Rheum Flashcards

1
Q

AI disease on immunosuppression
- general issues for mgmt

A

IMMUNOSUPPRESS BALNCE (control dis/prevent organ damage v S/E)
1. Ax disease activity regularly
- SLE: ?skin, jt, cytopenias; bloods - C3/C4, dsDNA; urine (nephritis)
2. Monitor for drug toxicity
- HCQ retinopathy (baseline then @5y + annual after), OP, bloods
3. CV RF modification
- Control systemic inflammation +/- minimise steroids
- Esp in RA/SLE
4. Cancer screen
- From dis risk + drug risk
- Annual skin, age/gender, dis specific (DM, Scleroderma)
5. Infection: minimise risk
- Vax (not live MMR, VZV, BCG); all inactivated (Pneumovax 5y)
6. Family planning (even from men: Mycophenolate, MTX)
7. Drug specific S/E (IL6 inh w/ lipids + G perf in RA)

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2
Q

Rheum long diseases

A
  1. SLE (multi system) - nephritis + renal disease, skin, inflam arthritis, cytopenias, serositis (20-45y women)
  2. Scleroderma (Raynauds, ILD, pulm HTN, GI
  3. Systemic vasculitis (inflam myositis - vasculitis of muscles) - multi system (pulm/renal, skin, arthritis) - DM ?underlying malignancy
  4. APLS - anticoagulation++
    RA
    Gout
    Drug mgmt & dis F/U
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3
Q

SLE - Rx options (Drugs)

A
  • HCQ : 80% on (dis modifying & sx controlling)
  • CS : cumulative dose over duration of dis (can fluctuate)
  • MMF (if renal)
  • MTX (occasionally used, wkly, if arthritis)
  • CYC : if hx then SEVERE dis prev (ie. aggressive nephritis or CNS)
  • AZA : not commonly used (unless can’t tolerate MMF)
  • Analgesia (NSAID)
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4
Q

SLE - tests

A

Disease activity (monitor 3monthy)
1. Anti-dsDNA
2. Low C3/C4
3. FBC - cytopenias
4. URINE

Dx:
ANA
- preceedes dis + must be +ve (>1:80)
- Other dis +ve (RA, SSc, PM/DM, RA, SjS, Graves/Hashimotos, PBC, lymphoproliferative, drugs)
Anti-dsDNA
- Disease activity
- Nephritis (+ TNFinduced SLE)
- Highly specific
ENA
- Ro/La (SjS + neonatal lupus)
- Sm: highly specific (renal & CNS dis)
Anticardiolipin Ab - prognostic

+ UEC, LFT - drug toxicity; ESR/CRP etc

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5
Q

Lupus nephritis - stages

A

2 : microscopic haematuria/proteinuria
3 + 4: H+P +/- HTN, CKD (+/- nephrotic syndrome)
5: Nephrotic syndrome
6: Progressive renal dysfxn, proteinuria, bland urine

Stage 1 is normal urine (only on bx)

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6
Q

Nephrotic syndrome

A
  • > 3g/day proteinuria
  • Hypo-albuminaemia
  • Oedema
  • Hyperlipidaemia
  • Thrombotic dis
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7
Q

RA - Rx options

A
  1. conventional synthetic
    * MTX (W if eGFR<30)
    * SSZ (hypersensitivity, agranulocytosis, azoospermia)
    * AIM to spare Pred - if needed <6mo only
  2. Biologic (if >2 synthetic for >6m) - combine with conSyn (MTX)
    * TNF-inh (infliximab, etancercept, adalimumab)
    * RTX; Abatacept, Tocilizumab (IL6 - suppresses CRP)
    * Jak-inh (Tofacitinib, Baricitinib) - C/I++, HZV reactivation, cytopen
    Nb - screen Tb prior (Qferon + CXR, Hep)
    * STATINS
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8
Q

RA - imaging

A
  1. Jt space narrowing → fusion/ankylosis
    1. Juxta-articular OP
    2. Marginal erosions
  2. Deformities (symmetric - ulnar dev, sublux)
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9
Q

RA - extra articular fx

A
  • OP
    • CVS (IHD risk similar to DM, pericarditis, HF, conduction)
    • Neuro: Entrapment (CTS-Median), MNM
    • Vasculitis
    • Eye: scleritis
    • Lung: pleural effusions (Exud), nodules, ILD (NSIP), Bronchiectasis
    • GI: hepatic (including Rx-related)
    • Renal (GN) w/ proteinuria, +/- Rx -related
    • Haem: Feltys (spleen, Leukopenia, RA), lymphoma (check LN)
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10
Q

RA - hx

Specific fx & diagnostic criteria

A

Specific contributing Fx
* Smoking (dose dependent & in ongoing)
* Dentition
Dx:
* Timeframe >6wks
* Serology
* No. Joints
* Acute phase reactants

Anti-CCP (prognostic including for ILD/CVS)

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