Session Information
Session Type: Abstract Submissions (ACR)
Background/Purpose: Allopurinol is the most commonly used urate-lowering therapy (ULT) in the world. Although allopurinol is FDA approved for up to 800 mg/d and EMEA authorized for up to 900 mg/d, the majority of patients with gout receive ≤300 mg/d. We describe physician, patient, and treatment characteristics in patients with gout treated with allopurinol.
Methods: Data from a quantitative survey of physicians in the United States (US), France, Germany, Italy, Spain, and the United Kingdom (UK) were assessed and results confirmed through in-depth chart audits. Initial and current allopurinol doses, presence of comorbid conditions, use of anti-inflammatory prophylaxis for flare prevention, serum uric acid (sUA), physician subspecialty, and patient factors were evaluated. Data on number of patients achieving target sUA <6 mg/dL were also collected. Results are presented as proportions or means and standard deviations (SD). Descriptive statistics and multivariable-adjusted logistic regression analyses were used to describe patients with sUA <6 mg/dL.
Results: In total, 251 rheumatologists and 250 primary care physicians were interviewed. Of 2505 patients, 1437 (57%) were treated with allopurinol.
Table 1 presents patient characteristics, treatment, and percent with sUA <6 mg/dL.
Table 1. Patients Treated with Allopurinol: Unadjusted Characteristics by Country |
||||||
|
France (n=146) |
Germany (n=180) |
Italy (n=167) |
Spain |
UK (n=137) |
US (n=621) |
Age, years (mean±SD) |
63±9.7 |
60±11.5 |
62±11.2 |
58±10.7 |
56±13.4 |
57±12.2 |
Male (n, %) |
112 (77) |
148 (82) |
139 (83) |
167 (90) |
118 (86) |
515 (83) |
Comorbidities (n, %) |
53 (36) |
106 (59) 40 (22) |
75 (45) |
91 (49) 13 (7) |
52 (38) |
348 (56) 112 (18) 81 (13) 143 (23) |
Allopurinol dosing (n, %) 300 mg/d >300 to <600 mg/d ≥600 mg/d |
74 (51) 64 (44) 5 (3.4) 3 (2.1) |
54 (30) 117 (65) 5 (2.8) 4 (2.2) |
47 (28) 104 (62) 9 (5.4) 8 (4.8) |
67 (36) 108 (58) 5 (2.7) 7 (3.8) |
29 (21) 62 (45) 27 (20) 19 (14) |
139 (22) 361 (58) 86 (14) 35 (5.6) |
Average allopurinol dose (mean±SD) |
239±97.2 |
261±96.9 |
279±119.0 |
249±116.8 |
347±168.5 |
303±129.3 |
Months on allopurinol (mean±SD) |
48±56.8 |
35±42.4 |
39±46.3 |
59±67.9 |
42±53.2 |
43±53.7 |
% sUA ≤6 mg/dL (n, %) |
57 (39) |
61 (34) |
62 (37) |
48 (26) |
92 (67) |
261 (42) |
Across all countries, the majority of patients were treated with ≤300 mg/d of allopurinol; ≤6.5% in France, Germany, and Spain were given >300 mg/d, whereas 10% in Italy, 19.6% in the US, and 34% in the UK achieved a dose >300 mg/d (p<0.01). Over 12 months, the number of patients achieving target sUA <6.0 mg/dL differed across the 6 countries (Spain < Germany < Italy Conclusion: Allopurinol is the most widely used ULT. Although it is approved for up to 800 mg/d in the US and 900 mg/d in the EU, the majority of patients are treated with ≤300 mg/d. On average, <50% of patients achieve sUA <6 mg/dL at any allopurinol dose.
Disclosure:
J. A. Singh,
Takeda and Savient,
2,
Savient, Takeda, Ardea, Regeneron, Allergan, URL pharmaceuticals, and Novartis,
5;
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.
« Back to 2013 ACR/ARHP Annual Meeting
ACR Meeting Abstracts - https://acrabstracts.org/abstract/use-of-high-dose-allopurinol-to-reach-serum-uric-acid-targets-in-patients-with-gout-across-multiple-countries/