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Efficacy of daprodustat for patients on dialysis with anemia: systematic review and network meta-analysis. | LitMetric

AI Article Synopsis

  • Chronic kidney disease (CKD) often leads to anemia, complicating treatment for dialysis-dependent patients, necessitating various therapies including daprodustat, rhEPO, and iron supplements.
  • This study aimed to evaluate whether daprodustat is more effective and safer than rhEPO and other standard treatments, using data from seven trials with a focus on systematic review and network meta-analysis.
  • Results showed that daprodustat (25-30 mg dosage) significantly improved serum hemoglobin and total iron binding capacity (TIBC) while reducing ferritin levels in these patients, indicating its potential superiority in managing anemia associated with CKD.

Article Abstract

Chronic kidney disease (CKD) is commonly complicated by anemia. Treating dialysis-dependent patients with anemia, including daprodustat and other inhibitors of prolyl hydroxylase of hypoxia-inducible factor, recombinant human erythropoietin (rhEPO), and iron supplements. We conducted this study to test our postulation; daprodustat is superior to rhEPO and other conventional treatments respecting efficacy and safety parameters. We made systematic search through PubMed, Web of Science, Scopus, and Cochrane. Seven unique trials were eventually included for systematic review; six of them with a sample size of 759 patients entered our network meta-analysis (NMA). Daprodustat 25-30 mg was associated with the greatest change in serum hemoglobin (MD=1.86, 95%CI= [1.20; 2.52]), ferritin (MD= -180.84, 95%CI= [-264.47; -97.20]), and total iron binding capacity (TIBC) (MD=11.03, 95%CI= [3.15; 18.92]) from baseline values. Dialysis-dependent patients with anemia had a significant increment in serum Hemoglobin and TIBC and a reduction in serum ferritin, in a dose-dependent manner, when administered daprodustat.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11143073PMC
http://dx.doi.org/10.11604/pamj.2024.47.114.37278DOI Listing

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