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DOI 10.1038/s41598-022-06261-0

Медицинская библиотека · Scientific reports · 2022

Ferric citrate hydrate is associated with a reduced cost of drugs and a smaller change in red blood cell distribution width.

Ito Kyoko, Yokoyama Keitaro, Nakayama Masaaki, Fukagawa Masafumi, Hirakata Hideki

СтатьяМногоцентровое исследованиеРандомизированное исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

The ASTRIO study was a randomised, multicentre, 24-week study that compared the effects of ferric citrate hydrate (FC) and non-iron-based phosphate binders (control) on anaemia management in haemodialysis (HD) patients receiving erythropoiesis-stimulating agents (ESAs). In that study, FC reduced the doses of ESAs and intravenous iron without affecting haemoglobin (Hb); however, the cost-effectiveness of FC was unclear. We retrospectively implemented a cost-effectiveness analysis comparing the incremental cost-effectiveness ratios (ICERs) in FC (n = 42) and control (n = 40) groups in patients with serum phosphate and Hb controlled within the ranges of 3.5-6.0 mg/dL and 10-12 g/dL, respectively. Costs included drug costs of phosphate binders, ESAs, and intravenous iron. Elevated red cell distribution width (RDW) has been reported to be associated with mortality in HD patients and was therefore used as an effectiveness index. The mean (95% confidence interval) differences in drug costs and RDW between the FC and control groups were US$ - 421.36 (- 778.94 to - 63.78, p = 0.02) and - 0.83% (- 1.61 to - 0.05, p = 0.04), respectively. ICER indicated a decrease of US$ 507.66 per 1% decrease in RDW. FC was more cost-effective than non-iron-based phosphate binders. Iron absorbed via FC could promote erythropoiesis and contribute to renal anaemia treatment.

Для цитирования: Ito Kyoko, Yokoyama Keitaro, Nakayama Masaaki, Fukagawa Masafumi, Hirakata Hideki. Ferric citrate hydrate is associated with a reduced cost of drugs and a smaller change in red blood cell distribution width.. Scientific reports. 2022. DOI: 10.1038/s41598-022-06261-0.

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