Background: Post-renal transplant anemia significantly impacts patient outcomes and quality of life. The only option available until recently was erythropoietin (EPO) that requires intravenous or subcutaneous injection. New class of drugs that are Hypoxia-Inducible Factor Prolyl Hydroxylase Inhibitor (HIF PHI) have become available and there is scarce data on their use in kidney transplant recipients (KTRs). Methods: This was prospective observational study which included 58 renal transplant recipients with anemia (Hb < 10 g/dL) who were started on either oral HIF PHI in the form of Desidustat (n=30) or EPO (n=28) based on nephrologist discretion. Adult KTRs with a hemoglobin (Hb) level of less than 10 gm/dl were included. Patients with acute graft dysfunction, bleeding and primary haematological diseases were excluded. Baseline clinical characteristics were recorded. Primary outcomes were change in Hb at 8 weeks in the two groups. Secondary outcomes included inflammatory markers (CRP, ESR), iron indices, and safety. Results: 58 patients were enrolled in the study; 30 received desidustat and 28 received erythropoietin. Both groups showed significant improvement in Hb from baseline to 2 months (Desidustat: 8.69 +/- 0.86 g/dL to 9.89 +/- 0.92 g/dL; EPO: 8.54 +/- 0.73 g/dL to 9.55 +/- 0.71 g/dL; p > 0.05). No significant differences were observed in inflammatory markers or iron indices. Both treatments were well-tolerated, with no reported adverse events. Conclusions: Desidustat demonstrated comparable efficacy and safety to EPO, with the added benefit of oral administration. It presents a promising alternative for anemia management in post-renal transplant patients.
Competing Interest StatementThe authors have declared no competing interest.
Clinical TrialCTRI/2024/08/072458
Funding StatementThis study did not receive any funding
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The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
Ethics committee of Post Graduate Institute of Medical Education and Research, Chandigarh gave ethical approval for this work
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