Gangaram Rajesh, Naicker Manogaran, Moodley Jagidesa
Department of Obstetrics and Gynaecology, Nelson R Mandela School of Medicine, University of KwaZulu-Natal, Private Bag 7, Congella 4013, South Africa.
Eur J Obstet Gynecol Reprod Biol. 2009 Jun;144(2):146-8. doi: 10.1016/j.ejogrb.2009.03.010. Epub 2009 Apr 15.
New developments in proteinuria assessment have included the use of spot urinary microalbumin to creatinine ratio measurements. This study determines the accuracy of spot urinary microalbumin to creatinine ratio dipsticks and conventional visual dipsticks compared to the 24h urinary protein (gold standard) to detect significant proteinuria in hypertensive pregnant women.
163 women presenting with pregnancy hypertension were recruited from antenatal clinics. On admission each participant had a spot urine sample tested using a semi-quantitative visual dipstick and a spot midstream urine sample collected and analysed using the semi-quantitative urinary microalbumin to creatinine ratio dipsticks read instrumentally on the Clinitek 50 urine chemistry analyser. A 24 h urinary protein estimation was then performed. The results of the urinary microalbumin to creatinine ratio dipsticks and the conventional visual dipsticks were compared to the 24 h urine protein. A urinary microalbumin to creatinine ratio of > or =300 mg/g (1+ to 4+ on urine dipsticks) was considered a positive result > or =0.3g/24 h was considered significant proteinuria.
The visual dipstick had a sensitivity of 51% (95% CI [0.41-0.61]) and specificity of 91% (95% CI [0.81-0.96]). The PPV and NPV was 89% (95% CI [0.77-0.95]) and 58% (95% CI [0.48-0.67]), respectively. The urinary microalbumin to creatinine ratio dipsticks had a sensitivity of 63% (95% CI [0.52-0.72]) and specificity of 81% (95% CI [0.70-0.89]). The PPV was 82% (95% CI [0.71-0.90]) and NPV was 62% (95% CI [0.51-0.71]).
Neither the visual dipstick nor the urinary microalbumin to creatinine ratio dipstick read on the Clinitek 50 system is accurate when compared to the total 24h urinary protein. Differences between the urinary microalbumin to creatinine ratio and 24h total urinary protein may be due to the variation in the albumin fraction of the total urinary protein of pre-eclampsia, technical problems with imprecision of the assay technique, and clinical causes of false positives and negatives. The improved sensitivity of the automated urinary microalbumin to creatinine ratio dipstick over the visual dipstick suggests it may be a suitable substitute for the visual dipstick in clinical practice.
蛋白尿评估的新进展包括使用随机尿微量白蛋白与肌酐比值测量。本研究确定与24小时尿蛋白(金标准)相比,随机尿微量白蛋白与肌酐比值试纸条和传统目视试纸条检测高血压孕妇显著蛋白尿的准确性。
从产前诊所招募163例妊娠高血压妇女。入院时,每位参与者使用半定量目视试纸条检测随机尿样,并收集和分析随机中段尿样,使用半定量尿微量白蛋白与肌酐比值试纸条在Clinitek 50尿液化学分析仪上进行仪器读取。然后进行24小时尿蛋白测定。将尿微量白蛋白与肌酐比值试纸条和传统目视试纸条的结果与24小时尿蛋白结果进行比较。尿微量白蛋白与肌酐比值>或=300mg/g(尿试纸条上为1+至4+)被视为阳性结果;>或=0.3g/24小时被视为显著蛋白尿。
目视试纸条的灵敏度为51%(95%CI[0.41-0.61]),特异性为91%(95%CI[0.81-0.96])。阳性预测值和阴性预测值分别为89%(95%CI[0.77-0.95])和58%(95%CI[0.48-0.67])。尿微量白蛋白与肌酐比值试纸条的灵敏度为63%(95%CI[0.52-0.72]),特异性为81%(95%CI[0.70-0.89])。阳性预测值为82%(95%CI[0.71-0.90]),阴性预测值为62%(95%CI[0.51-0.71])。
与24小时总尿蛋白相比,Clinitek 50系统上读取的目视试纸条和尿微量白蛋白与肌酐比值试纸条均不准确。尿微量白蛋白与肌酐比值和24小时总尿蛋白之间的差异可能是由于子痫前期总尿蛋白中白蛋白部分的变化、检测技术不精确的技术问题以及假阳性和假阴性的临床原因。自动化尿微量白蛋白与肌酐比值试纸条比目视试纸条灵敏度更高,这表明它可能是临床实践中目视试纸条的合适替代品。