The Impact of Nurse-led Programme With and Without Carotid Ultrasound on Addressing Cardiovascular Risk in Patients With Arthritis: a Prospective, Multicentre, Randomised, Controlled Trial
Overview
- Phase
- N/A
- Intervention
- Atorvastatin
- Conditions
- Arthritis, Rheumatoid
- Sponsor
- Chinese University of Hong Kong
- Locations
- 1
- Primary Endpoint
- change in Framingham risk score
- Status
- Withdrawn
- Last Updated
- 6 years ago
Overview
Brief Summary
Elevated CVD risk is a significant public health problem that contributes greatly to the increased morbidity and shortened lifespan of individuals with RA and PsA. Over the past decades, there has been great progress into the understanding of the severity of CVD risk in these patients but these risk factors are not well managed. The development of the high-risk strategy is therefore necessary, with more intensive therapy reserved for patients identified as high-risk, e.g. because they have high-risk FRS. However, these risk scores under-estimated CV risk in patients with RA and PsA. An intermediate approach is to use quantification of preclinical vascular disease to further identify high-risk patients. Results from this study will provide clinical implications in terms of detecting and managing cardiovascular morbidity in patients with RA and PsA.
Detailed Description
Objectives This study investigates the impact of a nurse-led programme on cardiovascular (CV) risk screening with and without carotid ultrasound for carotid plaque on CV risk factor control in asymptomatic rheumatoid arthritis (RA) and psoriatic arthritis (PsA) patients. Hypothesis The investigators hypothesize that CV risk stratification and management in RA and PsA may be improved by incorporation of carotid ultrasound to assess for carotid plaque.
Investigators
Lai-Shan Tam
Professor
Chinese University of Hong Kong
Eligibility Criteria
Inclusion Criteria
- •Patients with RA fulfilled the 2010 ACR/EULAR classification criteria or PsA fulfilled the Classification of Psoriatic Arthritis (CASPAR) criteria
- •aged between 18 and 75 will be recruited.
Exclusion Criteria
- •had a history of overt CVD (ie, symptomatic coronary artery disease \[CAD\] or ischemic stroke or transient ischemic attack or peripheral vascular disease)
- •had significant co-morbidities including severe renal impairment or severe deranged liver function
- •female of childbearing potential who are unwilling to use adequate contraception, pregnant or breastfeeding women
- •patients who are already taking lipid lowering therapy.
Arms & Interventions
Group 1 - FRS arm
Both group will participate in the nurse-led programme on CV risk screening and carotid ultrasound for carotid plaque assessment. Subjects in group 1 will initiate Atorvastatin treatment (20mg daily per oral) if their Framingham Risk Score \>10%
Intervention: Atorvastatin
Group 2 USG arm
Subjects in group 2 will initiate Atorvastatin treatment (20mg daily per oral) if they had carotid plaque upon carotid ultrasound findings..
Intervention: Atorvastatin
Outcomes
Primary Outcomes
change in Framingham risk score
Time Frame: 12 months
The Framingham Risk Score is a gender-specific algorithm used to estimate the 10-year cardiovascular risk of an individual. Individuals with low risk have 10% or less CHD risk at 10 years, with intermediate risk 10-20%, and with high risk 20% or more. Change in Framingham risk score between subject in two group will be evaluated. A positive change in score indicates increased CV risk, vice versa.
Secondary Outcomes
- Change in pulse wave velocity (PWV) in subjects(12 months)
- Change in augmentation index (AIX) in subjects(12 months)
- The number of measures taken against comorbidities(12 months)
- Changes in intima-media thickness (IMT)(12 months)
- Proportions of patients achieving remission(12 months)
- Change in individual modifiable risk factors levels(12 months)
- Proportion of plaque progression(12 months)