羧甲基铁诱发的低磷血症--一个病例系列。

IF 1.4 4区 医学 Q3 RHEUMATOLOGY ARP Rheumatology Pub Date : 2024-07-01 DOI:10.63032/DGZN9101
Carla Campinho Ferreira, Paulo Pereira, Margarida Correia, Emanuel Costa, Diogo Esperança Almeida, José Redondo Costa, Ana Roxo Ribeiro, Joana Leite Silva
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引用次数: 0

摘要

低磷血症可能会引起严重的并发症。根据其严重程度和持续时间,症状和体征的范围从疲劳到危及生命的事件,如严重横纹肌溶解和精神状态改变。长期后果包括骨软化症。低磷酸盐血症可能继发于父母铁的使用,主要与羧甲基麦芽糖铁(FCM)有关,发生率约为 45% 至 70%。我们描述了三例慢性缺铁性贫血患者的低磷血症,患者需要反复输注 FCM。患者到风湿病科就诊时出现了严重低磷血症的肌肉骨骼症状和长期低磷血症性骨质疏松症,并伴有骨折。我们旨在提高人们对羧甲基亚铁诱导的低磷血症的认识,文献中越来越多地描述了这种可导致严重残疾或潜在生命危险的不良事件。
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Ferric carboxymaltose-induced hypophosphatemia - a case series.

Hypophosphatemia may cause serious complications. Depending on its severity and duration, signs and symptoms range from fatigue to life-threatening events, like severe rhabdomyolysis and mental status changes. Long-term consequences include osteomalacia. Hypophosphatemia may be secondary to the use of parental iron, mostly associated with ferric carboxymaltose (FCM), with an incidence of around 45% to 70%. We describe three cases of hypophosphatemia in patients with chronic iron deficiency anemia, requiring repeated FCM infusions. The patients' presentation to the Rheumatology department included musculoskeletal symptoms of severe hypophosphatemia and long-term hypophosphatemic osteomalacia, with fractures. We aim to raise awareness for ferric carboxymaltose-induced hypophosphatemia, an entity increasingly described in the literature that can be responsible for severe disability or potentially life-threatening adverse events.

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