出血性综合征患儿血小板聚集功能横断面研究结果

O. Gordeeva, Albina V. Dobrotok, Mariia V. Volkova, N. L. Aleshenko, Vladimir S. Kargin, Irine Dzharkava, Nadezhda F. Zhdanovskaia
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The study was conducted on the basis of the Research Institute of Pediatrics and Children’s Health, Scientific Center No. 2, Petrovsky National Research Centre of Surgery in the period from January — until December 2022. 62 children were included in the study, of which 50 children were selected (21 boys and 29 girls) aged 2 years 3 months to 17 years 11 months. The median age was 9.4 (7.2; 13.4). Aggregometry was performed using an impedance semiautomatic aggregometer in whole blood.Results. Depending on the diagnosis, the children were divided into the following groups: cardiovascular diseases (CVD), lysosomal storage disorders (LSD), monogenic hereditary diseases (MHD), children with dysplastic syndrome (DS), children with pathology of the nervous system (NS). Hypoaggregation with thrombin-activating peptide (TRAP test) was detected in 28% of cases (n = 14), more often in children from the group with MHD — 10% (n = 5) and with the presenceof DS — 10% (n = 5). 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摘要

背景。早期诊断儿童血小板增多症是儿科的一个相关目标。诊断有助于预防出血、慢性出血性贫血后遗症的发生,降低血栓形成的风险。本研究的目的是在慢性病理的背景下评估有出血性综合征表现的儿童血小板聚集障碍的发生率。该研究是在彼得罗夫斯基国家外科研究中心第二科学中心儿科和儿童健康研究所的基础上进行的,时间为2022年1月至12月。62 名儿童被纳入研究,其中 50 名儿童(21 名男孩和 29 名女孩)年龄在 2 岁 3 个月至 17 岁 11 个月之间。年龄中位数为 9.4(7.2;13.4)岁。使用阻抗半自动聚集仪对全血进行聚集测定。根据诊断结果,儿童被分为以下几组:心血管疾病(CVD)、溶酶体贮积症(LSD)、单基因遗传病(MHD)、发育不良综合征(DS)患儿、神经系统病变(NS)患儿。28%的病例(14 人)检测到凝血酶活化肽(TRAP 试验)聚集过少,在 MHD 患儿组中更常见--10%(5 人),在 DS 患儿组中更常见--10%(5 人)。20%的病例(10 人)检测到二磷酸腺苷聚集过少(ADP 试验),14%的病例(7 人)检测到花生四烯酸聚集过多(ASPI 试验)。12%的病例(6 例)通过 TRAP 试验检测到过度聚集,8%的病例(4 例)通过 ADP 试验检测到过度聚集。18%的病例(9 人)通过 ASPI 试验检测出过度聚集。根据血小板聚集功能实验室检测的分析结果,半数以上的患儿在诱导剂的作用下出现血小板聚集功能低下,几乎半数患者出现血小板聚集功能亢进。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The results of the cross-sectional study of platelet aggregative function in children with hemorrhagic syndrome
Background. Early diagnosis of thrombocytopathies in children is a relevant objective of pediatrics. Diagnostics helps prevent the development of bleeding, chronic posthemorrhagic anemia, reduces the risk of thrombosis.The aim of the study is an assessment of the incidence of platelet aggregation disorders in children with manifestations of hemorrhagic syndrome against the background of chronic pathology.Methods. The study was conducted on the basis of the Research Institute of Pediatrics and Children’s Health, Scientific Center No. 2, Petrovsky National Research Centre of Surgery in the period from January — until December 2022. 62 children were included in the study, of which 50 children were selected (21 boys and 29 girls) aged 2 years 3 months to 17 years 11 months. The median age was 9.4 (7.2; 13.4). Aggregometry was performed using an impedance semiautomatic aggregometer in whole blood.Results. Depending on the diagnosis, the children were divided into the following groups: cardiovascular diseases (CVD), lysosomal storage disorders (LSD), monogenic hereditary diseases (MHD), children with dysplastic syndrome (DS), children with pathology of the nervous system (NS). Hypoaggregation with thrombin-activating peptide (TRAP test) was detected in 28% of cases (n = 14), more often in children from the group with MHD — 10% (n = 5) and with the presenceof DS — 10% (n = 5). Hypoaggregation with adenosine diphosphate (ADP test) was detected in 20% of cases (n = 10), with arachidonic acid (ASPI test) was detected in 14% (n = 7). Hyperaggregation with the TRAP test was detected in 12% (n = 6), with the ADP test detected in 8% of cases (n = 4). Hyperaggregation with ASPI test was detected in 18% of cases (n = 9).Conclusion. The analyzed results of laboratory tests of platelet aggregation function, hypoaggregation with inducers was observed in more than half of the children, hyperaggregation was observed was present in almost half of the patients.
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