首页> 外文期刊>Revista de Chimie >Chromogenic Limulus Amoebocyte Lysate Assay in Early Etiologic Diagnosis of Peritonitis in Patients on Continuous Ambulatory Peritoneal Dialysis
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Chromogenic Limulus Amoebocyte Lysate Assay in Early Etiologic Diagnosis of Peritonitis in Patients on Continuous Ambulatory Peritoneal Dialysis

机译:持续性非卧床腹膜透析患者的发色性Li虫变形细胞溶解物测定在早期病因诊断中的腹膜炎

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Although substantial progresses have been made in etiologic diagnosis of continuous ambulatory peritoneal dialysis (CAPD) peritonitis, the length of time until cultures are obtained remains unacceptable long; at least for the first 48 h, indiscriminate use of broad spectrum antibiotics is seen in clinical practice with various side effects and with high-rates of transfer on hemodialysis. Therefore, alternative methods for early etiological diagnosis are stringently needed. During a 4-years study, we conducted qualitative and quantitative chromogenic LAL (Limulus amoebocyte lysate) assay completed with beta-1,3-glucans blocking-sequence on 114 peritonitis episodes in 43 CAPD patients. The results were analyzed in parallel with the cultures of dialysate effluents. Sensitivity and specificity for Gram-negative peritonitis were evaluated in both tests; a receiver operating characteristic (ROC) plot was used to analyze the cutoff value for a maximum sensitivity and specificity of quantitative test in diagnosing Gram-negative infections. Screening LAL chromogenic test had a sensitivity of 92.7% and a specificity of 90.4% in establishing diagnosis of Gram-negative peritonitis. In quantitative LAL test (completed with blocking LAL-beta-1,3-glucans reaction), the ROC plot emphasized a sensitivity of 100% and a specificity of 95.89% at endotoxin levels of 0.423 EU/mL or greater. In conclusion, our study demonstrates a high sensitivity and specificity of chromogenic LAL assay for the detection of peritoneal Gram-negative peritonitis. Chromogenic LAL assay is a useful test in early diagnostic of peritonitis in CAPD patients and it should be recommended as a routine in clinical practice.
机译:尽管持续性非卧床腹膜透析(CAPD)腹膜炎的病因学诊断已取得实质性进展,但是直到获得培养物的时间仍然太长。至少在最初的48小时内,在临床实践中发现不加选择地使用广谱抗生素具有多种副作用,并且在血液透析中具有很高的转移率。因此,迫切需要早期病因诊断的替代方法。在为期4年的研究中,我们对43位CAPD患者的114例腹膜炎发作进行了定性和定量的生色LAL(Li变形细胞溶解物)测定,并采用β-1,3-葡聚糖阻断序列。与透析液流出物的培养平行地分析结果。两种测试均评估了革兰氏阴性腹膜炎的敏感性和特异性。接收者操作特征(ROC)图用于分析临界值,以在诊断革兰氏阴性感染时获得最大灵敏度和定量测试的特异性。 LAL显色试验的筛查对建立革兰氏阴性腹膜炎的诊断灵敏度为92.7%,特异性为90.4%。在定量LAL测试中(完成了阻断LAL-β-1,3-葡聚糖的反应),ROC图强调内毒素水平为0.423 EU / mL或更高时,灵敏度为100%,特异性为95.89%。总之,我们的研究表明,发色LAL检测对检测腹膜革兰氏阴性腹膜炎具有很高的敏感性和特异性。显色性LAL测定法是对CAPD患者腹膜炎进行早期诊断的有用测试方法,应建议在临床实践中将其作为常规方法使用。

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