Pridgeon Simon, Harding Christopher, Newton Douglas, Pickard Robert
Department of Urology, Freeman Hospital, Newcastle upon Tyne, UK.
Indian J Urol. 2007 Apr;23(2):114-8. doi: 10.4103/0970-1591.32058.
To evaluate the accuracy and diagnostic usefulness of a disposable flowmeter consisting of a plastic funnel with a spout divided into three chambers.
Men with lower urinary tract symptoms (LUTS) voided sequentially into a standard flowmeter and the funnel device recording maximum flow rate (Q(max)) and voided volume (V(void)). The device was precalibrated such that filling of the bottom, middle and top chambers categorized maximum input flows as <10, 10-15 and > 15 ml s(-1) respectively. Subjects who agreed to use the funnel device at home obtained readings of flow category and V(void) twice daily for seven days.
A single office reading in 46 men using the device showed good agreement with standard measurement of Q(max) for V(void) > 150 ml (Kappa = 0.68). All 14 men whose void reached the top chamber had standard Q(max) > 15 ml s(-1) (PPV = 100%, NPV = 72%) whilst eight of 12 men whose void remained in the bottom chamber had standard Q(max) < 10 ml s(-1) (PPV = 70%, NPV = 94%). During multiple home use by 14 men the device showed moderate repeatability (Kappa = 0.58) and correctly categorized Q(max) in comparison to standard measurement for 12 (87%) men.
This study suggests that the device has sufficient accuracy and reliability for initial flow rate assessment in men with LUTS. The device can provide a single measurement or alternatively multiple home measurements to categorize men with Q(max) < 15 ml s(-1).
评估一种由带有分为三个腔室的喷嘴的塑料漏斗组成的一次性流量计的准确性和诊断效用。
有下尿路症状(LUTS)的男性依次向标准流量计和漏斗装置排尿,记录最大尿流率(Q(max))和排尿量(V(void))。该装置预先校准,使得底部、中间和顶部腔室的填充分别将最大输入流量分类为<10、10 - 15和>15 ml s(-1)。同意在家使用漏斗装置的受试者连续七天每天两次获取流量类别和V(void)的读数。
46名男性在办公室单次使用该装置的读数与V(void)>150 ml时Q(max)的标准测量结果显示出良好的一致性(Kappa = 0.68)。所有14名排尿到达顶部腔室的男性标准Q(max)>15 ml s(-1)(阳性预测值 = 100%,阴性预测值 = 72%),而12名排尿留在底部腔室的男性中有8名标准Q(max)<10 ml s(-1)(阳性预测值 = 70%,阴性预测值 = 94%)。14名男性在家多次使用该装置期间,该装置显示出中等重复性(Kappa = 0.58),与12名(87%)男性的标准测量相比,正确分类了Q(max)。
本研究表明该装置对于评估有LUTS男性的初始尿流率具有足够的准确性和可靠性。该装置可以提供单次测量,也可以提供多次在家测量,以对Q(max)<15 ml s(-1)的男性进行分类。