Di Iorio B, Guastaferro P, Gironda A, Marano V, Morrongiello L, Cillo N, Zito B, Nigro F, Frieri A, Rubino R, Bellizzi V
U.O. di Nefrologia e Dialisi, Ospedale Civile di Ariano Irpino, ASL AV/1 (AV) - Dottorato di Ricerca in Scienze Nefrologiche, Seconda Universita' di Napoli, Napoli, Italy.
G Ital Nefrol. 2002 Sep-Oct;19(5):552-9.
Anemia is an important negative prognostic factor for dialysis patients, whose correction reduces hospitalisation and mortality. Besides, the presence of the thalassaemia minor (Thal-m) in haemodialysed patients causes erythropoietin resistance and more serious anemia. The goal of this study is the correction of anemia (Hb >11 g/dL) in haemodialysed Thal-m patients.
Multicentric, prospective and controlled 12-month study for the correction of anemia (up to values ranging from 11 to 12 g/dL) followed by a 12-month observation period. Ten Thal-m patients with inadequate anemia correction were studied after therapy with rHuEPO. Their age at the beginning of the study was 62.8+/-4 years while their dialytic age was 89+/-20 months.
During the study we observed no changes in dry weight (p=NS), no increase in interdialytic weight (p=NS), cardiac frequency (p=NS), serum albumin (p=NS), serum aluminium (p=NS), PTH (p=NS), URR (p=NS), flow FAV (p=NS), TSAT (p=NS) and ferritin (p=NS) (maintained at their optimal values by means of intravenous therapy with trivalent iron. The hypotensive therapy (1.6 drug/patient/year) required no modifications during the 24-month study. The rHuEPO dose varied from 200.3+/-94.3 to 286.6+/-116.2, 317.0+/-119.5, 446.9+/-142.3, and 407.0+/-130.5 U/kg/wk (p < 0.0001 vs. initial value) (from the start to the 3rd, 6th, 9th and 12th month, respectively). The dose was subsequently reduced to 385.2+/-119.7 U/kg/wk at 15 months (p < 0.0001 vs. initial value) and remained unchanged until the end of the study. Simultaneously, the Hb values at corresponding times were 9.2+/-0.9, 9.4+/-1.1, 10.2+/-1.4, 10.9+/-1.5, 11.2+/-1.4 and 11.0+/-1.4 (p=0.002 vs. initial value). The correction of anemia produced progressive reduction in cardiac mass from 141+/-12 to 120+/-10 and 110+/-8 g/mq at the beginning, 12th month and 24th month (p < 0.0001), respectively. During the study the hospitalisation time was 4.3+/-1.2 day/patient/year during the 3-month run-in period, 3.4+/-1.4 day/patient/year during the first year, and 3.1+/-1.1 day/patient/year during the second year (p=0.098).
In conclusion we can say that the question of Thal-m in dialysis patients cannot be ignored or underestimated. The rHuEPO dosage in these patients must be reassessed (a dose of 450 U/kg/wk corresponding to approximately 60,000 units/week is acceptable and does not produce an increase in side effects if the correction is done gradually); moreover, other factors responsible for EPO-resistance must be eliminated (hyperthyroidism, aluminium intoxication, iron overloaded or deficiency).
贫血是透析患者重要的不良预后因素,纠正贫血可降低住院率和死亡率。此外,血液透析患者中存在的轻型地中海贫血(Thal - m)会导致促红细胞生成素抵抗及更严重的贫血。本研究的目的是纠正血液透析的Thal - m患者的贫血(血红蛋白>11 g/dL)。
一项多中心、前瞻性、对照的12个月研究,旨在纠正贫血(血红蛋白值达到11至12 g/dL),随后进行12个月的观察期。对10例贫血纠正不足的Thal - m患者在接受重组人促红细胞生成素(rHuEPO)治疗后进行研究。研究开始时他们的年龄为62.8±4岁,透析龄为89±20个月。
在研究期间,我们观察到干体重无变化(p =无显著性差异),透析间期体重无增加(p =无显著性差异),心率(p =无显著性差异)、血清白蛋白(p =无显著性差异)、血清铝(p =无显著性差异)、甲状旁腺激素(p =无显著性差异)、尿素清除率(p =无显著性差异)、血流平均动脉压(p =无显著性差异)、转铁蛋白饱和度(p =无显著性差异)和铁蛋白(p =无显著性差异)(通过三价铁静脉治疗维持在最佳值)。在24个月的研究期间,降压治疗(1.6种药物/患者/年)无需调整。rHuEPO剂量从200.3±94.3变化至286.6±116.2、317.0±119.5、446.9±142.3和407.0±130.5 U/kg/周(与初始值相比,p < 0.0001)(分别从开始到第3、6、9和12个月)。随后在15个月时剂量降至385.2±119.7 U/kg/周(与初始值相比,p < 0.0001),并在研究结束前保持不变。同时,相应时间的血红蛋白值分别为9.2±0.9、9.4±1.1、10.2±1.4、10.9±1.5、11.2±1.4和11.0±1.4(与初始值相比,p = 0.002)。贫血的纠正使心脏质量从开始时的141±12逐渐降至第12个月时的120±10和第24个月时的110±8 g/m²(p < 0.0001)。在研究期间,3个月导入期的住院时间为4.3±1.2天/患者/年,第一年为3.4±1.4天/患者/年,第二年为3.1±1.1天/患者/年(p = 0.098)。
总之,我们可以说透析患者中Thal - m的问题不能被忽视或低估。这些患者的rHuEPO剂量必须重新评估(如果逐渐进行纠正,450 U/kg/周的剂量相当于约60,000单位/周是可接受的,且不会增加副作用);此外,必须消除其他导致促红细胞生成素抵抗的因素(甲状腺功能亢进、铝中毒、铁过载或缺乏)。