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1.
JAAPA ; 32(3): 25-31, 2019 Mar.
Article in English | MEDLINE | ID: mdl-30741851

ABSTRACT

Acute monoarthritis affects a single joint and has many potential underlying causes, including crystal deposition diseases, infection, trauma, and osteoarthritis. A comprehensive health history and physical examination can help narrow the list of differential diagnoses; judicious diagnostic testing can help pinpoint the diagnosis. Clinicians also must be able to recognize which patients require emergency referral to prevent long-term adverse consequences.


Subject(s)
Arthralgia/etiology , Arthritis/diagnosis , Arthritis/etiology , Acute Disease , Adrenal Cortex Hormones/adverse effects , Anticoagulants/adverse effects , Arthralgia/pathology , Arthritis/classification , Arthritis/pathology , Arthritis, Infectious/complications , Arthritis, Rheumatoid/complications , BCG Vaccine/adverse effects , Chondrocalcinosis/complications , Crystal Arthropathies/complications , Diagnosis, Differential , Diphosphonates/adverse effects , Diuretics/adverse effects , Gout/complications , Humans , Joints/pathology , Osteoarthritis/complications , Spondylarthropathies/complications
2.
BMJ ; 336(7644): 594-7, 2008 Mar 15.
Article in English | MEDLINE | ID: mdl-18296460

ABSTRACT

OBJECTIVES: To assess whether supplementation with antioxidants, folinic acid, or both improves the psychomotor and language development of children with Down's syndrome. DESIGN: Randomised controlled trial with two by two factorial design. SETTING: Children living in the Midlands, Greater London, and the south west of England. PARTICIPANTS: 156 infants aged under 7 months with trisomy 21. INTERVENTION: Daily oral supplementation with antioxidants (selenium 10 mug, zinc 5 mg, vitamin A 0.9 mg, vitamin E 100 mg, and vitamin C 50 mg), folinic acid (0.1 mg), antioxidants and folinic acid combined, or placebo. MAIN OUTCOME MEASURES: Griffiths developmental quotient and an adapted MacArthur communicative development inventory 18 months after starting supplementation; biochemical markers in blood and urine at age 12 months. RESULTS: Children randomised to antioxidant supplements attained similar developmental outcomes to those without antioxidants (mean Griffiths developmental quotient 57.3 v 56.1; adjusted mean difference 1.2 points, 95% confidence interval -2.2 to 4.6). Comparison of children randomised to folinic acid supplements or no folinic acid also showed no significant differences in Griffiths developmental quotient (mean 57.6 v 55.9; adjusted mean difference 1.7, -1.7 to 5.1). No between group differences were seen in the mean numbers of words said or signed: for antioxidants versus none the ratio of means was 0.85 (95% confidence interval 0.6 to 1.2), and for folinic acid versus none it was 1.24 (0.87 to 1.77). No significant differences were found between any of the groups in the biochemical outcomes measured. Adjustment for potential confounders did not appreciably change the results. CONCLUSIONS: This study provides no evidence to support the use of antioxidant or folinic acid supplements in children with Down's syndrome. TRIAL REGISTRATION: Clinical trials NCT00378456.


Subject(s)
Antioxidants/administration & dosage , Dietary Supplements , Down Syndrome/diet therapy , Leucovorin/administration & dosage , Administration, Oral , Developmental Disabilities/diet therapy , Developmental Disabilities/enzymology , Down Syndrome/enzymology , Glutathione Peroxidase/metabolism , Humans , Infant , Language Disorders/diet therapy , Language Disorders/enzymology , Patient Compliance , Psychomotor Disorders/diet therapy , Psychomotor Disorders/enzymology , Superoxide Dismutase/metabolism , Treatment Outcome
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