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going beyond STATE OF THE ARThritis
Gout, OA, RA, PsA, AS
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Gout
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2015 ACR-EULAR Gout Classification Criteria
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How I do it Hydrate aggressively: till urine is voluminous and clear
No medieval ages Colchicine regimens High/full dose NSAIDs/coxibs Steroids if swollen++ Intra-articular or tendon sheath; ultrasound-guided ideally; do NOT barbotage tophi Oral mg/kg BW/day Prednisolone x5 days RICE treatment Do not stop ULT OK to starting ULT Refer/admit: Comorbid: frail, elderly, dehydrated, renal-impaired/oliguric, congestive heart failure Complicated: febrile, septic arthritis/tenosynovitis suspected, tophaceous, neurological deficit
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How I do it Educate: Fear Factor (joint damage & disability, kidney failure, heart attack & stroke) Hydrate: till urine is clear Diet & Beverages: Karma Balancing; avoid fructose Metabolic screening: smoking, DM, hypertension, dyslipidaemia, obesity, psoriasis, OSA Uricosuric (Probenecid, Benzbromarone, Lesinurad, …Losartan, Atorvastatin, Gliflozins) as firstline: >80% under-excretors Contraindications: renal impairment, nephrolithiasis, fluid restriction, [hepatic dysfunction], [tophaceous] XOI (Allopurinol, Febuxostat) if uricosuric contraindicated or failed to achieve target: Warn about Allopurinol hypersensitivity reactions; HLA-B5801 assay start low, go slow, especially in renal impairment; go up to 800mg if necessary Combination Uricosuric + XOI to achieve target: <6 mg%, or <5 mg% if still flare Colchicine prophylaxis (with education) till 6 months flare-free and on-target Monitor LFT, UFEME, FBC, Cr, SUA
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Going beyond Consider atypical presentations:
Subacute Gout without visible tophi Chronic mechanical pain of tendons and entheses Advanced imaging evaluation: Ultrasound Double contour sign Juxta-articular erosion Hyperaemic rim around tophus Echogenic specks in effusion Dual-energy CT (DECT)
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osteoarthritis
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OA Management Guidelines
American College of Rheumatology 2012 recommendations for the use of nonpharmacologic and pharmacologic therapies in osteoarthritis of the hand, hip, and knee OARSI guidelines for the non-surgical management of knee osteoarthritis (2014) 2016 Patellofemoral pain consensus statement from the 4th International Patellofemoral Pain Research Retreat, Manchester. Part 1: Terminology, definitions, clinical examination, natural history, patellofemoral osteoarthritis and patient-reported outcome measures 2016 Patellofemoral pain consensus statement from the 4th International Patellofemoral Pain Research Retreat, Manchester. Part 2: recommended physical interventions (exercise, taping, bracing, foot orthoses and combined interventions) Osteoarthritis Treatment & Management (Medscape 2016)
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How I do it Identify source(s) of pain: history, examination, imaging
Identify precipitating/aggravating factor(s) Refer for biomechanical assessment and therapy SYSADOA/DMOAD 3-months’ trial: Glucosamine/Chondroitin Sulphate Avocado Soybean Unsaponifiables Strontium Ranelate Viscosupplementation Recurrent effusions: Exclude chronic infection (TB), tumour (PVNS), crystal deposition (MSU, CPPD) Consider colchicine, spironolactone, Methotrexate, IA steroid, lavage, synovectomy Going beyond the standard mile for the younger, active set
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Going beyond: T2T for OA Imaging to confirm diagnosis and quantify cartilage damage Imaging to pinpoint pain generator: MSUS for soft tissue pathologies (bursitis, tendinosis, enthesopathy, synovitis, crystal deposition) MRI for bone marrow oedema (BME) DECT for subclinical gouty deposits Targeted treatment of pathologies: BME: anti-resorptives Synovitis: IA steroid, viscosupplement, PRP/ACP Biomechanic assessment: strength training, taping, podiatry Full-thickness chondral defect: ACI/MSC repair/regeneration
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Rheumatoid arthritis
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2010 ACR/EULAR “Diagnostic Criteria” for RA
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2010 EULAR Recommendations for the Targeted Treatment of RA: A 3-Phase Approach
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2014 EULAR Recommendations for Treating RA to Target
Algorithm of treating rheumatoid arthritis (RA) to target based on the updated recommendations provided in the table 1 and discussed in detail in the 'Results' section. Indicated as separate threads are the main target (remission and sustained remission) and the alternative target (low-disease activity in patients with long-term disease and sustained low-disease activity), but the approaches to attain the targets and sustain them are essentially identical. Adaptation of therapy should be usually done by performing control examinations with appropriate frequency and using composite disease activity measures that comprise joint counts, but should take comorbidities and other patient factors into account. Setting the target as well start and adaptation of therapy should be done as a shared decision with the patient.
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2015 ACR Guideline for the Treatment of Early RA
2015 American College of Rheumatology recommendations for the treatment of Early rheumatoid arthritis (RA), defined as disease duration <6 months. ∗ = consider adding low‐dose glucocorticoids (≤10 mg/day of prednisone or equivalent) in patients with moderate or high RA disease activity when starting disease‐modifying antirheumatic drugs (DMARDs) and in patients with DMARD failure or biologic failure. † = also consider using short‐term glucocorticoids (defined as <3 months treatment) for RA disease flares. Glucocorticoids should be used at the lowest possible dose and for the shortest possible duration to provide the best benefit‐risk ratio for the patient. # = treatment target should ideally be low disease activity or remission. For the level of evidence supporting each recommendation, see the related section in the Results. This figure is derived from recommendations based on PICO (population, intervention, comparator, and outcomes) questions A.1 to A.12. For definitions of disease activity (categorized as low, moderate, or high) and descriptions, see Tables and . MTX = methotrexate. IF THIS IMAGE HAS BEEN PROVIDED BY OR IS OWNED BY A THIRD PARTY, AS INDICATED IN THE CAPTION LINE, THEN FURTHER PERMISSION MAY BE NEEDED BEFORE ANY FURTHER USE. PLEASE CONTACT WILEY'S PERMISSIONS DEPARTMENT ON OR USE THE RIGHTSLINK SERVICE BY CLICKING ON THE 'REQUEST PERMISSIONS' LINK ACCOMPANYING THIS ARTICLE. WILEY OR AUTHOR OWNED IMAGES MAY BE USED FOR NON-COMMERCIAL PURPOSES, SUBJECT TO PROPER CITATION OF THE ARTICLE, AUTHOR, AND PUBLISHER.
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2015 ACR Guideline for the Treatment of Established RA
2015 American College of Rheumatology (ACR) recommendations for the treatment of Established rheumatoid arthritis (RA), defined as disease duration ≥6 months, or meeting the 1987 ACR classification criteria . Due to complexity of management of established RA, not all clinical situations and choices could be depicted in this flow chart, and therefore we show the key recommendations. For a complete list of recommendations, please refer to the Results. ∗ = consider adding low‐dose glucocorticoids (≤10 mg/day of prednisone or equivalent) in patients with moderate or high RA disease activity when starting traditional disease‐modifying antirheumatic drugs (DMARDs) and in patients with DMARD failure or biologic failure. † = also consider using short‐term glucocorticoids (defined as <3 months treatment) for RA disease flares. Glucocorticoids should be used at the lowest possible dose and for the shortest possible duration to provide the best benefit‐risk ratio for the patient. # = treatment target should ideally be low disease activity or remission. ∗∗ = tapering denotes scaling back therapy (reducing dose or dosing frequency), not discontinuing it and if done, must be conducted slowly and carefully. For the level of evidence supporting each recommendation, see the related section in the Results. This figure is derived from recommendations based on PICO (population, intervention, comparator, and outcomes) questions B.1 to B.38. For definitions of disease activity (categorized as low, moderate, or high) and descriptions, see Tables and . MTX = methotrexate; TNFi = tumor‐necrosis factor inhibitor. IF THIS IMAGE HAS BEEN PROVIDED BY OR IS OWNED BY A THIRD PARTY, AS INDICATED IN THE CAPTION LINE, THEN FURTHER PERMISSION MAY BE NEEDED BEFORE ANY FURTHER USE. PLEASE CONTACT WILEY'S PERMISSIONS DEPARTMENT ON OR USE THE RIGHTSLINK SERVICE BY CLICKING ON THE 'REQUEST PERMISSIONS' LINK ACCOMPANYING THIS ARTICLE. WILEY OR AUTHOR OWNED IMAGES MAY BE USED FOR NON-COMMERCIAL PURPOSES, SUBJECT TO PROPER CITATION OF THE ARTICLE, AUTHOR, AND PUBLISHER.
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ACR-EULAR 2011 Definition of Remission
For clinical practice Boolean – SJC, TJC, PtGA all ≤1 Index-based – CDAI ≤2.8 CDAI=SJC+TJC+PhGA+PtGA For clinical trials Boolean – SJC, TJC, PtGA, CRP all ≤1 Index-based – SDAI ≤3.3 SDAI=SJC+TJC+PhGA+PtGA+ CRP (mg/dl)
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Going beyond… that’s how I’ve been doing it
Predicting who will develop RA: Ultrasound for early diagnosis of synovitis and tenosynovitis Trial of steroid Predicting who will do badly: Combine Fast-acting DMARD (steroid, targeted agents) for 3-6 months to induce remission Slow-acting DMARD (MTX, Leflunomide, Rituximab) for at least 1 year to maintain remission Intra-articular steroid Subcutaneous MTX 25-30mg/wk before combination csDMARDs Predicting who will respond to which targeted therapy: First Biologic: anti-TNF Anti-TNF failure: Switch class especially in primary failure Pan-JAK inhibitor as first choice Tapering: biologic-free before drug-free Flares: Search for triggers (eg infections, dysbiosis) Abridged re-induction Protracted maintenance for longer sustained remission
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Psoriatic arthritis
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2015 EULAR Recommendations for the Treatment of Psoriatic Arthritis
* anti-TNF or anti-IL12/23 or anti-IL17 or tsDMARD (+/- csDMARD) * *
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How I do it: going beyond a la RA
Screen for concomitant Gout/hyperuricaemia Screen for Metabolic Syndrome csDMARD (MTX, Leflunomide, Cyclosporin) as monotherapy or in combination with targeted therapy Steroids, if needed, preferably intra-articular Biologics: anti-TNF for joint-predominant, anti-IL17 or anti-12/23 for skin-predominant Severe disease: s/c MTX Loading dose monoclonal anti-TNF Refractory disease: Combination anti-TNF with anti-IL17 Evaluate for dysbiosis, weight gain, DM, HIV, malignancy New agents: Tofacitinib, Guselkumab Tapering and spontaneous remission
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Ankylosing spondylitis
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2012 ASAS Classification Criteria for Axial & Peripheral Spondyloarthritis (SpA)
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2010 ASAS/EULAR Recommendations for the Management of Spondyloarthritis
*anti-IL17A
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How I do it: going beyond a la PsA
Non-radiographic SpA treated like established AS, perhaps more urgently and aggressively Full dose NSAID/coxib is first-line for pure axial disease Sulfasalazine is preferred csDMARD in peripheral and extra-articular involvement Steroids, if needed, preferably intra-articular Biologics: monoclonal anti-TNF as first-line, anti-IL17 upon anti-TNF inadequate response Debatable whether continuing NSAID upon starting biologic confers benefit against ankylosis Secondary anti-TNF failure: Anti-biologic antibodies Dysbiosis: silent ileitis in 50%; check stool calprotectin, ASCA, KIV scopes Tapering to longterm maintenance vs on-demand treatment 70% flare within 6 months off biologic Flare triggers: infection, trauma, entheseal strain
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Fast & Furious Treat To Target Whatever It Takes
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The Rheuma Muse
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