Butler V P, Lindenbaum J
Am J Med. 1975 Apr;58(4):460-9. doi: 10.1016/0002-9343(75)90117-5.
Antibodies to digitalis glycosides have been elicited in experimental animals and have been utilized in the development of rapid, sensitive, specific and convenient radioimmunoassay methods for the clinical measurement of digoxin and other cardiac glycosides in man. The use of these assay methods has supplemented earlier studies with radiolabeled digitalis preparations and has made it possible to obtain much new information concerning factors which may contribute to the well known patient to patient variability in digitalis dosage requirements and in sensitivity to the toxic effects of cardiac glycosides. In some patients with a poor clinical response to digitalis, the finding of a serum concentration which is relatively low for the dose prescribed may suggest that true digitalis resistance is not present and may raise questions of poor patient compliance, tablet inadequacies, intestinal malabsorption, increased metabolic degradation or hyperthyroidism; if the cause of the low serum level cannot be identified or corrected, serial serum measurements should enable safe and rational upward adjustment of dosage. In some patients with digitalis toxicity, the finding of a serum level which is relativity high for the dose prescribed may suggest that the patient is not sensitive to digitalis but rather is excreting it slowly; in such instances in elderly patients (with decreased glomerular filtration rates) and in patients with renal disease, serial digitalis measurements are useful adjuncts to clinical observation in determining optimal digitalis dosage schedules. A knowledge of serum digitalis concentrations should enable us to develop sound principles for a more rational approach to the clinical administration of cardiac glycosides, especially in patients with unusually high dosage requirements or with unusual sensitivity to relatively small doses of digitalis.
在实验动物中已诱导出针对洋地黄苷的抗体,并已用于开发快速、灵敏、特异且便捷的放射免疫测定方法,用于临床测定人体中的地高辛和其他强心苷。这些测定方法的使用补充了早期用放射性标记洋地黄制剂进行的研究,并使得有可能获得许多新信息,这些信息涉及可能导致洋地黄剂量需求和对强心苷毒性作用敏感性在患者之间众所周知的个体差异的因素。在一些对洋地黄临床反应不佳的患者中,发现血清浓度相对于所开剂量较低,这可能表明不存在真正的洋地黄抵抗,并可能引发关于患者依从性差、片剂不足、肠道吸收不良、代谢降解增加或甲状腺功能亢进的问题;如果无法确定或纠正血清水平低的原因,连续血清测量应能安全合理地向上调整剂量。在一些洋地黄中毒的患者中,发现血清水平相对于所开剂量较高,这可能表明患者对洋地黄不敏感,而是排泄缓慢;在老年患者(肾小球滤过率降低)和肾病患者的此类情况下,连续洋地黄测量是确定最佳洋地黄给药方案时临床观察的有用辅助手段。了解血清洋地黄浓度应能使我们制定合理的原则,以更合理地临床应用强心苷,尤其是在剂量需求异常高或对相对小剂量洋地黄异常敏感的患者中。