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首页> 外文期刊>Peritoneal dialysis international: Journal of the International Society for Peritoneal Dialysis >Experience with a large dose (500 mg) of intravenous iron dextran and iron saccharate in peritoneal dialysis patients.
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Experience with a large dose (500 mg) of intravenous iron dextran and iron saccharate in peritoneal dialysis patients.

机译:腹膜透析患者使用大剂量(500毫克)静脉注射右旋糖酐铁和糖化铁的经验。

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OBJECTIVE: To compare efficacy in anemia correction and side effects of large doses of intravenous (IV) iron dextran and iron saccharate preparations in peritoneal dialysis (PD) patients. SETTING: Tertiary-care teaching hospital of University of Toronto. DESIGN: Retrospective analysis of 379 PD patients who attended PD clinics in past 5 years. Of these 379 patients, 62 were selected to receive IV iron based on ferrokinetic markers of iron deficiency, noncompliance to or ineffectiveness of oral iron, or increased erythropoietin (EPO) requirement. INTERVENTION: Sixty-one patients received two IV iron injections of 500 mg each, 1 week apart, 33 patients received iron dextran, 23 received iron saccharate, and 5 received both iron dextran and iron saccharate. One patient developed anaphylaxis to a test dose of iron dextran and was excluded from further therapy. Blood samples were collected before and 3 and 6 months after iron infusions. RESULTS: At 3 months, the group's average hemoglobin rose from 98.3+/-18.3 g/L to 110.6+/-16.4 g/L (p < 0.0001). Ferritin rose from 104.9+/-115.4 microg/L to 391.5+/-294.1 microg/L (p < 0.0001), and transferrin saturation from 0.17+/-0.07 to 0.26+/-0.19 (p z 0.0001). Erythropoietin requirements fell from 7278.7 IU/week to 5900 IU/week (p < 0.01). Five of the 34 patients who received iron dextran developed minor side effects and 1 patient had anaphylaxis to the test dose. Of the 23 patients who received iron saccharate, 1 had an anaphylactic reaction and 2 had transient chest pain, which subsided without therapy. Overall, there were more side effects with iron dextran (7.4% of injections) compared to the iron saccharate group (4.3% of injections), but this difference was statistically insignificant. Although statistically insignificant, there was an increase in the number of peritonitis episodes during the 6 months after IV iron infusion, especially with iron dextran, compared to the peritonitis episodes during the 6 months before iron infusions. CONCLUSION: Our study indicates that IV iron in PD patients is effective in restoring iron stores and in decreasing EPO requirements. One anaphylactic reaction occurred in each group. Our data suggest that as much caution be exercised with iron saccharate as with iron dextran. The slight trend toward increased peritonitis rates after iron infusions needs to be investigated in a larger group of patients.
机译:目的:比较腹膜透析(PD)患者大剂量静脉注射右旋糖酐铁和糖铁制剂在贫血纠正和副作用方面的疗效。单位:多伦多大学三级教学医院。设计:回顾性分析了过去5年中去过PD诊所的379名PD患者。在这379名患者中,根据铁缺乏,口服铁不服从或无效,或促红细胞生成素(EPO)需求增加的铁动力学标志物,选择了62名接受IV铁。干预:61例患者接受了两次静脉铁注射,每次500 mg,相隔1周; 33例患者接受了右旋糖酐铁,23例接受了蔗糖铁,5例同时接受了右旋糖酐铁和糖铁。一名患者对测试剂量的右旋糖酐铁过敏,因此被排除在进一步治疗之外。在输注铁之前和之后以及3和6个月收集血液样本。结果:在3个月时,该组的平均血红蛋白从98.3 +/- 18.3 g / L上升到110.6 +/- 16.4 g / L(p <0.0001)。铁蛋白从104.9 +/- 115.4 microg / L上升到391.5 +/- 294.1 microg / L(p <0.0001),转铁蛋白饱和度从0.17 +/- 0.07上升到0.26 +/- 0.19(p z 0.0001)。促红细胞生成素的需求量从7278.7 IU /周降至5900 IU /周(p <0.01)。接受右旋糖酐铁的34例患者中有5例出现了轻微的副作用,而1例患者对测试剂量有过敏反应。在接受糖精铁治疗的23例患者中,有1例出现过敏反应,有2例出现短暂性胸痛,这些症状未经治疗即消失。总体而言,右旋糖酐铁(注射剂的7.4%)比糖精铁组(注射剂的4.3%)有更多的副作用,但这种差异在统计学上不显着。尽管在统计学上无统计学意义,但与输铁前6个月的腹膜炎发作相比,静脉输注铁后6个月(尤其是右旋糖酐铁)腹膜炎发作的次数有所增加。结论:我们的研究表明,PD患者的IV铁可有效恢复铁存储并降低EPO需求。每组发生一种过敏反应。我们的数据表明,糖精铁和右旋糖酐铁要格外小心。大量患者需要研究输铁后腹膜炎发生率增加的轻微趋势。

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