Unité des Maladies Génétiques du Globule Rouge, APHP, Hôpitaux Universitaire Henri-Mondor, Créteil, France.
UPEC, Institut Mondor de Recherche Biomédicale (IMRB), Institut National de la Santé et de le Recherche Médicale (INSERM) U955, DHU A-TVB, Créteil, France.
Am J Hematol. 2016 Oct;91(10):989-94. doi: 10.1002/ajh.24460. Epub 2016 Jul 14.
Delayed hemolytic transfusion reaction (DHTR) is one of the most feared complications of sickle-cell disease (SCD). We retrospectively analyzed the clinical and biological features, treatments and outcomes of 99 DHTRs occurring in 69 referral center patients over 12 years. The first clinical signs appeared a median of 9.4 [IQR, 3-22] days after the triggering transfusion (TT). The most frequent DHTR-related clinical manifestation was dark urine/hemoglobinuria (94%). Most patients (89%) had a painful vaso-occlusive crisis and 50% developed a secondary acute chest syndrome (ACS). The median [IQR] hemoglobin-concentration nadir was 5.5 [4.5-6.3] g/dL and LDH peak was 1335 [798-2086] IU/L. Overall mortality was 6%. None of the patients had been receiving chronic transfusions. Among these DHTRs, 61% were developed in previously immunized patients, 28% in patients with prior DHTR. Among Abs detected after the TT in 62% of the episodes, half are classically considered potentially harmful. No association could be established between clinical severity and immunohematological profile and/or the type and specificity of Abs detected after the TT. Management consisted of supportive care alone (53%) or with adjunctive measures (47%), including recombinant erythropoietin and sometimes rituximab and/or immunosuppressants. Additional transfusions were either ineffective or worsened hemolysis. In some cases, severe intravascular hemolysis can be likely responsible for the vascular reaction and high rates of ACS, pulmonary hypertension and (multi)organ failure. In conclusion, clinicians and patients must recognize early DHTR signs to avoid additional transfusions. For patients with a history of RBC immunization or DHTR, transfusion indications should be restricted. Am. J. Hematol. 91:989-994, 2016. © 2016 Wiley Periodicals, Inc.
延迟性溶血性输血反应(DHTR)是镰状细胞病(SCD)最可怕的并发症之一。我们回顾性分析了 12 年来在 69 个转诊中心的 99 例 DHTR 患者的临床和生物学特征、治疗方法和结局。首次临床症状出现在触发输血(TT)后中位数 9.4 [IQR,3-22] 天。最常见的 DHTR 相关临床表现为深茶色尿/血红蛋白尿(94%)。大多数患者(89%)发生疼痛性血管阻塞性危象,50%发生继发性急性胸部综合征(ACS)。血红蛋白浓度最低点的中位数[IQR]为 5.5 [4.5-6.3] g/dL,LDH 峰值为 1335 [798-2086] IU/L。总体死亡率为 6%。没有患者正在接受慢性输血。在这些 DHTR 中,61%发生在以前免疫的患者中,28%发生在有过 DHTR 的患者中。在 TT 后检测到的 Abs 中,有 62%的 Abs 被认为具有潜在的危害性。在 TT 后检测到的 Abs 的临床严重程度、免疫血液学特征和/或类型和特异性之间,未发现任何关联。治疗包括单纯支持治疗(53%)或联合治疗(47%),包括重组促红细胞生成素,有时还包括利妥昔单抗和/或免疫抑制剂。额外的输血要么无效,要么使溶血恶化。在某些情况下,严重的血管内溶血可能是血管反应和 ACS、肺动脉高压和(多)器官衰竭的高发生率的原因。总之,临床医生和患者必须及早识别 DHTR 迹象,避免额外输血。对于有 RBC 免疫或 DHTR 病史的患者,应限制输血适应证。美国血液学杂志 91:989-994, 2016。© 2016 威利父子公司