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Sensitivities and predictive values of paraclinical tests for diagnosing multiple sclerosis
Authors:Graziella Filippini  Gian Carlo Comi  Vittorio Cosi  Luciana Bevilacqua  Massimo Ferrarini  Vittorio Martinelli  Roberto Bergamaschi  Massimo Filippi  Antonietta Citterio  Ludovico D'Incerti  Adriana Campi  Maurizio Sberna  Francesco Riti  Giuliano Avanzini  Nadia Colombo  Federico Zappoli  Giuseppe Scotti  Mario Savoiardo
Affiliation:(1) Istituto Nazionale Neurologico "ldquo"C. Besta"rdquo", Via Celoria 11, I-20133 Milan, Italy;(2) Istituto Scientifico H "ldquo"San Raffaele"rdquo", Milan, Italy;(3) Fondazione "ldquo"Istituto Neurologico C. Mondino"rdquo", Pavia, Italy;(4) Ospedale Niguarda, Milan, Italy
Abstract:The sensitivities and predictive values of visual, somatosensory, and brain auditory evoked potentials (EPs), cerebrospinal fluid oligoclonal banding (CSF-OB) and magnetic resonance imaging (MRI) were evaluated for the early diagnosis of clinically definite multiple sclerosis (CDMS). Paraclinical evidence of asymptomatic lesions allows a diagnosis of CDMS. Eighty-two patients in whom MS was suspected but diagnosis of CDMS was not possible entered the study prospectively. Paraclinical examinations were performed at entry. Patients were examined and underwent EPs every 6 months, and MRI yearly. After a mean follow-up of 2.9 years, 28 patients (34%) had developed CDMS (McDonald-Halliday criteria). The initial MRI was strongly suggestive of MS in 19 of these (68%), while 27 (96%) had at least one MS-like abnormality in the initial MRI. CSF-OB and EPs had lower sensitivities. CDMS developed during follow-up in 19 of the 36 patients (53%) who had an initial MRI strongly suggestive of MS but in only 1 of the 25 who had normal MRI when first studied. These results support previous conclusions that MRI is the most sensitive test for detecting white matter asymptomatic lesions, and the most predictive for the diagnosis of CDMS.Presented in part at the Third meeting of the European Neurological Society, Lausanne (Switzerland), June 1992
Keywords:Multiple sclerosis  Evoked potentials  Cerebrospinal fluid oligoclonal banding  Magnetic resonance imaging
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