Differences in Urodynamic Variables for Vesicoureteral Reflux Depending on the Neurogenic Bladder Type

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Abstract

INTRODUCTION

Unless appropriately treated, neurogenic bladder after spinal cord injury would lead to bladder deformity or other complications, such as vesicoureteral reflux (VUR), hydronephrosis, and renal failure [1]. VUR has been reported to occur due to higher intravesical pressure and urethral pressure, low bladder compliance, and thickening of the bladder wall resulting in changes at the vesicoureteric junction and intramural obliquity. Untreated VUR may lead to hydronephrosis and upper urinary tract infection, and ultimately cause renal failure [2].

According to the anatomic level of the lesion, neurogenic bladder after spinal cord injury is classified as suprasacral and infrasacral neurogenic bladder. Functionally, based on the results of urodynamic study during the filling phase, neurogenic bladders can be classified into detrusor overactive or underactive [3,4]. VUR occurs regardless of the type of neurogenic bladder. However, there are no well-designed studies assessing the differences in urodynamic study variables depending on the type of neurogenic bladder.

In the present study, we compared the urodynamic study variables at the onset of VUR between overactive and underactive bladders in patients with spinal cord injury who presented with VUR. In addition, based on the results of urodynamic study at the onset of VUR, we attempted to present the baseline data and the relevant guidelines for the optimal time of voiding by intermittent catheterization for the prevention of VUR in patients with neurogenic bladder.

MATERIALS AND METHODS

Three hundred twelve patients with spinal cord injury underwent urodynamic study and voiding cystourethrography on the same day from February 2008 to June 2011. Sixty-eight patients were confirmed to have VUR based on the international grading system [5] on voiding cystourethrography. Patients with peripheral neuropathy, those with an evidence of urinary tract infection, those who had concurrent brain injury, and those who were taking drugs that may affect the intravesical pressure, such as anticholinergics or cholinergics, were excluded. Finally, a total of 28 men were enrolled in the present study. In all of the study subjects, more than three months had elapsed since the onset of spinal cord injury. Mean age of the study subjects was 51.46±10.7 years. In these patients, a mean period of 92±103 months had elapsed since the spinal cord injury (Table 1).

Table 1

Demographic and clinical variables

The bladder was filled with a contrast medium using the drip infusion method and the infusion was controlled by an infusion pump at a rate of 50 mL/min. This was followed by assessment of the amount of contrast medium infused until the onset of VUR. A urodynamic study was also performed on the same day as voiding cystourethrography, and it was performed using Solar Gold (MMS, Enschede, The Netherlands). For performing these procedures, saline was infused into the bladder at room temperature at a rate of 24 mL/min using a two-lumen catheter.

Detrusor overactivity was defined according to the standardization of the 2002 International Continence Society, and it is defined as a condition in which there are spontaneous or provoked involuntary detrusor contractions [6]. There were 13 cases of detrusor overactivity and 15 cases of detrusor underactivity in this study.

The amount of contrast medium infused into the bladder at the onset of VUR was measured on the voiding cystourethrogram. The urodynamic variables, detrusor pressure and bladder compliance, the infused volume at the onset of VUR measured on a voiding cystourethrogram and cystometric capacity, maximum detrusor pressure, and bladder compliance during filling cystometry were recorded. We compared the urodynamic variables between the bladders with detrusor overactivity and detrusor underactivity. Statistical analysis was performed with the Mann-Whitney test using SPSS ver. 18.0 (SPSS Inc., Chicago, IL, USA).

RESULTS

In the detrusor overactivity group, the detrusor pressure, bladder volume, and bladder compliance at the onset of VUR were 19.23±20.96 cm H₂O, 120.38±88.56 mL, and 39.12±69.79 mL/cm H₂O, respectively. In the detrusor underactivity group, the detrusor pressure, bladder volume, and bladder compliance at the onset of VUR were 10.06±9.94 cm H₂O, 282.33±172.82 mL, and 68.60±134.57 mL/cm H₂O, respectively (Table 2).

Table 2

Comparison of urodynamic variables at the onset of vesicoureteral reflux between the two groups

The detrusor pressure, bladder volume, and bladder compliance during filling cystometry in the detrusor overactivity group were 62.00±29.96 cm H₂O, 230.61±79.42 mL, and 12.64±21.39 mL/cm H₂O, respectively. In the detrusor underactivity group, the detrusor pressure, bladder volume, and bladder compliance during filling cystometry were 25.04±20.73 cm H₂O, 457.06±141.93 mL, and 33.74±39.27 mL/cm H₂O, respectively (Table 3). At the onset of VUR, the bladder volume and bladder compliance, except for the detrusor pressure, showed a significant difference between the two groups. The detrusor pressure, bladder volume, and bladder compliance relative to the cystometric bladder capacity showed a significant difference between the two groups (p<0.05). The detrusor pressure, bladder volume, and bladder compliance at the onset of VUR relative to the cystometric bladder capacity did not any significant difference between the two groups (Table 4).

Table 3

Comparison of urodynamic variables during filling cystometry between the two groups

Table 4

Comparison of urodynamic ratios: the onset of vesicoureteral reflux vs. the cystometric capacity between the two groups

DISCUSSION

Ku et al. [7] reported that the incidence of VUR after spinal cord injury was 15.1%. Kaufman et al. [8] reported that the prevalence of VUR was 56% in patients with encephalocele whose intravesical pressure was relatively higher. Gerridzen et al. [9] reported that there were complications in the upper urinary tract among patients whose intravesical pressure was higher than 115 cm H₂O. McGuire et al. [10] demonstrated that there was a significant correlation between the leak point pressure of >40 cm H₂O and the risk of complications in the upper urinary tract. In addition, Hackler et al. [11] reported that among the 254 studied patients with spinal cord injury, the incidence of VUR was relatively higher in the low compliance group. Many studies have been conducted to examine the incidence of VUR following spinal cord injury, the causative factors of VUR, and the urodynamic study variables. However, there has been no study assessing the urodynamic variables at the onset of VUR in patients with spinal cord injury who had VUR.

In the current study, we compared the urodynamic study variables at the onset of VUR depending on the type of neurogenic bladder. Our results showed that the VUR occurred at a relatively lower capacity in the neurogenic bladder with detrusor overactivity than in the neurogenic bladder with detrusor underactivity. The bladder compliance at the onset of VUR was higher in the neurogenic bladder with detrusor underactivity. The detrusor pressure did not show any significant difference between the two types of neurogenic bladder. The detrusor pressure was 19.23±20.96 cm H₂O in the detrusor overactivity group and 10.06±9.94 cm H₂O in the detrusor underactivity group. This indicates that the VUR occurred at a lower pressure than that indicated by the well-known urodynamic study variables: leak point pressure of 40 cm H₂O [10], maximal detrusor pressure of 70 cm H₂O [12].

Both urodynamic study and voiding cystourethrography are routinely performed in different conditions from the physiological natural bladder filling. It can therefore be inferred that the results of these studies would be different from those obtained in physiological conditions. Filling rate of the filling media would affect the bladder compliance and the maximal cystometric capacity. Even at a lower filling rate of <20 mL/min, the detrusor pressure during bladder filling would be increased compared with that during natural bladder filling [13]. It is also known that the bladder compliance would be decreased with an increase in the filling rate [14]. In the current study, at a filling rate of 24 mL/min, we attempted to minimize the effects that may be generated during artificial filling. In addition, when a urodynamic study was performed twice consecutively, the bladder volume and compliance were increased during the second session as compared with those in the first session of bladder filling with saline [15]. In the current study, instead of a video-assisted urodynamic study, we presented the results of voiding cystourethrography and urodynamic study. This is one of the limitations of the present study that there is a lack of synchrony. Further studies are warranted to minimize these effects by performing a video-assisted urodynamic study.

In the current study, we performed urinalysis to exclude urinary tract infection that can affect bladder compliance and detrusor pressure on the same day as urodynamic study and voiding cystourethrography [16,17].

We conducted the current study only in male patients with spinal cord injury. It is known that there are sex-related differences in the VUR, and the incidence of VUR is relatively higher in women than in men [18]. This might be due to the anatomical differences, higher incidence of urinary tract infection, and a higher mean maximum detrusor pressure in women.

With regard to the type of neurogenic bladder depending on the level of spinal cord injury, Bors and Comarr [19] classified neurogenic bladder into the upper motor neuron bladders and lower motor neuron bladders depending on whether the level of injury was suprasacral or infrasacral. These authors reported that there was a higher prevalence of detrusor overactivity in cases of upper motor neuron injury and detrusor underactivity in cases of lower motor neuron injury. As compared with the other sites of spinal cord injury, the incidence of VUR has been reported to be relatively higher in cases of injury to the neurological level of T10-L2 [20]. However, there was no significant difference in the type of neurogenic bladder depending on the sites of spinal cord injury in our study.

It is known that the development of VUR is mainly due to factors, such as high leak point pressure [10] and high maximum detrusor pressure [12]. There are no established criteria for the optimal detrusor pressure for preventing injury to the upper urinary tract in patients with VUR.

We found that there was a significant difference in the results of the urodynamic study at the onset of VUR depending on the type of neurogenic bladder. It was also observed that the VUR occurred at a lower capacity in the neurogenic bladder with detrusor overactivity than in the neurogenic bladder with detrusor underactivity. Our results also showed that VUR occurred at a detrusor pressure of <40 cm H₂O, the leak point pressure which has been recognized so far as the critical level for the development of VUR in both types of neurogenic bladder.

In conclusion, there were differences in some urodynamic variables at the onset of VUR depending on the type of neurogenic bladder. The VUR occurred at a lower capacity in the neurogenic bladder with detrusor overactivity than in the neurogenic bladder with detrusor underactivity at the same pressure. VUR occurred at a lower intravesical pressure compared to that known as the critical detrusor pressure required for the development of VUR. Further studies are warranted to examine the role of detrusor pressure in order to effectively prevent the development of VUR. The results of our present study demonstrate that the detrusor pressure should be maintained lower than the well-known effective critical detrusor pressure for the prevention and treatment of VUR.

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