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Changes in and significance of platelet function and parameters in Kawasaki disease

机译:川崎病血小板函数与参数的变化和意义

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Kawasaki disease (KD) is a systemic febrile, inflammatory vascular disease of unknown etiology. The coronary artery abnormality (CAA) caused by KD has become the most commonly acquired heart disease in children. Initial treatment of intravenous immunoglobulin (IVIG) can reduce the incidence of CAA. Thrombocytosis is common during the course of KD, but changes in and significances of platelet function and parameters are unclear. In this study, we enrolled 120 patients, including 40 patients with KD, 40 febrile controls, and 40 afebrile controls. The platelet function was assessed using the platelet function analyzer (PFA)-200. Platelet parameters, including platelet count (PLT), mean platelet volume (MPV), platelet distribution width (PDW), and platelet hematocrit (PCT) were measured. In the febrile period, the PDW and MPV were lower in KD patients (P??0.05). The platelet function did not change significantly during the febrile period of KD but weakened in the defervescence phase. No significant differences between the CAA and normal groups, and between IVIG resistance and response groups. The diagnostic cutoff value of the PDW level for predicting KD was 10.85?fL with a sensitivity of 55% and a specificity of 77.5% (area under curve (AUC)?=?0.690, 95% confidence interval (CI): 0.574-0.806, P??0.01). Besides, the MPV level was 9.55?fL with sensitivity of 75% and specificity of 70% (AUC?=?0.733, 95%CI: 0.620-0.846, P??0.001). This is the first longitudinal study of platelet function changes in KD patients using PFA-200. Besides, lower PDW and MPV may be available markers for early diagnosis of KD.
机译:川崎病(KD)是一种全身性发热,炎症血管疾病的未知病因。 KD引起的冠状动脉异常(CAA)已成为儿童最常见的心脏病。静脉内免疫球蛋白(IVIG)的初始治疗可以降低CAA的发生率。在KD过程中血小板增生是常见的,但血小板功能和参数的变化和意义尚不清楚。在这项研究中,我们注册了120名患者,其中40例KD,40名发热对照和40名患者。使用血小板功能分析仪(PFA)-200评估血小板功能。测定血小板参数,包括血小板计数(PLT),平均血小板体积(MPV),血小板分布宽度(PDW)和血小板血细胞比容(PCT)。在发热期间,KD患者的PDW和MPV较低(P?<?0.05)。在KD的发热期间,血小板功能没有显着变化,但在渗透阶段削弱。 CAA和正常组之间没有显着差异,以及在IVIG抗性和响应组之间。预测Kd的PDW水平的诊断截止值为10.85?敏感性为55%,特异性为77.5%(曲线下面积(AUC)?= 0.690,95%置信区间(CI):0.0574-0.806 ,p?<?0.01)。此外,MPV水平为9.55?敏感度为75%,特异性为70%(AUC?= 0.733,95%CI:0.620-0.846,P?<0.001)。这是使用PFA-200的KD患者血小板功能变化的第一个纵向研究。此外,降低PDW和MPV可以是用于早期诊断KD的标记。

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