- Team approach
- Rheumatologists
- Therapists
- Surgeons
- Main objectives are
- Relief of pain
- Reduction or suppression of inflammation
- Minimising undesirable side effects
- Preservation of muscle & joint function
- Return to functional activities
- Patient education vital
- Drug therapy may take weeks to months to act
- Medical Treatment
- Nonspecific
- Patient Education
- Remissions & exacerbations occur
- Disability not inevitable
- Maintain realistic lifestyle
- Drugs take > 1 month to work
- Rest
- Can alleviate acute flare of Polyarthritis
- Reduces joint pain & swelling
- Admission may be warranted
- Splintage can rest joint flare-up
- Physical Therapy
- Maintain ROM
- Daily movement through range
- Daily gentle exercises
- Minimize muscle wasting
- Minimize deformity
- Anatomical positioning
- Eg. Sleep positioning » No pillows under knees
- Medications
- Aims
- Alleviate pain & swelling
- Modify course of disease
- Traditional & Modern
- Traditional is a 3 (4) tier pyramidal approach
- NSAID 1st
- DMARD’s 2nd
- Gold
- Penicillamine
- Chloroquine
- Sulfasalazine
- Cytotoxics 3rd
- Methotrexate
- Azathioprine
- Cyclophosphamide
- Steroids last
- Current trend is toward combination treatment
- Like Chemotherapy
- Traditional is a 3 (4) tier pyramidal approach
- Aims
- NSAID
- 1st -line therapy
- Cyclo-oxygenase inhibitor
- Used in almost all cases
- Alleviate pain & swelling
- Don’t modify course of disease
- Side effects troublesome
- Skin rashes
- Gastric ulceration
- Renal dysfunction
- Care if administering with
- Warfarin
- PUD
- Advancing age
- Recent evidence that high morbidity & mortality
- » Less use
- Disease-Modifying Anti-Rheumatic Drugs (DMARDs)
- 2nd-line therapy
- May allow improvement or even remission of symptoms
- Original rationale for usage unsure as fortuitous finding
- All slow acting
- Indications
- Clinical evidence of synovitis
- Inadequate response to NSAID
- Erosive disease on XR
- Types
- Gold salts
- Antimalarials – Chloroquine
- D-Penicillamine
- Sulphasalazine
- Activity related to
- Gold » Mononuclear cell inhibition
- D-Penicillamine » T-Lymphocyte inhibition
- Antimalarials » Stabilise lysosomal membranes & inhibit IL- I
- Sulphasalazine » Anti-folate activity
- Generally similar (see* for details)
- May be used sequentially & in combination
- Effective in 50-80%
- Improve symptoms & signs in medium term
- Some slowing of progress of disease
- Side effects & Toxicity is a problem » 30-40% of patients
- Rashes
- Stomatitis
- Dermatitis
- Leucopaenia
- Agranulocytosis
- Thrombocytopenia
- Nephrotic syndrome
- Glomerulonephritis
- Cholestatic jaundice
- Pulmonary
- Ocular – Macular degeneration in the antimalarials
- Regular urine & blood tests required to monitor toxicity » looking at FBC & Proteinuria
- *Gold Salts
- Inhibit monocyte function
- IM route (weekly)
- Need close monitoring
- Toxicity in 30-40%
- Screening with FBC & urinalysis
- Pancytopaenia & ARF
- *Penicillamine
- Modulates lymphocyte function
- Toxicity in 50%
- Similar profile to Gold
- *Antimalarials
- Chloroquine & Hydroxycholoroquine
- Stabilize lysosomal membranes
- Inhibit IL-1 function
- Less life-threatening toxicity
- Screen with Ocular examination for Macular degeneration
- *Sulphasalazine
- Anti-Folate activity
- Less side effects
- 3rd-line therapy tends to be Cytotoxics
- Indications
- 5-10% of RA patients with progressive disabling synovitis
- Three commonest
- Methotrexate
- Azothiaprine
- Cyclophosphamide
- Striking improvements seen
- MTX » Pneumonitis worst complication
- 70% benefit at 4-6/52
- Major side effects
- Should monitor carefully for marrow suppression & GIT toxicity
- Should not be given to child bearing aged women » Infertility & Teratogenesis
- Long term malignancy risk seen » Lymphoma with the cyclophosphamide and
- azathioprine but NOT Methotrexate
- » Current Trends
- More aggressive approach recently with DMARDs
- With the realization that NSAID are poor drugs
- & That rheumatoid arthritis is a very significant disease
- Traditional Management results only moderate
- With older age group dying within 10 years
- Erosions within 10 years
- MTX very effective
- Avara is the new replacement for MTX
- More aggressive approach recently with DMARDs
- Corticosteroids
- 4th-line therapy
- Oral
- Dramatically effective
- Act via
- Main glucocorticoid effect is ↑ protein synthesis especially Lipocortin
Lipocortin inhibits Phospholipase A2
Phopholipase important in releasing Arachadonic Acid
AA is catalysed by Cyclo-oxygenase & Lipoxygenase into PG & Leukotrienes
- Thus inhibits action of many proinflammatory products
- Prostaglandins
- Leukotrienes
- Cytokines (particularly interleukins)
- Effect on lymphocyte function
- In vivo effect not clear
- Indications
- Refractory disease
- As interim treatment waiting for DMARD’s to take effect
- Severe Non-Articular manifestations of RA
- Long-term side effects
- Osteoporosis
- HT & DM
- Operative complications
- Impaired wound healing
- Wound dehiscence
- Increased risk of infection
- Post-operative hypotension
- Cover required by replacement of oral dose
- With IV Hydrocortisone required with
- Pre-medication
- While unable to take oral dose
- Increase dose with infection
- With IV Hydrocortisone required with
- Intra-Articular steroids
- Useful for monoarticular & oligoarticular flares
- No more often than 3/12
- Sepsis rare with aseptic technique
- » Current Trends
- More people die from NSAID, hence more DMARDs
- Increasing role for steroids
- In principle better to stop steroids & DMARD’s prior to OT
- Stop steroids & DMARD’s in consultation with rheumatologist
- Have to balance against
- RA flares
- Inability to rehabilitate
- Pain
- Autologous Stem Cell Transplantation
- Can cure
- Mortality 1%
- Other Experimental Treatment
- Irradiation
- Cyclosporin A