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Plasma fibronectin as a marker of sepsis

机译:血浆纤连蛋白作为败血症的标志

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Objectives: To evaluate the value of plasma fibronectin (pFN) as a diagnostic marker of sepsis. Subjects and methods: Plasma FN was determined in patients showing sepsis-related symptoms who had blood cultures performed. These patients were assigned to one of two groups according to their clinical situation: (1) Clinical Septic Group: patients with sepsis according to American College of Chest Physicians/Society of Critical Care Medicine (ACCP/SCCM) criteria; (2) Fever Peak Group: patients who did not fulfil sufficient ACCP/SCCM criteria for sepsis. Two additional control groups were also established: (3) Non-infectious Diseases Control Group and (4) Healthy Control Group. Results: Plasma FN levels, microbiological and clinical data were compared among the different patient groups. For each group, the number of patients, median and mean pFN levels and the 95% confidence interval of the mean were: (1) n=43, 102?mg/l, 122?mg/l (100-144); (2) n=70, 185?mg/l, 207?mg/l (184-231); (3) n=22, 175?mg/l, 181?mg/l (151-211); and (4) n=22, 256?mg/l, 261?mg/l (229-292). Bonferroni's test of multiple comparisons was able to detect a significant difference between pFN concentrations corresponding to the septic group, compared to the remaining groups (pANOVA<0.001). Conclusion: Plasma FN appears to act as a marker of sepsis in that patients showed diminished pFN levels. Along with other clinical and laboratory variables, the use of this marker would allow a rapid diagnosis of sepsis and limit the number of blood cultures to be processed and the number of antibiotic prescriptions, particularly when symptoms are insidious and diagnosis is doubtful. We propose further and more complex studies using a higher number of patients.
机译:目的:评估血浆纤连蛋白(pFN)作为脓毒症诊断指标的价值。受试者和方法:对表现出败血症相关症状并进行血培养的患者进行血浆FN测定。这些患者根据其临床情况被分为两组之一:(1)临床败血症组:根据美国胸科医师协会/重症监护医学学会(ACCP / SCCM)标准的败血症患者; (2)发热高峰组:未达到脓毒症的足够ACCP / SCCM标准的患者。还建立了另外两个对照组:(3)非传染病对照组和(4)健康对照组。结果:比较了不同患者组的血浆FN水平,微生物学和临床数据。每组的患者人数,pFN中位数和平均值以及平均值的95%置信区间为:(1)n = 43,102?mg / l,122?mg / l(100-144); (2)n = 70,185μmg / l,207μmg/ l(184-231); (3)n = 22、175μmg / l,181μmg/ l(151-211); (4)n = 22,256μmg / l,261μmg/ l(229-292)。 Bonferroni的多重比较检验能够检测出与败血症组相对应的pFN浓度与其余各组之间的显着差异(pANOVA <0.001)。结论:血浆FN似乎是败血症的标志物,因为患者的pFN水平降低。与其他临床和实验室变量一起,使用此标记将可以快速诊断败血症,并限制要处理的血液培养物的数量和抗生素处方的数量,特别是在症状隐蔽且诊断不确定的情况下。我们建议使用更多的患者进行进一步和更复杂的研究。

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