Efficacy of etanercept in the treatment of acute, severe sciatica: a pilot study

被引:94
作者
Genevay, S [1 ]
Stingelin, S [1 ]
Gabay, C [1 ]
机构
[1] Univ Hosp Geneva, Div Rheumatol, CH-1211 Geneva 14, Switzerland
关键词
D O I
10.1136/ard.2003.016451
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Objectives: To explore the efficacy of a tumour necrosis factor alpha (TNFalpha) inhibitor ( etanercept, Enbrel) in patients with severe sciatica. Methods: A pilot study of etanercept was conducted in patients admitted to hospital for acute severe sciatica. Ten consecutive patients received three subcutaneous injections of etanercept ( 25 mg every 3 days) in addition to standard analgesia. Response was evaluated at day 10 ( T1) and week 6 (T2) using a visual analogue scale for leg pain (VASL) and for low back pain (VASB), and two validated functional scores: the Oswestry disability index (ODI) and the Roland Morris disability questionnaire (RMDQ). The control group consisted of 10 patients with severe sciatica, who took part in an observational study on IV methylprednisolone. Results: In the etanercept group all variables improved: VASB from 36 to 7; VASL from 74 to 12; RMDQ from 17.8 to 5.8, and ODI from 75.4 to 17.3; all p<0.001. Pain (VASL and VASB: p<0.001) and ODI (p<0.05) were significantly better in the etanercept group than in the methylprednisolone group. Conclusion: In this open, historical group controlled study, patients with severe sciatica had sustained improvement after a short treatment with etanercept that was better than standard care plus a short course of methylprednisolone. These results suggest that inhibition of TNFα is beneficial in the treatment of sciatica and support a pathological role for TNFα in the pathogenesis of sciatica. These results need to be confirmed by a randomised controlled trial.
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页码:1120 / 1123
页数:4
相关论文
共 21 条
[1]
mRNA expression of cytokines and chemokines in herniated lumbar intervertebral discs [J].
Ahn, SH ;
Cho, YW ;
Ahn, MW ;
Jang, SH ;
Sohn, YK ;
Kim, HS .
SPINE, 2002, 27 (09) :911-917
[2]
Influence of immunogenicity on the long-term efficacy of infliximab in Crohn's disease [J].
Baert, F ;
Noman, M ;
Vermeire, S ;
Van Assche, G ;
D'Haens, G ;
Carbonez, A ;
Rutgeerts, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (07) :601-608
[3]
DESCRIPTIVE EPIDEMIOLOGY OF LOW-BACK-PAIN AND ITS RELATED MEDICAL-CARE IN THE UNITED-STATES [J].
DEYO, RA ;
TSUIWU, YJ .
SPINE, 1987, 12 (03) :264-268
[4]
Fairbank J C, 1980, Physiotherapy, V66, P271
[5]
Anti-tumour necrosis factor agents and tuberculosis risk: mechanisms of action and clinical management [J].
Gardam, MA ;
Keystone, EC ;
Menzies, R ;
Manners, S ;
Skamene, E ;
Long, R ;
Vinh, DC .
LANCET INFECTIOUS DISEASES, 2003, 3 (03) :148-155
[6]
SPINAL NERVE ROOT COMPRESSION [J].
GARFIN, SR ;
RYDEVIK, B ;
LIND, B ;
MASSIE, J .
SPINE, 1995, 20 (16) :1810-1820
[7]
The role of inflammation in disk herniation-associated radiculopathy [J].
Goupille, P ;
Jayson, MIV ;
Valat, JP ;
Freemont, AJ .
SEMINARS IN ARTHRITIS AND RHEUMATISM, 1998, 28 (01) :60-71
[8]
2000 Volvo Award Winner in Basic Science Studies - Exogenous tumor necrosis factor-alpha mimics nucleus pulposus-induced neuropathology - Molecular, histologic, and behavioral comparisons in rats [J].
Igarashi, T ;
Kikuchi, S ;
Shubayev, V ;
Myers, RR .
SPINE, 2000, 25 (23) :2975-2980
[9]
Herniated lumbar intervertebral discs spontaneously produce matrix metalloproteinases, nitric oxide, interleukin-6, and prostaglandin E(2) [J].
Kang, JD ;
Georgescu, HI ;
McIntyreLarkin, L ;
StefanovicRacic, M ;
Donaldson, WF ;
Evans, CH .
SPINE, 1996, 21 (03) :271-277
[10]
Tumor necrosis factor-α monoclonal antibody, infliximab, used to manage severe sciatica [J].
Karppinen, J ;
Korhonen, T ;
Malmivaara, A ;
Paimela, L ;
Kyllönen, E ;
Lindgren, KA ;
Rantanen, P ;
Tervonen, O ;
Niinimäki, J ;
Seitsalo, S ;
Hurri, H .
SPINE, 2003, 28 (08) :750-753