Peedin Alexis R, Park Yara A, Mazepa Marshall A, Rollins-Raval Marian A, Brecher Mark E, Raval Jay S
Department of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, NC, USA.
Laboratory Corporation of America, Burlington, NC, USA.
Ther Apher Dial. 2018 Dec;22(6):662-665. doi: 10.1111/1744-9987.12713. Epub 2018 Sep 3.
Acquired thrombotic thrombocytopenic purpura (TTP) is characterized by microangiopathic hemolytic anemia, thrombocytopenia, and commonly ADAMTS13 deficiency. Patients with TTP and severe ADAMTS13 deficiency have high risk of disease recurrence, yet the ability to predict which patients will have recurrence remains limited. We assessed whether the presence of persistent schistocytes in TTP patients with severe ADAMTS13 deficiency at the time of daily therapeutic plasma exchange (TPE) discontinuation was predictive of disease recurrence. We retrospectively reviewed the electronic medical records of all patients with a diagnosis of TTP treated with TPE at our university medical center between August 1991 and April 2013. Exacerbation was defined as disease recurrence within 30 days of cessation of daily TPE, and relapse was defined as disease recurrence >30 days after cessation of daily TPE. Comparisons were performed with a two-sided Fisher's exact test or χ2 test. Of the 46 total TTP patients eligible for analysis, nine had residual schistocytosis (20%), four of the nine (44%) had exacerbations, and two of the nine (22%) relapsed. Of the 37 patients without residual schistocytosis, 16 (43%) had exacerbations and 11 (30%) relapsed. There were no statistically significant differences in the exacerbation or relapse rates with or without residual schistocytosis (P = 1.00 and 1.00, respectively). Residual schistocytes after discontinuation of daily TPE were not uncommon. The persistence of schistocytes had poor sensitivity, specificity, and both positive and negative predictive values. After the initial diagnosis of TTP is made, there is no reason to continue documenting the presence or absence of schistocytes.
获得性血栓性血小板减少性紫癜(TTP)的特征为微血管病性溶血性贫血、血小板减少,且通常存在ADAMTS13缺乏。TTP且伴有严重ADAMTS13缺乏的患者疾病复发风险高,但预测哪些患者会复发的能力仍然有限。我们评估了在每日治疗性血浆置换(TPE)停止时,严重ADAMTS13缺乏的TTP患者中持续存在裂体细胞是否可预测疾病复发。我们回顾性分析了1991年8月至2013年4月在我校医学中心接受TPE治疗的所有TTP患者的电子病历。病情加重定义为每日TPE停止后30天内疾病复发,病情复发定义为每日TPE停止后>30天疾病复发。采用双侧Fisher精确检验或χ2检验进行比较。在46例符合分析条件的TTP患者中,9例有残余裂体细胞增多(20%);这9例中的4例(44%)病情加重,9例中的2例(22%)复发。在37例无残余裂体细胞增多的患者中,16例(43%)病情加重,11例(30%)复发。有无残余裂体细胞增多的病情加重率或复发率无统计学显著差异(P分别为1.00和1.00)。每日TPE停止后残余裂体细胞并不少见。裂体细胞的持续存在敏感性、特异性以及阳性和阴性预测值均较差。在TTP初步诊断后,没有理由继续记录裂体细胞的有无。