Intensive Care Unit, Shanghai Jing'an District Zhabei Central Hospital, Shanghai, China.
Intensive Care Unit, Renhe Hospital, Baoshan District, Shanghai, China.
Allergol Immunopathol (Madr). 2024 May 1;52(3):17-21. doi: 10.15586/aei.v52i3.1039. eCollection 2024.
This study aims to investigate the relevance of platelet aggregation markers, specifically arachidonic acid (AA) and adenosine diphosphate (ADP), in relation to the prognosis of sepsis patients.
A cohort of 40 sepsis patients was included and stratified, based on their 28-day post-treatment prognosis, into two groups: a survival group (n = 31) and a severe sepsis group (n = 9. Then, their various clinical parameters, including patient demographics, platelet counts (PLT), inflammatory markers, and platelet aggregation rates (PAR) induced by AA and ADP between the two groups, were compared. Long-term health implications of sepsis were assessed using the Acute Physiologic Assessment and Chronic Health Evaluation II (APACHE II) score, and logistic regression analysis was conducted to evaluate the prognostic significance of PAR in sepsis patients.
Patients with severe sepsis exhibited significantly elevated levels of procalcitonin (PCT), platelet adhesion rates, and PAR induced by ADP (P < 0.05), but having lower PLT (P < 0.05), compared to those in the survival group. Logistic regression analysis demonstrated that PAR induced by ADP was a protective factor in predicting prognosis in sepsis patients (P < 0.01).
Activation of platelets in sepsis intensifies inflammatory response. Patients with sepsis whose ADP-induced PAR was < 60% displayed significant impairment in platelet aggregation function, and had higher mortality rate. Monitoring ADP-induced PAR is crucial for management of sepsis.
本研究旨在探讨血小板聚集标志物,特别是花生四烯酸(AA)和二磷酸腺苷(ADP),与脓毒症患者预后的相关性。
纳入了 40 例脓毒症患者,并根据其 28 天治疗后预后进行分层,分为存活组(n=31)和严重脓毒症组(n=9)。然后,比较了两组患者的各种临床参数,包括患者人口统计学、血小板计数(PLT)、炎症标志物和 AA 和 ADP 诱导的血小板聚集率(PAR)。使用急性生理和慢性健康评估 II(APACHE II)评分评估脓毒症的长期健康影响,并用逻辑回归分析评估 PAR 在脓毒症患者预后中的预测意义。
严重脓毒症组患者的降钙素原(PCT)、血小板黏附率和 ADP 诱导的 PAR 显著升高(P<0.05),而 PLT 水平显著降低(P<0.05),与存活组相比。逻辑回归分析表明,ADP 诱导的 PAR 是预测脓毒症患者预后的保护因素(P<0.01)。
脓毒症中血小板的激活加剧了炎症反应。ADP 诱导的 PAR<60%的脓毒症患者的血小板聚集功能明显受损,死亡率较高。监测 ADP 诱导的 PAR 对脓毒症的管理至关重要。