Gout Pharmacotherapy Ryan L Crass Pharm D PGY

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Gout Pharmacotherapy Ryan L. Crass, Pharm. D PGY 1 Pharmacy Resident UK Health. Care

Gout Pharmacotherapy Ryan L. Crass, Pharm. D PGY 1 Pharmacy Resident UK Health. Care ryan. crass@uky. edu

Learning Objectives 1. Understand the pathophysiology of and risk factors for the development of

Learning Objectives 1. Understand the pathophysiology of and risk factors for the development of gouty arthritis 2. Recognize clinical and laboratory findings consistent with the diagnosis of gout and how they are modified by treatment 3. Explain the different treatment modalities for acute gout attacks and long-term prophylaxis 4. Discuss the mechanisms, major adverse effects, and key drug-drug interactions for the primary medications used in the treatment and prevention of gout

“The Disease of Kings”

“The Disease of Kings”

Characterizing the Disease PATHOPHYSIOLOGY, MANIFESTATIONS, AND DIAGNOSIS

Characterizing the Disease PATHOPHYSIOLOGY, MANIFESTATIONS, AND DIAGNOSIS

Characterizing Gout • Gout is a spectrum of clinical features related to an excess

Characterizing Gout • Gout is a spectrum of clinical features related to an excess total body burden of uric acid • One of the most common adulthood rheumatic diseases – about 4% of U. S. adults (~ 8. 3 million people) Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1431 -1446.

Pathophysiology Hyperuricemia • Uric acid is byproduct of purine metabolism • Hyperuricemia occurs when

Pathophysiology Hyperuricemia • Uric acid is byproduct of purine metabolism • Hyperuricemia occurs when there is an imbalance in uric acid production and excretion – Defined as serum uric acid > 7 mg/d. L Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563.

Pathophysiology Hyperuricemia Overproduction Xanthine Oxidase Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563.

Pathophysiology Hyperuricemia Overproduction Xanthine Oxidase Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563. Underexcretion

Pathophysiology Gouty Arthritis • Precipitation of monosodium urate (MSU) crystals and activation of inflammation

Pathophysiology Gouty Arthritis • Precipitation of monosodium urate (MSU) crystals and activation of inflammation Hyperuricemia (> 7 mg/d. L) • Overproduction • Underexcretion Precipitation of MSU crystals • Temperature • p. H • Concentration Neutrophil infiltration and inflammation Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563. • Redness • Swelling • Pain • Warmth

Risk Factors • • Hyperuricemia* Male sex High purine diet (red meats, shellfish) Beer

Risk Factors • • Hyperuricemia* Male sex High purine diet (red meats, shellfish) Beer and alcohol Obesity and the metabolic syndrome CKD Solid organ transplantation *Hyperuricemia ≠ gout Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563. Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1431 -1446.

Risk Factors • Medications – Diuretics (thiazides, loops) – Calcineurin inhibitors – Low-dose salicylates

Risk Factors • Medications – Diuretics (thiazides, loops) – Calcineurin inhibitors – Low-dose salicylates – Niacin Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563. Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1431 -1446.

Clinical Manifestations Acute Gouty Arthritis (“Flare”) • Symptoms – Warmth/swelling – Severe Pain –

Clinical Manifestations Acute Gouty Arthritis (“Flare”) • Symptoms – Warmth/swelling – Severe Pain – Fever, leukocytosis • Location: – Usually monoarticular • Time course – Onset: Rapid – Peak: 8 -12 hours – Duration: 3 -10 days Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563. Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1431 -1446. Chronic Gouty Arhritis • Chronic Gout – Polyarticular involvement – Tophi = urate crystal aggregates – Nephropathy

Summary Disease Characteristics • The pathophysiology of gout is a dysregulation of the production

Summary Disease Characteristics • The pathophysiology of gout is a dysregulation of the production and/or excretion of uric acid • Gout commonly manifests as an acutely painful monoarticular arthritis with or without tophi formation • Modifiable risk factors include diet, lifestyle, medications, and hyperuricemia

Treatment ACUTE GOUTY ARTHRITIS

Treatment ACUTE GOUTY ARTHRITIS

General Principles • Maintenance ULT should be continued during attacks • Timing – Therapy

General Principles • Maintenance ULT should be continued during attacks • Timing – Therapy should be initiated within 24 hours AND – Continued until resolution of symptoms *ULT = Urate lowering therapy Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1447 -1461.

Pharmacotherapy Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1447 -1461.

Pharmacotherapy Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1447 -1461.

NSAIDs (naproxen, indomethacin, sulindac) Mechanism Inhibition of cyclooxygenase (COX) enzymes reducing prostaglandin synthesis Dose

NSAIDs (naproxen, indomethacin, sulindac) Mechanism Inhibition of cyclooxygenase (COX) enzymes reducing prostaglandin synthesis Dose Full antiinflammatory doses - Naproxen: 750 mg x 1, then 250 mg TID - Indomethacin: 50 mg TID - Sulindac: 200 mg BID Administration Take with food or dairy Adverse Events Common: dysepsia, hypetension, fluid retention Rare/Serious: GI bleeding, acute kidney injury Drug Interactions Antiplatelets/anticoagulants, antihypertensives, corticosteroids Pearls - Generally not used in combination with systemic steroids - Do not use salicylates as can disrupt uric acid levels - Antiinflammatory doses of other NSAIDs may be effective Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1447 -1461. Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563.

Systemic Corticosteroids (prednisone, prednisolone, methylprednisolone) Mechanism Broad range of effects leading to reduced neutrophil

Systemic Corticosteroids (prednisone, prednisolone, methylprednisolone) Mechanism Broad range of effects leading to reduced neutrophil infiltration and cytokine release Dose 1. Pulse: 0. 5 mg/kg/day x 5 -10 days 2. Taper: 0. 5 mg/kg/day x 2 -5 days, then taper over 7 -10 days 3. Methyprednisolone dose pack Administration Take with food and early in the day Adverse Events Common: hyperglycemia, hypertension, edema, insomnia Rare/Serious: delayed wound healing, osteoporosis Drug Interactions NSAIDS*, fluoroquinolones Pearls - Generally not used in combination with NSAIDs - May exacerbate underlying hypertension or diabetes - Consider adding intraarticular steroids to any modality if 1 -2 large joints affected Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1447 -1461. Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563.

Colchicine (Colcrys®) Mechanism Inhibits beta-tubulin polymyerization leading to decreased neutrophil chemotaxis and inflammation Dose

Colchicine (Colcrys®) Mechanism Inhibits beta-tubulin polymyerization leading to decreased neutrophil chemotaxis and inflammation Dose Acute Gout Attack: 1. 2 mg, then 0. 6 mg 1 -hour later. Prophylaxis dosing starting 12 hours later Prophylaxis: 0. 6 mg QD – BID Administration Take with a full class of water Adverse Events Common: GI distress (diarrhea, N&V) Rare/Serious: myelosuppression, myopathy Drug Interactions CYP 3 A 4/P-gp substrate (Avoid strong inducers/inhibitors) Pearls - Treatment generally titrated to diarrhea - Do not repeat treatment courses within 14 days - Contraindicated with renal or hepatic impairment AND a strong CYP 3 A 4/P-gp inhibitor Colcrys®. [package insert]: Philadelphia, PA. AR Scientific, INC; 2009.

Evaluating Response ULT should start 6 -8 weeks after resolution of acute attack Criteria

Evaluating Response ULT should start 6 -8 weeks after resolution of acute attack Criteria for Inadequate Response ↓ < 20% in pain score within 24 hours ↓ < 50% in pain score beyond 24 hours Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1447 -1461.

Summary: Acute Gouty Arthritis • Pharmacotherapy is the mainstay of acute gout treatment •

Summary: Acute Gouty Arthritis • Pharmacotherapy is the mainstay of acute gout treatment • NSAIDs, systemic cortiocosteroids, and colchcine are all first line options and choice of agent should be guided by patient-specific factors • Combination therapy can be used for severe attacks

Treatment MAINTENANCE URATE LOWERING THERAPY

Treatment MAINTENANCE URATE LOWERING THERAPY

Non-pharmacologic Therapy • Dietary and lifestyle modifications – Consume in moderation • Alcohol, red

Non-pharmacologic Therapy • Dietary and lifestyle modifications – Consume in moderation • Alcohol, red meat, shellfish, sweets – Weight loss – Tobacco cessation – Appropriate hydration • Minimize non-essential medications that may induce hyperuricemia Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1431 -1446.

Who should receive ULT? Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1431

Who should receive ULT? Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1431 -1446.

Which agents are first line? Khanna D, et al. Arthritis Care Res. 2012; 64(10):

Which agents are first line? Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1431 -1446.

Xanthine Oxidase Inhibitors Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563.

Xanthine Oxidase Inhibitors Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563.

Allopurinol (Zyloprim®) Mechanism Xanthine oxidase inhibitor (XOI) Dose Initial: 100 mg QD Titrate: q

Allopurinol (Zyloprim®) Mechanism Xanthine oxidase inhibitor (XOI) Dose Initial: 100 mg QD Titrate: q 2 -5 weeks until uric acid target achieved Max Dose: 800 mg/day divided Administration Take with or without meals Adverse Events Common: Rash, pruritis, transaminitis Rare/Serious: myelosuppression, hepatotoxicity, SJS/TEN Drug Interactions Purine antimetabolites (azathioprine, 6 -mercaptopurine), theophylline, didanosine Pearls - Dose is titrated up slowly to avoid acute gout flare - Dose is reduced by 50% in renal impairment - Hypersensitivity reaction more common with concurrent thiazides and in Asian populations (consider HLA-B*5801 screening) Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1447 -1461. Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563.

Febuxostat Febuxistat (Uloric®) Mechanism Xanthine oxidase inhibitor (XOI) Dose Initial: 40 mg QD Titrate:

Febuxostat Febuxistat (Uloric®) Mechanism Xanthine oxidase inhibitor (XOI) Dose Initial: 40 mg QD Titrate: may incease to 80 mg if not at goal in 2 weeks Max Dose: 120 mg/day Administration Take with or without meals Adverse Events Common: Rash, gout flare, transaminitis Rare/Serious: hepatotoxicity, thrombotic events, SJS/TEN Drug Interactions Purine antimetabolites (azathioprine, 6 -mercaptopurine), theophylline, didanosine Pearls - Consider in patients who do not tolerate allopurinol or have inadequate response (BRAND only) - Gout flares more common during initiation of therapy - Not renally eliminated Uloric®. [package insert]: Deerfield, IL. Takeda Pharmaceuticals America, Inc; 2013.

CONTRAINDICATION 6 -MP Theophylline Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563.

CONTRAINDICATION 6 -MP Theophylline Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563.

Uricosurics fenofibrate Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563.

Uricosurics fenofibrate Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563.

Probenecid Mechanism Inhibits the uric acid – organic anion transport pathway Dose Initial: 250

Probenecid Mechanism Inhibits the uric acid – organic anion transport pathway Dose Initial: 250 mg BID x 1 week Titrate: 500 mg/day increments every 4 weeks Max Dose: 2 g/day Administration Take with food and plenty of fluids Adverse Events Common: GI intolerance (dyspepsia, reflux), rash, acute gout Rare/Serious: nephrolithiasis Drug Interactions Significant – inhibits secretory elimination of anionic drugs Pearls - No benefit if Cr. CL < 30 -50 m. L/min - Can be used therapeutically to boost beta-lactam levels - Monitor urinary uric acid excretion before and during therapy - Contraindicated: history of nephrolithiasis Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1447 -1461. Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563.

Prophylaxis When Initiating ULT 6 -8 weeks after acute attack resolution Khanna D, et

Prophylaxis When Initiating ULT 6 -8 weeks after acute attack resolution Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1447 -1461.

Treatment-Resistant Gout • Referral to a rheumatologist – Refractory signs and symptoms – Difficulty

Treatment-Resistant Gout • Referral to a rheumatologist – Refractory signs and symptoms – Difficulty reaching serum uric acid target, particularly with renal impairment and trial of XOI – Multiple/serious adverse effects to treatment Khanna D, et al. Arthritis Care Res. 2012; 64(10): 1431 -1446.

Uricase Enzyme Rasburicase (Elitek®) Pegloticase (Krystexxa®) Teng GG, et al. Drugs. 2006; 66(12): 1547

Uricase Enzyme Rasburicase (Elitek®) Pegloticase (Krystexxa®) Teng GG, et al. Drugs. 2006; 66(12): 1547 -1563. Medicinal Chemistry

Hot Off the Press http: //www. fda. gov/News. Events/Newsroom /Press. Announcements/ucm 478791. htm

Hot Off the Press http: //www. fda. gov/News. Events/Newsroom /Press. Announcements/ucm 478791. htm

Lesinurad (Zurampic®) Probenecid Mechanism Selective inhibitor of URAT 1 and OAT 4 (diuretic-induced) Dose

Lesinurad (Zurampic®) Probenecid Mechanism Selective inhibitor of URAT 1 and OAT 4 (diuretic-induced) Dose 200 mg QD with a XOI Administration Take with food and plenty of fluids (2 L/day) at the same time as XOI Adverse Events Common: Headache, reflux, influenza Rare/Serious: Acute renal failure (monotherapy) Drug Interactions CYP 2 C 9 inhibitors/inducers Pearls - Contraindicated: monotherapy or with Cr. CL < 45 m. L/min - Limited experience and yet to define place in therapy Zurampic®. [package insert]: Wilmington, DE. Astra. Zeneca Pharmaceuticals LP; 2015.

Summary: Urate Lowering Therapy • Maintenance ULT is indicated in significant disease burden and

Summary: Urate Lowering Therapy • Maintenance ULT is indicated in significant disease burden and renal comorbidities • Xanthine oxidase inhibitors are the mainstay of therapy to target uric acid levels of at least < 6 mg/d. L • Uricosuric agents are alternatives to XOIs and useful adjuncts in resistant disease

Take Away Points • Gout is a common rheumatic disease that can be largely

Take Away Points • Gout is a common rheumatic disease that can be largely “cured” with pharmacotherapy • Medication selection during acute attacks should be guided by patient-specific factors • Maintenance ULT is largely well tolerated by some significant drug-drug interactions exist and most medications should be adjusted for renal dysfunction

Patient Case • Doran Martell is a 58 YOM with PMHx HTN, HLD, T

Patient Case • Doran Martell is a 58 YOM with PMHx HTN, HLD, T 2 DM, DVT who presents with a chief complaint of swelling and excruciating pain in his right foot.

Patient Case • Doran Martell supplies the following history – Diet: Eats shellfish frequently

Patient Case • Doran Martell supplies the following history – Diet: Eats shellfish frequently due to proximity to the sea, red meat on weekends – Et. OH: Drinks 3 -4 ales/day – Exercise: Little physical activity

Medications • • • ASA 325 mg q 4 -6 PRN pain Valsartan 160

Medications • • • ASA 325 mg q 4 -6 PRN pain Valsartan 160 mg QD HCTZ 25 mg QD Niacin OTC capsules QD Simvastatin 20 mg QHS Warfarin 5 mg QMWF & 2. 5 mg QTu. Th. Sa. Su

Patient Counseling • What modifiable risk factors could you counsel this patient on? •

Patient Counseling • What modifiable risk factors could you counsel this patient on? • Which medications may exacerbate gout?

Physical Exam Findings Erythema, tenderness, and swelling in the right great toe

Physical Exam Findings Erythema, tenderness, and swelling in the right great toe

Patient Case • Labs – A 1 c 5. 9% – Scr: 1. 4

Patient Case • Labs – A 1 c 5. 9% – Scr: 1. 4 (Cr. CL ~ 59 m. L/min) – LFTs: WNL – Uric Acid: 9 mg/d. L • Vitals – BP: 150/94 | HR: 87 | RR: 16

Medications • • • ASA 325 mg q 4 -6 PRN pain Valsartan 160

Medications • • • ASA 325 mg q 4 -6 PRN pain Valsartan 160 mg QD HCTZ 25 mg QD Niacin OTC capsules QD Simvastatin 20 mg QHS Warfarin 5 mg QMWF & 2. 5 mg QTu. Th. Sa. Su

Patient Case • With your neighbor discuss: – Which laboratory/physical exam findings are consistent

Patient Case • With your neighbor discuss: – Which laboratory/physical exam findings are consistent with acute gout? – Which medication(s) you want initiate for Doran Martell’s acute gout attack? Why?

Patient Case • One year later, Prince Doran returns to clinic for follow up

Patient Case • One year later, Prince Doran returns to clinic for follow up (he was swept away in wars and intrigue and missed his other follow ups). This is his physical exam today:

Patient Case • He is asymptomatic but has tophi on examination. He has made

Patient Case • He is asymptomatic but has tophi on examination. He has made the dietary and lifestyle modifications you discussed previously. What therapy would you like to initiate?

Questions?

Questions?