Anu K Devi, Pahuja Sangeeta, Sharma Geetika
Department of Immuno-Hematology and Blood Transfusion, Lady Hardinge Medical College and Associated Hospitals, New Delhi, India.
Asian J Transfus Sci. 2022 Jan-Jun;16(1):83-88. doi: 10.4103/ajts.ajts_138_20. Epub 2022 May 26.
The aim of pretransfusion testing (PTT) is to prevent the immune-mediated hemolytic reaction by the transfusion of incompatible donor red cells. The methods of PTT have evolved over the years and a new method of type and screen (T and S) was introduced, in which only ABO grouping, Rh typing, and antibody screening would be carried out with omission of routine Coombs crossmatch. Although T and S is an accepted method for PTT in developed countries, only a few studies in literature have evaluated its efficacy in India.
The aim of the study was to compare T and S method with conventional Coombs crossmatch method for PTT.
Two thousand and fifty samples were randomly selected from the samples received in blood bank for requisition of blood transfusion after taking informed consent. ABO blood grouping and Rh typing were performed for each recipient's sample. "T and S" and "Coombs crossmatch" were done simultaneously by two different persons without knowing the result of each test. A commercially available three cell panel was used for antibody screening, in which the recipient's plasma was reacted with red cells in the low ionic strength solution Coombs Gel card at 37°C by column agglutination technology.
Antibody screening was positive in 29 (1.41%) patients and negative in 2021 (98.59%) patients. Out of 29 patients, 27 had alloantibodies and 2 had autoantibody. Most common alloantibody found in our study was anti-D. Other antibodies found were anti-K, anti-C + D, anti-E, anti-C, anti-c, anti-Jk, and anti-Mi (a). Crossmatch on first attempt was compatible in 2028 (98.93%) patients and incompatible in 22 (1.07%) patients. Out of 29 patients who were positive for antibody screening, crossmatch was incompatible in nine patients. Crossmatch was compatible in twenty patients, who had positive antibody screen. However, crossmatch compatibility in these patients, reflect either absence of corresponding antigen or antigen present in low dose (heterozygous) in donor blood. On the other hand, out of 22 patients incompatible on first crossmatch, antibody screening was negative in 13 patients and was positive in only nine patients. Hence, 13 patients with antibody would have been missed by antibody screen alone. Kappa statistics was used to compare the efficacy of "type and screening" and "Coombs crossmatch." It showed κ =0.445 ( < 0.001) implying moderate agreement between the two variables of "T and S" and "Coombs crossmatch."
T and S is a scientifically better method but needs to be implemented with caution. We need to develop our own cell panels having adequate representation of indigenous antigen (including In, Mi (a), etc.,). Large-scale studies need to be done in India with indigenous screening cells to evaluate efficacy and safety of T and S method.
输血前检测(PTT)的目的是通过输注不相容供者红细胞来预防免疫介导的溶血反应。多年来,PTT的方法不断演变,一种新的血型鉴定和筛查(T和S)方法被引入,其中仅进行ABO血型分组、Rh血型鉴定和抗体筛查,省略了常规的抗人球蛋白交叉配血试验。尽管T和S方法在发达国家是一种被认可的PTT方法,但文献中仅有少数研究评估了其在印度的有效性。
本研究旨在比较T和S方法与传统抗人球蛋白交叉配血试验方法用于PTT的效果。
在获得知情同意后,从血库接收的输血申请样本中随机选取2050份样本。对每个受血者样本进行ABO血型分组和Rh血型鉴定。由两名不同的人员同时进行“T和S”及“抗人球蛋白交叉配血试验”,且彼此不知道对方的检测结果。使用市售的三细胞试剂板进行抗体筛查,在低离子强度溶液抗人球蛋白凝胶卡中,将受血者血浆与红细胞在37℃下通过柱凝集技术进行反应。
29例(1.41%)患者抗体筛查呈阳性,2021例(98.59%)患者呈阴性。在这29例患者中,27例有同种抗体,2例有自身抗体。本研究中发现的最常见同种抗体是抗-D。其他发现的抗体有抗-K、抗-C + D、抗-E、抗-C、抗-c、抗-Jk和抗-Mi(a)。首次交叉配血试验结果相合的患者有2028例(98.93%),不相合的有22例(1.07%)。在抗体筛查呈阳性的29例患者中,9例交叉配血不相合。20例抗体筛查呈阳性的患者交叉配血结果相合。然而,这些患者交叉配血结果相合,可能反映供者血液中不存在相应抗原或抗原呈低剂量(杂合子)存在。另一方面,在首次交叉配血不相合的22例患者中,13例患者抗体筛查呈阴性,仅9例呈阳性。因此,仅通过抗体筛查会漏诊13例有抗体的患者。使用Kappa统计量比较“血型鉴定和筛查”与“抗人球蛋白交叉配血试验”的有效性。结果显示κ =0.445(<0.001),这意味着“T和S”与“抗人球蛋白交叉配血试验”这两个变量之间存在中度一致性。
T和S方法在科学上是更好的方法,但需要谨慎实施。我们需要开发具有足够代表性的本土抗原(包括In、Mi(a)等)的细胞试剂板。需要在印度使用本土筛查细胞进行大规模研究,以评估T和S方法的有效性和安全性。