PATHFAST NT-proBNP(氨基末端 pro B 型利钠肽):一种新的即时检测分析方法的多中心评估。
PATHFAST NT-proBNP (N-terminal-pro B type natriuretic peptide): a multicenter evaluation of a new point-of-care assay.
机构信息
Department of Laboratory Medicine, University-Hospital, Padova, Italy.
出版信息
Clin Chem Lab Med. 2010 Jul;48(7):1029-34. doi: 10.1515/CCLM.2010.222.
BACKGROUND
The biochemical determination of cardiac natriuretic peptides, primarily brain natriuretic peptide (BNP) and the amino-terminal fragment of its pro-hormone proBNP (NT-proBNP), are reliable tools for diagnosing cardiac disease, establishing prognosis and evaluating the effectiveness of treatment. These biomarkers have proven to be of particular value in the management of chronic and acute heart failure patients, and in the outpatient and the emergency setting.
METHODS
A multicenter evaluation was performed to assess the practicability, and the analytical and clinical performance of a new point-of-care testing (POCT) PATHFAST NT-proBNP assay. This is an immunochemiluminescent assay using two polyclonal antibodies in a sandwich test format, and performed with a PATHFAST automated analyzer.
RESULTS
The limit of detection (mean+3 SD of the signal of 20 replicates of the zero calibrator obtained in one run) was 0.535 ng/L. An imprecision study, performed in accordance with the CLSI protocol, showed coefficients of variation of 4.0%-6.4% (within-run imprecision), 0.0%-3.4% (between-run imprecision), 5.5%-7.2% (between-day imprecision), 7.6%-8.9% (total imprecision). The method was linear to 28,755 ng/L. Slopes and intercepts ranged from 0.89 to 0.90 and from 10.96 to 22.85, respectively when lithium-heparin plasma samples (n=100) were used to compare the assay under evaluation with the routine laboratory methods (Dimension RxL, Stratus CS). When testing matched samples (n=52), a significant difference was found between the 50th percentile NT-proBNP concentration in K(2)EDTA whole blood, K(2)EDTA plasma, lithium-heparin plasma and serum. No significant interference was observed for NT-proBNP in lipemic (tryglicerides up to 28.54 mmol/L), icteric (total and conjugated bilirubin up to 513 and 13 micromol/L, respectively) or hemolyzed (hemoglobin up to 13.50 g/L) samples. The NT-proBNP concentration in a group of 180 healthy donors was significantly influenced by age and gender. In a selected population of patients (n=56) with acute dyspnea admitted to the emergency department, a marked reduction in cardiac natriuretic peptide concentrations was observed in hospitalized patients suffering from heart failure who had a better prognosis compared with those with a poorer prognosis (NT-proBNP mean Delta change, % from -22 to -71 vs. +9 to -11).
CONCLUSIONS
The satisfactory analytical and clinical performance of the PATHFAST NT-proBNP assay, together with its excellent practicability, suggests that it would be a reliable tool in clinical practice, in the emergency setting for point-of-care testing, as well as in the central laboratory.
背景
心脏利钠肽的生化测定,主要是脑利钠肽(BNP)和其前体激素 proBNP 的氨基末端片段(NT-proBNP),是诊断心脏疾病、确定预后和评估治疗效果的可靠工具。这些生物标志物在慢性和急性心力衰竭患者的管理、门诊和急诊环境中已被证明具有特别的价值。
方法
进行了一项多中心评估,以评估新的即时检验(POCT)PATHFAST NT-proBNP 检测的实用性以及分析和临床性能。这是一种使用两种多克隆抗体的免疫化学发光检测,采用 PATHFAST 自动化分析仪进行。
结果
检测限(在一个运行中获得的 20 个零校准品的信号的 3 SD 平均值)为 0.535ng/L。根据 CLSI 方案进行的不精密度研究显示,批内不精密度为 4.0%-6.4%,批间不精密度为 0.0%-3.4%,日间不精密度为 5.5%-7.2%,总不精密度为 7.6%-8.9%。方法的线性范围为 28755ng/L。当使用锂肝素血浆样本(n=100)与常规实验室方法(Dimension RxL,Stratus CS)比较评估中的检测方法时,斜率和截距分别为 0.89 至 0.90 和 10.96 至 22.85。当测试匹配样本(n=52)时,在 K2EDTA 全血、K2EDTA 血浆、锂肝素血浆和血清中的第 50 百分位 NT-proBNP 浓度之间发现了显著差异。在脂血(甘油三酯高达 28.54mmol/L)、黄疸(总胆红素和结合胆红素分别高达 513 和 13 微摩尔/L)或溶血(血红蛋白高达 13.50g/L)样本中,NT-proBNP 未观察到明显干扰。在 180 名健康供体的一组中,NT-proBNP 浓度显著受年龄和性别影响。在一组 56 名因急性呼吸困难而入住急诊科的急性呼吸困难患者中,与预后较差的患者相比,住院心力衰竭患者的心脏利钠肽浓度明显降低(NT-proBNP 平均变化百分比,从-22 到-71 与+9 到-11)。
结论
PATHFAST NT-proBNP 检测的分析和临床性能令人满意,加上其出色的实用性,表明它将是临床实践中的一种可靠工具,在急诊环境中的即时检验以及中心实验室中也是如此。