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1.
Ann Rheum Dis ; 69(1): 82-7, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19221399

ABSTRACT

OBJECTIVE: To assess whether the removal of aids/devices and/or help from another person in the Childhood Health Assessment Questionnaire (C-HAQ) leads to a significant change in the disability index (DI) score and responsiveness in juvenile idiopathic arthritis (JIA). METHODS: Changes in the C-HAQ DI score in a cross-sectional sample of 2663 children with JIA and in 530 active patients with JIA in a trial of methotrexate (MTX) were compared. RESULTS: Patients in the MTX trial had higher disease activity and disability than the cross-sectional sample. The frequency of aids/devices (range 1.2-10.2%) was similar between the two samples, while help (range 5.3-38.1%) was more frequently used in the MTX group. Correlation between disease severity variables and the two different C-HAQ DI scoring methods did not change substantially. There was a decrease in the C-HAQ DI score for both the cross-sectional (mean score from 0.64 with the original method to 0.54 without aids/devices and help, p<0.0001) and the MTX sample (mean score from 1.23 to 1.07, p<0.0001). A linear regression analysis of the original C-HAQ DI score versus the score without aids/devices and help demonstrated the substantial overlap of the different scoring methods. Responsiveness in the responders to MTX treatment did not change with the different C-HAQ DI scoring methods (range 0.86-0.82). CONCLUSION: The removal of aids/devices and help from the C-HAQ does not alter the interpretation of disability at a group level. The simplified C-HAQ is a more feasible and valid alternative for the evaluation of disability in patients with JIA.


Subject(s)
Arthritis, Juvenile/rehabilitation , Disability Evaluation , Self-Help Devices , Activities of Daily Living , Antirheumatic Agents/therapeutic use , Arthritis, Juvenile/drug therapy , Arthritis, Juvenile/physiopathology , Child , Child, Preschool , Cross-Sectional Studies , Female , Humans , Male , Methotrexate/therapeutic use , Reproducibility of Results , Severity of Illness Index , Treatment Outcome
2.
Clin Exp Rheumatol ; 19(4 Suppl 23): S163-7, 2001.
Article in English | MEDLINE | ID: mdl-11510323

ABSTRACT

We report herein the results of the cross-cultural adaptation and validation into the British language of the parent's version of two health related quality of life instruments. The Childhood Health Assessment Questionnaire (CHAQ) is a disease specific health instrument that measures functional ability in daily living activities in children with juvenile idiopathic arthritis (JIA). The Child Health Questionnaire (CHQ) is a generic health instrument designed to capture the physical and psychosocial well-being of children independently from the underlying disease. A total of 440 subjects were enrolled: 219 patients with JIA (17% systemic onset, 41% polyarticular onset, 33% extended oligoarticular subtype, and 9% persistent oligoarticular subtype) and 221 healthy children. The CHAQ clinically discriminated between healthy subjects and JIA patients, with the systemic, polyarticular and extended oligoarticular subtypes having a higher degree of disability, pain, and a lower overall well-being when compared to their healthy peers. Also the CHQ clinically discriminated between healthy subjects and JIA patients, with the systemic onset, polyarticular onset and extended oligoarticular subtypes having a lower physical and psychosocial well-being when compared to their healthy peers. In conclusion the British version of the CHAQ-CHQ is a reliable, and valid tool for the functional, physical and psychosocial assessment of children with JIA.


Subject(s)
Arthritis, Juvenile/diagnosis , Cross-Cultural Comparison , Health Status , Surveys and Questionnaires , Adolescent , Child , Cultural Characteristics , Disability Evaluation , Female , Humans , Language , Male , Psychometrics , Quality of Life , Reproducibility of Results , United Kingdom
4.
Br J Rheumatol ; 36(5): 594-8, 1997 May.
Article in English | MEDLINE | ID: mdl-9189063

ABSTRACT

Young people with conversion disorders require a different treatment approach compared with those who have organic illness. This paper describes a team approach which is based on detailed assessment, explanation of the vicious cycle, accepting the patient's symptoms, working towards achievable goals, encouraging bravery, rewarding 'wellness' behaviour, ignoring abnormal behaviour and supervising re-integration into school.


Subject(s)
Conversion Disorder/rehabilitation , Adolescent , Attitude , Conversion Disorder/physiopathology , Conversion Disorder/psychology , Exercise/physiology , Gait/physiology , Humans , Psychotherapy/standards
5.
Ann Rheum Dis ; 45(6): 464-74, 1986 Jun.
Article in English | MEDLINE | ID: mdl-3488035

ABSTRACT

To investigate the genetics of susceptibility to early onset pauciarticular juvenile chronic arthritis (JCA), 158 unrelated ethnic British patients with a mean disease onset of 3.2 years, together with controls, were tested for HLA-A, B, C, and DR antigens. Additionally, 117 patients were also investigated for complement Bf and C4 markers. New observations included an increased frequency of the C4B 2 allotype (p corrected (pc) less than 0.02) and C4A 4,B 2 phenotype (p less than 0.0005). Findings suggested a unique increase of the haplotype HLA-DRw8, Bf*S, C4A*4, C4B*2, HLA-B39, possibly predisposing to more severe disease. Strong positive associations were confirmed with HLA antigens A2 (pc = 2.5 X 10(-8)), DRw8 (pc = 3.5 X 10(-14)), DR5 (pc less than 0.02), DRw52 (pc = 2.8 X 10(-6)) and DR5, w8 phenotype (pc = 3.9 X 10(-6)), and negative associations with DR7 (pc = 5.8 X 10(-7)), DR4 (pc less than 0.002), and DRw53 (pc = 0.004). Antinuclear antibody (ANA) seropositivity correlated with DR5 (p less than 0.02), and in children with chronic iridocyclitis (CIR) Bw62 incidence was raised (p less than 0.03) and B44 reduced (p less than 0.03). HLA-A2 was found in 88% of ANA+, CIR+ patients (p less than 0.01). A significant excess of DR5, w8 heterozygotes was present (relative risk = 41.1) and a lack of corresponding homozygotes. Results are inconsistent with a recessive, dominant, or intermediate mode of inheritance of susceptibility, and favour the existence of at least two DR linked 'disease' genes. Moreover, there may be an interaction in heterozygotes of combinatorial factors associated with DR5 and DRw8 in enhancing susceptibility. Possible immunogenetic mechanisms underlying the observed associations with three antigen classes are discussed. Evidence here suggests a role for the HLA-DQ locus in determining susceptibility to this disease.


Subject(s)
Arthritis, Juvenile/genetics , Complement C4/genetics , Complement Factor B/genetics , Enzyme Precursors/genetics , HLA Antigens/genetics , Age Factors , Antibodies, Antinuclear/genetics , Arthritis, Juvenile/complications , Arthritis, Juvenile/immunology , Child , Child, Preschool , Female , Genetic Predisposition to Disease , Humans , Infant , Male , Phenotype , Uveitis, Anterior/etiology
6.
Clin Exp Rheumatol ; 3(1): 59-62, 1985.
Article in English | MEDLINE | ID: mdl-3978896

ABSTRACT

Indoprofen at 10-12 mg/kg body weight was compared with aloxiprin at 80 mg/kg body weight in children suffering from juvenile chronic arthritis. Indoprofen was significantly superior to aloxiprin in reducing soft tissue swelling and joint limitation and was effective in relieving pain and morning slowness and improving grip strength. The drug was well tolerated and is a satisfactory agent for the treatment of chronic arthritis in children.


Subject(s)
Arthritis, Juvenile/drug therapy , Indoprofen/therapeutic use , Phenylpropionates/therapeutic use , Arthritis, Juvenile/physiopathology , Aspirin/adverse effects , Aspirin/analogs & derivatives , Aspirin/therapeutic use , Child , Child, Preschool , Drug Evaluation , Gastrointestinal Diseases/chemically induced , Humans , Indoprofen/adverse effects
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