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10.1038/srep33082

http://scihub22266oqcxt.onion/10.1038/srep33082
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suck abstract from ncbi


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pmid27605442
      Sci+Rep 2016 ; 6 (ä): 33082
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  • Comparative efficacy and safety of urate-lowering therapy for the treatment of hyperuricemia: a systematic review and network meta-analysis #MMPMID27605442
  • Li S ; Yang H ; Guo Y ; Wei F ; Yang X ; Li D ; Li M ; Xu W ; Li W ; Sun L ; Gao Y ; Wang Y
  • Sci Rep 2016[Sep]; 6 (ä): 33082 PMID27605442 show ga
  • The prevalence of hyperuricemia and gout has been increasing, but the comparative effectiveness and safety of different treatments remain uncertain. We aimed to compare the effectiveness and safety of different treatments for hyperuricemia using network meta-analysis methodology. We systematically reviewed fifteen randomized controlled trials (involving 7,246 patients through January 2016) that compared the effects of different urate-lowering drugs (allopurinol, benzbromarone, febuxostat, pegloticase and probenecid) on hyperuricemia. Drug efficacy and safety, as outcomes, were measured by whether the target level of serum urate acid was achieved and whether any adverse events occurred, respectively. We derived pooled effect sizes expressed as odds ratios (ORs) and 95% confidence intervals (CIs). The efficacy and safety of the drugs were ranked by cumulative ranking probabilities. Our findings show that febuxostat, benzbromarone, probenecid, pegloticase, and allopurinol were all highly effective at reducing the risk of hyperuricemia compared to placebo. Febuxostat had the best efficacy and safety compared to the other drugs. Furthermore, febuxostat 120?mg QD was more effective at achieving urate-lowering targets (OR: 0.17, 95% CI: 0.12-0.24) and safer (OR: 0.72, 95% CI: 0.56-0.91) than allopurinol.
  • |Gout Suppressants/*therapeutic use [MESH]
  • |Gout/blood/drug therapy [MESH]
  • |Humans [MESH]
  • |Hyperuricemia/*blood/*drug therapy [MESH]
  • |Odds Ratio [MESH]
  • |Probability [MESH]
  • |Randomized Controlled Trials as Topic [MESH]


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