Laws H J, Göbel U, Christaras A, Janssen G
Department of Pediatric Oncology, Hematology and Immunology, Heinrich-Heine University Medical Center Düsseldorf.
Klin Padiatr. 2005 May-Jun;217(3):120-5. doi: 10.1055/s-2005-836506.
With the introduction of "hypertransfusion" regimens the extent of disease- and therapy-related hemosiderosis has become the survival limiting factor for patients with beta-thalassemia major as iron transferred with transfusions cannot be excreted by physiological means. Subsequent introduction of deferoxamine therapy for iron elimination and prophylaxis of hemosiderosis has improved prognosis and life quality of these patients considerably. We report our experience with seven adolescent patients with beta-thalassemia and ineffective subcutaneous therapy and severe hemosiderosis-related organ complications. For that reason they received i. v. intensified chelate therapy. The patients were given 70 to 120 mg/kg DFO 7 days a week continuously via a Port-a-cath or Hickman central venous line. Under high-dose i. v. DFO therapy, serum ferritin levels significantly decreased in all patients. Target serum ferritin levels of 3 000 ng/ml were reached after 12 to 20 months of treatment. In 3 of the 5 patients that were treated for longer than 43 months serum ferritin levels even dropped below 2 000 ng/ml. Serum ferritin levels also correlated well with SQUID examinations. Therefore, monitoring of serum ferritin may be useful to monitor patient's compliance and control intensified DFO therapy. Continuous administration of the intensified DFO therapy induced normalization of liver function and left ventricular cardiac function in all patients who are still alive. Two patients died due to cardiac decompensation. In five patients 19 episodes of central catheter-related infections were observed (1.5 infections per 1 000 catheter days). No DFO-associated allergic reactions nor irreversible organ dysfunction were observed. Our results indicate that intensified i. v. DFO therapy is an effective and safe method for treatment of severe organ dysfunction in patients with thalassemia major. The most severe problems are catheter-related infections and inconsistent long-term compliance.
随着“大量输血”方案的引入,与疾病和治疗相关的铁过载程度已成为重型β地中海贫血患者的生存限制因素,因为输血所输入的铁无法通过生理途径排出。随后引入的去铁胺疗法用于铁清除和预防铁过载,显著改善了这些患者的预后和生活质量。我们报告了7例青少年β地中海贫血患者皮下治疗无效且伴有严重铁过载相关器官并发症的治疗经验。因此,他们接受了静脉强化螯合治疗。通过植入式静脉输液港或希克曼中心静脉导管,每周7天持续给予患者70至120mg/kg的去铁胺。在高剂量静脉去铁胺治疗下,所有患者的血清铁蛋白水平均显著下降。治疗12至20个月后,血清铁蛋白水平达到了3000ng/ml的目标值。在5例治疗时间超过43个月的患者中,有3例血清铁蛋白水平甚至降至2000ng/ml以下。血清铁蛋白水平与超导量子干涉仪检查结果也具有良好的相关性。因此,监测血清铁蛋白可能有助于监测患者的依从性并控制强化去铁胺治疗。持续给予强化去铁胺治疗使所有存活患者的肝功能和左心室心功能恢复正常。2例患者因心脏代偿失调死亡。在5例患者中观察到19次中心导管相关感染(每1000导管日1.5次感染)。未观察到与去铁胺相关的过敏反应或不可逆器官功能障碍。我们的结果表明,强化静脉去铁胺治疗是治疗重型地中海贫血患者严重器官功能障碍的一种有效且安全的方法。最严重的问题是导管相关感染和长期依从性不一致。