Estudio comparativo de 2 formulaciones de hierro intravenoso en una Unidad de Hospital de Día

N. Cano , L. Oltra , J. Hinojosa
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引用次数: 2

Abstract

Objectives

To compare effectiveness, efficiency and safety of two parenteral iron formulations in patients with inflammatory bowel disease: ferric-carboximaltose vs ferric-sacarose.

Methods

Retrospective analysis of 72 patients undergoing intravenous iron treatment. Indications of treatment: hemoglobin < 10 g/dL and or ferritininemia < 100 μg/L. The need of transfusion of red blood cells pools was registered, meaning the immediate closure of the follow-up of the patient. Iron protocol administration: ferric-carboximaltose (40 patients): maximum dose 1000 mg in 15 minutes perfusion; ferric-sacarose (32 patients): maximum dose 200 mg in 1 hour perfusion.

Results

There were no significant differences in average levels of haemoglobin (Ferric-carboxymaltose 10.78 ± 2.06 mg/dL vs. Ferric-sucrose 10.14 ± 2.33 mg/dL), haematocrit (ferric-carboxymaltose 32.15 ± 3.24% vs. ferric-sucrose 30.47 ± 4.53%), MCV (ferric-carboxymaltose 72.40 ± 7.72 fL vs. ferric-sucrose 69.54 ± 8.46 fL) and MCH (ferric-carboxymaltose 25.43 ± 6.22 pg/dL vs. ferric-sucrose 23.75 ± 5.93 pg/dL). Average ferritin levels were higher in ferric-carboxymaltose group (246.74 ± 17.83 μg/L vs. 179.52 ± 21.36 μg/L; P=.023).

Adverse events registered in the administration of ferric-carboxymaltose were lower (2 urticarial reactions) vs. al ferric-sucrose (13 stomachache and headache cases); p < 0.001. 2 patients with ferric-carboxymaltose required blood transfusion vs. 6 patients with Ferric-sucrose group; p = 0.062. The number of administered dosages was significantly higher in ferric-sucrose group in a ratio ferric-sucrose/ferric-carboxymaltose of 3.39 dosages/patient. Ferric-carboxymaltose application reduced treatment cost in €948.46/patient.

Conclusions

Treatment with intravenous ferric-carboxymaltose shows an effectiveness profile not inferior to ferric-sucrose. Higher repletion of systemic stock and a better security profile. Related to posology, treatment shows to improve efficiency, reducing dosages, blood transfusion and cost per patient.

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医院日间单位两种静脉注射铁制剂的比较研究
目的比较两种肠外铁制剂治疗炎症性肠病患者的疗效、效率和安全性:铁-羧化麦芽糖与铁-糖糖。方法回顾性分析72例静脉铁治疗患者的临床资料。治疗指征:血红蛋白;10 g/dL和/或铁氨酸血症;100μg / L。需要输血的红细胞池被登记,这意味着立即结束对患者的随访。铁方案给药:铁-羧肟糖(40例):最大剂量1000 mg,灌注15分钟;糖糖铁(32例):灌注1小时最大剂量200mg。结果两组患者血红蛋白(铁-羧麦芽糖10.78±2.06 mg/dL vs铁-蔗糖10.14±2.33 mg/dL)、红细胞压积(铁-羧麦芽糖32.15±3.24% vs铁-蔗糖30.47±4.53%)、MCV(铁-羧麦芽糖72.40±7.72 fL vs铁-蔗糖69.54±8.46 fL)和MCH(铁-羧麦芽糖25.43±6.22 pg/dL vs铁-蔗糖23.75±5.93 pg/dL)的平均水平均无统计学差异。铁-羧麦糖组平均铁蛋白水平较高(246.74±17.83 μg/L vs. 179.52±21.36 μg/L);P = 0)。与铁-蔗糖相比,铁-羧麦糖组记录的不良事件(2例荨麻疹反应)较低(13例胃痛和头痛);p & lt;0.001. 羧基麦芽糖铁组输血2例,蔗糖铁组输血6例;p = 0.062。在铁-蔗糖/铁-羧麦芽糖比例为3.39剂/例的情况下,铁-蔗糖组给药次数显著增加。羧基麦芽糖铁的应用降低了治疗成本,为948.46欧元/例。结论静脉注射羧麦芽糖铁治疗的疗效不低于蔗糖铁。更高的系统库存充足率和更好的安全性。与病理学相关的是,治疗显示出提高效率、减少剂量、输血和每位患者的费用。
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