Rheumatology Flashcards

1
Q

What is the single most important diagnostic test in the inflamed joint?

A

arthrocentesis

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2
Q

A swollen, single joint: DDx until proven otherwise

A

septic arthritis

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3
Q

Septic arthritis: labs/Dx, DDx

A

Arthrocentesis
- Hold ABx until procedure completed
- do not perform on a prosthetic joint unless you talk to ortho first

DDx:
- trauma?
- underlying joint disease? Monoarthritis or poly arthritis?
- septic arthritis is almost always monoarticular, except if gonococcal

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4
Q

Risk factors for septic arthritis

A

Age >80
DM
prosthetic joints
skin infection overlying or close to the joint affected
known abnormal joint (e.g. rheumatoid joint)

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5
Q

septic arthritis: management

A

Blood cultures before ABx are given

ABx
- vancomycin - given empirically until culture data returns
- beta-lactam - given for gram negative (good penetrance into the synovium)

Surgery: wash out
- consult ortho surgery ASAP

Echocardiogram to assess for valvular vegetations

ABx for several weeks
- often nafcillin or oxacillin

If gonorrhea is suspected: genital NAAT
If Dx is uncertain: consult rheum to assist with management

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6
Q

gouty arthritis

A

acute monarticular inflammatory arthritis, most often the 1st MTP
Recurrence is common
Metabolic disease, where there is deposition of uric acid crystals in the tissues (synovium has a high affinity for this)
- caused by either overproduction or under excretion of uric acid

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7
Q

gouty arthritis: diagnosis

A

Joint fluid aspiration is the gold standard

identification of crystals with polarized light microscopy of the synovial fluid
- gout: monosodium urate crystals
- pseudogout: calcium pyrophosphate

Often based on clinical exam and history
Measuring the uric acid level is unreliable

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8
Q

primary gout

A

highly heritable
common in Pacific Islanders

Involves the underexcretion of uric acid

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9
Q

secondary gout: risk factors

A

Risk factors:
- hospitalized patients with high doses of diuretics
- kidney disease
- myeloma
- etoh
- consuming large amounts of purines (meats, gravies, foods with high yeast content)

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10
Q

gouty arthritis: S/Sx, imaging

A

Onset of an acute attack is typically sudden and nocturnal
Joint: hot, red, swollen, allodynia (light touch is exceedingly painful)
May have low grade fever

XR:
- joint space narrowing
- erosion
- soft tissue swelling

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11
Q

gouty arthritis: common precipitants

A

consumption of alcohol (specifically beer)
changes in medications (specifically diuretics)
fasting

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12
Q

gouty arthritis: treatment

A

NSAIDs
- if tolerated, full doses for 7-10 days

Colchicine:
- 1.2mg loading dose, followed by 0.6mg 1 hour later, then 0.6mg Q12h x14d
- often causes diarrhea
- adjust for CKD, risk for rhabdomylosis

Steroids
- for those who cannot tolerate NSAIDs
- dramatic effect (often within 1 hour)

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13
Q

gouty arthritis: management between attacks

A

Diet
- reduce purine consumption
- reduce EtOH intake

Medications
- avoid hyperuricemic medications (e.g. thiazide or loop diuretics)

Reduction of uric acid level
- allopurinol: 100mg/day, then titrated weekly until the uric acid level is <6.0; Never start during an attack, as it will cause paradoxical worsening of the attack
- febuxostat: 40mg/day, then titrated weekly until the uric acid level is <6.0; generally used in those who cannot tolerate allopurinol

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14
Q

axial spondyloarthritis

A

Formerly known as ankylosing spondylitis (ax-SpA)

Potentially disabling inflammatory arthritis of the spine, usually presenting as chronic back pain, almost always before the age of 45

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15
Q

axial spondyloarthritis: S/Sx, imaging

A

Lower back pain and stiffness that is typically worse at night and better upon rising

Xray: looks like bamboo

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16
Q

axial spondyloarthritis: treatment

A

NSAIDs
- helpful in mild cases

DMARDs
- biologics: TNF-inhibitors (etanercept), IL-17 monoclonal antibodies (drugs that end in -ab)
- small molecules (drugs that end in -ib)

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17
Q

reactive arthritis

A

A syndrome of large, weight bearing joint arthritis, and often extra-articular manifestations of conjunctivitis (or uveitis) and urethritis

“can’t see, can’t pee, can’t climb a tree”

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18
Q

reactive arthritis: presentation

A

Follows certain infections by about 1-4 weeks
- often follows GI infections (Shigella, Salmonella, Yersinia, or Campylobacter)
- some STDs (Chlamydia)
- some streptococcal infections

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19
Q

Systemic Lupus Erythematosus

A

A systemic inflammatory multi system disease, characterized by autoantibodies to nuclear antigens

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20
Q

Anti-nuclear antibodies (ANA)

A

Seen in 95% of SLE but not specific for SLE
Once this is found to be positive, no need to ever check it again

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21
Q

Anti-Smith (Anti-Sm)

A

Seen in 10-30% of SLE, but rarely seen with anything else; very highly specific for SLE

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22
Q

ANCA

A

highly specific for granulomatosis with polyangiitis

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23
Q

Systemic Lupus Erythematosus: treatment

A

Hydroxychloroquine (Plaquenil)
- essentially all cases of SLE should be on this

Corticosteroids (e.g. prednisone or methylprednisolone)
- especially helpful to manage a flare up of symptoms

Methotrexate
Azatioprine (Imuran)
Mycophenylate Mofetil (Cellcept)
Cyclophosphamide (Cytoxan)
Belimumab (Benlysta)
Voclosporine (Lupkynis)

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24
Q

CREST Syndrome

A

Calcinosis
Raynaud’s phenomenon
Esophageal dysmotility
Sclerodactyly
Telangiectasias

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25
Scleroderma renal crisis
**rheumatologic emergency** Abruptly develops severe hypertension AND one of the following: - increase in Cr by >50% over baseline or >120% of upper limit of normal - proteinuria >2+ - hematuria >2+ - thrombocytopenia (<100,000) - hemolysis - HA, SZ, LV failure, encephalopathy
26
Scleroderma renal crisis: risk factors
Rapidly progressive skin thickening within the first 2-3 years Steroid use (Prednisone >15mg/day) Anti-RNA Polymerase III Pericardial effusion
27
Scleroderma renal crisis: treatment
ACE Inhibitors
28
When a patient presents with kidney failure and hypertension, what should be included in your DDx?
scleroderma renal crisis
29
Scleroderma: treatment for Raynaud's
Avoid cold exposure, keep trunk warm Quit smoking Avoid certain medications Meds: - CCBs - ARBs - topical nitroglycerin - severe: sildenafil, IV prostacyclin
30
Scleroderma: treatment for esophageal dysmotility
PPI Refer to GI
31
Scleroderma: treatment for calcinosis
no good treatment
32
Scleroderma: treatment for telangiectasias
No good treatment Laser therapy
33
Scleroderma: treatment for pulmonary hypertension
CCBs, sildenafil, prostacyclin Lung-heart transplant Mycophenolate mofetil Azathioprine Prednisone (only if RNA Polymerase III negative) IV cyclophosphamide
34
Scleroderma: treatment if overall stable
Nothing
35
Scleroderma: treatment if overall rapidly progressing
Methotrexate Mycophenolate mofetil D-penicillamine (rarely used)
36
polymyalgia rheumatica: symptoms
Syndrome that involves multiple symptoms: - pain and stiffness in the neck, shoulders, upper arms, thighs, hips lasting weeks or months - fatigue - lack of appetite - anemia - overall feeling of illness or flu-like symptoms - low grade fever
37
polymyalgia rheumatica: treatment
prednisone (10-20mg/day) -Often patients have a response within hours. -slowly tapered off over months or years If no response, can exclude it from the DDx
38
giant cell arteritis (aka temporal arteritis): diagnosis
temporal arter biopsy
39
Many cases of acute MI in young adults have been attributed to ___ that went undiagnosed during childhood
Kawasaki disease
40
Meds that increase uric acid
hydrochlorothiazide salicylates pyrazinamide ethambutol nicotinic acid cyclosporin cytotoxic agents (e.g. chemo)
41
polymyalgia rheumatica
common chronic inflammatory disorder that is characterized by extended periods of morning stiffness in the hips, shoulders, neck, and thoracic spine
42
polymyalgia rheumatica is associated with a risk of...
giant cell arteritis
43
polymyalgia rheumatica: treatment
oral corticosteroids
44
polymyalgia rheumatica: diagnosis
Clinical Rapid response to low-dose steroids is considered diagnostic
45
giant cell arteritis (temporal arteritis)
inflammatory condition that can lead to permanent blindness Accounts for 15% of all FUO cases
46
giant cell arteritis (temporal arteritis): S/Sx
headache scalp tenderness visual complaints jaw claudication temporal artery: nodular, enlarged, or tender fever: may be as high as 40C (104F) chills, rigors
47
giant cell arteritis (temporal arteritis): labs/Dx
very high ESR (greater than assay) normal WBC temporal artery biopsy
48
normal ESR
men: 0-15 mm/hr women: 0-20 mm/hr
49
giant cell arteritis (temporal arteritis): management
prednisone referral
50
osteoarthritis
degenerative joint disease with slow destruction of the articular cartilage
51
osteoarthritis: inflammation
assymetrical
52
osteoarthritis: age
53-64 years
53
osteoarthritis: gender
men and women equally affected
54
osteoarthritis: joints
weight-bearing, fingers, hands, wrists swelling and edema no redness or "heat" Heberden's nodes (DIPs) Bouchard's nodes (PIPs)
55
osteoarthritis: stiffness/pain
better in the morning, worse throughout the day aggravated by activity, relieved by rest
56
rheumatoid arthritis
systemic autoimmune disease causing inflammation of connective tissue
57
rheumatoid arthritis: inflammation
symmetrical
58
rheumatoid arthritis: age
35-50 years
59
rheumatoid arthritis: gender
more common in women
60
rheumatoid arthritis: joints
PIPs MCPs wrists swelling and edema redness and "heat"
61
rheumatoid arthritis: stiffness/pain
worse in the morning, better throughout the day
62
rheumatoid arthritis: other s/sx
fatigue, weakness malaise anorexia weight loss
63
osteoarthritis: Dx
synovial aspirate normal, clear/yellow
64
osteoarthritis: x-ray findings
joint space narrowing osteophytes juxta-articular sclerosis subchondral bone
65
osteoarthritis: management
ASA APAP NSAIDs COX-2 inhibitors: celebrex
66
osteoarthritis: supportive care
weight loss cane on the opposite side ICE most heat physical therapy refer for joint replacement
67
rheumatoid arthritis: labs
ESR elevated ANA+
68
rheumatoid arthritis: Dx
synovial aspirate with inflammatory changes and WBCs
69
rheumatoid arthritis: x-ray finding
joint swelling progressive cortical thinning osteopenia joint space narrowing
70
rheumatoid arthritis: management
high-dose salicylates NSAIDs DMARDs -corticosteroids -methotrexate (monitor LFTs) -hydrochloroquine -gold salts injections
71
rheumatoid arthritis: supportive care
early rheumatologist referral rest PT surgery
72
axial spondyloarthritis: associated findings
aortic insufficiency IBD iritis
73
Sjögren's syndrome: Labs/Dx
+ANA ESR CBC rheumatoid factor anti-alpha-fodrin antibody Best test for diagnosis: salivary gland biopsy
74
Sjögren's syndrome: presentation
Dryness of the eyes and mouth (xerostomia) d/t immune mediated dysfunction of the lacrimal and salivary glands - Also seen with decreased mucus production involving the genitals and GI tract enlarged parotid gland
75
Sjögren's syndrome: treatment
Dry eyes: artificial tears Dry mouth: artificial saliva, gum chewing Prednisone