Treatment of low back pain with a herbal or synthetic anti-rheumatic:: a randomized controlled study.: Willow bark extract for low back pain

被引:68
作者
Chrubasik, S
Künzel, O
Model, A
Conradt, C
Black, A
机构
[1] Univ Freiburg, Dept Forens Med, D-79104 Freiburg, Germany
[2] Univ Sydney, Herbal Med Res & Educ Ctr, Sydney, NSW 2006, Australia
[3] Heidelberg Univ, Dept Med Biometry, D-69120 Heidelberg, Germany
[4] Univ Bristol, Bristol Royal Infirm, Dept Anaesthesia, Bristol BS2 8HW, Avon, England
关键词
low back pain; willow bark; COX-2; inhibitor; randomized controlled study;
D O I
10.1093/rheumatology/40.12.1388
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. To compare the effects of a proprietary extract of willow bark (Assalix) and a selective inhibitor (rofecoxib) of the enzyme cyclo-oxygenase-2 (COX-2). Methods. An open, randomized, post-marketing study was carried out in an out-patients clinic on two groups of patients aged 18 to 80 yr presenting over a 6-month period with acute exacerbations of low back pain. Using computer-generated random list, 114 patients were allocated to receive a daily dose of herbal extract containing 240 mg of salicin [PAID (phyto-anti-inflammatory drug) group] and 114 were allocated to receive 12.5 mg of the synthetic COX-2 inhibitor rofecoxib [NSAID (non-steroidal anti-inflammatory drug) group]. The doses were chosen according to existing recommendations. All patients were free to use whatever additional conventional treatments were thought necessary. The outcome measures were a modified Arhus index, its pain component and the Total Pain Index. Results. Groups were well matched. After 4 weeks of treatment, the Arhus index had improved by about 20%, its pain component by about 30% and the Total Pain Index by about 35%. The number of pain-free patients (visual analogue scale score <2) was about 20 in each group. About 60% of the patients in each group responded well to the treatment (as judged by an improvement of greater than or equal to30% in the Total Pain Index relative to its baseline). The improvement was also reflected reasonably well in the physicians' and patients' judgements of the effectiveness of treatment, which were largely concordant. Few patients of either group resorted to the additional conventional treatment options. The incidence of adverse events was similar in the two groups. Treatment with rofecoxib was about 40% more expensive than that with Assalix. Conclusion. There was no significant difference in effectiveness between the two treatments at the doses chosen. Treatment with Assalix was less expensive.
引用
收藏
页码:1388 / 1393
页数:6
相关论文
共 15 条
[1]  
Burton AK, 1998, BAILLIERE CLIN RHEUM, V12, P17
[2]  
Cannon GW, 2000, ARTHRITIS RHEUM-US, V43, P978, DOI 10.1002/1529-0131(200005)43:5<978::AID-ANR4>3.0.CO
[3]  
2-0
[4]   Potential economic impact of using a proprietary willow bark extract in outpatient treatment of low back pain:: An open non-randomized study [J].
Chrubasik, S ;
Künzel, O ;
Black, A ;
Conradt, C ;
Kerschbaumer, F .
PHYTOMEDICINE, 2001, 8 (04) :241-251
[5]   Treatment of low back pain exacerbations with willow bark extract: A randomized double-blind study [J].
Chrubasik, S ;
Eisenberg, E ;
Balan, E ;
Weinberger, T ;
Luzzati, R ;
Conradt, C .
AMERICAN JOURNAL OF MEDICINE, 2000, 109 (01) :9-14
[6]  
CHRUBASIK S, IN PRESS EUR J ANA S
[7]   A randomized trial of the efficacy and tolerability of the COX-2 inhibitor rofecoxib vs ibuprofen in patients with osteoarthritis [J].
Day, R ;
Morrison, B ;
Luza, A ;
Castaneda, O ;
Strusberg, A ;
Nahir, M ;
Helgetveit, KB ;
Kress, B ;
Daniels, B ;
Bolognese, J ;
Krupa, D ;
Seidenberg, B ;
Ehrich, E .
ARCHIVES OF INTERNAL MEDICINE, 2000, 160 (12) :1781-1787
[8]   Phyto-anti-inflammatories - A systematic review of randomized, placebo-controlled, double-blind trials [J].
Ernst, E ;
Chrubasik, S .
RHEUMATIC DISEASE CLINICS OF NORTH AMERICA, 2000, 26 (01) :13-+
[9]  
ESCOP (European Scientific Cooperative on Phytotherapy), ESCOP MON
[10]   The role of cytokines as inflammatory mediators in osteoarthritis: Lessons from animal models [J].
Goldring, MB .
CONNECTIVE TISSUE RESEARCH, 1999, 40 (01) :1-11