Interfering heterophile antibodies as the cause of persistently falsely elevated high-sensitivity troponin I on Alinity i: a case report.

IF 1.8
Ivana Lapić, Dunja Rogić, Dragana Šegulja, Sandra Jakšić Jurinjak, Željka Vogrinc, Sanja Kačkov, Fran Smaić, Indira Imširović, Lovorka Đerek
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Abstract

Hereby we describe a case of a 59-year-old female patient with persistently elevated high-sensitivity troponin I (hs-TnI) over the course of almost four years measured on Alinity i with the corresponding assay (Abbott Laboratories, Chicago, USA). The patient underwent multiple extensive cardiological evaluations, but none of them suggested acute or chronic cardiac damage. Therefore, interference in measurement was suspected by the attending cardiologist and a detailed, stepwise laboratory investigation was undertaken in the sample with initial hs-TnI result of 2077 ng/L. Serial sample dilutions (1:2,1:5,1:10) did not match the expected, calculated hs-TnI concentrations, yielding both huge positive biases (62, 109 and 139%, respectively) and absolute differences (639, 453 and 290 ng/L, respectively). Precipitation with polyethylene-glycol, pretreatment in heterophilic blocking tubes (HBT) and immunoglobulin G depletion yielded hs-TnI results below the assay's diagnostic cut-off (< 15.6 ng/L). Alternate hs-TnI immunoassays (Siemens Healthineers, Beckman Coulter and Snibe) and measurement with the high-sensitivity troponin T (hs-TnT) assay yielded results below assays' specific cut-off values. This investigation confirmed that results of hs-TnI obtained by the Abbott assay were spuriously elevated. Significant lowering of hs-TnI after HBT pretreatment indicated that heterophile antibodies are the most probable source of interference. Based on this finding, it was entered in the patient's medical record that future determinations of cardiac troponin should be performed with an alternate hs-TnI or hs-TnT assay. This case emphasizes that analytical interferences are usually immunoassay-dependent. Evaluation of laboratory results in the clinical context and close collaboration between laboratory and clinical staff is crucial for their recognition.

干扰性嗜异性抗体引起Alinity上高敏感肌钙蛋白I持续错误升高1例
在此,我们描述了一例59岁女性患者,其高敏感性肌钙蛋白I (hs-TnI)持续升高近四年,使用相应的检测方法(雅培实验室,芝加哥,美国)测量Alinity I。患者接受了多次广泛的心脏学评估,但没有一次显示急性或慢性心脏损伤。因此,主治心脏病专家怀疑测量受到干扰,并对初始hs-TnI结果为2077 ng/L的样本进行了详细的逐步实验室调查。连续样品稀释(1:2,1:5,1:10)与预期的计算hs-TnI浓度不匹配,产生了巨大的正偏差(分别为62,109和139%)和绝对差异(分别为639,453和290 ng/L)。用聚乙二醇沉淀,在异亲性阻断管(HBT)中预处理和免疫球蛋白G消耗产生的hs-TnI结果低于该检测的诊断临界值(< 15.6 ng/L)。替代的hs-TnT免疫测定(Siemens Healthineers, Beckman Coulter和Snibe)和高灵敏度肌钙蛋白T (hs-TnT)测定的结果低于测定的特定临界值。这项调查证实,雅培法获得的hs-TnI的结果是虚假的升高。HBT预处理后hs-TnI显著降低,表明嗜异性抗体是最可能的干扰源。基于这一发现,在患者的医疗记录中记录了未来心肌肌钙蛋白的测定应与hs-TnI或hs-TnT交替进行。这种情况强调分析干扰通常依赖于免疫测定。在临床环境中对实验室结果的评估以及实验室和临床工作人员之间的密切合作对他们的认可至关重要。
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