Kinoshita Teruhisa, Kondo Yuki, Sakazaki Yuka, Imaizumi Hiroki, Takimoto Norio, Ishitsuka Yoichi
Department of Pharmacy, Kariya Toyota General Hospital, 5-15 Sumiyoshi-cho, Kariya, Aichi 448-8505, Japan.
Department of Clinical Chemistry and Informatics, Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oehonmachi, Chuo-ku, Kumamoto 862-0973, Japan.
Bone Rep. 2024 Mar 26;21:101754. doi: 10.1016/j.bonr.2024.101754. eCollection 2024 Jun.
Intravenous iron replacement therapy is a common treatment for iron deficiency. Commonly used agents in this treatment include ferric carboxymaltose, ferric derisomaltose, and saccharated ferric oxide (SFO). These drugs are known to elevate fibroblast growth factor 23 levels, resulting in hypophosphatemia, but in past reports, hypophosphatemia attributable to SFO treatment has been associated mainly with prolonged administration over several weeks. The present study details our experience of a case of moderate hypophosphatemia (<2 mg/dL) in a 22-year-old woman who had no specific history of hypophosphatemia during the first 5 days of SFO treatment, and showed an increase in intact fibroblast growth factor 23 levels within the first week of treatment. Cases of hypophosphatemia have been reported as occurring as early as 1 week after the start of SFO administration in the Japanese Adverse Drug Event Report database. These cases, along with our case, underline the need for awareness of the possibility of hypophosphatemia from the early stage of SFO administration, regardless of the patient's age or dosage, as well as the need to monitor patients to prevent complications.
静脉补铁替代疗法是治疗缺铁的常用方法。该治疗中常用的药物包括羧基麦芽糖铁、异麦芽糖铁和含糖氧化铁(SFO)。已知这些药物会升高成纤维细胞生长因子23水平,导致低磷血症,但在过去的报告中,SFO治疗所致的低磷血症主要与数周的长期给药有关。本研究详细介绍了我们遇到的一例22岁女性发生中度低磷血症(<2mg/dL)的病例,该患者在SFO治疗的前5天无低磷血症的特殊病史,且在治疗的第一周内成纤维细胞生长因子23的完整水平升高。在日本药品不良事件报告数据库中,有报告称低磷血症病例早在SFO给药开始后1周就出现了。这些病例以及我们的病例强调,无论患者年龄或剂量如何,从SFO给药的早期阶段就需要意识到低磷血症的可能性,同时需要对患者进行监测以预防并发症。