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1.
Ann Rheum Dis ; 69(2): 325-31, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19773290

ABSTRACT

OBJECTIVES: To develop evidence-based EULAR recommendations for cardiovascular (CV) risk management in patients with rheumatoid arthritis (RA), ankylosing spondylitis (AS) and psoriatic arthritis (PsA). METHODS: A multidisciplinary expert committee was convened as a task force of the EULAR Standing Committee for Clinical Affairs (ESCCA), comprising 18 members including rheumatologists, cardiologists, internists and epidemiologists, representing nine European countries. Problem areas and related keywords for systematic literature research were identified. A systematic literature research was performed using MedLine, Embase and the Cochrane library through to May 2008. Based on this literature review and in accordance with the EULAR's "standardised operating procedures", the multidisciplinary steering committee formulated evidence-based and expert opinion-based recommendations for CV risk screening and management in patients with inflammatory arthritis. RESULTS: Annual CV risk assessment using national guidelines is recommended for all patients with RA and should be considered for all patients with AS and PsA. Any CV risk factors identified should be managed according to local guidelines. If no local guidelines are available, CV risk management should be carried out according to the SCORE function. In addition to appropriate CV risk management, aggressive suppression of the inflammatory process is recommended to further lower the CV risk. CONCLUSIONS: Ten recommendations were made for CV risk management in patients with RA, AS and PsA. The strength of the recommendations differed between RA on the one hand, and AS and PsA, on the other, as evidence for an increased CV risk is most compelling for RA.


Subject(s)
Arthritis, Psoriatic/complications , Arthritis, Rheumatoid/complications , Cardiovascular Diseases/etiology , Cardiovascular Diseases/prevention & control , Spondylitis, Ankylosing/complications , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Antihypertensive Agents/therapeutic use , Cholesterol/blood , Drug Administration Schedule , Evidence-Based Medicine/methods , Female , Glucocorticoids/administration & dosage , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Male , Risk Management/methods
2.
Clin Exp Rheumatol ; 27(4 Suppl 55): S124-6, 2009.
Article in English | MEDLINE | ID: mdl-19822058

ABSTRACT

Cardiovascular co-morbidity is now a recognised complication of chronic inflammation and an elevated acute phase response predisposes to hypertension, stroke and myocardial infarction. Dyslipidaemia is a feature of inflammatory joint diseases and is closely related to elevated CRP and Il-6 levels. Rheumatoid arthritis (RA) has an increased standardised mortality ratio largely attributable to cardiovascular risk. An increased although lesser, cardiovascular morbidity has also been observed in ankylosing spondylitis (AS) which has a similar abnormal lipid profile to that seen in RA. There is some evidence that therapeutic agents such as anti-tumour necrosis factor-alpha (TNF-alpha) drugs that down-regulate the acute phase response, also have an effect in reducing cardiovascular complications in RA and AS.


Subject(s)
Arthritis, Rheumatoid/epidemiology , Cardiovascular Diseases/epidemiology , Dyslipidemias/epidemiology , Spondylitis, Ankylosing/epidemiology , Antibodies, Monoclonal/therapeutic use , Antirheumatic Agents/therapeutic use , Arthritis, Rheumatoid/drug therapy , Arthritis, Rheumatoid/metabolism , Cardiovascular Diseases/drug therapy , Cardiovascular Diseases/metabolism , Comorbidity , Cytokines/metabolism , Dyslipidemias/drug therapy , Dyslipidemias/metabolism , Humans , Metabolic Syndrome/drug therapy , Metabolic Syndrome/epidemiology , Metabolic Syndrome/metabolism , Risk Factors , Spondylitis, Ankylosing/drug therapy , Spondylitis, Ankylosing/metabolism , Synovitis/metabolism , Tumor Necrosis Factor-alpha/antagonists & inhibitors
9.
Scott Med J ; 41(5): 147-9, 1996 Oct.
Article in English | MEDLINE | ID: mdl-8912986

ABSTRACT

Home enteral feeding (HEF) is increasingly used to achieve positive energy and nitrogen balance in children with chronic disease outside hospital. It should be considered when oral feeding cannot or should not be used, and when nutritional support is the sole reason for hospitalisation. In the West of Scotland 156 children (80 male, 76 female) cared for by the Royal Hospital for Sick Children in Glasgow received HEF between 1st September 1994 and 1995. They ranged in age from 0 months to 23 years. Indications for HEF were cystic fibrosis (21), cerebral palsy (17), other neurological disease (29), congenital/metabolic abnormalities (23), chronic renal failure (17), neoplastic disease (17), gastrointestinal/hepatic' disease (12), failure-to-thrive (10), and cardiorespiratory disease (10). Most children received feeds by nasogastric tube (59%) or gastrostomy (41%). One child had a jejunostomy. Feeding regimens were continuous infusion (52%), bolus feeding along (26%), and a combination of bolus and infusion (22%). 73% of patients had infusion pumps. Duration of HEF ranged from one month to 12 years. 78% of children received standard infant or enteral feeds, some receiving energy supplements. The remainder received 'disease-specific' or other special feeds. There was a 23% increase in the number of children receiving HEF during the year of the study. HEF represents an affective way of improving the nutritional status of children with chronic disease at home. It frees hospital beds and nursing resources, is well accepted by children and their families and is growing rapidly as an alternative to hospitalisation.


Subject(s)
Chronic Disease/therapy , Enteral Nutrition/methods , Home Nursing , Adolescent , Adult , Child , Child, Preschool , Enteral Nutrition/economics , Enteral Nutrition/statistics & numerical data , Female , Gastrostomy , Humans , Infant , Infant, Newborn , Intubation, Gastrointestinal , Jejunostomy , Male , Retrospective Studies , Scotland , Time Factors
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