Clinical Efficacy of Etanercept hip joint Injection in the Treatment of Patients with Ankylosing Spondylitis
Li We
Abstract
Li We
Abstract
Objective: To evaluate the short-term efficacy of etanercept hip joint injection in the treatment of patients with ankylosing spondylitis.Methods: 50 cases with ankylosing spondylitis admitted in our hospital from 2001 to 2011 were injected into hip joint with etanercept 50 mg once a week for a treatment course of 4 weeks under the high-frequency ultrasound.The Bath Ankylosing Spondylitis Functional Index(BASFI),Bath Ankylosing Spondylitis Disease Activity Index(BASDAI),spinal pain VAS,(PGA)VAS,nocturnal spinal pain VAS,ESR,C-reactive protein(CRP),Harris and possible adverse reaction were observed at week 0,2,4,8 respectively.Results: Compared with the baseline,the observation items were all significantly improved after 2,4 and 8 weeks' treatment.At 2nd week,60%(n=30),26%(n=13) and 16%(n=8) of the patients achieved ASAS20,ASAS50 and ASAS70,respectively.At 8th week,the percentage of patients achieving the ASAS20/50/70 were 64%(n=38),42%(n=21),30%(n=15)respectively.The percentage of responders,above 70 of Harris was 90%,above 80 was 60%,and above 90 was 30%.1 patient had no improvement.And there were 4 patients below 70,but had recuding clinical signs.Conclusion: Etanercept was clinically effective and well tolerated in the treatment of AS patients,which could provide fast action,reduce clinical signs and improve range of motion as well as quality of life.
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Objective: To evaluate the short-term efficacy of etanercept hip joint injection in the treatment of patients with ankylosing spondylitis.Methods: 50 cases with ankylosing spondylitis admitted in our hospital from 2001 to 2011 were injected into hip joint with etanercept 50 mg once a week for a treatment course of 4 weeks under the high-frequency ultrasound.The Bath Ankylosing Spondylitis Functional Index(BASFI),Bath Ankylosing Spondylitis Disease Activity Index(BASDAI),spinal pain VAS,(PGA)VAS,nocturnal spinal pain VAS,ESR,C-reactive protein(CRP),Harris and possible adverse reaction were observed at week 0,2,4,8 respectively.Results: Compared with the baseline,the observation items were all significantly improved after 2,4 and 8 weeks' treatment.At 2nd week,60%(n=30),26%(n=13) and 16%(n=8) of the patients achieved ASAS20,ASAS50 and ASAS70,respectively.At 8th week,the percentage of patients achieving the ASAS20/50/70 were 64%(n=38),42%(n=21),30%(n=15)respectively.The percentage of responders,above 70 of Harris was 90%,above 80 was 60%,and above 90 was 30%.1 patient had no improvement.And there were 4 patients below 70,but had recuding clinical signs.Conclusion: Etanercept was clinically effective and well tolerated in the treatment of AS patients,which could provide fast action,reduce clinical signs and improve range of motion as well as quality of life.
Key concepts: Ankylosing spondylitis, Medicine, Etanercept, BASDAI, BASFI, Spondylitis, Quality of life (healthcare), Surgery