Management of gout: American College of Rheumatology guideline

Published On 2021-02-03 15:13 GMT   |   Update On 2021-02-03 15:13 GMT

Duration of ULT

  • Continuing ULT indefinitely over stopping ULT is conditionally recommended.

Recommendations for patients receiving ULT medications

  • Testing for the HLA–B*5801 allele prior to starting allopurinol is conditionally recommended for patients of Southeast Asian descent (e.g., Han Chinese, Korean, Thai) and for African American patients, over not testing for the HLA–B*5801 allele.
  • Universal testing for the HLA–B*5801 allele prior to starting allopurinol is conditionally recomm - ended against in patients of other ethnic or racial background over testing for the HLA–B*5801 allele.
  • As noted above, starting allopurinol in daily doses of ≤100 mg (and lower doses in patients with CKD) is strongly recommended over starting at a higher dose.
  • Allopurinol desensitization is conditionally recommended for patients with a prior allergic response to allopurinol who cannot be treated with other oral ULT agents.
  • Switching to an alternative oral ULT agent, if available and consistent with other recommendations in this guideline, is conditionally recommended for patients taking febuxostat with a history of CVD or a new CVD-related event.
  • Checking urinary uric acid is conditionally recommend against for patients considered for or receiving uricosuric treatment.
  • Alkalinizing the urine is conditionally recommended against for patients receiving uricosuric treatment.

Changing ULT strategy

  • Switching to a second XOI over adding a uricosuric agent is conditionally recommended for patients taking their first XOI, who have persistently high SU concentrations (>6 mg/dl) despite maximum-tolerated or FDA-indicated XOI dose, and who have continued frequent gout flares (>2 flares/year) OR who have nonresolving subcutaneous tophi.
  • Switching to pegloticase over continuing current ULT is strongly recommended for patients with gout for whom XOI treatment, uricosurics, and other interventions have failed to achieve the SU target, and who continue to have frequent gout flares (≥2 flares/year) OR who have nonresolving subcutaneous tophi.
  • Switching to pegloticase over continuing current ULT is strongly recommended against for patients with gout for whom XOI treatment, uricosurics, and other interventions have failed to achieve the SU target, but who have infrequent gout flares (<2 flares/year) AND no tophi.

Gout flare management

  • Using colchicine, NSAIDs, or glucocorticoids (oral, intraarticular, or intramuscular) as appropriate firstline therapy for gout flares over IL-1 inhibitors or adrenocorticotropic hormone (ACTH) is strongly recommended for patients experiencing a gout flare.
  • Given similar efficacy and a lower risk of adverse effects, low-dose colchicine over high-dose colchicine is strongly recommended when colchicine is the chosen agent.
  • Using topical ice as an adjuvant treatment over no adjuvant treatment is conditionally recommended for patients experiencing a gout flare.
  • Using an IL-1 inhibitor over no therapy (beyond supportive/analgesic treatment) is conditionally recommended for patients experiencing a gout flare for whom the above antiinflammatory therapies are either ineffective, poorly tolerated, or contraindicated.
  • Treatment with glucocorticoids (intramuscular, intravenous, or intraarticular) over IL-1 inhibitors or ACTH is strongly recommended for patients who are unable to take oral medications.

Management of lifestyle factors

  • Limiting alcohol intake is conditionally recommended for patients with gout, regardless of disease activity.
  • Limiting purine intake is conditionally recommended for patients with gout, regardless of disease activity.
  • Limiting high-fructose corn syrup intake is conditionally recommended for patients with gout, regardless of disease activity.
  • Using a weight loss program (no specific program endorsed) is conditionally recommended for those patients with gout who are overweight/ obese, regardless of disease activity.
  • Adding vitamin C supplementation is conditionally recommended against for patients with gout, regardless of disease activity.

Management of concurrent medications

  • Switching hydrochlorothiazide to an alternate antihypertensive when feasible is conditionally recommended for patients with gout, regardless of disease activity.
  • Choosing losartan preferentially as an antihypertensive agent when feasible is conditionally recommended for patients with gout, regardless of disease activity.
  • Stopping low-dose aspirin (for patients taking this medication for appropriate indications) is conditionally recommended against for patients with gout, regardless of disease activity
  • Adding or switching cholesterol-lowering agents to fenofibrate is conditionally recommended against for patients with gout, regardless of disease activity.

"Using GRADE methodology and informed by a consensus process based on evidence from the current literature and patient preferences, this guideline provides direction for clinicians and patients making decisions on the management of gout," concluded the authors.

"2020 American College of Rheumatology Guideline for the Management of Gout," is published in the journal Arthritis & Rheumatology.

DOI: https://onlinelibrary.wiley.com/doi/abs/10.1002/art.41247

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USA: The American College of Rheumatology has released 2020 guideline for the management of gout. 

The guideline, published in the journal Arthritis & Rheumatology, is intended provide guidance for the management of gout, including indications for and optimal use of urate lowering therapy (ULT), treatment of gout flares, and lifestyle and other medication recommendations. 

Recommendations

Indications for pharmacologic ULT

  • Initiating ULT is strongly recommended for gout patients with any of the following: ≥1 subcutaneous tophi; evidence of radiographic damage (any modality) attributable to gout; OR frequent gout flares, with frequent being defined as ≥2 annually.
  • Initiating ULT is conditionally recommended for patients who have previously experienced >1 flare but have infrequent flares.
  • Initiating ULT is conditionally recommended against in patients with gout experiencing their first gout flare.
  • Initiating ULT is conditionally recommended for patients with comorbid moderateto-severe CKD (stage ≥3), SU concentration >9 mg/ dl, or urolithiasis.
  • Initiating ULT is conditionally recommended against in patients with asymptomatic hyperuricemia.

Recommendations for choice of initial ULT for patients with gout

  • Treatment with allopurinol as the preferred first-line agent, over all other ULTs, is strongly recommended for all patients, including those with moderate-to-severe CKD (stage ≥3).
  • The choice of either allopurinol or febuxostat over probenecid is strongly recommended for patients with moderate-to-severe CKD (stage ≥3).
  • The choice of pegloticase as a first-line therapy is strongly recommended against.
  • Starting treatment with low-dose allopurinol (≤100 mg/day and lower in patients with CKD [stage ≥3]) and febuxostat (≤40 mg/day) with subsequent dose titration over starting at a higher dose is strongly recommended.
  • Starting treatment with low-dose probenecid (500 mg once to twice daily) with subsequent dose titration over starting at a higher dose is conditionally recommended.
  • Administering concomitant antiinflammatory prophylaxis therapy (e.g., colchicine, nonsteroidal antiinflammatory drugs [NSAIDs], prednisone/ prednisolone) over no antiinflammatory prophylaxis therapy is strongly recommended.
  • Continuing concomitant antiinflammatory prophylaxis therapy for 3–6 months is strongly recommended.

Timing of ULT initiation

  • When the decision is made that ULT is indicated while the patient is experiencing a gout flare, starting ULT during the gout flare over starting ULT after the gout flare has resolved is conditionally recommended.
  • A treat-to-target management strategy that includes ULT dose titration and subsequent dosing guided by serial SU measurements to achieve a target SU, over a fixed-dose ULT strategy, is strongly recommended for all patients receiving ULT.
  • Achieving and maintaining an SU target of < 6mg/dl over the use of no target is strongly recommended for all patients receiving ULT.
  • Delivery of an augmented protocol of ULT dose management by nonphysician providers to optimize the treat-to-target strategy that includes patient education, shared decision-making, and treat-to-target protocol is conditionally recommended for all patients receiving ULT.
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Article Source : Arthritis & Rheumatology

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