Sunteți pe pagina 1din 6

Applicability of Perineal Sonography in

Anatomical Evaluation of Bladder Neck


in Women with and without Genuine
Stress Incontinence

Gin-Den Chen, MD,1 Tsaung-Hsien Su, MD,2 Long-Yau Lin, MD1

1
Department of Obstetrics & Gynecology, Chung Shan Medical & Dental College
Hospital, 23, section 1, Taichung-Kang Road, Taichung, Taiwan
2
Urodynamic Unit, Department of Obstetrics & Gynecology, Mackay Memorial Hospital, Taiwan

Received 1 August 1995; accepted 7 November 1996

Abstract: Thirty-seven patients with proven genuine stress incontinence (GSI) un-
derwent ultrasound study to evaluate the bladder neck position relative to the sym-
physis pubis. Sixty-five continent women including 40 parous and 25 nulliparous
women were recruited as a control group. Several parameters were found to be statis-
tically different between incontinent and control groups ( P , 0.01). If 28 degrees or
13 mm were used as the cut-off point for rotational angle (RA) and descent of bladder
neck (DBN), the sensitivity, specificity, and positive and negative predictive values
were 73.0%, 76.9%, 64.3%, and 83.3%, respectively. The specificity and positive pre-
dictive value for GSI increased to 83.1% and 67.6% if these two parameters were used
together. Perineal sonography is valuable in assessing anatomic change of the bladder
neck, but it is not a sensitive tool for predicting GSI.  1997 John Wiley & Sons, Inc.
J Clin Ultrasound 25:189–194, 1997
Keywords: perineal sonography; rotational angle; bladder neck descent; urinary
stress incontinence

Poor anatomic support of the bladder base and nography7–9 have been used to assess the dy-
urethrovesical junction, incompetence of the vesi- namic changes of the urethrovesical junction and
cal neck, and urethral function were considered proximal urethra for a decade as an alternative
important factors in uncomplicated genuine to conventional radiological techniques. How-
stress urinary incontinence.1 The movement of ever, their shortcomings, such as impaired reso-
the bladder neck beyond the intra-abdominal lution of image, distortion of the anatomical fea-
pressure transmission zone prevents pressure tures, requirement of urethral catheterization for
transmission to the bladder neck and proximal detecting the bladder neck and exact determina-
urethra to compensate for the pressure transmit- tion of the position of the bladder neck, are still
ted to the bladder in case of a sudden increase of not clearly resolved.
abdominal pressure which might contribute to The purposes of this study were to evaluate
the urine leakage.2 objective parameters of the dynamic changes of
Transrectal,3 transvaginal,4–6 and perineal so- the bladder neck among patients with genuine
stress incontinence (GSI), to develop diagnostic
criteria for differentiating various groups of pa-
Correspondence to: G.-D. Chen tients, and to assess the predictability of GSI us-
 1997 John Wiley & Sons, Inc. CCC 0091-2751/97/040189-006 ing perineal sonography.
VOL. 25, NO. 4, MAY 1997 189
CHEN ET AL

MATERIALS AND METHODS about 150–250 mL, and the voiding volume was
Thirty-seven patients with proven GSI by urody- checked after the procedure was completed.
namic study but without marked cystocele or ur- A sagittal scan was performed to evaluate the
ethrocele underwent ultrasound study to evalu- symphysis pubis (SP), the bladder, the vesico-
ate the bladder neck relative to the symphysis urethral junction (VUJ), the proximal urethra,
pubis. The ages of patients ranged from 24 to 46 and other pelvic organs. If the bladder neck could
(mean: 35.6) years and parity ranged from 1 to 4 not be shown in the initial sectional plane, the
(median: 2). Sixty-five continent women, includ- patient was asked to cough slightly to permit fur-
ing 40 cases with vaginal delivery history and 25 ther searching for the bladder neck. The patient
nullipara, were recruited as a control group (con- was then asked to perform a Valsalva maneuver
trol group 1, C1). The 40 cases with vaginal de- or cough, and the picture was frozen at the point
livery were further defined as control group 2 of maximal bladder neck rotational descent. Pic-
(C2). The age of the participants with vaginal de- tures were taken at rest and during maximal
livery history ranged from 23 to 49 (mean: 37.5) straining during this sequence of events. All of
years and parity ranged from 1 to 4 (median: 2). the scanning procedures were recorded on vid-
The same procedures were performed on the con- eotape.
trol groups after they had received the regular The rotational angle (RA) and descent of the
abdominal or transvaginal sonographic exami- bladder neck (DBN) during maximal straining
nation. were determined by using an arbitrary line
Perineal sonography was performed by using drawn at 120 degrees from midline of SP, drawn
a convex probe (3.5 MHz, Aloka 650 scanner). from the inferior margin of SP (Figure 1). The
The probe enclosed in a condom was positioned inferior margin of SP was used as the reference
just adjacent to the perineum and between the point for RA. The distance between the inferior
labia majora at rest. The patient was placed in a margin of the SP and bladder neck was mea-
supine position and straightened her legs sponta- sured at rest (Dr) and during maximal straining
neously. The bladder neck was identified without (Ds). The distance of the bladder neck from the
urethral catheterization. The bladder capacity arbitrary line (DBN) was described at rest (r)
was set at self-comfortably full sensation level, and during maximal straining (s). The DBN was

FIGURE 1. Diagram showing the relationships of symphysis pubis and the location of the bladder neck and
bladder at rest and during maximal straining. SP 5 symphysis pubis, BN 5 bladder neck, Dr 5 distance of
the bladder neck and the inferior margin of the symphysis pubis at rest, Ds 5 distance of the bladder neck
and the inferior margin of the symphysis pubis during maximal straining, r 5 distance of the bladder neck
and the arbitrary line at rest, s 5 distance of the bladder neck and the arbitrary line during maximal straining,
120 degrees 5 the angle between the middle line of the symphysis pubis and the arbitrary line.

190 JOURNAL OF CLINICAL ULTRASOUND


BLADDER NECK IN WOMEN

defined as r minus s. This arbitrary line was There were no significant differences in the
compared with the line drawn from the lower measured parameters between continent women
margin of SP to the inferior margin of the 5th in the two selected control groups (C1 and C2).
sacral vertebra, which serves as a reference line The parameters of Dr, Ds, r, s, RA, and DBN
in the lateral chain-cystogram.10 were significantly different between the GSI
The parameters Dr, Ds, r, s, RA, and DBN group and each of the selected control groups
were compared between the incontinent and con- (Table 1).
trol groups. The Student t test was used in the Descent of bladder neck was statistically sig-
statistical analysis to compare the parameters nificantly larger during the Valsalva maneuver
between the incontinent and continent groups. or coughing in the GSI group (17.6 6 7.3 vs
The significant level was set at P , 0.01. The 9.0 6 6.9; 17.6 6 7.3 vs 11.2 6 5.4 mm, all p ,
cut-off points of Dr, Ds, RA, and DBN were eval- 0.01). During maximal straining, the RA of blad-
uated through the receiver operating characteris- der neck in the GSI group was statistically sig-
tic (ROC) curves to determine the highest sensi- nificantly larger than that in the continent group
tivity and the lowest false predictive value. The (42.9 6 19.7 vs 17.7 6 15.0; 42.9 6 19.7 vs
ability of perineal sonography to predict GSI was 22.7 6 13.4 degrees, all p , 0.01).
expressed in sensitivity, specificity, and pre- The cut-off points for RA and DBN of bladder
dictive values. neck were found to be 28 degrees and 13 mm
from their receiver operating characteristic
(ROC) curves, respectively (Figure 3). The cut-off
RESULTS points for evaluating Dr and Ds were found to be
The dynamic changes of bladder neck and the in- meaningless through ROC analysis. If either 28
formation of the anatomic relationships of blad- degrees or 13 mm was used as a cut-off point for
der neck, proximal urethra, and other pelvic RA and DBN, the sensitivity, specificity, and pos-
organs during straining could be clearly demon- itive and negative predictive values were 73.0%,
strated in sonographic scanning as shown in Fig- 76.9%, 64.3%, and 83.3%, respectively. Combin-
ure 2. ing these two parameters, the specificity and pos-

FIGURE 2. Ultrasound images showing the relationships of the symphysis pubis and the location of the bladder at rest and during maximal
straining. SP 5 symphysis pubis, BL 5 bladder, BN 5 bladder neck, U 5 urethra, Cx 5 cervix of uterus, V 5 vagina, R 5 rectum. Oblique dotted
line 5 the middle line of the symphysis pubis, transverse dotted line 5 an arbitrary line drawn at 120 degrees from the inferior margin of the
symphysis pubis.

VOL. 25, NO. 4, MAY 1997 191


CHEN ET AL

TABLE 1 the hazard of radiation exposure. Also, it is more


Comparison of Parameters Between GSI and
reproducible than radiological measurements.
Control Groups
The vaginal probe was proven to reduce the
Control likelihood of detecting incontinence in women
GSI (C1 5 65) with GSI or reduce the severity of GSI diag-
TCH (N 5 37) (C2 5 40) P Value
nosed. It might be inappropriate in assessing the
Dr (mm) 26.8 6 4.0 29.3 6 3.3 P , 0.01 descent and mobility of the bladder neck and
29.5 6 3.6 P , 0.01
Ds (mm) 19.4 6 3.5 23.0 6 3.8 P , 0.01
urogenital prolapse, because the vaginal probe
22.4 6 3.9 P , 0.01 may directly contact, and thus compress, the va-
RA (degrees) 42.9 6 19.7 17.6 6 14.9 P , 0.01 ginal wall.11 On the contrary, by using the convex
22.7 6 13.6 P , 0.01 probe adjacent to the perineum and between the
r (mm) 18.2 6 5.6 21.3 6 5.4 P , 0.01
22.3 6 4.6 P , 0.01 labia majora, normal pelvic floor anatomy is not
S (mm) 0.6 6 6.8 12.3 6 8.5 P , 0.01 distorted nor the bladder neck mobility impeded.
11.4 6 6.0 P , 0.01 Therefore, the dynamic changes of the bladder
DBN (mm) 17.6 6 7.3 9.0 6 6.9 P , 0.01
11.2 6 5.4 P , 0.01
neck and the relative changes of other pelvic or-
gans can be clearly shown in the sonographic ex-
Dr: distance between bladder neck and lower margin of symphysis
pubis at rest.
amination.
Ds: distance between bladder neck and lower margin of symphysis Schaer et al8 found that some landmarks re-
pubis during straining. lating to the bladder neck could not be demon-
RA: rotational angle of bladder neck.
r: distance between bladder neck and arbitrary line at rest.
strated satisfactorily at rest and during the Val-
s: distance between bladder neck and arbitrary line during salva maneuver, especially in measuring the
straining. funneling of the bladder neck and severe bladder
DBN: descent of bladder neck. base descent. They considered these results to be
P value , 0.01 was statistically significantly different by Student
t test. The parameters of C1 and C2 group were not statistically signifi- a typical phenomenon illustrating the difference
cantly different by Student t test. between ultrasound and x-ray techniques. Ultra-
sound portrays a thin cut through the female pel-
vis, whereas x-ray assessment scans all layers of
itive predictive value for GSI could be increased the pelvic region with the potential risk of a mis-
to 83.1% and 67.6% (Table 2). leading assessment of the anatomy when not per-
formed correctly.9
Because our cases had proven GSI by urody-
DISCUSSION namic study without marked pelvic relaxation,
the above phenomenon could be ruled out in this
Ultrasound has been advocated as an alterna- study. When the position of the bladder neck
tive to videocystourethrography in several could not be clearly shown in the image during
studies.2–6,12,13 There were some benefits, such as straining, the patient was asked to cough and
no x-ray exposure and less expense. Perineal so- perform the Valsalva menuever repeatedly. Thus
nography could be performed repeatedly without the point of maximal bladder neck rotational de-

FIGURE 3. Diagram of cut-off point for rotational angle (left) and descent of the bladder neck (right) as shown in receiver operating characteristics
curve analysis.

192 JOURNAL OF CLINICAL ULTRASOUND


BLADDER NECK IN WOMEN

TABLE 2
Sensitivity, Specificity, and Positive and Negative Predictive Values for
Diagnosis of GSI

DBN . 13 mm and
DBN . 13 mm RA . 28 Degree RA . 28 Degree
(%) (%) (%)
Sensitivity 73.0 73.0 62.2
Specificity 76.9 76.9 83.1
Positive 64.3 64.3 67.6
predictive value
Negative 83.3 83.3 79.4
predictive value
DBN: descent of bladder neck.
RA: rotational angle of bladder neck.

scent could be reached. Conclusively, perineal so- 4.0 vs 29.3 6 3.3 or 29.5 6 3.6. Ds: 19.4 6 3.6 vs
nography can provide a reproducible result for 23.0 6 3.8 or 22.4 6 3.9), but there was consider-
determining the dynamic change of the bladder able overlap. Nevertheless, Dr was significantly
neck area. longer than Ds in the GSI compared with the se-
Gordon et al9 have found similar results be- lected control groups.
tween perineal ultrasound scanning and x-ray If two of three criteria (angle at rest .95 de-
chain urethrocystography in evaluating the blad- grees, BS ,2.3 cm, and mobility .20 degrees)
der neck position in GSI patients. Furthermore, are regarded as the diagnostic criteria of inconti-
the experience of Mackay Memorial Hospital in- nence, the sensitivity was 84% and the specificity
dicated that an arbitrary line drawn at 120 de- 82% using vaginal ultrasonography in the study
grees from the lower margin of the symphysis of Mouritsen et al.12 The sensitivity of transrectal
pubis axis in introital ultrasound could replace ultrasonic evaluation of women with stress uri-
the pubo-sacral line in chain cystourethrography. nary incontinence (when 1 cm drop of the
A close correlation was found between this arbi- urethrovesical junction is considered as the up-
trary line and the pubo-sacral line in chain cys- per normal limit) was 86% and the specificity
tourethrography in a previous report.10 By using was 91% in the report of Bergman et al.13
this arbitrary line, the mobility of bladder neck In our study, the diagnostic cut-off points for
and proximal urethra could be shown in perineal RA and DBN were set as 28 degrees and 13 mm
sonography just as in chain cystourethrography. in diagnosing the GSI. The sensitivity, specific-
This procedure has been suggested as a suitable ity, and positive and negative predictive values
alternative to conventional radiological tech- were 73.0%, 76.9%, 64.3%, and 83.3%, respec-
niques in the evaluation of mobility of the blad- tively. The specificity and positive predictive
der neck. Our method could easily and directly value for GSI could be increased to 83.1% and
provide information on the dynamic changes of 67.6% only if these two criteria were considered
the bladder neck and the anatomic relationships together.
of the bladder neck in the absence of urethral In conclusion, perineal sonography can detect
catheterization, which might introduce an iatro- the realistic movement of the bladder neck with-
genic infection and distort the urethral profile. out restricting it by the presence of the probe.
In this study, the movement of the bladder This offers real-time dynamic scanning of the re-
lationship between pelvic anatomic changes at
neck was shown as a semicircular movement
rest and during straining. It is valuable in as-
with the tip of the symphysis pubis as the center
sessing anatomic change of the bladder neck, in
and a line from the tip to the bladder neck as
GSI patients. However, there is not sufficient ev-
the radius (BS). This finding was similar to the
idence to use perineal sonography in predicting
description of Mouritsen et al.12
GSI.
These parameters in the two selected control
groups are not significantly different. In conti-
nent women, parity seems to make little contri- REFERENCE
bution to the mobility of the bladder neck (Table 1. Summitt RL Jr, Bent AE, Ostergard DR: The
1). pathophysiology of genuine stress incontinence.
The Dr and Ds were significantly different be- Int Urogynec J 1:12–17, 1990.
tween the GSI and continent groups (Dr: 26.8 6 2. Johnson JD, Lamensdorf H, Hollander IN, et al:
VOL. 25, NO. 4, MAY 1997 193
CHEN ET AL

Use of transvaginal endosonography in the evalu- 8. Schaer GN, Koechli OR, Schuessler B, et al. Peri-
ation of women with stress urinary incontinence. neal ultrasound for evaluating the bladder neck in
J Urol 147:421–425, 1992. urinary stress incontinence. Obstet Gynecol
3. Bergman A, Mckenzie CJ, Richmond J, et al: 85:220–224, 1995.
Transrectal ultrasound versus cystography in the 9. Gordon D, Pearce M, Norton P, et al: Comparison
evaluation of anatomical stress urinary inconti- of ultrasound and lateral chain urethrocystogra-
nence. Br J Urol 62:228–234, 1988. phy in the determination of bladder neck descent.
4. Richmond DH, Suther J: Transrectal ultrasound Am J Obstet Gynecol 160:182–185, 1989.
scanning in urinary incontinence: the effect of the 10. Hwu YM, Su TS, Yang JM, et al: In comparison of
probe on urodynamic parameters. Br J Urol vaginal introital sonography and chain cys-
64:582–585, 1989. tourethrography in patients with genuine stress
5. Quinn MJ, Beynon J, Mortenson NJMcC, et al: incontinence. 1992 Annual Convention of the Soci-
Transvaginal endosonography: a new method to ety of Ultrasound in Medicine of the Republic of
study the anatomy of the lower urinary tract in China. JUMROC 9(3):190, 1992.
urinary stress incontinence. Br J Urol 62:414– 11. Wise BG, Burton G, Cutner A, et al: Effect of vagi-
418, 1988. nal ultrasound probe on lower urinary tract func-
6. Koebl H, Bernaschek G: A new method for sono- tion. Br J Urol 70:12–16, 1992.
graphic urethrocystography and simultaneous 12. Mouritsen L, Rasmussen A: Bladder neck mobility
pressure-flow measurements. Obstet Gynecol evaluated by vaginal ultrasonography. Br J Urol
74:417–422, 1989. 71:166–171, 1993.
7. Creighton SM, Pearce JM, Stanton SL: Perineal 13. Bergman A, Ballard CA, Plat LD: Ultrasonic eval-
video-ultrasonography in the assessment of vagi- uation of urethrovesical junction in women with
nal prolapse: early observations. Br J Obstet Gyne- stress urinary incontinence. J Clin Ultrasound
col 99:310–313, 1992. 16:295–300, 1989.

194 JOURNAL OF CLINICAL ULTRASOUND

S-ar putea să vă placă și