Corticosteroids in chronic inflammatory demyelinating polyneuropathy

被引:0
作者
van Lieverloo, G. G. A. [1 ]
Peric, S. [2 ]
Doneddu, P. E. [3 ]
Gallia, F. [3 ]
Nikolic, A. [2 ]
Wieske, L. [1 ]
Verhamme, C. [1 ]
van Schalk, I. N. [1 ]
Nobile-Orazio, E. [3 ]
Basta, I [2 ]
Eftimov, F. [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Amsterdam, Netherlands
[2] Univ Belgrade, Clin Ctr Serbia, Sch Med, Neurol Clin, Belgrade, Serbia
[3] Milan Univ, Humanitas Clin & Res Ctr, Dept Med Biotechnol & Translat Med, Neuromuscular & Neuroimmunol Serv, Milan, Italy
关键词
CIDP; (Cortico)steroids; Immunosuppressive treatment; Peripheral nerve disorder; INTRAVENOUS IMMUNOGLOBULIN; POLYRADICULONEUROPATHY; METHYLPREDNISOLONE; DEXAMETHASONE; GUIDELINE;
D O I
10.1007/s00415-018-8948-y
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Chronic inflammatory demyelinating polyneuropathy (CIDP) can be treated with corticosteroids or intravenous immunoglobulins. Various corticosteroid regimens are currently used in CIDP, but it is unknown whether they are equally efficacious. In this retrospective study, we compared efficacy and safety of three corticosteroid regimens in CIDP patients. Methods We included treatment naive patients that fulfilled the EFNS/PNS criteria for CIDP. Patients were treated with corticosteroids according to the local protocol of three CIDP expertise centres. Corticosteroid regimens consisted of daily oral prednisolone, pulsed oral dexamethasone, or pulsed intravenous methylprednisolone. Outcomes were number of responders to treatment, remission rate of treatment responders, overall probability of 5-year remission, and the occurrence of adverse events. Results A total of 125 patients were included. Sixty-seven (54%) patients received daily prednisone or prednisolone, 37 (30%) pulsed dexamethasone, and 21 (17%) pulsed intravenous methylprednisolone. Overall, 60% (95% CI 51-69%) responded to corticosteroids, with no significant difference between the three treatment regimens (p = 0.56). From the 75 responders, 61% (95% CI 50-73%) remained in remission, during a median follow-up of 55 months (range 1-197 months). The probability of responders reaching 5-year remission was 55% (95% CI 44-70%), with no difference between the three groups. Adverse events leading to a change in treatment occurred in ten patients (8%). Two patients had a serious adverse event. Conclusion Corticosteroids lead to improvement in 60% of patients and to remission in 61% of treatment responders. There were no differences between treatment modalities in terms of efficacy and safety.
引用
收藏
页码:2052 / 2059
页数:8
相关论文
共 24 条
[1]   Outcomes validity and reliability of the modified Rankin scale: Implications for stroke clinical trials - A literature review and synthesis [J].
Banks, Jamie L. ;
Marotta, Charles A. .
STROKE, 2007, 38 (03) :1091-1096
[2]   2017 American College of Rheumatology Guideline for the Prevention and Treatment of Glucocorticoid-Induced Osteoporosis [J].
Buckley, Lenore ;
Guyatt, Gordon ;
Fink, Howard A. ;
Cannon, Michael ;
Grossman, Jennifer ;
Hansen, Karen E. ;
Humphrey, Mary Beth ;
Lane, Nancy E. ;
Magrey, Marina ;
Miller, Marc ;
Morrison, Lake ;
Rao, Madhumathi ;
Robinson, Angela Byun ;
Saha, Sumona ;
Wolver, Susan ;
Bannuru, Raveendhara R. ;
Vaysbrot, Elizaveta ;
Osani, Mikala ;
Turgunbaev, Marat ;
Miller, Amy S. ;
McAlindon, Timothy .
ARTHRITIS CARE & RESEARCH, 2017, 69 (08) :1095-1110
[3]   A nationwide retrospective analysis on the effect of immune therapies in patients with chronic inflammatory demyelinating polyradiculoneuropathy [J].
Cocito, D. ;
Paolasso, I. ;
Antonini, G. ;
Benedetti, L. ;
Briani, C. ;
Comi, C. ;
Fazio, R. ;
Jann, S. ;
Mata, S. ;
Mazzeo, A. ;
Sabatelli, M. ;
Nobile-Orazio, E. .
EUROPEAN JOURNAL OF NEUROLOGY, 2010, 17 (02) :289-294
[4]   Long-term remission of CIDP after pulsed dexamethasone or short-term prednisolone treatment [J].
Eftimov, F. ;
Vermeulen, M. ;
van Doorn, P. A. ;
Brusse, E. ;
van Schaik, I. N. .
NEUROLOGY, 2012, 78 (14) :1079-1084
[5]   Intravenous immunoglobulin for chronic inflammatory demyelinating polyradiculoneuropathy [J].
Eftimov, Filip ;
Winer, John B. ;
Vermeulen, Marinus ;
de Haan, Rob ;
van Schaik, Ivo N. .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2013, (12)
[6]   Chronic inflammatory demyelinating polyradiculoneuropathy: update on clinical features, phenotypes and treatment options [J].
Eftimov, Filip ;
van Schaik, Ivo .
CURRENT OPINION IN NEUROLOGY, 2013, 26 (05) :496-502
[7]   Chronic inflammatory demyelinating polyneuropathy disease activity status: recommendations for clinical research standards and use in clinical practice [J].
Gorson, Kenneth C. ;
van Schaik, Ivo N. ;
Merkies, Ingemar S. J. ;
Lewis, Richard A. ;
Barohn, Richard J. ;
Koski, Carol L. ;
Cornblath, David R. ;
Hughes, Richard A. C. ;
Hahn, Angelika F. ;
Baumgarten, Mona ;
Goldstein, Jonathan ;
Katz, Jonathan ;
Graves, Michael ;
Parry, Gareth ;
van Doorn, Pieter A. .
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2010, 15 (04) :326-333
[8]   Corticosteroids for chronic inflammatory demyelinating polyradiculoneuropathy [J].
Hughes, Richard A. C. ;
Mehndiratta, Man Mohan ;
Rajabally, Yusuf A. .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2017, (11)
[9]   Intravenous immunoglobulin for chronic inflammatory demyelinating polyradiculoneuropathy: the ICE trial [J].
Hughes, Richard A. C. .
EXPERT REVIEW OF NEUROTHERAPEUTICS, 2009, 9 (06) :789-795
[10]   INTEROBSERVER AGREEMENT IN THE ASSESSMENT OF MUSCLE STRENGTH AND FUNCTIONAL ABILITIES IN GUILLAIN-BARRE-SYNDROME [J].
KLEYWEG, RP ;
VANDERMECHE, FGA ;
SCHMITZ, PIM .
MUSCLE & NERVE, 1991, 14 (11) :1103-1109