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1.
Mod Rheumatol ; 23(3): 529-37, 2013 May.
Article in English | MEDLINE | ID: mdl-22752535

ABSTRACT

OBJECTIVES: Adalimumab, a fully human anti-tumor necrosis factor monoclonal antibody, was retrospectively evaluated for its effect on musculoskeletal manifestations and health-related quality of life in patients with psoriatic arthritis (PsA) during daily clinical practice. METHODS: Patients who initiated adalimumab therapy after March 2010 were followed for at least 24 weeks with the clinical outcome measures. Eleven patients, all men with a mean age of 45.4 years, had mean psoriasis durations of 16.2 and 8.4 years at baseline. RESULTS: After 24 weeks, 72.7, 63.6, and 45.5 % of the patients met the ACR 20, 50, and 70 response criteria, respectively, while 81.8 % achieved the PsA response criteria. Disease Activity Score using the 28-joint count and CRP declined from 3.2 ± 1.2 at baseline to 1.3 ± 0.4 at week 24 (P < 0.01). The Bath Ankylosing Spondylitis Disease Activity Index and Bath Ankylosing Spondylitis Functional Index scores also decreased significantly (both P values were <0.01). After 24 weeks, three out of eight dimensions of the Medical Outcomes Study 36-Item Short Form Health Survey and Physical Component Summary were significantly improved (all P values were <0.05). CONCLUSIONS: Adalimumab exerted its effect as early as week 4, and it was sustained until the end of the 24-week observation period in the PsA patients.


Subject(s)
Antibodies, Monoclonal, Humanized/therapeutic use , Antirheumatic Agents/therapeutic use , Arthritis, Psoriatic/drug therapy , Spondylitis, Ankylosing/drug therapy , Adalimumab , Adult , Arthritis, Psoriatic/psychology , Disability Evaluation , Health Status , Humans , Male , Middle Aged , Quality of Life , Retrospective Studies , Severity of Illness Index , Treatment Outcome
2.
Clin Orthop Relat Res ; 468(4): 1173-7, 2010 Apr.
Article in English | MEDLINE | ID: mdl-19657703

ABSTRACT

Abnormal reactions accompanied by bone formation in the osteoarticular region induced by long-term administration of etretinate have been reported. We treated a patient who received continuous treatment of psoriatic erythroderma with etretinate for 7 years, and who had an osseous bridge that extended across the acetabulum over the femur on both sides. The patient experienced a major gait disturbance and eventually was unable to walk. Functional gait was restored by resecting the ossified regions and radiotherapy. Histologic sections of the ossified lesions showed enchondral ossification in the ligament attachment site in the joint margin, with advancing ossification along the articular capsule; the pattern was similar to that in diffuse idiopathic skeletal hyperostosis. This is the first report of an osseous bridge associated with long-term administration of etretinate extending across the acetabulum over the femur on both sides.


Subject(s)
Calcinosis/chemically induced , Dermatitis, Exfoliative/drug therapy , Etretinate/adverse effects , Keratolytic Agents/adverse effects , Ligaments, Articular/drug effects , Psoriasis/drug therapy , Acetabulum/pathology , Aged , Calcinosis/pathology , Calcinosis/surgery , Dermatitis, Exfoliative/complications , Femur/pathology , Hip Joint/drug effects , Hip Joint/pathology , Hip Joint/surgery , Humans , Ligaments, Articular/pathology , Ligaments, Articular/surgery , Male , Psoriasis/complications , Range of Motion, Articular , Recovery of Function
3.
Arch Orthop Trauma Surg ; 122(2): 73-9, 2002 Mar.
Article in English | MEDLINE | ID: mdl-11880906

ABSTRACT

We performed posterior lumbar interbody fusion (PLIF) on 7 patients with rheumatoid spondylitis (RA) of the lumbar spine with severe low-back pain and/or cauda equina symptoms, and evaluated the effectiveness of PLIF for the lumbar spinal instability in RA secondary to destruction of the anterior elements, including vertebral endplates and the apophyseal joint. The subjects were 7 patients with classic RA, 2 men and 5 women, mean age 65 years old, and the mean duration of RA was 21 years. All had severe low-back pain and difficulty with walking. According to the ARA classification, the patients were at stage 3 or worse and in class 3. Diagnostic imaging including magnetic resonance imaging (MRI), tomography, myelography, and computed tomographic myelography (CTM) of the lumbar spine clearly delineated pathology, destruction of the vertebral endplate, subluxation, and cauda compression which can be well treated with PLIF. We performed L4/5PLIF (5 cases), L3/4 and L4/5 PLIF (2 cases), and posterior fixation with instruments for anterior column repair and stabilization and posterior decompression. Autografts (all cases) and Brantigan IF cage (2 cases) were used. Stable fixation of the lumbar spine was achieved after surgery, and improvement in gait and activities of daily living were achieved through the relief of low-back pain and radicular pain; the mean duration of follow-up was 22 months. Postoperative, plain radiography, CT, and MRI revealed the enlargement of the lumbar canal and fusion and incorporation of grafted bone, but in some cases, collapse of graft, migration of pedicle screw, instability of adjacent level, and collapse of adjacent vertebra were noted. PLIF with spinal instruments is a preferred treatment for rheumatoid spondylitis of the lumbar spine, but in the mutilating type of RA with severe osteoporosis, PLIF in combination with a long fixation system and/or augmentation of the vertebral bodies might be needed.


Subject(s)
Lumbar Vertebrae/surgery , Spinal Fusion/methods , Spondylitis, Ankylosing/diagnosis , Spondylitis, Ankylosing/surgery , Aged , Female , Follow-Up Studies , Humans , Lumbar Vertebrae/diagnostic imaging , Magnetic Resonance Imaging , Male , Middle Aged , Myelography , Recovery of Function , Severity of Illness Index , Spinal Fusion/adverse effects , Tomography, X-Ray Computed , Treatment Outcome
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