Unit of Anesthesia and Intensive Care, Department of Medicine (DIMED), University of Padua, Padua, Italy.
Unit of Thrombotic and Hemorrhagic Diseases, Department of Medicine (DIMED), University of Padua, Padua, Italy.
Minerva Anestesiol. 2019 Jun;85(6):625-634. doi: 10.23736/S0375-9393.18.12782-9. Epub 2018 Nov 22.
Microparticles (MP) have been largely studied as potential biomarkers in septic shock (SS) though their biological and clinical relevance is still unclear. This case-control study describes the trend of various MP subtypes during SS to evaluate their possible association with severity of illness and sepsis-related complications (disseminated intravascular coagulation [DIC] and acute kidney injury [AKI]).
Forty patients admitted to the Intensive Care Unit with SS and 40 matched healthy volunteers were recruited. AnnexinV+, E-selectin+, thrombomodulin (TM+), leukocyte-derived (CD45+, CD36+) and platelet-derived MP (PMP-expressed as PMP/platelets ratio) were measured by flow-cytometry at baseline, on day 1, 3 and 7 after diagnosis. Severity of illness was assessed by Sequential Organ Failure Assessment Score, duration of vasoactive support and mechanical ventilation. Sepsis-related complications were considered.
Overall, septic patients showed higher levels of all MP considered compared to controls. TM+MP were significantly lower in more severe sepsis, while CD36+MP and PMP/platelets ratio were significantly increased in patients requiring longer vasoactive support and mechanical ventilation. As for sepsis-related complications, a higher PMP/platelets ratio in patients who developed DIC and increased E-selectin+MP in subjects who developed AKI were observed. PMP/platelets ratio at baseline was significantly associated with longer vasoactive support (OR=1.59 [1.05-2.42]), longer mechanical ventilation (OR=1.6 [1.06-2.42]) and DIC occurrence (OR=1.45 [1.08-1.96]).
A global response through extra-vesiculation of endothelial cells, leukocytes and platelets during the early stages of SS was confirmed. The cellular activation was detected until day 3 after diagnosis. PMP/platelets ratio at diagnosis may be useful to evaluate SS severity and DIC occurrence.
微粒(MP)已被广泛研究作为感染性休克(SS)的潜在生物标志物,但其生物学和临床相关性仍不清楚。本病例对照研究描述了 SS 期间各种 MP 亚型的趋势,以评估它们与疾病严重程度和与败血症相关的并发症(弥散性血管内凝血[DIC]和急性肾损伤[AKI])的可能关联。
招募了 40 名因 SS 入住重症监护病房的患者和 40 名匹配的健康志愿者。在基线、诊断后第 1、3 和 7 天,通过流式细胞术测量膜联蛋白 V+、E-选择素+、血栓调节蛋白(TM+)、白细胞衍生(CD45+、CD36+)和血小板衍生 MP(PMP 表示为 PMP/血小板比值)。使用序贯器官衰竭评估评分、血管活性支持和机械通气的持续时间来评估疾病严重程度。考虑了与败血症相关的并发症。
总体而言,与对照组相比,所有考虑的 MP 在败血症患者中水平更高。在更严重的败血症中,TM+MP 显著降低,而在需要更长时间血管活性支持和机械通气的患者中,CD36+MP 和 PMP/血小板比值显著增加。对于与败血症相关的并发症,观察到发生 DIC 的患者的 PMP/血小板比值升高,以及发生 AKI 的患者的 E-选择素+MP 增加。在基线时,PMP/血小板比值与较长时间的血管活性支持(OR=1.59 [1.05-2.42])、较长时间的机械通气(OR=1.6 [1.06-2.42])和 DIC 发生(OR=1.45 [1.08-1.96])显著相关。
在 SS 的早期阶段,通过内皮细胞、白细胞和血小板的囊泡外溢证实了全身性反应。在诊断后第 3 天仍检测到细胞激活。在诊断时的 PMP/血小板比值可能有助于评估 SS 的严重程度和 DIC 的发生。