Jackson K W
Clin Chem. 1978 Dec;24(12):2135-8.
Each of 65 laboratories analyzed 10 whole-blood samples for erythrocyte protoporphyrin by one or more of several analytical procedures. These procedures were of two types: (a) extraction of protoporphyrin from the erythrocytes into ethyl acetate/acetic acid, re-extraction into hydrochloric acid, and fluorometric measurement; or (b) direct reading in a portable fluorometer (hematofluorometer), with no pretreatment of the blood sample. Interlaboratory correlation was generally poor, especially between laboratories using extraction procedures. Hematofluorometric results intercorrelated better, but they had a low bias as compared to the extraction approach. Nationwide standardization of the test is required to assure satisfactory interlaboratory performance and to identify laboratories whose results are sufficiently accurate to be used for interpretations according to guidelines set forth by the Center for Disease Control for erythrocyte protoporphyrin testing.
65个实验室分别通过几种分析方法中的一种或多种,对10份全血样本进行红细胞原卟啉分析。这些方法分为两类:(a) 从红细胞中提取原卟啉至乙酸乙酯/乙酸中,再提取至盐酸中,并进行荧光测定;或(b) 直接用便携式荧光计(血液荧光计)读取,血液样本无需预处理。实验室间的相关性普遍较差,尤其是采用提取方法的实验室之间。血液荧光计测量结果之间的相关性更好,但与提取方法相比,偏差较小。需要在全国范围内对该检测进行标准化,以确保实验室间的检测结果令人满意,并识别出其结果足够准确、可根据疾病控制中心制定的红细胞原卟啉检测指南用于解读的实验室。