Neurological Deficits During Treatment With Tumor Necrosis Factor-Alpha Antagonists

被引:36
作者
Nozaki, Kenkichi [1 ]
Silver, Richard M. [2 ]
Stickler, David E. [1 ]
Abou-Fayssal, Nada G. [1 ]
Giglio, Pierre [1 ]
Kamen, Diane L. [2 ]
Daniel, Rodney [2 ]
Judson, Marc A. [3 ]
机构
[1] Med Univ S Carolina, Dept Neurosci, Div Adult Neurol, Charleston, SC 29425 USA
[2] Med Univ S Carolina, Dept Med, Div Rheumatol & Immunol, Charleston, SC 29425 USA
[3] Med Univ S Carolina, Dept Med, Div Pulm Crit Care Allergy & Sleep Med, Charleston, SC 29425 USA
关键词
Tumor necrosis factor-alpha antagonist; Etanercept; Infliximab; Adalimumab; Neurological deficits; RHEUMATOID-ARTHRITIS; INFLIXIMAB THERAPY; GUILLAIN-BARRE; DEMYELINATION; PATIENT; ONSET;
D O I
10.1097/MAJ.0b013e31822b7bb8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Neurological deficits that occur during treatment with tumor necrosis factor (TNF)-alpha antagonists are rare, and their clinical features have not been fully elucidated. Methods: Retrospective review of medical records of 9 patients who were given TNF-alpha antagonists, subsequently developed neurological deficits and were cared for at the Medical University of South Carolina between January 2002 and May 2010. Adverse drug reaction probability scale was used for the assessment of their causal connection. Results: The underlying diseases for which TNF-alpha antagonists were administered included rheumatologic disorders (4), sarcoidosis (3), psoriasis (1) and Crohn's disease (1). Etanercept, infliximab or adalimumab was administered to these patients. Neurological complications included central or peripheral demyelination (5), antiphospholipid syndrome/central nervous system lupus (1), Epstein-Barr virus encephalitis (1), axonal sensory polyneuropathy (1) and small fiber polyneuropathy (1). TNF-alpha antagonists were discontinued in 8 patients and clinical improvement was seen in 3 of them. Additional therapies were given in 4 patients. An adverse drug reaction probability score suggested probable (3/9) and possible (6/9) causal relationships. Conclusions: Neurological deficits that develop during treatment with TNF-alpha antagonists are relatively rare but important potential complications of these drugs. Determining if the relationship between the neurological deficits and TNF-alpha antagonist therapy is causal can be challenging and can impact patient care.
引用
收藏
页码:352 / 355
页数:4
相关论文
共 31 条
[1]  
[Anonymous], 1999, Neurology, V53, P457
[2]  
Bensouda-Grimaldi L, 2007, J RHEUMATOL, V34, P239
[3]   Guillain-Barre in a patient with ankylosing spondylitis secondary to ulcerative colitis on infliximab therapy [J].
Bouchra, Amine ;
Benbouazza, Karima ;
Hajjaj-Hassouni, Najia .
CLINICAL RHEUMATOLOGY, 2009, 28 :S53-S55
[4]   Herpes Simplex Encephalitis during Treatment with Tumor Necrosis Factor-α Inhibitors [J].
Bradford, Russell D. ;
Pettit, April C. ;
Wright, Patty W. ;
Mulligan, Mark J. ;
Moreland, Larry W. ;
McLain, David A. ;
Gnann, John W. ;
Bloch, Karen C. .
CLINICAL INFECTIOUS DISEASES, 2009, 49 (06) :924-927
[5]   Etanercept (Enbrel®) therapy for chronic inflammatory demyelinating polyneuropathy [J].
Chin, RL ;
Sherman, WH ;
Sander, HW ;
Hays, AP ;
Latov, N .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2003, 210 (1-2) :19-21
[6]   Caution with the use of cyclosporin in pregnancy [J].
Dor, R ;
Blanshard, C .
GUT, 2003, 52 (07) :1070-1070
[7]   Acute motor and sensory axonal neuropathy and concomitant encephalopathy during tumor necrosis factor-alpha antagonist therapy [J].
Faivre, Anthony ;
Franques, Jerome ;
De Paula, Andre Maues ;
Gutierrez, Mariana ;
Bret, Sandie ;
Aubert, Sandrine ;
Attarian, Shahram ;
Pouget, Jean .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2010, 291 (1-2) :103-106
[8]   Multiple sclerosis onset during etanercept treatment [J].
Gomez-Gallego, Maria ;
Meca-Lallana, Jose ;
Fernandez-Barreiro, Andres .
EUROPEAN NEUROLOGY, 2008, 59 (1-2) :91-93
[9]   Lewis-Sumner syndrome associated with infliximab therapy in rheumatoid arthritis [J].
Hooper, Davyd R. ;
Tarnopolsky, Mark A. ;
Baker, Steven K. .
MUSCLE & NERVE, 2008, 38 (04) :1318-1325
[10]  
Jarand J, 2006, J RHEUMATOL, V33, P1018