Gordon B, Tarantolo S, Ruby E, Stephens L, Lynch J, Kessinger A, Haire W
Department of Pediatrics, University of Nebraska Medical Center, Omaha 68198-2168, USA.
Bone Marrow Transplant. 1998 Nov;22(10):999-1003. doi: 10.1038/sj.bmt.1701464.
Organ dysfunction following hematopoietic stem cell transplantation (HSCT) may be a manifestation of a systemic inflammatory response. We speculate that part of the platelet transfusion requirement in HSCT patients results from this systemic inflammatory response, and increased transfusion requirement would be associated with, or precede, organ dysfunction. We studied 199 adults undergoing autologous (n=173) or allogeneic (n=26) HSCT. Patients with CNS (P=0.008) or pulmonary (P=0.002) dysfunction, or with VOD (P=0.05) received a higher mean number of platelet transfusions per week than patients who did not have these dysfunctions. Furthermore, a higher number of platelet transfusions during any 1 week period was significantly associated with development of pulmonary (P=0.0002) or renal (P < 0.0001) dysfunction in the following week. This predictive value was strongest early in the HSCT course, but remained significant over all 4 weeks. In multivariate analysis the number of platelet transfusions during the previous week was independently predictive for development of pulmonary dysfunction in week 2 (P=0.01) and week 3 (P=0.055). We believe that occurrence of increased platelet transfusion requirement prior to onset of dysfunction is consistent with the concept that an antecedent inflammatory response results in both platelet consumption and various organ dysfunctions. Increased platelet transfusion requirement may act as an early marker of subsequent organ dysfunction. Additionally, there may be a direct role of platelets in the development and progression of organ dysfunction in HSCT patients.
造血干细胞移植(HSCT)后出现的器官功能障碍可能是全身炎症反应的一种表现。我们推测,HSCT患者部分血小板输注需求源于这种全身炎症反应,而输注需求增加可能与器官功能障碍相关或先于器官功能障碍出现。我们研究了199例接受自体(n = 173)或异体(n = 26)HSCT的成年人。患有中枢神经系统(P = 0.008)或肺部(P = 0.002)功能障碍,或患有肝静脉闭塞病(VOD,P = 0.05)的患者,每周平均接受的血小板输注次数高于未出现这些功能障碍的患者。此外,在任何1周内较高的血小板输注次数与下一周出现肺部(P = 0.0002)或肾脏(P < 0.0001)功能障碍显著相关。这种预测价值在HSCT病程早期最强,但在整个4周内均保持显著。在多变量分析中,前一周的血小板输注次数可独立预测第2周(P = 0.01)和第3周(P = 0.055)肺部功能障碍的发生。我们认为在功能障碍发生前血小板输注需求增加的情况与以下概念一致,即先前的炎症反应导致血小板消耗和各种器官功能障碍。血小板输注需求增加可能是随后器官功能障碍的早期标志物。此外,血小板可能在HSCT患者器官功能障碍的发生和发展中起直接作用。