RELATIONSHIP BETWEEN DETRUSOR INSTABILITY AND URETHRAL RESISTANCE

 

Authors:

J. Groen, J.L.H.R. Bosch

   

Institution:

University Hospital Rotterdam, Rotterdam, The Netherlands

     

Conference:

ICS 2000 Tampere

       

Type:

Informally discussed posters

         

Category:

Bladder Overactivity

                 

AIMS.

Sacral neuromodulation is a treatment option for patients with detrusor instability [1]. This method has also been shown to decrease urethral resistance during voiding [2]. We previously found that urethral resistance was higher in a group of females with detrusor instability than in females with mixed incontinence or stress incontinence or females without a demonstrable cause of the incontinence and postulated that functional obstruction could be a potential cause of instability [3]. In the present study, we examined the relationship between the decrease of urethral resistance and that of the grade of instability in patients with detrusor instability treated with neuromodulation. In addition, we examined if the symptomatic changes as derived from voiding / incontinence diaries depended on urethral resistance. Such a study might contribute to the understanding of the role of voiding characteristics in the signs and symptoms of detrusor instability.

 

METHODS.

Neuromodulation is applied at our department since 1990. Voiding / incontinence diaries and cystometric studies with subsequent pressure / flow studies before and 6 months after the operation are part of the evaluation. Cystometry is done in the supine and standing position and, after implantation, with the stimulator on and off. The pressure / flow studies are done in the standing position. Only patients with symptoms of urge incontinence and urodynamically demonstrated detrusor instability who had passed the 6 month evaluation period were included in the present study. The maximum detrusor pressure Pmax during the filling phase was used as the parameter characterising the grade of instability. Urethral resistance was characterised by URA. In addition, the maximum flow rate Qmax and the associated detrusor pressure pQmax were determined. The measurements in the standing position and, after implantation, with the neurostimulator on, were used. Three categories of symptomatic success were defined: a more than 90% decrease in the number of pads used per day or the number of incontinence episodes per day was considered a cure, a decrease between 50 and 90% was considered a partial success and a decrease of less than 50% was considered a failure.

 

RESULTS.

Of the 47 patients implanted so far, 44 (38 women, 6 men, mean age 46 years) underwent the 6 month follow-up examinations. Symptomatically, 23 patients were cured, 15 were a partial success and in 6 treatment failed. The table summarises the mean values and interquartile ranges of the urodynamic parameters for all patients and for the symptomatic categories separately. On average, Pmax as well as URA decreased significantly (paired t-test: p=0.004 and p<0.0005, respectively). Qmax increased significantly (p=0.007). The change in pQmax, however, was not significant (p=0.19). The high initial mean values of URA and pQmax in the patients who failed were caused by one patient only: they were 19 and 39 cm H2O, respectively, in the remaining 5 patients. None of the parameters listed in the table demonstrated significant differences between the symptomatic categories (unpaired t-tests, Kruskal-Wallis test). The figure demonstrates the relationship between the changes in Pmax and URA. The Pearson correlation coefficient r was 0.27, which was not significant (p=0.081). The Spearman rank correlation coefficient rho, however, was 0.34, which was significant (p=0.024). No dependence of the relationship on the symptomatic category was found. The relationship between the changes in Pmax and those in the voiding pressure pQmax looked very similar, but significance was reached in both tests (r = 0.52, rho = 0.54, p<0.0005).

 

 

 

All (44)

Cure (23)

Partial (15)

Fail (6)

Pmax

before

42 (25 - 56)

47 (25 - 59)

37 (25 - 50)

35 (22 - 56)

(cm H2O)

after

30 (10 - 45)

30 (17 - 41)

33 (14 - 45)

28 (6 - 48)

 

change

-12 (-27 - -1)

-18 (-30 - -2)

-5 (-20 - 4)

-7 (-16 – 0)

URA

before

21 (14 – 26)

18 (14 – 19)

22 (11 – 28)

28 (14 – 39)

(cm H2O)

after

16 (11 – 20)

15 (12 – 20)

16 (12 – 22)

18 (8 – 31)

 

change

-5 (-8 – 1)

-3 (-5 – 1)

-5 (-11 – 2)

-10 (-19 - -1)

pQmax

before

39 (27 – 50)

38 (27 – 50)

38 (29 – 52)

47 (26 – 69)

(cm H2O)

after

36 (25 – 44)

36 (21 – 57)

37 (24 – 45)

37 (21 – 57)

 

change

-3 (-11 – 6)

-2 (-8 – 6)

-1 (-10 – 10)

-10 (-24 – 4)

Qmax

before

13 (8 – 17)

15 (9 – 17)

10 (5 – 12)

12 (7 – 18)

(ml/s)

after

16 (10 – 20)

17 (11 – 22)

14 (10 – 17)

14 (8 – 20)

 

change

3 (-1 – 5)

2 (-1 – 4)

4 (1 – 9)

2 (-1 – 6)

 

DISCUSSION.

This study confirms that neuromodulation reduces the grade of instability as well as the urethral resistance during voiding. The correlation between these two entities, however, was weak. If the voiding pressure would be considered a measure of urethral resistance, the decrease of the instability could be ”explained” by a decrease of the resistance for about 25% (coefficient of determination r2). It has been shown that symptomatic changes only poorly correlate with changes of the grade of instability [1]. It might be hypothesised that the symptomatic outcome is correlated more strongly with voiding phase characteristics than with filling phase characteristics. This study does not give evidence supporting that hypothesis. Apparently non-urodynamic factors play a significant role in the success of neuromodulation.

 

[1]. Curr.Opin.Urol. 8: 287-291, 1998               [3]. Neurourol.Urodynam. 17: 386-388, 1998

[2]. Neurourol.Urodynam. 14: 502-504, 1995