Jiang F, Wilhite T R, Smith C H, Landt M
Department of Pediatrics, Washington University School of Medicine, St. Louis Children's Hospital, MO 63110, USA.
Ther Drug Monit. 1995 Apr;17(2):184-8. doi: 10.1097/00007691-199504000-00014.
We have evaluated the new Roche digoxin "On Line" procedure for use in a pediatric population with particular interest in the potential for interference by digoxin-like immunoreactive factor (DLIF). An initial study comparing digoxin values obtained with the new Roche procedure with determinations on an Abbott TDx, American Dade Stratus, and COBAS-FARA using Microgenics Cedia reagents, found good correlations with these established methods. The Roche method was suitably precise and utilized either serum or plasma. Interference by DLIF was assessed by analyzing specimens from patients not receiving digoxin but likely to contain DLIF, with the argument that non-zero values represent cross-reactivity of anti-digoxin antibodies with DLIF endogenous to these specimens. When specimens from neonates, women with second/third trimester pregnancies, and patients with renal and liver failure were assayed with the Roche, Stratus, and TDx methods, all three methods measured DLIF in some specimens, but the Roche method possessed the lowest overall DLIF interference. The modest extent of DLIF interference and the requirement of a small amount of specimen make the Roche method superior in monitoring digoxin in a pediatric population.
我们评估了罗氏新型地高辛“在线”检测方法在儿科人群中的应用,特别关注地高辛样免疫反应因子(DLIF)的干扰可能性。最初的一项研究将罗氏新方法测得的地高辛值与使用Microgenics Cedia试剂在雅培TDx、美国达德Stratus和COBAS-FARA上的测定值进行了比较,发现与这些既定方法具有良好的相关性。罗氏方法具有适当的精密度,可使用血清或血浆。通过分析未接受地高辛但可能含有DLIF的患者的样本,评估了DLIF的干扰情况,理由是非零值代表抗地高辛抗体与这些样本内源性DLIF的交叉反应。当使用罗氏、Stratus和TDx方法检测新生儿、妊娠中晚期妇女以及肾衰竭和肝衰竭患者的样本时,所有三种方法在一些样本中均检测到了DLIF,但罗氏方法总体上对DLIF的干扰最低。DLIF干扰程度适中且所需样本量少,使得罗氏方法在监测儿科人群地高辛方面更具优势。