Neanaey Wafaa A, Deghady Akram A, Nafea Dalia A, Fahmy Nada M, Gouda Asmaa M
Clinical Pathology Department, Alexandria University, Alexandria, Egypt.
Internal Medicine Department, Hematology Unit, Alexandria University, Alexandria, Egypt.
Oman Med J. 2022 Jul 31;37(4):e402. doi: 10.5001/omj.2022.81. eCollection 2022 Jul.
Platelet refractoriness complicates the platelet transfusion, which is essential for managing thrombocytopenia in patients with hematological disorders. It is associated with adverse clinical outcomes and increased health care costs. We conducted a prospective study to determine the effectiveness of cross-matched compatible platelets in a group of patients refractory to platelets from random donors and to evaluate human leukocyte antigen (HLA)-mediated refractoriness.
This prospective study was conducted on 40 patients with different hematological disorders requiring platelet transfusions who were refractory to random platelets and presented to the hematology unit of Alexandria's main university hospitals between May 2020 and March 2021. They received 60 ABO-compatible platelet transfusions, either leuco-reduced or random donor platelets, stored for no more than 72 hours. A solid-phase red cell adherence technique (SPRCA) was used for platelet crossmatching. The corrected count increment (CCI) was used to monitor the effectiveness of each platelet transfusion with a cut-off value of 5 × 10/µL at 1 hour and 2.5 × 10/µL at 24 hours. Anti-HLA antibodies were assessed using the enzyme-linked immunosorbent assay technique.
Out of 60 cross matches, 47 (78.3%) were compatible, and 13 (21.7%) were incompatible. Among 47 compatible results, 30 (63.8%) showed adequate CCI and 17 (36.2%) showed inadequate CCI at 1-hour post-transfusion. Among the incompatible results, 3 (23.1%) had adequate CCI and 10 (76.9%) had inadequate CCI. Significant improvements were found in the mean CCI when comparing cross-matched compatible platelets and incompatible platelets at 1hour or 24 hours (0.009 and < 0.001, respectively). From the 40 studied patients, HLA alloimmunization was present in 18 patients (45.0%) and absent in the remaining 22 patients (55.0%). In the absence of HLA alloimmunization, patients showed significantly better responses at 1 hour and 24 hours (0.001 and 0.015, respectively). There was better sensitivity of platelet crossmatching with random donor platelet concentrates than single donor platelet concentrates.
Platelet crossmatching using SPRCA and HLA screening are effective and rapid tools for better management of patients' refractory to platelet transfusions.
血小板输注无效使血小板输注变得复杂,而血小板输注对于治疗血液系统疾病患者的血小板减少至关重要。它与不良临床结局及医疗费用增加相关。我们进行了一项前瞻性研究,以确定交叉配型相合的血小板在一组对随机供者血小板无效的患者中的有效性,并评估人类白细胞抗原(HLA)介导的输注无效情况。
这项前瞻性研究针对2020年5月至2021年3月期间在亚历山大主要大学医院血液科就诊的40例需要血小板输注且对随机血小板无效的不同血液系统疾病患者。他们接受了60次ABO相合的血小板输注,要么是白细胞滤除血小板,要么是随机供者血小板,储存时间不超过72小时。采用固相红细胞黏附技术(SPRCA)进行血小板交叉配型。校正计数增加值(CCI)用于监测每次血小板输注的有效性,1小时时的临界值为5×10/µL,24小时时为2.5×10/µL。使用酶联免疫吸附测定技术评估抗HLA抗体。
在60次交叉配型中,47次(78.3%)相合,13次(21.7%)不相合。在47次相合结果中,30次(63.8%)在输血后1小时显示CCI充足,17次(36.2%)显示CCI不足。在不相合结果中,3次(23.1%)CCI充足,10次(76.9%)CCI不足。在1小时或24小时比较交叉配型相合的血小板和不相合的血小板时,平均CCI有显著改善(分别为0.009和<0.001)。在40例研究患者中,18例(45.0%)存在HLA同种免疫,其余22例(55.0%)不存在。在无HLA同种免疫的情况下,患者在1小时和24小时显示出明显更好的反应(分别为0.001和0.015)。与单采血小板浓缩物相比,随机供者血小板浓缩物的血小板交叉配型敏感性更高。
使用SPRCA进行血小板交叉配型和HLA筛查是有效且快速的工具,有助于更好地管理对血小板输注无效的患者。