Gelfand Erwin W, Hanna Kim
National Jewish Medical and Research Center, Denver, Colorado 80206, USA.
J Clin Immunol. 2006 May;26(3):284-90. doi: 10.1007/s10875-006-9014-6. Epub 2006 May 31.
The incidence and severity of infusion-related adverse events (AEs) after infusions of IGIV-C, 10%, (Gamunex) at 0.14 mL/kg/min versus 0.08 mL/kg/min (standard rate) were compared. Patients with confirmed PID received two infusions 3-4 weeks apart with IGIV-C, 10% 400-600 mg/kg. Patients received their first infusion at 0.08 or 0.14 mL/kg/min and their second infusion 3-4 weeks later at the alternate rate, at an established step-wise rate increase. Ninety-seven of 100 patients remained valid for safety assessment. There were three infusion-related reactions at the standard rate and five at the increased rate. The incidence of all reported AEs was similar for both rates. Despite the time required for step-wise increases in infusion rate, the increased rate resulted in a shortened overall infusion time. Increasing the rate of infusion of IGIV-C, 10% by 75% up to 0.14 mL/kg/min (840 mg/kg/h) was well tolerated, suggesting safe administration of IGIV-C, 10% at this rate.
比较了以0.14 mL/kg/分钟与0.08 mL/kg/分钟(标准速率)输注10%的静脉注射免疫球蛋白(IGIV-C,商品名Gamunex)后与输注相关的不良事件(AE)的发生率和严重程度。确诊为原发性免疫缺陷病(PID)的患者每隔3 - 4周接受两次10%的IGIV-C输注,剂量为400 - 600 mg/kg。患者第一次输注时速率为0.08或0.14 mL/kg/分钟,3 - 4周后第二次输注时采用交替速率,并按既定的逐步增加速率进行。100名患者中有97名仍可进行安全性评估。标准速率下有3例与输注相关的反应,增加速率下有5例。两种速率下所有报告的不良事件发生率相似。尽管输注速率逐步增加需要时间,但增加速率导致总体输注时间缩短。将10%的IGIV-C输注速率提高75%至0.14 mL/kg/分钟(840 mg/kg/小时)耐受性良好,表明以该速率安全给予10%的IGIV-C。