Devgun Manjit S, Chan Man Khun, El-Nujumi Adil M, Abara Rosemary, Armbruster David, Adeli Khosrow
Clinical Laboratories, Department of Biochemistry, NHS Lanarkshire, Wishaw General Hospital, 50 Netherton Street, Wishaw ML2 0DP, Scotland, UK.
Clinical Biochemistry Division, Department of Pediatric Laboratory Medicine, the Hospital for Sick Children, Toronto, Ontario, Canada.
Clin Biochem. 2015 Jan;48(1-2):93-6. doi: 10.1016/j.clinbiochem.2014.10.011. Epub 2014 Nov 7.
Measurement of total and direct bilirubin is routinely performed for the differential diagnosis of hyperbilirubinemias. The diagnostic efficiency of a test is dependent on the chosen clinical decision limit. This study is designed to address the clinical decision limits for direct bilirubin.
Routine laboratory method was used to measure total and direct bilirubin in children up to the age of 18years. Case study data and serum from a group of healthy children were analyzed and statistical exercise was performed to establish decision limits.
The reference interval for total bilirubin was 1-12μmol/L and for direct bilirubin 1-9μmol/L with the median direct bilirubin of 3μmol/L. In 17% of children with non-pathological jaundice, median total bilirubin was 173μmol/L, median direct bilirubin was 8μmol/L and median direct bilirubin percent was 49%. From birth direct bilirubin percentage decreased until total bilirubin was 41μmol/L, then it remained at ≤10%. Albumin increased with age, and was on average 2.4g/L higher when measured using bromocresol-green compared with bromocresol-purple. An increased amount of direct bilirubin was observed when albumin (detected using the bromocresol-purple method) was >35g/L.
Direct bilirubin concentration of ≥10μmol/L should be used to consider the presence of conjugated hyperbilirubinemia provided that total bilirubin is also above the reference interval. A high direct bilirubin percentage is unlikely to offer any clinical value when total bilirubin is not increased. It is, however, a useful diagnostic tool when there is a persistence of hyperbilirubinemia or when total bilirubin increases during times of stress with direct bilirubin >10%.
总胆红素和直接胆红素的检测常用于高胆红素血症的鉴别诊断。一项检测的诊断效率取决于所选择的临床决策界限。本研究旨在确定直接胆红素的临床决策界限。
采用常规实验室方法检测18岁以下儿童的总胆红素和直接胆红素。分析一组健康儿童的病例研究数据和血清,并进行统计学分析以确定决策界限。
总胆红素的参考区间为1 - 12μmol/L,直接胆红素为1 - 9μmol/L,直接胆红素中位数为3μmol/L。在17%非病理性黄疸儿童中,总胆红素中位数为173μmol/L,直接胆红素中位数为8μmol/L,直接胆红素百分比中位数为49%。从出生起,直接胆红素百分比下降,直至总胆红素达到41μmol/L,然后保持在≤10%。白蛋白随年龄增加,与使用溴甲酚紫法相比,使用溴甲酚绿法测量时平均高2.4g/L。当白蛋白(使用溴甲酚紫法检测)>35g/L时,观察到直接胆红素量增加。
如果总胆红素也高于参考区间,直接胆红素浓度≥10μmol/L应被视为存在结合胆红素血症。当总胆红素未升高时,高直接胆红素百分比不太可能具有任何临床价值。然而,当高胆红素血症持续存在或在应激状态下总胆红素升高且直接胆红素>10%时,它是一种有用的诊断工具。