- Have at least 1 joint with definite clinical synovitis
- With the synovitis not better explained by another disease
Classification criteria for rheumatoid arthritis (add the score of categories A-D; a score of 6/10 is needed definite rheumatoid arthritis)
Key RF = rheumatoid factor
- ACPA = anti-cyclic citrullinated peptide antibody
Factor Scoring
A. Joint involvement
1 large joint 0
2 - 10 large joints 1
1 - 3 small joints (with or without the involvement of large joints) 2
4 - 10 small joints (with or without the involvement of large joints) 3
10 joints (at least 1 small joint) 5
B. Serology (at least 1 test result is needed for classification)
Negative RF and negative ACPA 0
Low-positive RF or low-positive ACPA 2
High-positive RF or high-positive ACPA 3
C. Acute-phase reactants (at least 1 test result is needed for classification)
Normal CRP and normal ESR 0
Abnormal CRP or abnormal ESR 1
Rheumatoid arthritis Prognostic Features
A number of features have been shown to predict a poor prognosis in patients with rheumatoid arthritis, as listed below Poor prognostic features
- Rheumatoid factor positive
- Poor functional status at presentation
- Hla dr4
- X-ray: early erosions (e.g. After < 2 years)
- Extra-articular features e.g. Nodules
- Insidious onset
- Anti-ccp antibodies
In terms of gender, there seems to be a split in what the established sources state is associated with a poor prognosis. However, both the American College of Rheumatology and the recent NICE guidelines (which looked at a huge number of prognosis studies) seem to conclude that female gender is associated with a poor prognosis.
Rheumatoid arthritis management
The management of rheumatoid arthritis (RA) has been revolutionized by the introduction of disease-modifying therapies in the past decade. NICE has issued a number of technology appraisals on the newer agents and released general guidelines in 2009. Patients with evidence of joint inflammation should start a combination of disease-modifying drugs (DMARD) as soon as possible. Other important treatment options include analgesia, physiotherapy, and surgery.
Initial therapy
- In the 2009 NICE guidelines, it is recommended that patients with newly diagnosed active RA start a combination of DMARDs (including methotrexate and at least one other DMARD, plus short-term glucocorticoids)
DMARDs
- Methotrexate is the most widely used DMARD. Monitoring of FBC & lfts is essential due to the risk of myelosuppression and liver cirrhosis. Other important side-effects include pneumonitis
- Sulfasalazine
- Leflunomide
- Hydroxychloroquine
TNF-inhibitors
- The current indication for a TNF-inhibitor is an inadequate response to at least two DMARDs including methotrexate
- Etanercept: recombinant human protein, acts as a decoy receptor for TNF-α, subcutaneous administration, can cause demyelination, risks include reactivation of tuberculosis
- Infliximab: monoclonal antibody, binds to TNF-α and prevents it from binding with TNF receptors, intravenous administration, risks include reactivation of tuberculosis
- Adalimumab: monoclonal antibody, subcutaneous administration
Rituximab
- An anti-cd20 monoclonal antibody results in B-cell depletion
- Two 1g intravenous infusions are given two weeks apart
- Infusion reactions are common
Abatacept
- Fusion protein that modulates a key signal required for activation of T lymphocytes
- Leads to decreased T-cell proliferation and cytokine production
- Given as an infusion
- Not currently recommend by NICE
Rheumatoid Arthritis complications
A wide variety of extra-articular complications occur in patients with rheumatoid arthritis (RA):
- Respiratory: pulmonary fibrosis, pleural effusion, pulmonary nodules, bronchiolitis obliterans, methotrexate pneumonitis, pleurisy
- Ocular: keratoconjunctivitis sicca (most common), episcleritis, scleritis, corneal ulceration, keratitis, steroid-induced cataracts, chloroquine retinopathy
- Osteoporosis
- Ischaemic heart disease: ra carries a similar risk to type 2 diabetes mellitus
- Increased risk of infections
- Depression
Less common
- Felty's syndrome (RA + splenomegaly + low white cell count)
- Amyloidosis