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Basic Concepts
inflammatory vs non-inflammatory
-autoimmune vs OA
signs of inflammation
warmth
swelling
eryhtema
AM stiffness x 30+ mins
CRP/ESR→elevated
synovial fluid/synovium+inflammation
number of joints involved
what joints involved
Rheumatoid Arthritis (RA)
PP: chronic+systemic autoimmune condition→causes joint pain
multiple smaller joints in a symmetric distribution
RF:
genetic
human leukocyte antigen (HLA) genes
female
40-50y/o
non-genetic
smoking
environmental
-silica
-dust
gut health
diet
CM: symmetric joint pain
-early→small joints
-late→large joints
AM stiffness x 30+ minutes
-reoccur after increased mobility
warmth of joint (inflamed tissue)
joint erythema
loss of range of motion (ROM)
deformities (complications→late dx)
ulnar deviation/”drift”
boutonniere
swan neck
plantar subluxation
hallux valgus
other organ involvement
DX: RF
anti-citrullinated peptide antibodies (ACPA/anti-CCP)
HLA-B27
inflammatory markers
ESR
CRP
XRay
osteopenia
-decreased bone density
erosions
soft tissue swelling
joint space narrowing
US
soft tissue changes
swelling
MRI
bone+soft tissue abnormalities
TX:
prophx
DMARDS
bDMARDS
pain relief
NSAIDS
glucocorticoids
rheumatology referral
Methotrexate+Folate
MX: DMARDS
MOA: dx-modifying anti-rheumatic drugs
I: RA
AE: GI upset
LFT→increased
DX (x3 months): CBC
CMP
CRP
ESR
-more frequent in beginning
CI: child bearing
hepatitis
alcohol
bactrim
amoxicillin
probenecid
Sulfasalazine
MX: DMARDS
MOA: disease modifying anti-rheumatic drugs
I: RA
AE: GI upset
DX (x3 months): CBC
CMP
CRP
ESR
-more frequent in beginning
CI: ASA
G6PD
Hydrochloroquinolone
MX: DMARDS
MOA: disease modifying anti-rheumatic drugs
I: RA
AE: none
chronic→retina involvement
DX (x3 months): CBC
CMP
CRP
ESR
-more frequent in beginning
CI: retina issue
Leflunomide
MX: DMARDS
MOA: disease modifying anti-rheumatic drugs
I: RA
AE: diarrhea
rash
hair loss
DX (x3 months): CBC
CMP
CRP
ESR
-more frequent in beginning
CI: child bearing
Biologic DMARDS (bDMARDs): MOA+MX
affect epcific pathway of inflammation→decrease active inflammation+prevent joint damage
block cytokine tumor necrosis factor (TNF)
etanercept
infliximab
adalimumab
golimumab
certolizumab pegol
suppress t cells
abatacept
suppress b cells
rituximab
block cytokin IL-6
tocilizumab
sarilumab
JAK inhibitors
baricitinib
upadacitinib
tofacitinib
Biologic DMARDS (bDMARDs): General
ROA: duration→indefinite
-x3-6 months to produce effect
if sick+next dose due→wait
AE: injection site rxn
increased RF of infxn
MS
leukemia
black box warning→JAK
heart-related events
cancer
blood clots
death
DX:
before tx
CBC
CMP
quantiferon TB gold
hep B/C
after tx (Q3 months)
CBC
CMP
CRP
ESR
CI: h/o cancer
MS
hepatitis B
hepatitis C
TB
TNF→HF
Rheumatoid Arthritis (RA): Dx+Tx
DX
DAS28-ESR
thorough hx+PE
good note writing
TX
NP: PT/OT
diet
deformities→surgery
MX: NSAIDS
glucocorticoids
intra-articular steroid injections
omega-3 supplements
Rheumatoid Arthrits (RA): Complications
ulnar deviation
boutonniere
swan neck
plantar subluxation of metatarsal head+hallux valgus
rheumatoid nodules
excessive amount of inflammatory exudate inside synovial cavity
formation of cysts→drain→fistula
rupture→spread of inflammation
baker cyst
rheumatoid nodules
extrasynovial→out
collection of inflammatory cells
areas of pressure/trauma→extensor surfaces
20-30%
organ involvement
-sclera
-heart
-lung
Rheumatoid Arthrits (RA): Organ System Complications
opthalmology
scleritis
episcleritis
cardiac
valvular deformities
pericardial effusion
pericarditis
aortitis
-aortic regurgitation
-rupture
pulmonary
fibrosis
ILD
pleural effusion
GI
splenomegaly
-+neutropenia→felty syndrome
hematology
lymphadenopathy
anemia
vasculitis→thrombosis/nrecrosis
-MI
-CVA
-kidney damage
-rayndaud phenomenon
MSK
deformities
atlantoaxial subluxation→myelopathy
-spares rest of spine+SI joints
muscle atrophy
septic arthritis
neurology
nerve entrapment
Rheumatoid Arthritis (RA): Prognosis
early+aggresive tx→better outcome
systemic impact→decreased
joint damage→decreased
decreased developement of deformity/disability
control HTN+DM+obesity
no smoking
Oligoarticular Juvenile Idiopathic Arthritis (JIA)
PP: chronic inflammatory dx→causes joint pain in childhood
duration→6+ weeks
RF: genetic susceptibility→HLA
E: m/c form
r/o other dxs
u16 y/o
CM:
up to 4 joints
medium-large joints
asymmetrical
uveitis
no systemic sxs
Systematic Juvenile Idiopathic Arthritis (sJIA)
PP: chronic inflammatory dx→causes joint pain in childhood
duration→6+ weeks
RF: genetic susceptibility→HLA
E: r/o other dxs
u16 y/o
CM:
1+ joints+fever+at least 1 of below
sore thrat
rash
-salmon-colored
-macular
-nonpruitic
-chest+abdomen or pressure areas
serositis
lymphadenopathy
hepatomegaly
splenomegaly
small-large joint involvement
-any #
-can be asx at onset
high fever 2x/day→returns to normal/subnormal
DX: anemia
leukocytosis
ferritin→elevated
Polyarticular Juvenile Idiopathic Arthritis (JIA)
PP: chronic inflammatory dx→causes joint pain in childhood
duration→6+ weeks
RF: genetic susceptibility→HLA
E: 2nd m/c form
r/o other dxs
u16 y/o
CM:
5+ joints
small-large joints
symmetrical
Ethesitis-Related Juvenile Idiopathic Arthritis (JIA)
PP: chronic inflammatory dx→causes joint pain in childhood
duration→6+ weeks
RF: genetic susceptibility→HLA
male
10+ y/o
E: 2nd m/c form
r/o other dxs
u16 y/o
CM:
5+ joints
large joints→lower extremities
-low back
-SI joints
enthesitis→inflammation at tendon/ligament
-tibia tubercle
-heel
Psoriatic Juvenile Idiopathic Arthritis (JIA)
PP: chronic inflammatory dx→causes joint pain in childhood
duration→6+ weeks
RF: genetic susceptibility→HLA
male
10+ y/o
E: 2nd m/c form
r/o other dxs
u16 y/o
CM:
psoriatic:
± psoriasis+2 of the following:
dactylitis→”sausage digit”
nail changes
1st degree FHx of psoriasis
Undifferentiated Juvenile Idiopathic Arthritis (JIA)
PP: chronic inflammatory dx→causes joint pain in childhood
duration→6+ weeks
RF: genetic susceptibility→HLA
male
10+ y/o
E: 2nd m/c form
r/o other dxs
u16 y/o
CM:
undifferentiated:
don’t meet criteria of other subgroups
meet criteria for 2+ subgroups
JIA Dx
labs
RF
anti-CCP
ANA
HLA-B27
CRP
ESR
CBC
CMP
synovial fluid
imaging
XRay
US
MRI
JIA NP Tx
PT/OT
shoe lift
diet
eye exam x 4 months post-arthritis onset
ANA+→slit lamp exam q3 months
ANA→slit lamp exam q6 months
primary care
NSAIDS
pediatric rheumatology referral
JIA Mx Tx
sx relief→NSAIDS
naproxen
ibuprofen
meloxicam
prophx→DMARDS
methotrexate
leflunolide
prophx→bDMARDS
block chemokine tumor necrosis factor (TNF):
-etanercept
-infliximab
-infliximab
-adalimumab
block IL-1:
-anakinra
-canakinumab
block IL-6→tocilizumab
suppress b cells→rituximab
supresss t cells→abatacept
janus kinase (JAK) inhibitors
DMARD/bDMARD DX (q3 months):
CBC
CMP
CRP
ESR
corticosteroids
IA injections
opthalmic drops
JIA Complications
blindness
ankylosing spondylitis
leg-length discrepancy
macrophage activation syndrome (MAS)
coagulopathy
pancytopenia
liver dysfxn
JIA Prognosis
varies depending on subgroup
highest rate of remission→oligoarticular JIA+seronegative
highest rate of chronic+erosive dx
RF+ dx
systemic sxs last longer than 6m
Psoriatic Arthritis (PsA)+Primary Care Tx
RF: genetics→HLA
non-genetic→environmental trigger
-trauma
-smoking
-infxn
-gut health
E: HLA-B27
CM: asymmetric
larger joint
enthesitis→inflammation at tendon/ligament/joint capsule insertion point
ocular inflammation
finger/toe dactylitis
nail changes
uveitis
IBD/IBD-like sxs
DX:
autoantibodies→absent
RF
anti-CCP
HLA-B27 testing
CRP
ESR
uric acid→elevated
XRay
osteopenia
ethesophyte
erosions
soft tissue swelling
joint space narrowing→”pencil-in-cup” deformity
US
soft tissue changes
swelling
MRI→bone+soft tissue abnormalities
TX:
primary care
NSAIDS
glucocorticoids
rheumatology referral
PsA Mx Tx
sx relief→NSAIDS
naproxen
ibuprofen
meloxicam
glucocorticoids
intra-articular steroid injections
prophx→DMARDS
methotrexate
sulfasalazine
prophx→bDMARDS
block chemokine tumor necrosis factor (TNF):
-etanercept
-infliximab
-infliximab
-adalimumab
-golimumab
-certolizumab
block IL-12+23→ustekinumab
block IL-17:
-secukinumab
-ixekizumab
-brodalumab
-bimekizumab
block IL-23:
-guselkumab
-risankizumab
phosphodiesterase 4 inhibitors→apremilast
janus kinase (JAK) inhibitors:
-tofacitinib
-upadacitinib
bDMARD DX:
pre-initiation
CBC
CMP
quantiferon TB gold
hepatitis B+C
post-initiation (q3 months)
CBC
CMP
CRP
ESR
PsA Tx: bDMARDS
ROA: duration→indefinite
timing→3-6 months for tx
AE: injection site rxn
increased infxn risk
MS
leukemia
DX:
pre-initiation
CBC
CMP
quantiferon TB gold
hepatitis B+C
post-initiation (q3 months)
CBC
CMP
CRP
ESR
CI: h/o cancer
MS
hepatitis B
hepatitis C
TB
black box warning→JAK
heart-related events
cancer
blood clots
death
Pt edu→sick+next dose due→wait
PsA NP Tx
PT/OT
diet
deformities→surgery
PsA Prognosis
earlier+aggressive tx→better outcome
systemic impact→decreased
joint damage→decreased
decreased development of deformities+disabilities
Ankylosing Spondylitis (AS)
PP: HLA-B27 gene mutation→autoimmune axial spine→stiffening→fusion
-intervertebral joints
-facet joints
-sacroiliac joints
RF: HLA-B27
men
u40-45 y/o→20-30 y/o
trauma
smoking
gut health
E: radiographic (AS)
non-radiographic
CM: sacroilitis→inflammation of sacroiliac joints
peripheral joint pain
dactylitis
syndesmophytes→enthesis formed on top of previous enthesis
low back pain+stiffness
gradual onset
AM stiffness 1+ hr
improves with exercise
enthesitis→tendon/ligament insertion point inflammation
costosternal
-chest pain
-restricted chest movement
ischial tuberosity→pain with sitting
achilles
-walking pain
-limp
plantar fasciitis→heel pain
dactylitis
uveitis
DX: HLA-B27
RF
anti-CCP
CRP
ESR
XRay
“shiny corner sign”→annulus firbosus attaches to vertebra→inflammation+sclerosis
“bamboo spine”
-later finding
MRI
erosion
sacroilitis/narrowing of joint spaces→joint fusion
AS NP Tx
NSAIDs
corticosteroid injections→not recommended
glucocorticoids
postural training
PT
diet
end-stage dx+deformities→surgery
AS Mx Tx
sx relief
NSAIDS
glucocorticoids
prophx
DMARDS
bDMARDS
primary care
NSAIDS
glucocorticoids
rheumatology referral
DMARDS
methotrexate
sulfasalazine
bDMARDS
block chemokine tumor necrosis factor (TNF):
etanercept
infliximab
adalimumab
golimumab
certolizumab pegol
IL-12+23→ustekinumab
IL-17A
secukinumab
ixekizumab
IL-23
guselkumab
risankizumab
JAK inhibitors
tofacitinib
upadacitinib
AS Complications
progressively decreasing back ROM+chest expansion
posture change→hyperkyphosis
“bamboo spine”
cardiac
aortic regurgitation
AV conduction defects
aortic root widening
pulmonary fibrosis
neurologic→cauda equina syndrome
mental health→mood disorders
AS Prognosis
early+aggressive tx→decreased development of deformities/disabilities→better outcome
systemic impact→decreased
joint damage→decreased
hips involvement→worse prognosis
Reactive Arthritis (ReA)
PP: infxn→inflammatory arthritis
RF: HLA-B27
young men
GI
shigella
salmonella
yersinia
campylobacter
GU
chlamydia
ureaplasma
CM: post-dysentery/STI
-1-4 weeks prior
beginning→systemic sxs
fever
wt loss
oligoarthritis
1+ joints
asymmetric
lower+larger+wt-bearing joints
conjunctivitis
uveitis
stomatitis
balanitis
keratoderma blennorrhagicum
enthesitis
nail changes
urethritis
cervicitis
DX: clinical
HLA-B27
RF
anti-CCP
infxn→synovial fluid→negative
CBC
CMP
CRP
ESR
ReA Tx
glucocorticoids
DMARDS
methotrexate
sulfasalazine
bDMARDS
TNF inhibitors
block IL-17s
primary care
find infxn
if STI→abx
NSAIDS
rheumatology referral
ReA Complications+Prognosis
C: uveitis
cardiac
carditis
aortic regurgitation
P: tx x days-weeks
arthritis→persists several months
sxs can reoccur
can become chronic