Chen K S, Leu M L, Huang C C
Department of Internal Medicine, Chang Gung Memorial Hospital, Taipei, Taiwan, R.O.C.
Changgeng Yi Xue Za Zhi. 1995 Sep;18(3):248-53.
Six chronic hemodialysis patients suffering from iron overload (serum ferritin ranged between 2053-15704 mu g/L) were treated with human recombinant erythropoietin (EPO) alone for eighteen months. An initial rapid decrease of serum ferritin was observed in all six patients when the loading dose of EPO was given. Three patients (Cases 4, 5, 6) who suffered from chronic blood loss maintained a continuous decline of serum ferritin in the subsequent stage of maintenance dose EPO therapy, however, the decrease of serum ferritin became sluggish under a maintenance dose in the other three patients (Cases 1, 2 and 3). The serum ferritin eventually decreased to a satisfactory level (975-1761 mu g/L) in Cases 4, 5 and 6, whereas it remained high (4232-8196 mu g/L) in Cases 1, 2, and 3 who had higher basal levels of serum ferritin (5641-15704 mu g/L) and a plateau of response under a maintenance dose of EPO. These three patients were then treated with EPO and phlebotomy. Their serum ferritin decreased quickly from 6752 +/- 1264 mu g/L to 2454 +/- 482 mu g/L after six months of phlebotomy therapy; it was a dramatic improvement in contrast to the stagnant response under a maintenance dose of EPO alone. Our experience indicates that EPO therapy alone has its limitations in treating severe iron overload. Although there is an initial rapid decrease of serum ferritin during the period of the loading dose, the response might become stagnant during the period of maintenance dose. Phlebotomy effectively eliminated the excessive iron stores in these refractory cases. Therefore, we suggest that phlebotomy be considered in severe iron overload if a stagnant response is observed under a maintenance dose EPO therapy.
六名患有铁过载(血清铁蛋白范围在2053 - 15704μg/L之间)的慢性血液透析患者单独接受重组人促红细胞生成素(EPO)治疗18个月。在给予EPO负荷剂量时,所有六名患者均观察到血清铁蛋白最初迅速下降。三名患有慢性失血的患者(病例4、5、6)在维持剂量EPO治疗的后续阶段血清铁蛋白持续下降,然而,其他三名患者(病例1、2和3)在维持剂量下血清铁蛋白下降变得缓慢。病例4、5和6的血清铁蛋白最终降至满意水平(975 - 1761μg/L),而病例1、2和3的血清铁蛋白仍居高不下(4232 - 8196μg/L),他们的血清铁蛋白基础水平较高(5641 - 15704μg/L),且在EPO维持剂量下反应呈平台期。然后对这三名患者进行EPO和放血治疗。放血治疗六个月后,他们的血清铁蛋白从6752±1264μg/L迅速降至2454±482μg/L;与单独使用EPO维持剂量时的停滞反应相比,这是一个显著的改善。我们的经验表明,单独使用EPO治疗严重铁过载有其局限性。尽管在负荷剂量期间血清铁蛋白最初迅速下降,但在维持剂量期间反应可能会停滞。放血有效地消除了这些难治性病例中过多的铁储存。因此,我们建议,如果在EPO维持剂量治疗下观察到反应停滞,对于严重铁过载应考虑放血治疗。