriptors

Abstract

Overdiagnosis of Parkinson's disease (PD) is suggested by specialist review of community diagnosis, and in postmortem studies. In specialist centers 4 to 15% of patients entered into clinical trials as early PD do not have functional imaging support for a PD diagnosis. In a European multicenter, prospective, longitudinal study, we compared clinical diagnosis with functional SPECT imaging using [123I]FP‐CIT (DaTSCAN™, GE Healthcare). Repeat observations were performed over 3 years in patients with tremor and/or parkinsonism in whom there was initial diagnostic uncertainty between degenerative parkinsonism and nondegenerative tremor disorders. Video‐recording of clinical features was scored independently of functional imaging results by two blinded clinicians at 36 months (= gold standard clinical diagnosis). Three readers, unaware of the clinical diagnosis, classified the images as normal or abnormal by visual inspection. The main endpoint was the sensitivity and specificity of SPECT imaging at baseline compared with the gold standard. In 99 patients completing the three serial assessments, on‐site clinical diagnosis overdiagnosed degenerative parkinsonism at baseline in diagnostically uncertain cases compared with the gold standard clinical diagnosis (at 36 months), the latter giving a sensitivity of 93% and specificity of 46%. The corresponding baseline [123I]FP‐CIT SPECT results showed a mean sensitivity of 78% and a specificity of 97%. Inter‐reader agreement for rating scans as normal or abnormal was high (Cohen's $\hat{\kappa}$ = 0.94–0.97). © 2008 Movement Disorder Society

Url:
DOI: 10.1002/mds.22108

Links to Exploration step

ISTEX:82F70FF4E28E22E0A207F3F5207597591906AA0A

Le document en format XML

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<name sortKey="Ulm, Gudrun" sort="Ulm, Gudrun" uniqKey="Ulm G" first="Gudrun" last="Ulm">Gudrun Ulm</name>
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<title level="j">Movement Disorders</title>
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<div type="abstract" xml:lang="en">Overdiagnosis of Parkinson's disease (PD) is suggested by specialist review of community diagnosis, and in postmortem studies. In specialist centers 4 to 15% of patients entered into clinical trials as early PD do not have functional imaging support for a PD diagnosis. In a European multicenter, prospective, longitudinal study, we compared clinical diagnosis with functional SPECT imaging using [123I]FP‐CIT (DaTSCAN™, GE Healthcare). Repeat observations were performed over 3 years in patients with tremor and/or parkinsonism in whom there was initial diagnostic uncertainty between degenerative parkinsonism and nondegenerative tremor disorders. Video‐recording of clinical features was scored independently of functional imaging results by two blinded clinicians at 36 months (= gold standard clinical diagnosis). Three readers, unaware of the clinical diagnosis, classified the images as normal or abnormal by visual inspection. The main endpoint was the sensitivity and specificity of SPECT imaging at baseline compared with the gold standard. In 99 patients completing the three serial assessments, on‐site clinical diagnosis overdiagnosed degenerative parkinsonism at baseline in diagnostically uncertain cases compared with the gold standard clinical diagnosis (at 36 months), the latter giving a sensitivity of 93% and specificity of 46%. The corresponding baseline [123I]FP‐CIT SPECT results showed a mean sensitivity of 78% and a specificity of 97%. Inter‐reader agreement for rating scans as normal or abnormal was high (Cohen's $\hat{\kappa}$ = 0.94–0.97). © 2008 Movement Disorder Society</div>
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<note type="content">*Potential conflict of interest: Financial support has been received by Klaus Tatsch, Jan Booij, Paul Kemp, Ray Chaudhuri, Wolfgang Oertel, Jim Patterson, Hani Benamer, Oliver Pogarell, Vicky Marshall, and Donald Grosset from GE Healthcare (manufacturers of [123I]FP‐CIT).</note>
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