Rheumatoid arthritis Flashcards

1
Q

epidemiology

A

prevalence RA: 0,5-1%

two-egg sibling: 5%

one-egg sibling: 15-20%

compromised class II HLA molecule - human leukocyte antibody especially HLA-DR 4 develop more RA than normal population

developement is a summation of genetic dispostion, risks and triggers

risks:

  • fammilary disorder - strong for ACPA positive patients
  • obesity
  • age (40-60)
  • females
  • smokers
  • coffeine

most common: antigens from an infection (bacteria and virus) intiate the disease

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2
Q

articular manifestiations

A
  • morning stiffness
  • symmetrical polyarthritis (PIP and MCP)
  • also wrist, shoulder, hip, knee
  • hand and wrist > 90%
  • at the beginning without radiographs changing - morning stiffness and swelling
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3
Q

extra articular manifestions

A
  • skin nodulars (especially RF positive - extensor surface of hand and food)
  • heart

pericarditis, conduction disorders

  • lung

nonspecific interstitial pneumonia (NSIP)

usual interstitial pneumonia (UIP)

cryptogenic organising pneumonia

follicular bronchiolitis

  • eyes
  • haematologic effects

anemia, thrombocytosis, elevated CRP and ESR

  • blood vessels

small and medium vessels, rheumatoid vasculitis

  • felty syndrome

splenomegalie, leukopenie, absolute granulocytopenie - seropositive RA

  • chauffard syndrome

great lymphomes

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4
Q

EULAR classification

A

EULAR - European alliance of associations for rheumatology classification

A - joint involvement

1 large joint - 0

2-10 large joints 1

1-3 small joints 2

4-10 small joints 3

>10 joints 5

B- Serology

neg RF and neg ACPA 0

low pos RF and low pos ACPA 2

high pos RF and high pos ACPA 3

C - acute phase reactants (erythrocytes sedimentation rate)

no CRP and no ESR 0

high CRP and high ESR 1

D - duration of disease

< 6 weeks 0

> 6 weeks 1

more than 6 points is a manifested RA

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5
Q

laboratory

A
  • RF and ACPA typical
  • ANA maybe
  • anemia
  • thrombocytosis
  • elevated ESR and CRP

pathophysiology with ACPA pos. or ACPA neg.

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6
Q

management

medicals

A
    1. step corticosteoids + conventional synthetic disease modyfiying antirheumatic drugs (csDMARD)
  • MTX first step for active RA
  • Hydroxychloroquine (HCQ - low disease activity - absence of poor prognosis)
  • TNF inhibitors (csDMARD with negative response)
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7
Q

histology

A

3 zones

a - central: necrotic area, composed of fibrin

b - surrounding: histocytes and fibroblasts (palisades with radiating columns)

c - outer layer: chronic inflammatory infiltration

rheumatoid vasculitis:

extra-articular manifestation involves small and medium sized vessels (positive ANA are common)

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8
Q

x-rays

A

periarticular osteopenia:

  • marginal erosions
  • subchondral cyst formation (maybe large cysts)
  • juxta-articular osteopenia
  • subluxation
  • dislocation
  • deviation
  • ankylosis
  • DRUJ are involved in 30% in early stage RA and 75% in late stage RA
  • look at the age: maybe juvenile idiopathic arthritis
  • Geode cysts: subchondral cysts maybe open the joint (not typical in RA: DD calciumpyrophosphate dihydrate disease (CPPD), avascular necrosis)

x-ray changes in time:

  1. waist of the scaphoid - very early
  2. ulnar styloid - early
  3. DRUJ - early
  4. radiocarpal
  5. midcarpal (palmar than dorsal)
  6. radial angulation (carpal ulnar shift - radioscaphocapitate and radio lunate ligament damage)
  7. MCP
  8. Thumb

common:

radiocarpal > midcarpal

palmar > dorsal

RSL-Fusion common possible

instable DRUJ - ulnar dorsal luxation

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9
Q

diagnostic criteria

A
  1. morning stiffness - 1 hour
  2. soft tissue swelling - 3 or more joints
  3. soft tissue swelling - symmetric
  4. soft tissue swelling hand - MCP, PIP, wrist joint
  5. subcutaneous nodules - rheumatoid nodules
  6. seropositive - RF positive
  7. typical radiographics findings - periarticular erosions

4 of 7 must present to the diagnosis for a RA

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10
Q

DMARD

disease modyfying antirheumatic drugs

A

conventional:

MTX, Azathioprine, Leflunomide, Plaquenil, Sulfasalazide, Gold

biologic:

TNF-alpha (Enbrel, Remicade, Lumira)

IL-1-inhibitors

monoclonal antibodies

perioperative management:

Corticosteroids: continue

MTX: continue

conventionals DMARD - normally continue

biologic DMARD - hold for 2-4 weeks before and after surgery

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11
Q

soft tissue manifestion

A

CTS:

rice bodies through chronic tenosynovitis - not minimal

total synovektomie (DD: mycobacteria infections)

caused by microinfarcts in the synovial - rice bodies are fibrin blocks with palisate surrounding histiocytes

trigger finger:

normally the A1-pulley - tenosynovitis!!!

other impressions of infectious tissues

rheumatic nodules in pulleys

if possible no operation (release of the pulley leads to increase of ulnar deviation with a little bow stringing)

extensor ruptures - common!!!

MCP-movement:

phalanx dislocation (tightness with the intrinsic mechanism)

extensor tendon rupture (bony disorder dorsal at the wrist and DRUJ)

sagittal band rupture with tendon luxation

PIN palsy at the elbow through periarticular rheumatoid infections

tendon transfer:

always FDS over RADIAL site (ulnar deviation of the rheumatoid hand)

FCU and FCR not long enough

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12
Q

surgery treatment

A

fusion and arthroplasty lead to pain relief

more complications with arthroplasty especially with wrist athroplasty

normally:

  • wrist fusion
  • MCP arthroplasty - silicone
  • PIP fusion
  • DIP (rare) fusion

DRUJ:

  • Darrach-OP: long ulnar with dorsal luxation - leads to tendon ruptur on the dorsum of the hand
  • osteotomy proximal to the simoid notch and remove the ulnar head
  • maybe fixation with a tendon slip from the ECU through the ulna stump
  • stump instability is common with radial-ulnar-impingement
  • no support of the carpus of the ulnar side
  • ggf. sauve-kapandji op with ulnar support
  • ulnar prothesis not for RA, instable DRUJ
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13
Q

surgery treatment II

A

hand involvement

  • 70% hand involvement in the first 2y, 90 in 10y
  • DIP joint is normally spared

typical:

  • periarticular erosions and osteopenia
  • joint space narrowing
  • blood:
  • ACPA pos., ESR elvated, CRP elevated, positive RF (IgM targets FC portion of normal IgG - elevated in 75-80% of RA patients)
  • joint fluid: complement decreased, RF elevates
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14
Q

surgery treatment III

A

PIP-joint:

collateral ligament involvement - synovitis and disruption of extensor mechanism

boutonniere deformity:

central slip and triangular ligament is involved - lateral band subluxation to volar - boutonniere

swan neck:

volar plate and palmar plate failure - central slip overwhelms palmar failure - swan neck deformity

early repair of boutonniere:

only repair, when passive motion is complete and no arthritis changes in the joint

if not: fusion or arthroplasty (silicone is better than pyrocarbon prosthesis - only 11-13% revisons, good pain relief, minimal improvement in motion)

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15
Q

reasons of ulnar deviation of the fingers

A
  • joint synovitis - radial band and volar plate strechting
  • ulnar intrinsics contracts
  • lax collateral ligaments also allow ulnar drift
  • wrist radial deviation worsens vectors
  • flexor tendon eventually drift ulnary
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16
Q

reasons for MCP extension lag

A
  • extendor tendon rupture
  • volar dislocation of the proximal phalanx
  • radial sagittal band rutpure with ulnar subluxation of extensors
  • PIN palsy
  • locked MCP joint due osteophyte, bony prominence

repair:

synovectomy

extensor centralization

intrinsic release

MCP-arthroplasty

repair of radial collateral ligament of index finger complicated reha protocols probably over-rated, better extension, most patiens satisfied, most implants fractures over the time, recurrence of the deformity over the time

17
Q

thumb

A

Type I - boutonniere (starts at MCP - most common)

MCP and IP fusion

Type II - boutonniere and CMC luxation

MCP and IP fusion - synovectomy

Type III - swan neck (starts in the CMC joint - 2. most common)

CMC arthroplasty with MCP fusion

Type IV - game keepers thumb - ulnar instability

synovectomy, UCL reconstruction or prodeed to fusion

Tpye V - swan neck deformity with MCP disease

stabilize MCP in flexion (capsulodesis in flexion or fusion)

Type VI - arthritis mutilans

fusion of all joints

18
Q

Caput ulnae syndrome

A

synovitis DRUJ

ECU subluxation

supination of carpal bones from ulna

volar subluxation of carpus, ulna stays dorsally prominent

extensor tendon rupture

treatment:

Darrach or Bower OP

relocate ECU with a flap from the retinaculum extensorum

Sauve-Kapandji preserves TFCC - good option for younger patients

19
Q

wrist

A

ECRL to ECU - stabilize the force vector on the ulnar side (Clayton OP)

radiolunate fusion (Channay OP)

wrist fusion and darrach OP (execellent outcomes)

arthroplasty (if there is reasonable pre-op motion of the wrist)

20
Q

juvenile rheumatoid arthritis (JRA)

A

age < 16

  • polyarticular: 5 or more joints (35-40%)
  • pauciarticular: 4 joints or less (40-50%)

(need to check for uveitis to safe vision - especially common in grils ANA positive)

  • systemic: Still’s disease (20%)

fever, anemia, heptosplenomegaly - usually RF negative

common clinical features:

  • wrist arthritis produces flexion contracture
  • wrist deviates ULNARY instead of radially
  • MCP joints go RADIAL and get stuck in EXTENSION (opposite to adult’s disease)