Rheumatology and bone disease Flashcards

(50 cards)

1
Q

What is rheumatology?

A

Branch of medicine dealing with joint, bone and muscle disease
Diseases normally inflammatory
Most diseases are autoimmune with systemic manifestations
Can present either with arthritis or thro’ systemic (oral) features
Rheumatologists need to look in the mouth, dentists need to know when to refer to rheumatology
*** AND GRAPH

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2
Q

Rheumatic disease overview

A
Non- inflammatory
-osteoarthritis
Inflammatory
-rheumatoid Arthritis
-reactive arthritis/ seronegative arthritis
-systemic lupus erythematosus
-vasculitis
-scleroderma
-behcets
-dermatomyositis/ polymyositis
**
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3
Q

Oral manifestations necessary to diagnosis

A

Sjögrens Syndrome
-primary
-secondary
Behcets Disease

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4
Q

Rheumatoid arthritis

A

Disease of synovial joints
Affects 1% population
Auto-immune, systemic inflammatory illness
Symmetrical joint inflammation and deformity
“Extra-articular” features

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5
Q

Rheumatoid arthritis: the pain

A

Inflammatory joint pain

  • early morning stiffness (>30 min)
  • stiffness after rest
  • ease with use/ exercise
  • swelling
  • may have “flu-like” symptoms
  • anti-inflammatory drugs: NSAIDs e.g. Ibuprofen - may be helpful
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6
Q

Sjögren’s syndrome

-“sicca syndrome” or Mikulicz’s disease

A

Auto-immune inflammatory disorder of exocrine glands
-lacrimal, salivary, nasal, laryngeal, tracheal and vaginal glands.
-xerostomia + keratoconjunctivitis sicca
Marked lymphocytic infiltration destroying the gland architecture and function
Affected glands may be initially swollen, inflamed, tender and later atrophic

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7
Q

Inflammation

A

Red (rubor)
Hot (calor)
Painful (dolor)
Swollen (tumour)

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8
Q

Rheumatoid arthritis can lead to

A

Progressive joint deformity

  • Z thumb deformity
  • Swelling and subluxation of MCPJs
  • Spares DIPJs
  • Ulnar deviation of fingers (e.g. swan neck deformity)
  • “Boggy” swelling (could be warm and tender but quite firm)
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9
Q

Sjögren’s syndrome histology (biopsy)

A

Lymphotic infiltration of salivary gland showing disruption of the normal glandular architecture

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10
Q

Rheumatoid arthritis: extra-articular features

A
Lungs
-nodules (collection of inflammatory cells)
-lung fibrosis
-pleural effusions
CV
-pericardial inflammation/ effusions
-myocarditis
-valve inflammation
Kidneys
-amyloidosis
Skin
-rheumatoid nodules
-vasculitis
Secondary Sjögren's syndrome
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11
Q

Blood tests: rheumatoid arthritis

A

Anaemia (normocytic, normochromic?)
High/ low platelets
High inflammatory marker
-C reactive protein (CRP), erythrocyte sedimentation rate (ESR)
Auto-antibodies
-up to 75% positive for RF (rheumatoid factor) and/ or anti-CCP (cyclic citrullinated peptide)

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12
Q

Xrays - rheumatoid arthritis

A
Early
-osteopenia (thinning) around joints: "periarticular osteopenia"
-soft tissue swelling
Late
-erosions
-joint space narrowing
-subluxation/ dislocation
-fusion ("ankylosis")
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13
Q

Treatment for rheumatoid arthritis: immediate relief

A

NSAIDs e.g. Ibuprofen
Steroids
-injected into joint/ IM/ IV/ oral

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14
Q

Treatment for rheumatoid arthritis: control of disease (immunosuppressive)

A

DMARDs (Disease Modifying Anti-Rheumatic Drugs)
-e.g. methotrxate, sulfasalazine, leflunomide, hydroxychloroquine
Biologic drugs (all either SC or IV injections so will not appear on pt’s prescription list from GP)
-anti TNF (tumour necrosis factor) e.g. Infliximab, Adalimumab, Etanercept
-B cell depletion (anti CD20) e.g. Rituximab
-others e.g. Tocilizumab (anti IL 6), Abatacept (T cell blocker), Jak

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15
Q

Side effects of rheumatoid arthritis treatment

A
Infection
-all increase risk
-for biologic drugs: reactivation of TB
Bone Marrow Toxicity
-low white cell count/ low platelets/ pancytopenia
Hepatotoxic
-abnormal liver tests (rise in enzymes)
Gastric upset 
-nausea, diarrhoea, flatulence
Skin rashes
*advise all pts to stop dmards/ biologic drugs for duration of course of antibiotics and for up to 2 weeks afterwards*
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16
Q

Methotrexate (DMARD)

A

Prescribed as once weekly dose: 15-25 mg/wk (2.5mg tabs)
Never co-prescribe with Trimethoprim/ Septrin
-risk of severe bone marrow suppression: all anti-folate drugs
Lung complications
-pneumonia
-fibrosis?
Renally excreted
-reduce dose/ stop or contact us if pt develops new renal impairment
Contra-indicated in both men and women pre-conception
Nausea, mouth ulcers

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17
Q

Biologic drugs

A

Much greater infection risk
-stop 2 weeks prior to surgery/ significant procedure
-restart 2 weeks later or when wounds healing
-remember to ask your pt if they are on on of these
-contact us
Reactivation of TB/ Hep B & C
Relatively contra-indicated if pt develops cancer
May cause/ exacervate MS (anti-TNF)

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18
Q

“Rheumatoid neck”

A

Erosive change at C1/ C2 (and lower levels)
Leading to subluxation at atlanto-axial level or at subaxial levels or both
Important to recognise “rheumatoid neck” because instability can lead to neurological deficit from spinal cord compression
-neck slightly off to one side
May be a problem with intubation or positioning a pt in dental chair

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19
Q

Anatomy of atlanto-axial joint / subluxation

A

Dens can push back into SC and cause injury (of C2 - axis)
-usually preotected by ligament, this is disrupted by erosive change in rheumatoid arthritis
Atlas (C1)

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20
Q

Rheumatoid pts in dental chair

A

Ask about neck pain
Ask about known “rheumatoid neck”
When positioning pt, check no new neck pain develops or neurological symptoms such as pins and needles/ numbness in arms/ hands/ legs
Pre-intubation: flexion and extension xrays of cervical spine and discuss with anesthetist

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21
Q

Caries/ gingivitis in RA

A

Poor hand/ neck/ shoulder function can impair dental hygiene
Immuno-suppressive drugs may compound this
Remember many RA pts have co-existent osteoporosis, so may well be on bisphosphonates too (jaw necrosis)
> evidence that gingivitis/ caries may be trigger for RA in genetically susceptible individuals

22
Q

JIA: Juvenile idiopathic arthritis

A

Inflammatory arthritis occurring before age of 16
Up to 40% “grow out of it” by adulthood
Many different patterns of arthritis
Jaw underdevelopment
-TMJ inflammation leads to altered mandibular growth
-malocclusion, micrognathia
-pain, biomechanical problems

23
Q

Sponyloarthropathy

A
Akylosing spondilitis
Reactive arthritis
Enteropathic arthritis (Crohns/ UC)
Psoriatic arthritis
--all overlapping and all associated with genetic tissue type HLA B27)
24
Q

Akylosing spondilitis

A

Inflammatory spinal pain
-progressive new bone formation/ calcification in spine = severe limitation of movement –> bamboo spine
-sacro-ilitis
More common in men than women
Biologic drugs
Can have rigid, fused neck (risk of fracture) and/ or atlanto-axial subluxation

25
Common features of spondyloarthropathy
``` Enthesitis -inflammation of junction between tendon/ ligament and bone -e.g. achilles tendon, tennis elbow Dactylitis -"sausage finger" or "sausage toe" -combination of joint and tendon sheath inflammation Skin/ nail psoriasis Psoriatic arthritis DIPJ involvement Inflammatory eye disease -iritis (anterior uveitis) IBD -Crohns/ UC Large joint oligoarthritis ```
26
Psoriatic arthritis
Psoriasis: common skin condition that speeds up the life cycle of skin cells. It causes cells to build up rapidly on the surface of the skin Doesn't spare DIPJ Nail pitting Dactylitis
27
Osteoarthritis
Degenerative process, probably with exaggerated repair response Leads to pain, stiffness, deformity, < joint movement, joint instability > with age Occupation/ hobbies > risk E.g. footballers - knees, typists - hands and wrists
28
X-rays in OA
Los of joint space Osteophytes Sub-chondral sclerosis
29
OA treatment
``` Physiotherapy/ exercises Weight loss (lower limb joints) Paracetamol, co-codamol, NSAIDS Surgery as final resort -for uncontrolled pain -joint failure e.g. knee giving way ```
30
Gout
Hot, red, swollen, painful Type of arthritis Can be in any joint Urate crystals precipitate out from bloodstream into joints/ soft tissues Induces intense neutrophil-led inflammatory response -needle shaped urate crystals
31
Why does gout happen?
Pt has high serum urate (before attack; urate may be falsely low during attack) Causes of high urate: -genetic predisposition (enzyme defects) -renal impairment -diuretics -dehydration -inter-current illness -high alcohol/ fructose/ red meat/ shellfish diet -part of "metabolic syndrome" - central obesity, diabetes, high BP, high cholesterol
32
Treatment of gout
``` Acute -NSAIDs -Colchicine -steroids Prevention of future attacks -urate lowering drugs e.g. allopuinol and febuxostat (both xanthine oxidase inhibitors) ```
33
Severe chronic gout
Chronic polyarticular tophaceous gout
34
CT diseases
Group of rare auto-immune systemic diseases Certain common features Can be life-threatening, usually due to organ involvement -e.g. renal failure (glomerulonephritis), lung fibrosis, myocarditis, cerebral involvement (vascular occlusion or vasculitis) Associated with "auto-antibodies" - antibodies directed against "self" More common in women
35
CT diseases examples
``` SLE (lupus) Scleroderma Primary Sjogren's Polymyositis/ dermatomyositis *all associated with anti-nuclear antibody (ANA)* ```
36
Common features of CT disease
Raynauds - vasocontriction fingers and toes in response to cold -triphasic colour change Mouth ulcer Cardio respiratory disease
37
SLE
Non-erosive arthritis -no erosions Butterfly rash Photosensitivity
38
Scleroderma or "systemic sclerosis"
Progressive skin thickening and tightening -e.g. oral tethering Severe Raynaud's -often leading to digital ulcers, frank tissue necrosis (digital gangrene) Can be limited to hands, feet and face (limited systemic sclerosis LcSSc) Or widespread (Diffuse systemic sclerosis DcSSc) Telangiesctasia (including inside lips), microstomia
39
LcSSc
Also associated with pulmonary hypertension, severe acid reflux Telangiectasia, microstomia & oral tethering
40
DcSSc
Associated with pulmonary fibrosis (often life threatening) | “Scleroderma renal crisis” – hypertensive acute renal failure
41
Sjogren's syndrome
Primary -occurring on its own without an associated rheumatic illness but with its own systemic manifestations Secondary -occurring with rheumatic illness e.g. RA, SLE etc. -associated with other auto-immune disorder including interstitial lung disease, auto-immune liver disease etc.
42
Primary Sjogren's
Dry eyes and mouth Associated with Ro and La antibodies High immunoglobulins, high ESR, positive Rheumatoid Factor Fatigue, joint pain
43
Rare but serious complications of primary Sjogrens
Vasculitis (inflammation of BVs) Renal involvement (renal tubular acidosis) Neurological involvement (peripheral neuropathy) Associated with primary biliary cirrhosis (inflammation and stricture of bile ducts) 9x increase in risk of lymphoma
44
atrophy Sjogren's
Atrophic, shrunken parotid gland | Atrophic, "shiny" glossitis
45
Polymyositis and dermatomyositis
2 diseases associated with inflammation of muscles Causes weakness of arms and thighs Painless wasting of these muscles Both can be associated with lung fibrosis
46
Polymyositis
Muscle involvement only
47
Dermatomyositis
Muscles and skin Photosensitivity/ purple "heliotrope" rash around eyes Strong association with internal malignancy Swollen red face, mucosal lesions, lymphotic infiltrations of muscle fibres
48
Treatment for CT diseases
Different for each but include: -NSAIDs/ steroids DMARDS Cytotoxic drugs (for life-threatening complications) e.g. cyclophosphamide Biologic drug e.g. Rituximab (anti-TNF drugs contra-indicated in SLE)
49
Xerostomia
Due to a marked reduction in saliva production from all the salivary glands. Causes difficulty with chewing or swallowing food, articulation, food lodges in recesses, increased risk of dental caries, altered taste. Oral mucosa and tongue may be sore, reddened, “burn”, saliva is typically scanty and sticky
50
Keratoconjunctivitis sicca
Common symptom complex - dry, itchy, red, sore, photophobic eyes - < tear secretion leading to conjunctival ulcers - blinking painful and irritable - eyes commonly feel “gritty"