Fishbane S, Lynn R I
Division of Nephrology, Winthrop-University Hospital, Mineola, NY.
Am J Kidney Dis. 1995 Mar;25(3):426-32. doi: 10.1016/0272-6386(95)90104-3.
The optimal method for diagnosing iron deficiency in end-stage renal disease is an area of controversy. This study compared the use of zinc protoporphyrin (ZPP) with the use of conventional tests for determination of iron deficiency when evaluating the need for intravenous iron therapy in hemodialysis patients maintained on erythropoietin (EPO). A baseline survey was performed in all hemodialysis patients at the Baumritter Kidney Center (Bronx, NY), measuring ZPP, ferritin, transferrin saturation (TSAT), mean corpuscular volume, and hematocrit. Patients with ZPP > or = 90 mumol/mol heme or ferritin less than 100 ng/mL were considered likely to be iron deficient and were treated with 1,000 mg of intravenous iron dextran over 10 hemodialysis treatments. The positive predictive values of ferritin and ZPP for predicting a response to intravenous iron dextran were similar (73% v 83%, respectively; two-tailed, P = 0.48). To determine the sensitivity and specificity of the tests, patients were divided into two groups at the end of the study period: those in whom iron therapy was required (n = 23) (patients treated with intravenous iron dextran who had a 5% increase in hematocrit or a decrease in erythropoietin dose of > or = 2,000 U/treatment) and those in whom iron therapy was not required (n = 24) (patients either treated with intravenous iron dextran without a response [n = 9] or patients whose initial ZPP and ferritin levels were not suggestive of iron deficiency and who maintained a stable hematocrit and erythropoietin dose during the study period [n = 15]).(ABSTRACT TRUNCATED AT 250 WORDS)
诊断终末期肾病缺铁的最佳方法是一个存在争议的领域。本研究在评估接受促红细胞生成素(EPO)治疗的血液透析患者静脉补铁治疗需求时,比较了使用锌原卟啉(ZPP)与使用传统检测方法来测定缺铁情况。在纽约州布朗克斯区的鲍姆里特肾脏中心,对所有血液透析患者进行了基线调查,测量ZPP、铁蛋白、转铁蛋白饱和度(TSAT)、平均红细胞体积和血细胞比容。ZPP≥90μmol/mol血红素或铁蛋白低于100ng/mL的患者被认为可能缺铁,并在10次血液透析治疗中接受1000mg静脉右旋糖酐铁治疗。铁蛋白和ZPP预测静脉右旋糖酐铁治疗反应的阳性预测值相似(分别为73%和83%;双侧,P = 0.48)。为确定检测的敏感性和特异性,在研究期结束时将患者分为两组:需要铁治疗的患者(n = 23)(接受静脉右旋糖酐铁治疗且血细胞比容增加5%或促红细胞生成素剂量降低≥2000U/次的患者)和不需要铁治疗的患者(n = 24)(接受静脉右旋糖酐铁治疗但无反应的患者[n = 9]或初始ZPP和铁蛋白水平不提示缺铁且在研究期内血细胞比容和促红细胞生成素剂量保持稳定的患者[n = 15])。(摘要截短至250字)