波多黎各大学医院血液透析患者的贫血管理。

Heana E Ocasio, Hector Diaz, José L Cangiano, Rafael Báez, Erick Suárez
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摘要

终末期肾病常并发贫血。缺铁性贫血发生在大多数血液透析患者中,继发于当使用刺激剂治疗贫血时,红细胞生成加速导致铁需求增加。本研究的目的是确定在我们单位接受血液透析的患者中贫血和铁储备的患病率;确定其治疗方法和效果。对53例门诊血液透析患者进行为期3个月的病历评估。记录患者血红蛋白、铁蛋白、铁、总铁结合力及转铁蛋白饱和度。91%的患者有动脉高血压,62%的患者有糖尿病。三个月期间的贫血患病率分别为34%、57%和47%。只有21%的人群转铁蛋白饱和度低于20%,没有人的铁蛋白低于200ng /ml。在整个研究过程中,大多数患者采用铁和促红细胞生成素(ESAs)联合治疗。尽管用铁和esa治疗,贫血的患病率仍然升高。然而,在三个月内,56%的贫血患者在观察期结束时血红蛋白水平升高。53%的患者连续3个月接受铁治疗或esa治疗,只有2例患者转铁蛋白饱和度低于20%。在我们的人群中,esa的低反应性与缺铁无关,而是与疾病的发病率有关。
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Anemia management among hemodyalisis patients at the University Hospital in Puerto Rico.

End-stage renal disease is frequently complicated with anemia. Iron deficiency anemia occurs in most hemodialysis patients secondary to increased iron demand driven by the accelerated erythropoiesis that occurs when stimulating agents are administered as treatment of the anemia. The purpose of this study was to determine the prevalence of anemia and iron stores in patients undergoing hemodialysis at our unit; identify their treatment and effectiveness. Medical records of fifty-three patients undergoing ambulatory hemodialysis were evaluated for three months. Patient's hemoglobin, ferritin, iron, total iron binding capacity and percent transferrin saturation were recorded. 91% patients had arterial hypertension and 62% were diabetic. The prevalence of anemia was 34%, 57% and 47% during the three-month period respectively. Only 21% of the population had transferrin saturation less than 20% and none had ferritin below 200 ng/ml. Throughout the study, the majority of patients were managed with combination of iron and erythropoietin stimulating agents (ESAs). The prevalence of anemia remained elevated despite treatment with iron and ESAs. However, 56% of anemic patients throughout the three months showed an increase in hemoglobin levels by the end of the observation period. 53% of patients were treated with iron alone or with ESAs for the three consecutive month periods and only two had transferrin saturation less than 20%. In our population, ESAs low responsiveness is not related to iron deficiency but to the morbidity of their disease.

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