First steps to understanding the free and invasive maximum flow rate discrepancy

Arevalo D1, López L1, Gallegos H2, Dell'Oro A1, Calvo C1

Research Type

Clinical

Abstract Category

Urodynamics

Abstract 142
Urodynamics
Scientific Podium Short Oral Session 8
Thursday 8th September 2022
15:42 - 15:50
Hall D
Urodynamics Techniques Voiding Dysfunction Mixed Urinary Incontinence
1. Pontificia Universidad Católica de Chile, 2. Hospital Sótero del Rio
Online
Presenter
C

Carlos Calvo

Links

Abstract

Hypothesis / aims of study
This study aims to compare the parameters of free and invasive uroflowmetry among female patients with different referral diagnoses in order to describe if the known difference between these two measurements varies in different clinical settings.
Study design, materials and methods
This is a cross-sectional study. We reviewed Urodynamic studies performed from 2015 to 2021 in an academic hospital in Chile. Urodynamics were conducted following ICS good practices. Female adult patients with lower urinary tract symptoms were selected. Only patients who voided at least 150 ml in both free and invasive flowmetry were included. Patients with high-grade prolapse were excluded. Depending on the referral diagnosis and clinical suspicion patients were classified into 5 different groups (they could be part of more than one group): voiding dysfunction, mixed urinary incontinence, isolated stress urinary incontinence (SUI), isolated overactive bladder-urge incontinence (OAB) and prior anti-incontinence surgery. Each patient was asked to urinate with the same sensation they would do at home for a non-invasive uroflowmetry (measuring free maximum flow (fQMax). The cystometry was conducted using a 6 Fr double lumen catheter for bladder filling and measurement of intravesical pressure, and a rectal balloon catheter was installed to measure abdominal pressure. Warm saline solution was infused at a rate between 10-50 ml/min. Finally, a pressure-flow study (PFS) was carried out to evaluate invasive maximum flow (iQmax). Both Qmax measures were manually corrected. Comparison of both uroflowmetries (free and invasive) was conducted for the whole sample through Spearman's rank correlation coefficient and intraclass correlation coefficient (ICC).The difference between both Qmax (fQmax-iQmax=𝚫Qmax) was calculated. Then, 𝚫Qmax was assessed among the different groups to see if there were any significant associations using  U Mann-Whitney. Numbers are shown with median and interquartile range and were evaluated with non-parametric tests using IBM SPSS version 23.0 and two-tailed p-values <0.05 was considered as statistically significant.
Results
891 urodynamic studies from female patients were reviewed and 407  patients met the inclusion criteria forming the analysis group. Overall, patients’ mean age was 53.9+-12 years, other socio demographic information is shown in table 1. Our population had a referral diagnosis of: voiding dysfunction (VD) (6.6%), mixed urinary incontinence (MUI) (61.7%), stress urinary incontinence (SUI) (24.6%), overactive bladder (OAB) (7.4%) and prior anti-incontinence surgery (13.3%). They had a median of 2 vaginal deliveries (IQR 3). 12.8% complained of vaginal bulge. They used a median of 3 pads/day (IQR 3) and their daily and nightly micturitions were 7(IQR 5) and 1 (IQR 2), respectively. 
 
Free Qmax was higher (30 ml/sec) and correlated poorly (r: 0271, p<0.001) with the iQmax (17 ml/sec). The F-Test to assess reliability of the two measurement tools showed there was a systematic error when measuring Qmax (p<0.001). Intraclass correlation coefficient (ICC) showed that only 14.8% of the variability among the measurement tools corresponded to a random error, in other words most variability was explained by systematic error. 
The comparison between both fQMax and iQmax is shown in Table 2. The whole group had a median of 12 ml/sec difference between both micturitions. This contrast behaved differently among the groups, showing that voiding dysfunction patients had a much lighter difference  (only 5 ml/sec), whereas patients with SUI showed a deeper difference with 17 ml/sec.
Interpretation of results
There is a bad correlation between free and invasive Qmax(1,2) and the systematic error shown by these two tools makes them not interchangeable. Theories proposed to explain this big gap includes that a catheter may provoke: a) diminution of the cross-sectional area of the urethra; b) a poor urethral-pelvic floor relaxation; and c) a urethra-bladder reflex leading to a poor detrusor contraction(1-3). Our results let us hypothesize that different urethras react variably to instrumentalization. Low resistance bladder outlets like in SUI patients seem to be more affected by the presence of the catheter, while patients with a presumed impaired urethral relaxation, like in voiding dysfunction, seem to be affected to a lesser extent.
Concluding message
Maximum flow rate in free and invasive measurement are not interchangeable, the latter is around 12 ml/sec lesser than the former. The presence of a urethral catheter importantly affects the measurement of urine maximum flow rate. This phenomenon varies among different kinds of patients.
Figure 1 Table 1: Clinical and demographic characteristics
Figure 2 Table 2: Comparison of Free and Invasive flowmetry between patients in different clinical groups according to the referral diagnosis/clinical suspicion.
References
  1. Groutz A, Blaivas JG, Sassone AM. Detrusor pressure uroflowmetry studies in women: effect of a 7Fr transurethral catheter. J Urol. 2000 Jul;164(1):109-14. PMID: 10840435.
  2. Valentini, F.A., Robain, G., Hennebelle, D.S. et al. Decreased maximum flow rate during intubated flow is not only due to urethral catheter in situ. Int Urogynecol J 24, 461–467 (2013). https://doi.org/10.1007/s00192-012-1856-2
  3. Harding C, Horsburgh B, Dorkin TJ, Thorpe AC. Quantifying the effect of urodynamic catheters on urine flow rate measurement. Neurourol Urodyn. 2012 Jan;31(1):139-42. doi: 10.1002/nau.21188. Epub 2011 Sep 26. PMID: 21953734.
Disclosures
Funding None Clinical Trial No Subjects Human Ethics Committee Comité de Ética de la Pontificia Universidad Católica de Chile Helsinki Yes Informed Consent No
Citation

Continence 2S2 (2022) 100254
DOI: 10.1016/j.cont.2022.100254

17/04/2024 19:34:29