Terra Patrícia Oliveira Cunha, De Santis Gil Cunha, Prado Júnior Benedito de Pina Almeida, Oliveira Luciana Correa
Department of Medical Imaging, Hematology, and Oncology, Ribeirão Preto Medical School, University of São Paulo, São Paulo, Brazil; Regional Blood Center of Ribeirão Preto, Ribeirão Preto Medical School, University of São Paulo, São Paulo, Brazil.
Department of Medical Imaging, Hematology, and Oncology, Ribeirão Preto Medical School, University of São Paulo, São Paulo, Brazil; Regional Blood Center of Ribeirão Preto, Ribeirão Preto Medical School, University of São Paulo, São Paulo, Brazil.
Hematol Transfus Cell Ther. 2024 Nov;46 Suppl 5(Suppl 5):S24-S31. doi: 10.1016/j.htct.2023.11.006. Epub 2023 Dec 30.
Immune thrombotic thrombocytopenic purpura (iTTP) is characterized by acute systemic microvascular thrombosis and is associated with a high morbidity and mortality, especially in delayed diagnosis (later than 6-7 days from symptoms). iTTP data in Brazil is scarce, so we aimed to characterize the clinical presentation and identify predictors of death risk in patients with this disease in Brazil.
In this single-center retrospective study the patients who underwent therapeutic plasma exchange (TPE) for presumptive or confirmed iTTP were evaluated regarding the epidemiological, clinical, laboratorial characteristics and management.
A total of 50 patients (90 % female), with median age (IQR) of 34.1 (27-47) years, were enrolled, of which 12 (24 %) died. The most frequent symptoms were neurological (96 %), bleeding (76 %), gastrointestinal (52 %), fever (38 %), and cardiovascular (22 %). Neurological focal deficit and cardiovascular symptoms were more frequently observed in the non-survivor group (P = 0.0019 and P = 0.007, respectively). The mean ± SD number of days from beginning of symptoms to first TPE was 12.22 ± 7.91. We identified an association regarding mortality rate with a score MITS ≥ 2 points (P = 0.04), a higher indirect bilirubin (P = 0.0006), a higher number of transfused red blood cell units (P = 0.025), and platelet transfusion (P = 0.027).
Delayed diagnosis appears to be associated with a higher frequency of neurological symptoms and mortality. Intensity of hemolysis and signs of organ ischemia, such as cardiovascular symptoms and focal neurological deficit, are indicators of death risk.
免疫性血栓性血小板减少性紫癜(iTTP)的特征是急性全身性微血管血栓形成,且发病率和死亡率较高,尤其是在诊断延迟(症状出现后6 - 7天以后)的情况下。巴西关于iTTP的数据稀缺,因此我们旨在描述巴西该病患者的临床表现并确定死亡风险的预测因素。
在这项单中心回顾性研究中,对因疑似或确诊iTTP接受治疗性血浆置换(TPE)的患者进行了流行病学、临床症状、实验室检查特征及治疗管理方面的评估。
共纳入50例患者(90%为女性),中位年龄(四分位间距)为34.1(27 - 47)岁,其中12例(24%)死亡。最常见的症状为神经系统症状(96%)、出血(76%)、胃肠道症状(52%)、发热(38%)和心血管系统症状(22%)。非存活组中神经系统局灶性缺损和心血管系统症状更为常见(分别为P = 0.0019和P = 0.007)。从症状出现到首次进行TPE的平均天数±标准差为12.22 ± 7.91。我们发现死亡率与MITS评分≥2分(P = 0.04)、间接胆红素升高(P = 0.0006)、输注红细胞单位数量增加(P = 0.025)以及血小板输注(P = 0.027)相关。
诊断延迟似乎与神经系统症状频率增加和死亡率升高有关。溶血强度和器官缺血迹象,如心血管系统症状和局灶性神经缺损,是死亡风险的指标。