Gong A K
Department of Pediatrics, University of Texas Health Science Center, San Antonio 78284-7812.
Crit Care Med. 1995 Jan;23(1):193-201. doi: 10.1097/00003246-199501000-00030.
a) To evaluate the performance of a compact, new instrument that uses disposable cuvettes to measure total hemoglobin concentration, oxygen content, and the relative concentrations of oxy- and methemoglobin in 50-microL blood samples; b) to determine whether the instrument can be used for near-patient assessment of methemoglobinemia; and c) to ascertain whether problems commonly encountered in neonatal blood samples affect the instrument's performance.
Prospective study, in which the test instrument was compared with a standard method. Samples of whole blood with and without bilirubin, fetal hemoglobin, and hemolysis were analyzed on the new (test) instrument and on a widely used cooximeter (OSM3 hemoximeter, Radiometer; reference instrument).
In vitro analyses of blood samples in clinical and university laboratories.
There was a close linear correlation between the methomoglobin measurements of the test instrument and those measurements of the reference instrument (slope = 0.989; r2 = .989). The average difference in mean assay values between the reference instrument and the test instrument was -0.59%, i.e., < 1% methemoglobin. Repeated measurements indicated the precision was 0.5% methemoglobin. Complete hemolysis of the sample reduced the methemoglobin reading by only 0.40%. Adding bilirubin (10 to 11 mg/dL [171 to 188.1 mumol/L]), increased the methemoglobin reading by 0.23%, increased the oxyhemoglobin reading by 0.45%, and increased total hemoglobin by 0.21 g/dL. Fetal hemoglobin also had minimal effects on the readings.
The test instrument is fast and easy to operate. No sample preparation or pipetting is required. To operate the instrument, the user simply connects a syringe containing the blood sample to one of the disposable cuvettes, injects 50 microL of blood into the cuvette, and inserts the cuvette into the instrument. The test instrument automatically detects the presence of the cuvette, analyzes the sample, and displays the results in < 10 secs. The findings in this study indicate that the test instrument has sufficient accuracy for near-patient testing in intensive care units. The errors introduced by hemolysis, fetal hemoglobin, and bilirubin were too small to be of clinical importance. Thus, the test instrument is essentially unaffected by complications commonly encountered in neonatal blood. The capacity of the test instrument to measure methemoglobin makes it particularly useful if inhaled nitric oxide therapy becomes a standard clinical practice.
a)评估一种新型紧凑型仪器的性能,该仪器使用一次性比色皿测量50微升血样中的总血红蛋白浓度、氧含量以及氧合血红蛋白和高铁血红蛋白的相对浓度;b)确定该仪器是否可用于对高铁血红蛋白血症进行床旁评估;c)确定新生儿血样中常见的问题是否会影响该仪器的性能。
前瞻性研究,将测试仪器与标准方法进行比较。对含有和不含胆红素、胎儿血红蛋白及溶血的全血样本,在新型(测试)仪器和广泛使用的血氧计(OSM3血氧计,Radiometer;参考仪器)上进行分析。
临床和大学实验室对血样进行体外分析。
测试仪器的高铁血红蛋白测量值与参考仪器的测量值之间存在密切的线性相关性(斜率 = 0.989;r2 = 0.989)。参考仪器与测试仪器的平均测定值平均差异为 -0.59%,即高铁血红蛋白 < 1%。重复测量表明精密度为高铁血红蛋白0.5%。样本完全溶血仅使高铁血红蛋白读数降低0.40%。添加胆红素(10至11mg/dL [171至188.1μmol/L])使高铁血红蛋白读数增加0.23%,使氧合血红蛋白读数增加0.45%,使总血红蛋白增加0.21g/dL。胎儿血红蛋白对读数的影响也极小。
测试仪器操作快速简便。无需样本制备或移液。要操作该仪器,用户只需将装有血样的注射器连接到一个一次性比色皿上,将50微升血液注入比色皿,然后将比色皿插入仪器。测试仪器会自动检测比色皿的存在,分析样本,并在不到10秒内显示结果。本研究结果表明,测试仪器在重症监护病房进行床旁检测具有足够的准确性。溶血、胎儿血红蛋白和胆红素所引入的误差过小,无临床意义。因此,测试仪器基本不受新生儿血样中常见并发症的影响。如果吸入一氧化氮治疗成为标准临床实践,测试仪器测量高铁血红蛋白的能力使其特别有用。