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Applicability and reproducibility of condom catheter method for measuring isovolumetric bladder pressure

To report on the applicability, reproducibility, and adverse events of the noninvasive condom catheter method in the first 730 subjects of a longitudinal survey of changes in urinary bladder contractility secondary to benign prostatic hyperplasia, in which 1300 men will be evaluated three times in 5...

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Bibliographic Details
Published in:Urology (Ridgewood, N.J.) N.J.), 2004, Vol.63 (1), p.56-60
Main Authors: Huang Foen Chung, J.W.N.C., Bohnen, A.M., Pel, J.J.M., Bosch, J.L.H.R., Niesing, R., van Mastrigt, R.
Format: Article
Language:English
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Summary:To report on the applicability, reproducibility, and adverse events of the noninvasive condom catheter method in the first 730 subjects of a longitudinal survey of changes in urinary bladder contractility secondary to benign prostatic hyperplasia, in which 1300 men will be evaluated three times in 5 years using this method. Subjects were recruited by general practitioners, general publicity, and e-mail. Only those meeting the study criteria were entered in the study. If the free flow rate exceeded 5.4 mL/s, at least two consecutive condom pressure measurements were attempted using the condom catheter method. The condom pressure measured reflected the isovolumetric bladder pressure, a measure of urinary bladder contractility. The reproducibility of the method was quantified by a difference plot of the two maximal condom pressures measured in each subject. In 618 (94%) of 659 eligible participants, one condom pressure measurement was completed; two measurements were done in 555 (84%). The maximal condom pressure ranged from 28 to 228 cm H 2O (overall mean 101, SD 34). A difference between the two pressures of less than ±21 cm H 2O was found in 80%. The mean difference was −1 cm H 2O (SD 18), significantly different from 0. Some adverse events such as terminal self-limiting hematuria were encountered. The condom catheter method is very suitable for large-scale use. It has a success rate of 94% and a reproducibility comparable to that of invasive pressure flow studies.
ISSN:0090-4295
1527-9995
DOI:10.1016/j.urology.2003.08.030