Weisbach V, Skoda P, Rippel R, Lauer G, Glaser A, Zingsem J, Zimmermann R, Eckstein R
Department of Transfusion Medicine and Hemostaseology, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen, Germany.
Transfusion. 1999 May;39(5):465-72. doi: 10.1046/j.1537-2995.1999.39050465.x.
This study was performed to evaluate the capacity of oral and intravenous (i.v.) iron administration during autologous blood donation (ABD) to improve the efficacy of ABD and to prevent the need for allogeneic blood transfusion in patients without iron deficiency who are undergoing major elective surgery for which a minimum of 3 autologous units have been ordered.
One hundred twenty-three patients were enrolled in an open-labeled, randomized, controlled trial and assigned to three treatment groups: patients in Group 1 received 3 x 100 mg of Fe2+ per day given orally for 5 weeks before operation; patients in Group 2 received 200 mg of Fe3+ given intravenously after each donation combined with initial i.v. iron supplementation in patients with hemoglobin under 15 g per dL; and patients in Group 3 were in the control group that received no iron medication. A modest ABD program involving weekly phlebotomy and threshold hemoglobin values for donation of 11.5 g per dL in women and 12.0 g per dL in men was performed.
Ninety patients, 15 women and 15 men in each of the three groups, completed the study. The mean net red cell production during ABD was no higher (p>0.2) in the iron-treated groups (Group 1: 473 +/- 178 mL; Group 2: 436 +/- 170 mL; Group 3 (controls): 397 +/- 174 mL). The mean number of autologous units donated per patient did not differ (p>0.7) among the groups (Group 1: 3.1 +/- 0.6; Group 2: 2.9 +/- 0.7; Group 3: 3.0 +/- 0.7). The proportion of patients who needed allogeneic blood transfusion showed no significant (p>0.4) advantage for iron treatment, (Group 1: 7%; Group 2: 20%; Group 3: 10%).
In non-iron-deficient patients undergoing modest ABD without erythropoietin therapy, neither oral nor i.v. application of iron during the preoperative period enhances the success of preoperative ABD.
本研究旨在评估在自体献血(ABD)期间口服和静脉注射铁剂,以提高ABD的疗效,并防止在没有缺铁的患者中进行至少3个自体单位预定的大型择期手术时需要异体输血。
123例患者参加了一项开放标签、随机、对照试验,并被分配到三个治疗组:第1组患者在术前5周每天口服3×100mg Fe2+;第2组患者每次献血后静脉注射200mg Fe3+,并对血红蛋白低于15g/dL的患者进行初始静脉补铁;第3组患者为对照组,不接受铁剂治疗。实施了一个适度的ABD计划,包括每周采血,女性献血的血红蛋白阈值为11.5g/dL,男性为12.0g/dL。
90例患者完成了研究,三个组各有15名女性和15名男性。在铁剂治疗组中,ABD期间的平均净红细胞生成量没有更高(p>0.2)(第1组:473±178mL;第2组:436±170mL;第3组(对照组):397±174mL)。各组患者每人捐献的自体单位平均数没有差异(p>0.7)(第1组:3.1±0.6;第2组:2.9±0.7;第3组:3.0±0.7)。需要异体输血的患者比例在铁剂治疗方面没有显著优势(p>0.4)(第1组:7%;第2组:20%;第3组:10%)。
在没有促红细胞生成素治疗的情况下进行适度ABD的非缺铁患者中,术前口服或静脉应用铁剂均不能提高术前ABD的成功率。