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  4. The net clinical benefits of febuxostat versus allopurinol in patients with gout or asymptomatic hyperuricemia – A systematic review and meta-analysis
 
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The net clinical benefits of febuxostat versus allopurinol in patients with gout or asymptomatic hyperuricemia – A systematic review and meta-analysis

Journal
Nutrition, Metabolism and Cardiovascular Diseases
Journal Volume
29
Journal Issue
10
Pages
1011-1022
Date Issued
2019
Author(s)
Liu, Cheng-Wei
Chang, Wei-Cheng
Lee, Chiao-Chin
Shau, Wen-Yi
Hsu, Fu-Shun
MAN-LING WANG  
Chen, Tsung-Chih
CHIAO LO  
HWANG, JUEY-JEN  
DOI
10.1016/j.numecd.2019.06.016
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85069976056&doi=10.1016%2fj.numecd.2019.06.016&partnerID=40&md5=fabb1176d205ae82ce8c9d0352429e86
https://scholars.lib.ntu.edu.tw/handle/123456789/621306
Abstract
Background and aims: Systemic reviews and meta-analyses suggest hyperuricemia is a cardiovascular risk factor. The effects of xanthine oxidase inhibitors on cardiac outcomes remain unclear. We assessed the effects of febuxostat and allopurinol on mortality and adverse reactions in adult patients with hyperuricemia. Methods and results: PubMed and EMBASE were searched to retrieve randomized controlled trials of febuxostat and allopurinol from January 2005 to July 2018. The meta-analysis consisted of 13 randomized controlled trials with a combined sample size of 13,539 patients. Febuxostat vs. allopurinol was not associated with an increased risk of cardiac-related mortality in the overall population (OR: 0.72, 95% CI: 0.24-2.13, P = 0.55). Regarding adverse skin reactions, the patients receiving febuxostat had significantly fewer adverse skin reactions than those receiving allopurinol treatment (OR: 0.50, 95% CI: 0.30-085, P = 0.01). Compared with allopurinol, febuxostat was associated with an improved safety outcome of cardiac-related mortality and adverse skin reactions (OR: 0.72, 95% CI: 0.55-0.96, P = 0.02). The net clinical outcome, composite of incident gout and the safety outcome, was not different significantly in the patients receiving febuxostat or allopurinol (OR: 1.04, 95% CI: 0.76-0.1.42, P = 0.79). In sensitivity analyses, a borderline significance was found in the patients randomized to febuxostat vs. allopurinol regarding cardiac-related mortality (OR: 1.29, 95% CI: 1.00-1.67, P = 0.05) after the CARES study was included. Conclusion: Febuxostat vs. allopurinol was associated with the improved safety outcome and have comparable mortality and net clinical outcome in patients with hyperuricemia. Registration number: PROSPERO(CRD42018091657).
Subjects
Allopurinol
Febuxostat
Hyperuricemia
Randomized-controlled trial
SDGs

[SDGs]SDG3

Publisher
Elsevier B.V.
Type
journal article

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