Yang Yao-Jong, Sheu Bor-Shyang, Lee Shui-Cheng, Wu Jiunn-Jong
Department of Pediatrics, Medical College, National Cheng Kung University, Tainan, Taiwan.
J Gastroenterol Hepatol. 2007 Mar;22(3):335-9. doi: 10.1111/j.1440-1746.2006.04453.x.
The high cost of the 13C-urea breath test (UBT) limits its wide application for both epidemiological and clinical studies for diagnosing Helicobacter pylori infection. This study examined if a lower-dose UBT, applying 1 mg/kg of bodyweight (maximum 25 mg, UBT(25)), could introduce cost savings while preserving high diagnostic yields for primary H. pylori infection.
Children aged less than 16 years were recruited after obtaining consent. Those children with administration of antibiotics or proton pump inhibitors within 1 month of the tests were excluded. Positive tests for both the UBT with 50 mg urea (UBT(50)) and the H. pylori stool antigen (HpSA) were qualifying criteria for H. pylori infection. Negative results for both indicated non-infection. The UBT(25) was conducted 1 week after the UBT(50). The cut-off points for the UBT(25) ranging from 2delta to 5delta were examined for their sensitivity, specificity and accuracy rates.
A total of 153 children were recruited (55% male; mean age 9.1 +/- 3.5 years). Both the UBT(50) and HpSA test were positive in 18 (13.1%) and negative in 119 children, respectively. The sensitivity and specificity of the UBT(25) were optimally achieved at 88.9% (95% confidence interval [CI]: 71.4-100) and 95.0% (95% CI: 91.1-99.9), judged with a cut-off point at 3.5delta. The diagnostic accuracy was significantly higher for children older than 7 years than for those younger than 7 years (98%vs 85%, P = 0.009).
Lower-dose UBT titration by bodyweight can cut costs while maintaining a highly reliable method to screen primary H. pylori infection in children older than 7 years, which is generally beyond school age.
13C尿素呼气试验(UBT)成本高昂,限制了其在幽门螺杆菌感染流行病学及临床研究中的广泛应用。本研究旨在探讨低剂量UBT(按体重1mg/kg给药,最大剂量25mg,即UBT(25))在降低成本的同时,能否保持对原发性幽门螺杆菌感染的高诊断率。
征得同意后招募16岁以下儿童。排除在检测前1个月内使用过抗生素或质子泵抑制剂的儿童。尿素50mg的UBT(UBT(50))和幽门螺杆菌粪便抗原(HpSA)检测均为阳性是幽门螺杆菌感染的合格标准。两者均为阴性则表明未感染。UBT(25)在UBT(50)后1周进行。研究了UBT(25)从2δ到5δ的不同截断点的敏感性、特异性和准确率。
共招募153名儿童(55%为男性;平均年龄9.1±3.5岁)。UBT(50)和HpSA检测均为阳性的有18名儿童(13.1%),均为阴性的有119名儿童。以3.5δ为截断点判断,UBT(25)的敏感性和特异性分别达到最佳的88.9%(95%置信区间[CI]:71.4 - 100)和95.0%(95%CI:91.1 - 99.9)。7岁以上儿童的诊断准确率显著高于7岁以下儿童(98%对85%,P = 0.009)。
按体重进行低剂量UBT滴定可降低成本,同时维持一种高度可靠的方法来筛查7岁以上(通常已超出学龄)儿童的原发性幽门螺杆菌感染。