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DOI 10.1111/jcpt.13156

Медицинская библиотека · Journal of clinical pharmacy and therapeutics · 2020

Efficacy and safety of urate-lowering treatments in patients with hyperuricemia: A comprehensive network meta-analysis of randomized controlled trials.

Sun Shan-Shan, Zhang Dong-Hu, Shi Yue, Lin Cheng-Jiang, Lin Jian-Yang

СтатьяСистематический обзорNetwork Meta-AnalysisПеревод в очереди

Аннотация

WHAT IS KNOWN AND

OBJECTIVE

Hyperuricemia (HUA) and gout are considerable public health problems because of their increasing incidence and interactions with other diseases. We aimed to evaluate the efficacy and safety of urate-lowering therapies (ULTs) for patients.

METHODS

A systematic literature review was conducted, and a network meta-analysis was performed on the included studies using the Markov Chain Monte Carlo simulation method and a Bayesian statistical framework. We calculated surface under the cumulative ranking curve (SUCRA) values and performed clustered ranking to combine the efficacy and safety results.

RESULTS

Twenty-two randomized controlled studies were identified for the efficacy analysis, and 20 studies were identified for the safety analysis. Compared with the placebo, the ULTs were efficient and safe. Febuxostat 120 mg/d and allopurinol 200 mg/d had the highest SUCRA scores for efficacy and safety, respectively. Clustered ranking results showed that febuxostat 120 mg/d was the best in terms of efficacy and safety, topiroxostat 120/160 mg/d was similar to febuxostat 80 mg/d in terms of efficacy but safer, and allopurinol was not inferior to topiroxostat.

WHAT IS NEW AND

CONCLUSION

Febuxostat had the best efficacy and safety results among the tested agents, and topiroxostat and allopurinol appeared to have fewer adverse events.

Для цитирования: Sun Shan-Shan, Zhang Dong-Hu, Shi Yue, Lin Cheng-Jiang, Lin Jian-Yang. Efficacy and safety of urate-lowering treatments in patients with hyperuricemia: A comprehensive network meta-analysis of randomized controlled trials.. Journal of clinical pharmacy and therapeutics. 2020. DOI: 10.1111/jcpt.13156.

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