Antimalarials in Rheumatic Diseases
Identifieur interne : 003748 ( Main/Exploration ); précédent : 003747; suivant : 003749Antimalarials in Rheumatic Diseases
Auteurs : R. O. Day ; P. Sambrook ; G. D. Champion ; G- G. GrahamSource :
- Australian and New Zealand Journal of Medicine [ 0004-8291 ] ; 1982-12.
English descriptors
- Teeft :
- Adverse effects, Antimalarial, Antimalarials bind, Arthritis, Arthritis rheum, Chloroquine, Clin, Clinical pharmacology, Complement deficiency, Complement system, Creatinine clearance, Cumulative dose, Daily dosages, Daily dose, Discoid lupus, Further studies, Gastrointestinal, Gold thiomalate, Hydroxychloroquine, Immune response, Individual components, Lupus, Lupus erythematosus, Older patients, Ophthalmological examination, Ophthalmological safety, Other drugs, Plasma concentrations, Renal, Renal failure, Retinal toxicity, Rheum, Rheumatic, Rheumatic diseases, Rheumatoid, Rheumatoid anhntis, Rheumatoid arthritis, Semin arthritis rheum, Serum chloroquine, Side effects, Systemic lupus erythematosus, Toxicity, Whole blood.
Abstract
Abstract: The use of antimalarials in rheumatoid arthritis (RA) and systemic lupus erythematosis (SLE) has declined over recent years due to concern over retinal toxicity and the impression that this class of drugs is relatively ineffective in rheumatic diseases. Recent reviewsr‐3 suggest that this position should be changed. Firstly, there is now good evidence for the efficacy of these drugs in RA and secondly strict control of the daily dosage and careful ophthalmological surveillance can almost eliminate the risk of serious retinal toxicity.
Url:
DOI: 10.1111/j.1445-5994.1982.tb02658.x
Affiliations:
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Le document en format XML
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<term>Antimalarials bind</term>
<term>Arthritis</term>
<term>Arthritis rheum</term>
<term>Chloroquine</term>
<term>Clin</term>
<term>Clinical pharmacology</term>
<term>Complement deficiency</term>
<term>Complement system</term>
<term>Creatinine clearance</term>
<term>Cumulative dose</term>
<term>Daily dosages</term>
<term>Daily dose</term>
<term>Discoid lupus</term>
<term>Further studies</term>
<term>Gastrointestinal</term>
<term>Gold thiomalate</term>
<term>Hydroxychloroquine</term>
<term>Immune response</term>
<term>Individual components</term>
<term>Lupus</term>
<term>Lupus erythematosus</term>
<term>Older patients</term>
<term>Ophthalmological examination</term>
<term>Ophthalmological safety</term>
<term>Other drugs</term>
<term>Plasma concentrations</term>
<term>Renal</term>
<term>Renal failure</term>
<term>Retinal toxicity</term>
<term>Rheum</term>
<term>Rheumatic</term>
<term>Rheumatic diseases</term>
<term>Rheumatoid</term>
<term>Rheumatoid anhntis</term>
<term>Rheumatoid arthritis</term>
<term>Semin arthritis rheum</term>
<term>Serum chloroquine</term>
<term>Side effects</term>
<term>Systemic lupus erythematosus</term>
<term>Toxicity</term>
<term>Whole blood</term>
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<front><div type="abstract" xml:lang="en">Abstract: The use of antimalarials in rheumatoid arthritis (RA) and systemic lupus erythematosis (SLE) has declined over recent years due to concern over retinal toxicity and the impression that this class of drugs is relatively ineffective in rheumatic diseases. Recent reviewsr‐3 suggest that this position should be changed. Firstly, there is now good evidence for the efficacy of these drugs in RA and secondly strict control of the daily dosage and careful ophthalmological surveillance can almost eliminate the risk of serious retinal toxicity.</div>
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<name sortKey="Graham, G G" sort="Graham, G G" uniqKey="Graham G" first="G- G." last="Graham">G- G. Graham</name>
<name sortKey="Sambrook, P" sort="Sambrook, P" uniqKey="Sambrook P" first="P." last="Sambrook">P. Sambrook</name>
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