Correlation between obesity-related measurements and initial and initial resting intravesical and abdominal pressures in urodynamic study using air-charged catheter system

Shen S1, Zeng X1, Zhang J1, Shen H1, Luo D1, Fan Y1

Research Type

Clinical

Abstract Category

Urodynamics

Abstract 593
Open Discussion ePosters
Scientific Open Discussion Session 33
Friday 29th September 2023
13:05 - 13:10 (ePoster Station 1)
Exhibit Hall
Urodynamics Techniques Prospective Study Voiding Dysfunction
1. Department of Urology, Institute of Urology, West China Hospital, Sichuan University, No. 37 Guo Xue Xiang, Chengdu, Sichuan, 610041, P.R. China
Presenter
Links

Poster

Abstract

Hypothesis / aims of study
To firstly establish the initial (before pressure equilibrium) and initial resting intravesical and abdominal pressure of air-charged catheter (ACC) system urodynamic study (UDS) testing, to assess the correlation between these pressures and obesity-related measurements, and to estimate if obesity-related measurements can be a guide to interpret initial and initial resting pressures in the UDS testing.
Study design, materials and methods
This study was conducted in our UDS center from August 2022 to October 2022. Local ethics committee approval was obtained, and written informed consent was obtained. Patients with non-neurogenic lower urinary tract symptoms (LUTS) referred for UDS were prospectively enrolled. Conventional pressure flow studies were carried out in the sitting position with a Laborie Triton equipment using the ACC system (Laborie & Co, Canada) following Good Urodynamic Practice (GUP) guidelines published by the International Continence Society (ICS) [1,2]. All patients were asked to empty the bladder before UDS. Intravesical dual lumen catheter (T-DOC 7FD, Laborie) and single lumen rectal catheter (T-DOC 7FA, Laborie) were used to measure intravesical pressure (Pves) and abdominal pressure (Pabd). Catheters were inserted in the open position and the connector then switched to the “charge” position after the transducer exposed to the surrounding atmospheric pressure were set to zero [1,2]. We recorded the initial Pves and Pabd at this moment. Then we clicked Pabd = Pves for pressure equilibrium. The initial resting Pves, Pabd, and calculated detrusor pressure (Pdet = Pves − Pabd) were recorded after confirming the ‘‘live’’ signal tracing (the same pressure transmission while coughing) before filling. After the UDS procedure, BMI, weight, fat, muscle, and visceral fat grade were recorded using Direct Segmental Multi-Frequency Bioelectrical Impedance Analysis Method (InbodyH20B) (patients were asked to wear light clothing). The abdominal sebum thickness and waistline were also recorded. The initial and initial resting pressures were also expressed as 50% range (equivalent to the interquartile range). The correlation between initial and initial resting pressures and obesity-related measurements, including abdominal sebum thickness, waistline, BMI, weight, height, fat, and visceral fat grade, was studied using Pearson correlation coefficient. Then we used multiple linear regression analysis for further investigation (weight, height, and fat were not considered because of the effect of multicollinearity). Data was processed with the SPSS 24.0 and statistical significance was defined as P < 0.05.
Results
Ninety-eight patients aged 56±16 were studied. The 50% range of the initial Pves ranged between 27.0 - 34.0 cmH2O and Pabd ranged between 35.0 - 46.0 cmH2O. While the initial resting Pves, Pabd, and Pdet ranged between 24.0 - 33.0, 24.0 - 32.0, and -1.0 - 1.0 cmH2O, respectively, which falls closely in line with the previous similar type of study [3]. Analysis of Pearson correlation coefficient revealed a significant correlation between initial pressures and obesity-related measurements. Initial Pves was positively correlated with abdominal sebum thickness, waistline, BMI, visceral fat grade, weight, and fat, with no significant correlation with height. The initial Pabd showed high correlation with abdominal sebum thickness, waistline, BMI, visceral fat grade, weight, and fat, while there was no correlation with height and muscle. Related factors were included in the multiple linear regression analysis. The results of the multiple linear regression analysis indicating a significant correlation between initial Pves and abdominal sebum thickness and BMI (r=0.651, p=0.041 and p=0.004, respectively), but no correlation with waistline and visceral fat grade. The results of the multiple analysis also show only visceral fat grade maintained a significant correlation with initial Pabd (r=0.679, p=0.021) (shown in Figure 1). For the initial resting pressures, we only analyzed the correlation between initial resting Pves and obesity-related measurements, because the value of initial resting Pabd was close to the initial resting Pves after the pressure equilibrium procedure. The results of Pearson’s correlation coefficient indicated a significant correlation between initial resting Pves and abdominal sebum thickness, waistline, BMI, visceral fat grade, weight, muscle, and fat, with no significant correlation with height. Regardless of weight, height, and fat, only BMI maintained a significant correlation with initial resting Pves over the multiple analysis (r = 0.608, P=0.007) (shown in Figure 1).
Interpretation of results
Our results firstly revealed that the obesity-related indexes were positively correlated with the corresponding bladder and rectal pressures in the ACC system. In the UDS procedure, if the initial value of Pabd is lower than the estimated value based on the obesity index of the patient, it should be considering whether the insertion depth of the rectal catheter is not enough. If it is higher than the estimated range, it should be considering whether the bowel preparation is inadequate or whether there is abnormal rectal contraction (e.g., neurogenic rectum, intestinal hyperperistalsis, etc.), or whether the balloon tip reaches the rectal wall. After adjusting the possible problems according to the situation, ensure that the initial or initial resting Pabd and Pves values are within the normal range estimated based on the obesity index, a good initial and initial resting pressure quality control can be better obtained. A good quality urodynamic trace can only be obtained when the procedure is started under a good quality control.
Concluding message
Our original study firstly carried out the values of both initial and initial resting pressures in the ACC system UDS testing. Our single center results were in accordance with the literature and reflected a good baseline quality control [3]. Though currently there is still a lack of the estimating model, our study showed the obesity-related measurements might be used as a guide to interpret the initial and initial resting pressures in urodynamic testing, and might provide a reference for the quality control of these pressures.
Figure 1 Figure 1. Correlation of abdominal sebum thickness, waistline, BMI, and visceral fat grade with intravesical and abdominal pressure (results of multiple linear regression analysis).
References
  1. Rosier P, Schaefer W, Lose G, Goldman HB, Guralnick M, Eustice S, Dickinson T, Hashim H (2017) International Continence Society Good Urodynamic Practices and Terms 2016: Urodynamics, uroflowmetry, cystometry, and pressure-flow study. Neurourol Urodyn 36 (5):1243-1260. doi:10.1002/nau.23124
  2. Schäfer W, Abrams P, Liao L, Mattiasson A, Pesce F, Spangberg A, Sterling AM, Zinner NR, van Kerrebroeck P (2002) Good urodynamic practices: uroflowmetry, filling cystometry, and pressure-flow studies. Neurourol Urodyn 21 (3):261-274. doi:10.1002/nau.10066
  3. Deng H, Liao L, Wu J, Li X, Pang D, Liu Q, Wang X, Li X, Liang Yn, Zhou Z, Luo R, He P (2023) Typical value ranges and signal patterns in patients with neurogenic bladder: Quality control in urodynamics using an air-charged catheter system. Neurourology and Urodynamics 42 (1):113-122. doi:https://doi.org/10.1002/nau.25055
Disclosures
Funding none Clinical Trial Yes Registration Number The study was registered in the Chinese Clinical Trials Registry (Trial No. ChiCTR2300068280). RCT No Subjects Human Ethics Committee Ethics Committee on Biomedical Research, West China Hospital of Sichuan University, No.2021183 Helsinki Yes Informed Consent Yes
20/11/2024 07:40:53