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カイダ ケンイチ
KAIDA Kenichi
海田 賢一 所属 埼玉医科大学 医学部 総合医療センター 脳神経内科 職種 教授 |
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| 論文種別 | 学術雑誌(原著) |
| 言語種別 | 英語 |
| 査読の有無 | 査読あり |
| 表題 | International Guillain-Barré Syndrome Outcome Study: protocol of a prospective observational cohort study on clinical and biological predictors of disease course and outcome in Guillain-Barré syndrome |
| 掲載誌名 | 正式名：Journal of the Peripheral Nervous System ISSNコード：15298027 |
| 出版社 | Blackwell Publishing Inc. |
| 巻・号・頁 | 22(2),68-76頁 |
| 著者・共著者 | Bart C. Jacobs,Bianca van den Berg,Christine Verboon,Govindsinh Chavada,David R. Cornblath,Kenneth C. Gorson,Thomas Harbo,Hans-Peter Hartung,Richard A. C. Hughes,Susumu Kusunoki,Pieter A. van Doorn,Hugh J. Willison,the IGOS Consortium,B. C. Jacobs,R. A.C. Hughes,D. R. Cornblath,K. C. Gorson,H. P. Hartung,S. Kusunoki,P. A. van Doorn,H. J. Willison,M. van Woerkom,B. van den Berg,C. Verboon,J. Roodbol,B. C. Jacobs,R. C. Reisin,S. W. Reddel,Z. Islam,B. Islam,Q. D. Mohammad,P. van den Bergh,T. E. Feasby,Y. Z. Wang,T. Harbo,Y. Péréon,H. P. Hartung,H. C. Lehmann,E. Dardiotis,E. Nobile-Orazio,S. Kusunoki,N. Shahrizaila,B. C. Jacobs,B. van den Berg,C. Verboon,K. Bateman,I. Illa,L. A. Querol,S. T. Hsieh,H. J. Willison,G. Chavada,A. Davidson,K. C. Gorson,J. M. Addington,S. Ajroud-Driss,H. Andersen,G. Antonini,S. Attarian,U. Badrising,F. A. Barroso,L. Benedetti,A. Beronio,M. Bianco,D. Binda,C. Briani,J. Bürmann,I. R. Bella,T. E. Bertorini,R. Bhavaraju-Sanka,T. H. Brannagan,M. Busby,S. Butterworth,M. Campagnolo,C. Casasnovas,G. Cavaletti,C. S. Chao,S. Chen,S. Chetty,K. G. Claeys,J. A. Cohen,M. E. Conti,J. S. Cosgrove,M. C. Dalakas,M. M. Dimachkie,U. Dillmann,C. Domínguez González,K. Doppler,C. Dornonville de la Cour,A. Echaniz-Laguna,F. Eftimov,C. G. Faber,R. Fazio,C. Fokke,T. Fujioka,E. A. Fulgenzi,G. Galassi,T. Garcia,M. Garnero,M. P.J. Garssen,C. J. Gijsbers,J. M. Gilchrist,H. J. Gilhuis,J. M. Goldstein,N. Goyal,V. Granit,A. Grapperon,G. Gutiérrez Gutiérrez,L. Gutmann,R. D.M. Hadden,J. V. Holbech,J. K.L. Holt,C. Homedes Pedret,M. Htut,K. Jellema,I. Jericó Pascual,K. Kaida,S. Karafiath,H. D. Katzberg,L. Kiers,B. C. Kieseier,K. Kimpinski,R. P. Kleyweg,N. Kokubun,N. A. Kolb,K. Kuitwaard,S. Kuwabara,J. Y. Kwan,S. S. Ladha,L. Landschoff Lassen,V. Lawson,D. Ledingham,L. Léon Cejas,C. A. Luciano,S. T. Lucy,M. P.T. Lunn,A. Magot,H. Manji,C. Marchesoni,G. A.M. Marfia,C. Márquez Infante,E. Martinez Hernandez,G. Mataluni,M. Mattiazi,C. J. McDermott,G. D. Meekins,J. Miller,M. S. Monges,M. C.J. Montero,G. Morís de la Tassa,C. Nascimbene,C. Neumann,R. J. Nowak,P. Orizaola Balaguer,M. Osei-Bonsu,E. B.L. Pan,J. Pardo Fernandez,M. Pasnoor,M. T. Pulley,Y. A. Rajabally,S. Rinaldi,C. Ritter,R. C. Roberts,I. Rojas-Marcos,S. A. Rudnicki,G. M. Sachs,J. P.A. Samijn,L. Santoro,D. S. Saperstein,A. Savransky,H. Schneider,A. Schenone,M. J. Sedano Tous,Y. Sekiguchi,K. A. Sheikh,N. J. Silvestri,S. H. Sindrup,C. L. Sommer,B. Stein,A. M. Stino,A. Spyropoulos,J. Srinivasan,H. Suzuki,S. W. Taylor,H. Tankisi,D. Tigner,P. T. Twydell,F. Valzania,P. van Damme,A. J. van der Kooi,G. W. van Dijk,T. van der Ree,R. van Koningsveld,J. D. Varrato,F. H. Vermeij,J. J.G.M. Verschuuren,L. H. Visser,M. V. Vytopil,W. Waheed,M. Wilken,C. Wilkerson,P. W. Wirtz,Y. Yamagishi,E. M. Yiu,L. Zhou,S. Zivkovic |
| 発行年月 | 2017/06 |
| 概要 | Guillain-Barré syndrome (GBS) is an acute polyradiculoneuropathy with a highly variable clinical presentation, course, and outcome. The factors that determine the clinical variation of GBS are poorly understood which complicates the care and treatment of individual patients. The protocol of the ongoing International GBS Outcome Study (IGOS), a prospective, observational, multicenter cohort study that aims to identify the clinical and biological determinants and predictors of disease onset, subtype, course and outcome of GBS is presented here. Patients fulfilling the diagnostic criteria for GBS, regardless of age, disease severity, variant forms, or treatment, can participate if included within 2 weeks after onset of weakness. Information about demography, preceding infections, clinical features, diagnostic findings, treatment, course, and outcome is collected. In addition, cerebrospinal fluid and serial blood samples for serum and DNA is collected at standard time points. The original aim was to include at least 1,000 patients with a follow-up of 1–3 years. Data are collected via a web-based data entry system and stored anonymously. IGOS started in May 2012 and by January 2017 i |
| DOI | 10.1111/jns.12209 |
| PMID | 28406555 |