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首页> 外文期刊>European Journal of Obstetrics, Gynecology and Reproductive Biology: An International Journal >Accuracy of the spot urinary microalbumin:creatinine ratio and visual dipsticks in hypertensive pregnant women.
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Accuracy of the spot urinary microalbumin:creatinine ratio and visual dipsticks in hypertensive pregnant women.

机译:高血压孕妇中尿微量白蛋白:肌酐比值和视觉试纸的准确性。

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OBJECTIVES: 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. STUDY DESIGN: 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. RESULTS: 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]). CONCLUSION: 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.
机译:目的:蛋白尿评估的新进展包括使用尿微量白蛋白与肌酐比值测量。这项研究确定了与24小时尿蛋白(金标准)相比,现货尿微量白蛋白与肌酐比率试纸和常规视觉试纸的准确性,以检测高血压孕妇中的重要蛋白尿。研究设计:从产前诊所招募了163名患有妊娠高血压的妇女。入院时,每位参与者都有使用半定量视觉试纸测试的尿液现货样本,并使用在Clinitek 50尿液化学分析仪上仪器读取的半定量尿微量白蛋白与肌酐比值试纸收集并分析了中游尿液样本。然后进行24小时尿蛋白评估。将尿微量白蛋白与肌酐比值试纸和常规视觉试纸的结果与24小时尿蛋白进行比较。尿微量白蛋白与肌酐的比率>或= 300 mg / g(尿浸量尺为1+到4+)被认为是阳性结果,或> 0.3g / 24 h被认为是显着的蛋白尿。结果:视觉试纸的灵敏度为51%(95%CI [0.41-0.61]),特异性为91%(95%CI [0.81-0.96])。 PPV和NPV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的敏感性为63%(95%CI [0.52-0.72]),特异性为81%(95%CI [0.70-0.89])。 PPV为82%(95%CI [0.71-0.90]),NPV为62%(95%CI [0.51-0.71])。结论:与总的24h尿蛋白相比,在Clinitek 50系统上读取的视觉试纸和尿微量白蛋白/肌酐比率试纸都不准确。尿微量白蛋白与肌酐比值与24h总尿蛋白之间的差异可能是由于先兆子痫前总尿蛋白中白蛋白含量的变化,测定技术不精确的技术问题以及假阳性和阴性的临床原因。自动化尿微量白蛋白对肌酐比率试纸的敏感性高于视觉试纸,表明它可能是临床实践中视觉试纸的合适替代品。

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