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AIM To assess the correlation between the send-out enzymelinked immuno sorbent assay(ELISA) and the point-ofcare(POC) calprotectin test in pediatric inflammatory bowel disease(IBD) patients.METHODS We prospectively collected stool samples in pediatric IBD patients for concomitant send-out ELISA analysis and POC calprotectin testing using the Quantum Blue?(QB) Extended immunoassay. Continuous results between 17 to 1000 μg/g were considered for comparison. Agreement between the two tests was measured by a Bland-Altman plot and statistical significance was determined using Pitman’s test.RESULTS Forty-nine stool samples were collected from 31 pediatric IBD patients. The overall means for the rapid and ELISA tests were 580.5 and 522.87 μg/g respectively. Among the 49 samples, 18(37.5%) had POC calprotectin levelsof ≤ 250 μg/g and 31(62.5%) had levels > 250 μg/g.Calprotectin levels ≤ 250 μg/g show good correlation between the two assays. Less correlation was observed at quantitatively higher calprotectin levels. CONCLUSION In pediatric IBD patients, there is better correlation of between ELISA and POC calprotectin measurements at clinically meaningful, low-range levels. Future adoption of POC calprotectin testing in the United States may have utility for guiding clinical decision making in real time.
AIM To assess the correlation between the send-out enzymelinked immuno sorbent assay (ELISA) and the point-ofcare (POC) calprotectin test in pediatric inflammatory bowel disease (IBD) patients. METHODS We prospectively collected soil samples in pediatric IBD patients for concomitant send -out ELISA analysis and POC calprotectin testing using the Quantum Blue® (QB) Extended immunoassay. Continuous results between 17 to 1000 μg / g were considered for comparison. Agreement between the two tests was measured by a Bland-Altman plot and statistical significance was determined using Pitman’s test. PCRULTS Forty-nine stool samples were collected from 31 pediatric IBD patients. The overall performance of the rapid and ELISA tests were 580.5 and 522.87 μg / g respectively. Among the 49 samples, 18 (37.5%) had POC calprotectin Levels of ≤ 250 μg / g and 31 (62.5%) had levels> 250 μg / g. Calprotectin levels ≤ 250 μg / g show correlation between the two assays. Less correlation was observed at quantitative ly higher calprotectin levels. CONCLUSION In pediatric IBD patients, there is better correlation between ELISA and POC calprotectin measurements at clinically meaningful, low-range levels. Future adoption of POC calprotectin testing in the United States may have utility for guiding clinical decision making in real time.