Rheumatology Flashcards
RA
- what is most accurate test
- what joint is spared in RA
- what do you need to check before starting mAb
- role of steroids
1. RF is nonspecific anti-CCP is >95% specific 2.SI joint 3. NSAIDS and DMARDS 1st: MTX 2nd: if MTX fails add TNF antag: infliximab, adalimumab, cetrolizumab, etanercept
- hydroxychloroquine for mid RA
- Hep B and Tb
- use acutely as bridge to DMARDs. don’t use long term
AE
- MTX
- hydroxychloroquince
- BM suppression, pneumonitits, liver dx
2. retinopathy (eye exams)
what do the following all have in common?
- Ankylosing Spondylitis
- Reactive Arthritis (aka reiters)
- Psoriatic Arthritis
- Juvenile rheumatoid Arthritis
they’re all inflammatory arthritic conditions that are RF negative, have predilection for the spine, involve SI joint and are associated with HLA-B27
- Ankylosing Spondylitis
presentation: young, male pt with spine/back stiffness. pm pain worse. relief when leaning forward. can lead to kyphosis and diminished chest expansion. rare: uveitis, aortitis, restrictive lung disease
diag: MRI spine with attn. to SI joint
treatment: NSAIDs, infliximab/adalimumab
NO STEROIDS
- Reactive Arthritis
presentation: symmetric arthritis with hx of urethritis/cervicitis or GI infection. +/- fever, fatigue, weight loss, penile head lesion, conjunctivitis, skin lesion
diag. can’t see, can’t pee, can’t climb a tree & hx of chlamydia, shigella, Yersinia, salmonells, campylobacter
treatment: NSAIDs
- Psoriatic Arthritis
presentation: joint involvement + hx of psoriasis, dactylitis, DIP involvement, nail pitting, enthesitis
no diag test
treat: NSAIDs first, if fails then anti-TNF agents - Juvenile rheumatoid Arthritis
presentation: salmon colored rash, fever, polyarteritis, myalgias, lymphadenopathy. sometimes high LFTs and hepatosplenomegaly
diag: super high ferritin, high WBC, RF (-), ANA (-)
treatment: NSAIDS, if fails then steroid bridge to MTX or anti-TNF agents
Whipple dx
presents with diarrhea, fat malabsorption, weight loss, joint pain.
bowel biopsy with PCR shows PAS+
treat with TMX-SMX
SLE
- what is best test to follow the severity of a flare up
- serology to check
- treatment
- drug induced-common drugs
- complement levels drop during flare up
anti-ds DNA rises during flare up - ANA, RF, anti-ds DNA, Anti-smith, anti-RO (fetal heart block), anti SSA, complement, ESR
anti-ds DNA and anti-SM specific for SLE. anti smith more specific.
- acute flare up: prednisone
joint pain: NSAIDs. hydroxychloroquine if NSAIDs fail
severe: belimumab, cyclophosphamide, azathioprine
nephritis: steroids and MMF
- hydralazine, INH, procainamide
will have +ANA and +anti-histone antibodies
NO RENAL or CNS involvement
normal complement and anti-ds DNA levels
Sjogrens Syndrome
- presentation
- diag
- treatment
- woman with dry mouth, dry eyes, sensation of sand under eyelids, poor sense of smell & taste
- most accurate: lip biopsy
schirmer test: decreased wetting of paper help to eye
serology: ANA, RF, anti-Ro/SSA, Anti-La/SSB - treat by keeping eyes and mouth moist
pilocarpine (everywhere) and cevimeline (salivary only) increase ACTH which increases oral and ocular secretions
Scleroderma
Systemic
Diffuse
Systemic
ususally woman; skin (tight, fibrous, sclerodactyly,
Raynauds, mild and symmetric joint pain
Diffuse
lung: fibrosis, pulmonary HTN
heart: restrictive cardiomyopathy and premature CAD
renal: malignant HTN
GI: esophageal dysmotility, wide mouth colonic diverticula
diagnosis : no single test. look for + ANA, antiScl 70 (antitopoisomerase)
treatment: none will stop dx progression
renal: ACEI
pulmonary: bosetan, prostacyclin analogs, sildafenil
GI: PPIs
lung: cyclophosphamide
Raynauds: CCBs
CREST
= limited scleroderma this form of scleroderma presents with Calcinosis of fingers Raynauds Esophageal dysmotility Scleodactyly Telangiectasia
anti-centromere antibodies more often than antiScl 70
doesn’t present with joint pain, heart/lung/kidney problems
eosinophilic Fascitis
looks like scleroderma but its not
high eosinophils
treat with steroids
Poly and Dermatomyositis
diag
significance of anti-Jo
what is most common serious complication
diag: abnormal EMG, high aldolase, high CPK
muscle biopsy is most accurate
anti-Jo-1 indicates higher risk of interstitial lung dx
malignancy is most common serious complication
treat with steroids
fibromyalgia
treatment
exercise
milnacipran, duloxetine, pregabalin
tricyclic antidepressants work but more side effects
Polymyalgia Rheumatica
presentation
women>50 lots of pain and stiffness of proximal MUSCLES! more pain than weakness! pain of muscles not joints
diag: high ESR
normal CPK, aldolase, EMG, muscle biopsy
treat with steroids
Vasculitis
treatment
steroids
if fail, then cyclophosphamide, azathioprine/6MP, MTX
Polyarteritis Nodosa
same stuff as vasculitis but following is different:
abdominal pain, pericarditis, HTN, renal involvement, testicular involvement
diag: angiography of abdominal vessels
most accurate skin/muscle/sural nerve biopsy
treatment :prednisone and cyclophosphamide
Granulomatosis with Polyangitis
vasculitis + upper & lower respiratory findings
+C-ANCA
treat with prednisone and cyclophosphamide