Rheumatology: Arthritic Disorders

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36 Terms

1
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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

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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

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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

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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

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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

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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

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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


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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

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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

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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


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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


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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

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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


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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

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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


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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


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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


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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


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JIA Dx

labs

  • RF

  • anti-CCP

  • ANA

  • HLA-B27

  • CRP

  • ESR

  • CBC

  • CMP

synovial fluid

imaging

  • XRay

  • US

  • MRI


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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


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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


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JIA Complications

blindness

ankylosing spondylitis

leg-length discrepancy

macrophage activation syndrome (MAS)

  • coagulopathy

  • pancytopenia

  • liver dysfxn


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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


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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


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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


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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

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PsA NP Tx

PT/OT

diet

deformities→surgery

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PsA Prognosis

earlier+aggressive tx→better outcome

  • systemic impact→decreased

  • joint damage→decreased

  • decreased development of deformities+disabilities


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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


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AS NP Tx

NSAIDs

corticosteroid injections→not recommended

glucocorticoids

postural training

PT

diet

end-stage dx+deformities→surgery

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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


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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

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AS Prognosis

early+aggressive tx→decreased development of deformities/disabilities→better outcome

  • systemic impact→decreased

  • joint damage→decreased

  • hips involvement→worse prognosis


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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

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ReA Tx

glucocorticoids

DMARDS

  • methotrexate

  • sulfasalazine

bDMARDS

  • TNF inhibitors

  • block IL-17s

primary care

  • find infxn

  • if STI→abx

  • NSAIDS

  • rheumatology referral


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ReA Complications+Prognosis

C: uveitis

cardiac

  • carditis

  • aortic regurgitation

P: tx x days-weeks
arthritis→persists several months
sxs can reoccur
can become chronic