Rand Royden N
Department of Pathology, University of Pennsylvania, and William Pepper Laboratory, Hospital of the University of Pennsylvania, Philadelphia, Pa. 19104.
J Res Natl Bur Stand A Phys Chem. 1972 Sep-Oct;76A(5):499-508. doi: 10.6028/jres.076A.044.
It is obvious that erroneous data reported to a physician may adversely affect patient welfare. Currently, acceptable limits of accuracy and precision are poorly defined. It should be recognized, however, that the spectrophotometric measurement step in an appropriate analytical procedure is critical and inapparent error may occur. Spectrophotometric measurements, both manual and automated, are extensively used in the clinical chemistry laboratory. At least 1,000,000 such measurements per day on rather diverse equipment are made in this country; yet, few standards exist. Results of intra-lab surveys suggests that performance could be improved. The various ways in which spectrophotometry is used will be illustrated and a discussion of possible errors resulting from nonstandardized instrumentation will follow. There is pressing need for well defined and easily usable standards for wavelength, photometric accuracy, photometric linearity, stray light, as well as NBS specifications for optical cuvettes.
显然,向医生报告的错误数据可能会对患者的健康产生不利影响。目前,准确度和精密度的可接受限度定义不明确。然而,应该认识到,在适当的分析程序中,分光光度测量步骤至关重要,可能会出现不明显的误差。分光光度测量,无论是手动还是自动的,在临床化学实验室中都被广泛使用。在这个国家,每天在相当多样的设备上进行至少100万次这样的测量;然而,几乎没有相关标准。实验室内部调查结果表明,测量性能有待提高。将说明分光光度法的各种使用方式,并讨论因仪器未标准化而可能产生的误差。迫切需要为波长、光度准确度、光度线性、杂散光以及光学比色皿的国家标准局规范制定明确且易于使用的标准。