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Cardiovascular risk and rheumatoid arthritis: clinical practice guidelines based on published evidence and expert
Thao Pham1, Laure Gossec, Arnaud Constantin
1Service de rhumatologie, CHU de la Conception, Marseille, France.
Insights
Rheumatoid arthritis (RA) patients face increased cardiovascular disease risk due to persistent inflammation. Guidelines recommend evaluating and managing this risk, considering specific treatments like methotrexate and TNFalpha antagonists, while correcting modifiable factors.
Area of Science:
- Rheumatology
- Cardiology
- Clinical Practice Guidelines
Background:
- Rheumatoid arthritis (RA) is associated with a significant excess burden of cardiovascular disease (CVD) morbidity and mortality.
- Persistent inflammation in RA is recognized as an independent cardiovascular risk factor.
Purpose of the Study:
- To establish evidence-based clinical practice guidelines for evaluating and managing cardiovascular risk in patients with rheumatoid arthritis.
- To provide expert recommendations for optimizing cardiovascular health in RA patients.
Main Methods:
- A Delphi procedure was utilized by a scientific committee to formulate key questions.
- Literature searches were conducted to gather evidence addressing these questions.
- Recommendations were developed by a panel of experts based on the synthesized evidence.
Main Results:
- RA is an independent cardiovascular risk factor, with inflammation exacerbating risk.
- Cardiovascular risk assessment and correction of modifiable factors are crucial for RA patients.
- Specific recommendations address glucocorticoid use, methotrexate's potential protective effects, TNFalpha antagonists in heart failure, LDL-cholesterol targets, statin therapy, and aspirin use for prevention.
Conclusions:
- Clinical guidelines emphasize proactive cardiovascular risk management in RA patients.
- Treatment decisions should consider the impact on cardiovascular health, including the benefits and risks of specific RA therapies.
- Integrated management of RA and cardiovascular risk factors is essential for improving patient outcomes.
Objective:
To develop clinical practice guidelines for the evaluation and management of cardiovascular risk in patients with rheumatoid arthritis (RA), using the evidence-based approach and expert opinion.
Methods:
Recommendations were developed using the evidence-based approach and expert opinion: A scientific committee used a Delphi procedure to select five questions, which formed the basis for developing the recommendations; Evidence providing answers to the five questions was sought in the literature; Based on this evidence, recommendations were developed by a panel of experts.
Results:
The recommendations were as follows: 1) In patients with RA, attention should be given to the risk of cardiovascular disease, which is responsible for an excess burden of morbidity and mortality; 2) It must be recognized that RA may be an independent cardiovascular risk factor. Persistent inflammation is an additional risk factor; 3) The cardiovascular risk should be evaluated, and modifiable risk factors should be corrected; 4) In patients with RA requiring glucocorticoid therapy, the need for cardiovascular risk minimization is among the reasons that mandate the use of the minimal effective dose; 5) It should be recognized that methotrexate may protect against cardiovascular mortality in patients with RA; 6) It should be recognized that TNFalpha antagonists remain contraindicated in patients with RA and severe heart failure. TNFalpha antagonists do not seem to worsen moderate heart failure and may protect against cardiovascular mortality; 7) AFSSAPS recommendations about LDL-cholesterol objectives should be followed, with active RA being counted as a cardiovascular risk factor; 8) In patients with RA, statin therapy should be considered only when cholesterol levels are elevated despite appropriate dietary treatment; 9) RA per se does not indicate aspirin for primary prevention. When aspirin is used for secondary prevention, it should be recognized that concomitant treatment with nonsteroidal antiinflammatory drugs (NSAIDs) may decrease the antiplatelet effects and increase the gastrointestinal side effects of aspirin therapy.
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