Medical University of Innsbruck, Department of Medicine I, Gastroenterology, Hepatology and Endocrinology, Anichstrasse 35, A-6020, Innsbruck, Austria.
Medical University of Innsbruck, Department of Medicine I, Gastroenterology, Hepatology and Endocrinology, Anichstrasse 35, A-6020, Innsbruck, Austria.
Mol Aspects Med. 2020 Oct;75:100862. doi: 10.1016/j.mam.2020.100862. Epub 2020 May 19.
Intravenous infusions of iron have evolved from a poorly effective and dangerous intervention to a safe cornerstone in the treatment of iron deficiency. Modern iron formulations are composite nanoparticles composed of carbohydrate ferric oxy-hydroxides. Iron dextran, iron derisomaltose (formely known as iron isomaltoside 1000), ferric carboxymaltose, ferrumoxytol, iron sucrose and sodium ferric gluconate can be infused at different doses and allow correction of total iron deficit with single or repeated doses in 1-2 weeks depending on the specific formulation. All iron preparations are associated with a risk of severe infusion reactions. In recent prospective clinical trials, the risk of moderate to severe infusion reactions was comparable among all modern preparations affecting <1% of patients. Hence, intravenous iron therapy is reserved for iron deficiency anemia patients with intolerance or unresponsiveness of oral iron. As per European drug label, intravenous iron may also be preferred when rapid correction of the iron deficit is required. In patients with inflammation, iron-deficiency should also be suspected as anemia cause when transferrin saturation is low because serum ferritin can be spuriously normal. The main treatment target for i.v. iron is an improvement of the quality of life, for which hemoglobin is a surrogate marker. An emerging complication affecting 50-74% of patients treated with ferric carboxymaltose in prospective clinical trials is hypophosphatemia - or more accurately the 6H syndrome (hyperphosphaturic hypophosphatemia triggered by high fibroblast growth factor 23 that causes hypovitaminosis D, hypocalcemia and secondary hyperparathyroidism). These biochemical changes can cause severe and potentially irreversible clinical complications, such a bone pain, osteomalacia and fractures. Individual selection of the appropriate iron therapy and evaluation of treatment response are mandatory to safely deliver improved outcome through intravenous iron therapies.
静脉输注铁剂已从一种疗效差且危险的干预手段发展为治疗缺铁症的安全基石。现代铁制剂是由碳水化合物铁氧羟化物组成的复合纳米颗粒。右旋糖酐铁、铁低聚糖(以前称为异麦芽糖铁 1000)、羧基麦芽糖铁、ferrumoxytol、蔗糖铁和葡甲胺铁可在不同剂量下输注,并可根据特定制剂在 1-2 周内单次或重复剂量纠正总铁缺乏。所有铁制剂都与严重输注反应的风险相关。在最近的前瞻性临床试验中,所有现代制剂引起的中度至重度输注反应风险在 1%以下的患者中相当。因此,静脉铁治疗仅用于口服铁不耐受或无效的缺铁性贫血患者。根据欧洲药品标签,当需要快速纠正铁缺乏时,也可以选择静脉铁治疗。在炎症患者中,由于转铁蛋白饱和度低,铁缺乏也应怀疑为贫血的原因,因为血清铁蛋白可能会出现假性正常。静脉铁的主要治疗目标是提高生活质量,血红蛋白是其替代标志物。在前瞻性临床试验中,接受羧基麦芽糖铁治疗的患者中出现了一种新的并发症,即低磷血症,或更准确地说是 6H 综合征(由高成纤维细胞生长因子 23 触发的高磷尿低磷血症,导致维生素 D 缺乏、低钙血症和继发性甲状旁腺功能亢进)。这些生化变化可引起严重且潜在不可逆转的临床并发症,如骨痛、骨软化症和骨折。必须进行个体化选择适当的铁治疗并评估治疗反应,以通过静脉铁治疗安全地改善预后。