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Authordc.contributor.authorLee, Ikjae 
Authordc.contributor.authorKuo, Hui-Chien 
Authordc.contributor.authorAban, Inmaculada B. 
Authordc.contributor.authorCutter, Gary R. 
Authordc.contributor.authorMcPherson, Tarrant 
Authordc.contributor.authorKaminski, Henry J. 
Authordc.contributor.authorSussman, Jon 
Authordc.contributor.authorStrobel, Philipp 
Authordc.contributor.authorOger, Joel 
Authordc.contributor.authorCea Muñoz, Gabriel 
Authordc.contributor.authorHeckmann, Jeannine M. 
Authordc.contributor.authorEvoli, Amelia 
Authordc.contributor.authorNix, Wilfred 
Authordc.contributor.authorCiafaloni, Emma 
Authordc.contributor.authorAntonini, Giovanni 
Authordc.contributor.authorWitoonpanich, Rawiphan 
Authordc.contributor.authorKing, John O. 
Authordc.contributor.authorBeydoun, Said R. 
Authordc.contributor.authorChalk, Colin H. 
Authordc.contributor.authorBarboi, Alexandru C. 
Authordc.contributor.authorAmato, Anthony A. 
Authordc.contributor.authorShaibani, Aziz I. 
Authordc.contributor.authorKatirji, Bashar 
Authordc.contributor.authorLecky, Bryan R. F. 
Authordc.contributor.authorBuckley, Camilla 
Authordc.contributor.authorVincent, Angela 
Authordc.contributor.authorDias-Tosta, Elza 
Authordc.contributor.authorYoshikawa, Hiroaki 
Authordc.contributor.authorWaddington-Cruz, Marcia 
Authordc.contributor.authorPulley, Michael T. 
Authordc.contributor.authorRivner, Michael H. 
Authordc.contributor.authorKostera-Pruszczyk, Anna 
Authordc.contributor.authorPascuzzi, Robert M. 
Authordc.contributor.authorJackson, Carlayne E. 
Authordc.contributor.authorVerschuuren, Jan J. G. 
Authordc.contributor.authorMassey, Janice M. 
Authordc.contributor.authorKissel, John T. 
Authordc.contributor.authorWerneck, Lineu C. 
Authordc.contributor.authorBenatar, Michael 
Authordc.contributor.authorBarohn, Richard J. 
Authordc.contributor.authorTandan, Rup 
Authordc.contributor.authorMozaffar, Tahseen 
Authordc.contributor.authorConwit, Robin 
Authordc.contributor.authorMinisman, Greg 
Authordc.contributor.authorSonett, Joshua R. 
Authordc.contributor.authorWolfe, Gil I. 
Admission datedc.date.accessioned2021-03-30T18:45:08Z
Available datedc.date.available2021-03-30T18:45:08Z
Publication datedc.date.issued2020
Cita de ítemdc.identifier.citationNeurology Volumen: 95 Número: 6 Páginas: E755-E766 Aug 2020es_ES
Identifierdc.identifier.other10.1212/WNL.0000000000010031
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/178864
Abstractdc.description.abstractTo examine whether sustained minimal manifestation status (MMS) with complete withdrawal of prednisone is better achieved in thymectomized patients with myasthenia gravis (MG). Methods This study is a post hoc analysis of data from a randomized trial of thymectomy in MG (Thymectomy Trial in Non-Thymomatous Myasthenia Gravis Patients Receiving Prednisone Therapy [MGTX]). MGTX was a multicenter, randomized, rater-blinded 3-year trial that was followed by a voluntary 2-year extension for patients with acetylcholine receptor (AChR) antibody-positive MG without thymoma. Patients were randomized 1:1 to thymectomy plus prednisone vs prednisone alone. Participants were age 18-65 years at enrollment with disease duration less than 5 years. All patients received oral prednisone titrated up to 100 mg on alternate days until they achieved MMS, which prompted a standardized prednisone taper as long as MMS was maintained. The achievement rate of sustained MMS (no symptoms of MG for 6 months) with complete withdrawal of prednisone was compared between the thymectomy plus prednisone and prednisone alone groups. Results Patients with MG in the thymectomy plus prednisone group achieved sustained MMS with complete withdrawal of prednisone more frequently (64% vs 38%) and quickly compared to the prednisone alone group (median time 30 months vs no median time achieved, p < 0.001) over the 5-year study period. Prednisone-associated adverse symptoms were more frequent in the prednisone alone group and distress level increased with higher doses of prednisone. Conclusions Thymectomy benefits patients with MG by increasing the likelihood of achieving sustained MMS with complete withdrawal of prednisone. Classification of evidence This study provides Class II evidence that for patients with generalized MG with AChR antibody, those receiving thymectomy plus prednisone are more likely to attain sustained MMS and complete prednisone withdrawal than those on prednisone alone.es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherLippincott Williams & Wilkinses_ES
Sourcedc.sourceNeurologyes_ES
Keywordsdc.subjectAlternate-day prednisonees_ES
Keywordsdc.subjectMyasthenia-gravises_ES
Keywordsdc.subjectDouble-blindes_ES
Keywordsdc.subjectRandomized-triales_ES
Keywordsdc.subjectFollow-upes_ES
Keywordsdc.subjectMulticenteres_ES
Keywordsdc.subjectTherapyes_ES
Keywordsdc.subjectGlucocorticoidses_ES
Keywordsdc.subjectResponsivenesses_ES
Keywordsdc.subjectResponsivenesses_ES
Keywordsdc.subjectAzathioprinees_ES
Títulodc.titleMinimal manifestation status and prednisone withdrawal in the MGTX triales_ES
Document typedc.typeArtículo de revistaes_ES
dcterms.accessRightsdcterms.accessRightsAcceso a solo metadatoses_ES
Catalogueruchile.catalogadorcrbes_ES
Indexationuchile.indexArtículo de publicación ISI
Indexationuchile.indexArtículo de publicación SCOPUS


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