Mintz P D, Haines A L, Sullivan M F
Transfusion. 1982 Mar-Apr;22(2):107-10. doi: 10.1046/j.1537-2995.1982.22282177114.x.
In order to determine the frequency and cause of an incompatible crossmatch found in specimens for which the antibody detection test was nonreactive, 261, 136 crossmatches performed on 116,278 patient samples from approximately 46,000 different patients were reviewed. One-hundred and one patients were identified whose sera were incompatible in at least one crossmatch following a nonreactive antibody detection test. The cause of the incompatibility was determined in 69 of these. Incompatibility was detected only after 37 degrees C incubation and/or after the antiglobulin phase in 36 (52%). Incompatibility was detected after an immediate-spin and/or incubation at room temperature in 33 (48%). Serologic evaluation did not identify the cause of the incompatibility in 16 of the 101 patients. In eight of these 16 the incompatibility was noted only after 37 degrees C incubation and/or after the antiglobulin phase. Detailed serologic evaluation was not performed on 16 of the 101 patients (all of whose sera were incompatible with only 1 donor unit). In 12 of these 16, the incompatibility was detected only after the antiglobulin phase.
为了确定在抗体检测试验呈阴性的标本中发现的交叉配血不相容的频率和原因,我们回顾了对来自约46,000名不同患者的116,278份患者样本进行的261,136次交叉配血。在抗体检测试验呈阴性后,有101名患者的血清在至少一次交叉配血中不相容。其中69名患者的不相容原因已确定。36例(52%)仅在37℃孵育和/或抗球蛋白试验阶段后检测到不相容。33例(48%)在立即离心和/或室温孵育后检测到不相容。血清学评估未能确定101例患者中16例的不相容原因。在这16例中的8例中,仅在37℃孵育和/或抗球蛋白试验阶段后才发现不相容。101例患者中有16例(其所有血清仅与1个供体单位不相容)未进行详细的血清学评估。在这16例中的12例中,仅在抗球蛋白试验阶段后检测到不相容。