Rheum Flashcards
What are you prescribing for fibromyalgia?
Neuropathic meds:
1st - amitryptilline 25mg
Or duloxetine or pregabalin.
List some side effects of alendronate and bisphosphonate?
Osteonecrosis of jaw
Oesophagitis - careful posture when taking meds
Gastric ulcers
what are the clincial features of RA?
o Stiffness worse in the morning -> better with exercise
o Swan neck, boutonnière (late features), Z-thumb, ulnar deviation at MCPJ
name some exra-articular features of RA?
Eyes episcleritis, keratoconjunctivitis sicca
Heart pericarditis
Lungs fibrosis, rheumatoid nodules
Hands De Quervain’s tenosynovitis, Carpal tunnel, trigger finger
Spleen splenomegaly [Felty’s syndrome]
Kidney - amyloidosis
Feet - Peripheral neuropathy
what are the features of felty syndrome?
- Splenomegaly !
- Anaemia
- Neutropenia!
- Thrombocytopenia
- Rheumatoid Arthritis !
how do we ivx RA?
o Bloods: FBC (anaemia, ↓PMN, ↑plat), ↑ESR, ↑CRP SJC = swollen JC
RhF: +ve in 70% JC = Joint Count
Anti-CCP: 90-95% specific, 80% sensitive
ANA: +ve in 30%
o Imaging: XR (baseline), USS (synovitis)
How do we monitor disease activity in RA?
CRP,
Disease activity score 28; DAS 28
TJC/SJC; tender/swollen joint count (feeds into das28)
- If DAS-28 >5.1, consider stepping up management
- If pain/CRP/DAS, offer simple analgesics
outline of Mx for RA?
o 1st line conventional DMARD (cDMARD) monotherapy ± short course bridging prednisolone
DMARD medications = methotrexate, sulfasalazine, MMF, hydroxychloroquine, leflunomide,
o 2nd line (DAS/CRP increasing);
[2x DMARDs in combination]
o 3rd line (DAS/CRP increasing):
biologics (bDMARD)
Etanercept, Infliximab, Adalimumab, Rituximab
± cDMARD (TNFa-inhibitors, B-cell/T-cell depletion)
Once remission is achieved, keep them on a low dose of the dmard
Mx for flare ups in RA?
o Corticosteroids (PO, IM; methylprednisolone acetate, triamcinolone acetonide) ± NSAIDs
what are the principles of RA mx?
With a new diagnosis, start steroid then wean off steroids starting dmard. Takes 12weeks to kick in hence bridging prednisolone for 6weeks.
If someone is taking methotrexate, they MUST be given folate- take on a different day. Once weekly methotrexate.
If you start methotrexate and they have side effects, just change to another first line eg hydroxychloroquine - not this is the only first line NOT considered an immunosuppressant so no vaccines, regular blood tests needed. Need once yearly flu jab, no live vaccines.
If disease persists after some months on 1st line drug then change to 2nd lines, anti-tnf drugs then make inhibitors.
Doctors DO actually give nsaids with methotrexate, a small amount - some may not though.
Drs usually start pt on 2 dmards straight away. Trial period is 6 months during which remission is expected. If very mild just start on 1 dmard, must try for 6 months before changing to another dmard. If 2 dmards don’t work then biologics.
what are some notable points about RA mx and pregnancy>
Notes about methotrexate:
Must stop for 3 months before trying to get pregnant. Swap to sulfasalazine.
list the causes fo fracture?
Causes of fracture:
Hypogonadism in males - low testosterone (that’s why we ask if they shave regularly, libido etc)
Osteomalacia- malabsorption; coealiac etc, diet
Medications - steroids, diabetes drugs - gliflozins
Breast cancer drugs - lefloxazole?
Myeloma
Osteoporosis
In osteoporosis, which bisphosphonates do we prescribe?
Alendronate, risidronate - 1st line.
Risidronate usually better tolerated.
Teriparatide - very expensive. Only if fractures, unresponsive to bisphophonates.
what counts as significant morning stiffness
when it last 30mins more
what do we give upon a new diagnosis of Rheumatoid condition eg polymyalgia?
give prednisolone 15mg
Steroid dosing.
What dose of pred given in these circumstances:
- Life threatening asthma or cold
- Temporal arthritis
- Life threatening asthma or cold give 40mg prednisolone
- Temporal arthritis give 60mg prednisolone.
GCA usually secondary to polymyalgia rheumatica.
GCA is most common vasculitis.
Differentiating features of RA vs OA osteoarthritis on Xray?
Rheumatoid - LESS: Loss of joint space - proximal joints more Erosions (periarticular) Soft tissue swelling Subluxation & deformity
OA - LOSS: Loss of joint space Osteophytes Subchondral sclerosis Subchondral cysts
Clinical Features of OA?
Presents with joint pain and stiffness that is typically worse with activity.
Pain following use, improves with rest
Unilateral
No systemic upset
Weight-bearing joints (knee, hip)
Hands: DIPJ (Herbedens nodes), PIPJ (Bouchards nodes),
CMCJ! (squaring at base of thumb)
Knee giving way/locking sometimes
Reduced ROM
Usually elderly!
How does Polyarteritis nodosa present?
Mx?
Polyarteritis nodosa- widespread ischaemic and infarcts -> headaches, gangrene, foot drop etc.
Is a vasculitis
Give Prednisolone and cyclophosphamide
How does Churg Strauss / eGPA present?
ivx?
- Eosinophilia
- Asthma (late-onset)
- Vasculitis (incl. RPGN)
ivx: +ve pANCA
How do we mx neuropathic pain?
o 1st line neuropathic pain -> amytriptyline, pregabalin
o 1st line diabetic neuropathy -> duloxetine
options include ; gabapentin
o 1st line trigeminal neuralgia -> carbamazepine
Clinical features fibromyalgia ?
o Chronic, widespread musculoskeletal pain and tenderness
o Fatigue
o Poor concentration
o Sleep disturbance
o Low mood
o Morning stiffness? - note; in fibro, pain may lead to perceived reduction in ROM but truly can be overcome
ivx and mx of Fibromyalgia?
Ex: feel tender points
Ivx: normal
Mx: educate, CBT, graded exercise programmes, amitryptyline/pregabalin/venlafaxine
What are the forms of vasculitis?
• Large vessel:
o GCA / temporal arteritis
o Takayasu’s arteritis
• Medium vessel:
o Polyarteritis nodosa
o Kawasaki’s disease Chapel-Hill criteria [2012]
• Small vessel:
o pANCA Churg-Strauss (eGPA), microscopic polyangiitis
o cANCA Wegener’s Granulomatosis (GPA)
o ANCA –ve HSP, Goodpasture’s, cryoglobulinaemia
how would temproal arteritis present?
scalp tenderness, jaw claudication, headache, amaurosis fugax (ant. ischaemic optic neuropathy)
How do we mx temproal arteritis?
o Ix:
USS temporal artery (halo sign; if -ve -> temporal artery biopsy) ->, ESR raised, ALP raised, plts raised
o Mx:
40-60mg, PO prednisolone (immediately; before ix . taper down)
?Aspirin
-> PPI + alendronate (for 2 years)
Visual symptoms -> IV methylprednisolone
how would polymyalgia rheumatica present?
manifests as PAIN and morning STIFFNESS involving the neck, shoulder girdle, and/or pelvic girdle in individuals older than age 50 years.
NO WEAKNESS
varying degrees of muscle tenderness, shoulder/hip bursitis, and/or oligoarthritis
About 15% to 20% of patients with PMR have giant cell arteritis