Orgad Tamar, Abu-Rahma Isra, Rekhtman David, Hashavya Saar, Milman Peri, Slae Mordechai, Davidovics Zev, Wilschanski Michael, Birimberg-Schwartz Liron
Department of Pediatric Gastroenterology, Hadassah Medical Center and Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Department of Pediatric Emergency Medicine, Hadassah Medical Center, Hebrew University of Jerusalem, Jerusalem, Israel.
J Pediatr Gastroenterol Nutr. 2025 Sep;81(3):683-689. doi: 10.1002/jpn3.70119. Epub 2025 Jun 17.
Pediatric acute pancreatitis (AP) is a growing clinical concern with a wide spectrum of severity, from mild episodes to life-threatening conditions. Traditional diagnostic methods primarily rely on serum amylase and lipase measurements, which are invasive and can be challenging in children. This study is the first to evaluate the diagnostic accuracy of the urine trypsinogen-2 dipstick test (UTDT) as a noninvasive test for diagnosing pediatric AP.
This prospective study included 28 pediatric patients (31 episodes) presenting with acute abdominal pain at a tertiary medical center from November 2022 to October 2024. AP was diagnosed based on the International Study Group of Pediatric Pancreatitis: In Search for a Cure (INSPPIRE) criteria. Urine samples were collected either within the first 24 hours (h) or later during hospitalization. UTDT sensitivity and specificity were calculated and compared to serum amylase and lipase levels.
Of the 31 episodes, 19 (61%) were confirmed as AP, and 12 (39%) were attributed to other causes. The UTDT had an overall sensitivity of 68% and specificity of 100%. Sensitivity increased to 87% when urine samples were collected within 24 h of admission. In non-AP cases, UTDT consistently produced negative results, with the high specificity supporting its reliability in distinguishing AP from other conditions.
The UTDT demonstrates promise as a rapid, noninvasive diagnostic tool for pediatric AP, particularly when used early in the disease course. Its high specificity and ease of use suggest that it may serve as an alternative to invasive blood tests once validated through larger-scale studies. Further research is needed to confirm these findings and establish the role of UTDT in clinical practice.
小儿急性胰腺炎(AP)是一个日益受到临床关注的问题,其严重程度范围广泛,从轻度发作到危及生命的情况。传统的诊断方法主要依赖血清淀粉酶和脂肪酶测量,这些方法具有侵入性,对儿童来说可能具有挑战性。本研究首次评估尿胰蛋白酶原-2试纸检测(UTDT)作为诊断小儿AP的非侵入性检测方法的诊断准确性。
这项前瞻性研究纳入了2022年11月至2024年10月在一家三级医疗中心因急性腹痛就诊的28例儿科患者(31次发作)。根据国际小儿胰腺炎研究组:寻求治愈方法(INSPPIRE)标准诊断AP。在入院后的前24小时内或住院后期收集尿液样本。计算UTDT的敏感性和特异性,并与血清淀粉酶和脂肪酶水平进行比较。
在这31次发作中,19次(61%)被确诊为AP,12次(39%)归因于其他原因。UTDT的总体敏感性为68%,特异性为100%。当在入院后24小时内收集尿液样本时,敏感性提高到87%。在非AP病例中,UTDT始终产生阴性结果,高特异性支持其在区分AP与其他病症方面的可靠性。
UTDT作为小儿AP的快速、非侵入性诊断工具显示出前景,特别是在疾病病程早期使用时。其高特异性和易用性表明,一旦通过大规模研究验证,它可能成为侵入性血液检测的替代方法。需要进一步研究以证实这些发现并确定UTDT在临床实践中的作用。