Hurley J C
Division of Infectious Diseases, Children's Hospital & Medical Center, Seattle, Washington 98105-0371.
J Clin Microbiol. 1994 Sep;32(9):2120-7. doi: 10.1128/jcm.32.9.2120-2127.1994.
The Limulus amebocyte lysate (LAL) assay is a sensitive method for detecting endotoxin. Using gram-negative (GN) bacteremia as the basis for comparison, concordance with endotoxemia in 45 studies could be expressed as an odds ratio. Calculation of summary odds ratios by the Mantel-Haenszel-Peto method indicated that the concordance of the results was no higher by the chromogenic LAL assay than by the gelation version, and the sensitivity was improved by only 11% (62 versus 51%). Endotoxemia was detected in 77 (68%) of 114 patients with bacteremia caused by an organism that was not a member of the family Enterobacteriaceae, whereas endotoxemia was detected in only 120 (45%) of 269 patients with bacteremia caused by a member of the family Enterobacteriaceae or an anaerobe (P < 0.001). This difference was also apparent for patients with GN bacteremia for whom a fatal outcome had been recorded. The prevalence of GN bacteremia in the tested population and the type of etiological agent are critical and previously unrecognized variables which affect the interpretation of the LAL test in patients with suspected sepsis.
鲎试剂检测法是一种检测内毒素的灵敏方法。以革兰氏阴性菌血症作为比较基础,45项研究中鲎试剂检测法与内毒素血症的一致性可用比值比来表示。采用Mantel-Haenszel-Peto法计算汇总比值比表明,显色鲎试剂检测法与凝胶法相比,结果的一致性并无更高,且灵敏度仅提高了11%(分别为62%和51%)。在114例由非肠杆菌科细菌引起菌血症的患者中,77例(68%)检测到内毒素血症,而在269例由肠杆菌科细菌或厌氧菌引起菌血症的患者中,仅120例(45%)检测到内毒素血症(P<0.001)。对于记录有致命结局的革兰氏阴性菌血症患者,这种差异也很明显。受试人群中革兰氏阴性菌血症的患病率以及病原体类型是影响疑似脓毒症患者鲎试剂检测结果解读的关键且此前未被认识到的变量。