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Abstract Number: 1185

More Than One-Third Of Patients Reach Serum Urate Target and Continue To Report Multiple Flares

Dinesh Khanna1, Puja Khanna2, Chris Storgard3, Scott Baumgartner4 and Robert Morlock5, 1Division of Rheumatology, University of Michigan, Ann Arbor, MI, 2Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI, 34939 Directors Place, Ardea Bioscience, San Diego, CA, 4Ardea Biosciences, San Diego, CA, 5Ardea Bioscience, San Diego, CA

Meeting: 2013 ACR/ARHP Annual Meeting

Keywords: gout, rheumatologic practice, treatment and uric acid

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Session Information

Title: Metabolic and Crystal Arthropathies I

Session Type: Abstract Submissions (ACR)

Background/Purpose: Gout is a common inflammatory arthritis, and its worldwide prevalence is increasing. EULAR and ACR guidelines recommend a target serum urate (sUA) ≤6 mg/dL. We describe US and EU physician, patient, and treatment characteristics in patients treated with xanthine oxidase inhibitor (XOI) therapy who achieve sUA ≤6 mg/dL yet have 2 or more physician-confirmed gout flares per year.

Methods: A large survey of more than 500 physicians across the US and EU was conducted. Data was confirmed through in-depth chart audits, which assessed diagnosis, comorbid conditions, disease severity, and laboratory results of the last 5 patients with gout that they treated. Disease severity was measured using a physician global assessment (mild, moderate, or severe), flare counts, joint damage, and presence of tophi. Type and dose of XOI, length of current treatment, compliance, physician type, and patient sociodemographic factors were identified. Comorbidities were captured using chart review and analyzed as present or absent. Descriptive and multivariate statistics described patients having 2 or more flares per year (excluding treatment initiation flares) in patients achieving sUA ≤6 mg/dL.

Table 1. Demographics: Patients With Most Recent sUA Level ≤6 mg/dL

 

≥2 Flares

(n=122)

≤1 Flare

(n=233)

Total

(n=355)

Sex (male)

87%

79%

81%

Age (years)

60.22

58.93

59.37

Number of flares (last 12 months)*

3.11

0.43

1.35

Most recent sUA level (mg/dL)

5.20

5.16

5.18

12-month average sUA level (mg/dL)*

6.34

5.84

6.01

Tophi*

31%

19%

23%

Treated with allopurinol

72%

74%

74%

Treated with febuxostat

28%

26%

27%

Months on current urate-lowering therapy

36.78

37.19

37.05

Rheumatologist management

65%

69%

67%

*p<0.05.

Results: In total, 251 rheumatologists and 250 primary care physicians were interviewed. Of 2505 patients with gout, 82% were male and the average age was 58 (SD=12) years; 1826 (73%) patients were treated with a XOI. Of these, 811 (44%) had at least one assessment of sUA ≤6 mg/dL and 305 (38%) reported 2 or more flares in the last 12 months (Table). A backward stepwise multivariate model predicting patients classified as controlled (sUA ≤6 mg/dL) and continuing to flare (2 or more flares in the last year) found physician-reported and chart-documented coexisting comorbidities, including chronic kidney disease (OR 2.8; p<0.01), alcoholism (OR 3.6; p<0.01), and diabetes mellitus (OR 1.9; p<0.05). There was no difference by XOI or physician type. Results were similar for patients with single or multiple sUA assessments ≤6 mg/dL during the study period.

Conclusion: Less than 50% of patients treated with a XOI alone achieved sUA target. Of the patients achieving a sUA level of ≤6 mg/dL, more than one-third reported 2 or more flares in a 12-month period despite being treated with the same ULT for more than 3 years. Frequent flares and greater tophaceous burden requires treatment to an even lower urate target than 6.0 mg/dL.


Disclosure:

D. Khanna,

Savient, NIH,

2,

University of Michigan,

3,

AstraZeneca, Takeda, Savient,

5;

P. Khanna,
None;

C. Storgard,

AstraZeneca,

1,

Ardea Biosciences, a wholly owned subsidiary of AstraZeneca,

3;

S. Baumgartner,

Stock options AstraZeneca,

1,

Full time employment Ardea Biosciences, a wholly owned subsidiary of AstraZeneca,

3;

R. Morlock,

Employee of Ardea Biosciences, Inc,

3.

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