Urodynamics: Indications, techniques, interpretation, and clinical utility


Introduction to urodynamics

The term urodynamics means observation of the changing function of the lower urinary tract (LUT) over time. Specifically, urodynamic studies are a number of interactive diagnostic tests that can be used to obtain functional information about bladder filling, urine storage, and voiding.

To understand the fundamental value of urodynamics, one should realize that the female bladder responds similarly to a variety of pathologies. Symptoms do not always accurately reflect the physiologic state of the bladder. For example, a patient may feel that her bladder is full when it is nearly empty, or that her bladder is contracting when it is not. The validity of any urodynamic diagnosis is linked to the patient’s symptoms and the reproduction of these symptoms during the testing session. To obtain the most accurate, clinically relevant interpretation of urodynamic studies, the urodynamicist should clearly understand LUT function and should correlate urodynamic data with other clinical information. Ideally, the urodynamicist should be the physician who takes the history, reviews the voiding diary, performs the physical examination, interprets other tests, explains the diagnosis, and develops a reasonable management plan.

Results of urodynamic investigations should be recorded in a way that can be communicated among physicians and other health care personnel. For this reason, the recommendations detailed in the standardization reports of the International Continence Society (ICS) should be followed ( ).

Normal bladder physiology

A prerequisite to performing and interpreting a urodynamic study is having a full understanding of normal LUT function (see Chapter 3 ). During filling, a normal adult bladder should act as a low-pressure reservoir. It has the inherent ability of responding to filling (when done at a physiologic rate) with an almost imperceptible change in intravesical and detrusor pressure ( P det ). This high compliance of the bladder is due primarily to its elastic and viscoelastic properties. During filling, the bladder outlet should be closed and remain closed even during increases in intraabdominal pressure. There is a gradual increase in urethral pressure during bladder filling contributed to in part by the striated sphincter of the urethra and perhaps also by smooth sphincteric elements as well. This can be detected by measuring urethral pressure but also can be seen on electromyography (EMG). The normal opening vesical pressure in an adult female bladder should be in the range of 2 to 6 cm H 2 O, with it only increasing to approximately 10 cm H 2 O at maximum capacity.

Bladder filling should be associated with appropriate sensation. Most women will feel a first sensation of bladder filling between 75 and 150 mL, feel an urge to void between 300 and 400 mL, and have a maximum capacity or strong desire to void between 400 and 700 mL. Although many factors are involved in the initiation of micturition in adults, it is intravesical pressure that creates the sensation of distention that is primarily responsible for the initiation of a normal voluntarily induced emptying of the bladder. This also involves inhibition of the striated sphincter of the urethra and an inhibition of all aspects of any spinal sympathetic reflexes evoked during filling. A decrease in outlet resistance occurs with adaptive shaping and funneling of the relaxed bladder outlet, leading to efficient voiding. Fig. 11.1 demonstrates a storage and micturition reflex in a neurologically intact female.

Fig. 11.1, A , Typical storage reflex in a neurologically intact woman; note increased electromyographic ( EMG ) activity during filling, coughing, straining, and an uninhibited detrusor contraction. This indicates an intact synergistic pelvic floor response. B , Typical micturition reflex in a neurologically intact woman. Note complete loss of EMG activity simultaneous with an increase in detrusor pressure at initiation of voiding. IDC , Involuntary detrusor contraction; P abd , intraabdominal pressure; P det , detrusor pressure; P ure , urethral pressure; P ves , intravesical pressure.

Functional classification of lower urinary tract dysfunction

To be able to formulate the appropriate questions to be answered by a urodynamic study, the clinician must have a clear understanding of the possible or potential causes of symptoms. The functional classification of LUT dysfunction as proposed and popularized by is a simple, clinically relevant way of classifying LUT dysfunction. Wein proposed that functional abnormalities of the LUT can be broadly divided into failure of the bladder to adequately store urine or failure of the bladder to adequately empty. Failure of the bladder to store urine results from bladder overactivity (involuntary contractions or decreased compliance), decreased outlet resistance (sphincter deficiency), heightened or altered sensation, or a combination of these various abnormalities. Failure of the bladder to empty results from decreased bladder contractility, increased outlet resistance, or a combination of both. Finally, a combined dysfunction of failure to store and empty is also potentially feasible.

To use a functional classification appropriately, there must be an understanding of the physiology of urine storage and voiding, as well as knowledge regarding the various disease states that can cause LUT dysfunction. The advantage of a simple classification such as this is that it helps to clarify treatment options for a given patient. Simply determining whether there is a problem with storage, emptying, or both, as well as assessing bladder and urethral (outlet) function, can commonly lead to a correct urodynamic diagnosis with institution of appropriate therapy. The clinician should always focus on the urodynamic finding that is most likely to explain a particular symptom, and, more importantly, how a particular finding may ultimately affect the patient and her subsequent treatment. See Box 11.1 for a variety of disease states categorized using this classification.

Box 11.1
ISD , Intrinsic sphincter deficiency; SUI , stress urinary incontinence.
Modified Functional Classification of Voiding Dysfunction

Failure to store

  • 1.

    Bladder abnormality

    • A.

      Detrusor overactivity

      • i.

        Involuntary contractions

        • a.

          Idiopathic

        • b.

          Inflammatory

        • c.

          Outlet obstruction

        • d.

          Neurogenic

      • ii.

        Impaired compliance

        • a.

          Neurogenic

        • b.

          Fibrosis

        • c.

          Idiopathic

      • iii.

        Combination

    • B.

      Bladder hypersensitivity

      • i.

        Infection/inflammation

      • ii.

        Idiopathic

      • iii.

        Psychologic

      • iv.

        Neurogenic

      • v.

        Combination

  • 2.

    Incompetent outlet

    • A.

      Urodynamic SUI

      • i.

        Anatomic (hypermobility)

      • ii.

        ISD

      • iii.

        Combination

    • B.

      Neurologic disease

      • i.

        ISD

Failure to empty

  • 1.

    Bladder abnormality

    • A.

      Neurogenic

    • B.

      Idiopathic

    • C.

      Myogenic

    • D.

      Psychogenic

  • 2.

    Outlet abnormality

    • A.

      Anatomic

      • i.

        Obstruction—post–incontinence surgery

      • ii.

        Distortion—(e.g., pelvic organ prolapse)

      • iii.

        External compression

    • B.

      Functional

      • i.

        Smooth sphincter dyssynergia

      • ii.

        Striated sphincter dyssynergia

      • iii.

        Dysfunctional voiding

    • C.

      Combination

Role of urodynamics in clinical practice

Although urodynamic testing has been frequently used in the evaluation of women with LUT dysfunction, level 1 evidence–based “indications” for its use are surprisingly few. The clinical question that must always be asked is whether the results of a urodynamic evaluation will either alter the outcome of the proposed management plan or be able to identify a potentially life-threatening situation (e.g., neurogenic voiding dysfunction). Urodynamic studies should be considered in clinical situations in which the testing is felt to be needed to make an accurate diagnosis, to assist in making an appropriate treatment plan, or to determine the impact of a disease state that has the potential to cause irreversible damage to the urinary tract, such as spinal cord injury. summarized the role of urodynamics in clinical practice by listing the following situations in which urodynamic studies should be considered:

  • 1.

    To identify or rule out factors contributing to LUT dysfunction and assess their relative importance.

  • 2.

    To obtain information about other aspects of LUT dysfunction.

  • 3.

    To predict the consequences of LUT dysfunction on the upper urinary tract.

  • 4.

    To predict the outcome, including undesirable side effects, of a contemplated treatment.

  • 5.

    To confirm the effects of an intervention or understand the mode of action of a particular type of treatment (especially a new one).

  • 6.

    To understand the reasons for failure of previous treatments for symptoms or for LUT function in general.

Urodynamic equipment

The ICS has developed recommendations for the minimum requirements for the equipment used to conduct urodynamic studies. These include three measurement channels (two for pressure and one for flow), a display on either a printer or a monitor, and a method of secure storage of the recorded pressures ( ). The infused volume and voided volume may be recorded graphically or numerically. There also must be a method of event recording to mark information about sensation, leakage, and additional comments during the study. Cystometry transducers are devices that convert an applied pressure into an electrical signal. Pressure to be measured may be transmitted indirectly to the transducer using an open-ended or sealed catheter filled with liquid or gas or directly when the transducer is small and mounted on the tip of the catheter (microtip transducer). The transducer is normally calibrated against atmospheric pressure, with a zero reference level being the superior edge of the symphysis pubis. The customary unit of measurement for pressure during urodynamics is cm H 2 O. The standard catheter for routine urodynamics is a transurethral double-lumen catheter ( ). The urethral catheters should be as small as possible, but not so small as to dampen pressure transmission or limit the desired filling rate. The smallest available is a 6-French double-lumen catheter; this allows the fill and void sequence to be repeated without recategorization.

More recently, air-charged catheters have become popular for pressure measurement. These catheters have miniature air-filled balloons placed circumferentially around a polyethylene catheter. The catheters are disposable and single-use. Practical advantages over fluid-filled pressure lines revolve around the fact that there is no hydrostatic pressure effect to account for, so there is no need to position anything at the level of the symphysis pubis or to flush the system through to exclude air, which is essential when using a fluid-filled system. With that said, many urodynamic “standard measurements” have been determined using fluid-filled systems. There are few studies directly comparing air-charged catheters with standard fluid-filled catheters; however, current evidence suggests the two are not interchangeable. One comparative study found that air-charged catheters consistently produce higher mean pressures than water-filled catheters and suggested that caution must be used when comparing urodynamic parameters using air-charged and water-filled catheters ( ). Another study found that pressure recordings from air-charged catheters and fluid-filled systems appear to be interchangeable for some urodynamic parameters, such as intravesical pressure ( P ves ) at Valsalva maneuver, if the baseline pressure is compensated, but not for fast-changing pressure signals such as coughs ( ).

Although it is beyond the scope of this chapter to discuss the various commercially available urodynamic systems, most are computer-based digital systems that allow for easy data storage and post-processing. Available systems can range in price from several thousand dollars to more than $100,000 for a video urodynamic system. Despite constant nuanced improvements in systems and software, the clinician performing the study remains the most important constant in data collection and interpretation. In certain clinical settings, a simple three-channel system ( Fig. 11.2 ) may be adequate, whereas large referral centers that evaluate complex cases or have a high percentage of patients with neurogenic bladder may require a more sophisticated system with the potential for video assessment ( Fig. 11.3 ). Several modern urodynamic systems that are wireless and use Bluetooth technology have become available. These systems have the advantage of allowing more patient flexibility and privacy, as the catheters are not tethered to the urodynamic machine, because the signal can be sent wirelessly (up to 30 m) from the transducer to the urodynamic machine.

Fig. 11.2, Subtracted cystometry. Intravesical and intraabdominal pressures are measured, and true detrusor pressure is electronically derived ( P ves − P abd ). P ves , Bladder pressure; Pabd , abdominal pressure; Pdet , detrusor pressure.

Fig. 11.3, Multichannel urodynamics. Intravesical, intraabdominal, and intraurethral pressures are measured. True detrusor pressure ( P det ) and urethral closure pressure ( P ucp ) are electronically derived. Electromyography ( EMG ) and flow studies are also performed. P ves , Bladder pressure; P abd , abdominal pressure; P det , detrusor pressure; P ure , urethral pressure; P ucp , urethral closure pressure.

Performing a urodynamic evaluation

Urodynamic procedures should be performed with a clear indication and with a specific question or questions that hopefully can be answered by the study. The procedure must be performed interactively with the patient and should include continuous and careful observation of the collected data. Artifacts are best corrected as they occur, because they are often difficult to correct after the study is completed. It is valuable for the urodynamicist to have a clear understanding of the patient’s symptoms and pertinent physical examination findings, practical experience with the equipment being used, and an understanding of quality control, with the ultimate goal of determining whether the questions that the procedure attempted to answer have been appropriately addressed. Obviously, a prerequisite to this is a good understanding of pertinent anatomy and physiology of the LUT, as well as the biomechanics and physics of the urodynamic study. The test should be explained to the patient in advance. Although complications are rare, certain morbidities such as urinary retention, hematuria, urinary tract infection, and pain can occur.

Based on the American Urological Association (AUA) “Best Practice Policy Statement,” assuming the preprocedure urine is negative for a urinary tract infection, preprocedure antibiotic prophylaxis is not indicated except in high-risk patients ( Box 11.2 ). The antimicrobial agents of choice are fluoroquinolones or trimethoprim/sulfamethoxazole. In patients who are allergic to both medications, the alternatives include a combination of aminoglycosides and ampicillin, first- or second-generation cephalosporin, or amoxicillin/clavulanate ( ). If a preprocedure urinary tract infection is diagnosed, the condition should be treated before the procedure. The American Heart Association no longer recommends the use of antibiotic prophylaxis before genitourinary procedures solely to prevent infective endocarditis. For patients who have had previous orthopedic surgery, there is no indication for antibiotic prophylaxis if the urine culture is negative and patients are not high risk.

Box 11.2
Risk Factors for Infection

Advanced age

Anatomic anomalies of the urinary tract

Poor nutritional status

Smoking

Chronic corticosteroid use

Immunodeficiency

Externalized catheters

Colonized endogenous/exogenous material

Distant coexistent infection

Prolonged hospitalization

Because micturition is normally a private act, the study setting should be quiet, to provide as little distraction as possible. The number of observers should be limited to as few as possible to minimize patient embarrassment.

A list of problems or questions that should be solved or answered by the urodynamic studies should be made before any testing is performed. A good practice is to decide on the questions before starting the study and then potentially design the study to answer those questions with the idea of customizing every study to a specific patient and her issues. It is also important to explain to the patient exactly why the tests are being performed and how the results may affect the treatment plan that will be proposed. The following is a brief description of the various tests that can be performed during a urodynamic evaluation.

  • 1.

    Postvoid residual (PVR) urine volume: This is an objective assessment of how well a woman empties her bladder. It can be performed by ultrasound, bladder scan, or direct catheterization. An elevated PVR indicates a problem with emptying but does not really provide any information regarding the etiology of the dysfunction. A persistently elevated PVR may prompt further testing. Although no specific number has been agreed on to define what a normal PVR is, most would agree that a PVR less than 50 mL or a PVR less than 80% of the total bladder volume would be considered normal.

  • 2.

    Uroflowmetry is a measurement of the rate of urine flow over time ( Fig. 11.4 ). It is also an assessment of bladder emptying. A normal uroflow is a bell-shaped curve ( Fig. 11.5 ). When the flow rate is reduced, or the pattern is altered, this may indicate bladder underactivity or bladder outlet obstruction (BOO).

    Fig. 11.4, Special commode and flowmeter used for spontaneous uroflowmetry.

    Fig. 11.5, Graphic representation of normal uroflow curve.

  • 3.

    Cystometrogram (CMG): Filling cystometry is the method by which the pressure/volume relationship of the bladder is measured during bladder filling. The test starts when filling commences and ends when the patient and urodynamicist decide that permission to void has been given. Although single-channel cystometry has been described, it is recommended that subtracted CMG be performed using the total vesical pressure and abdominal pressure by catheter placements in the bladder and rectum or vagina to calculate the true P det , which is the vesical pressure minus the abdominal pressure. Also, leak point pressure measurements are obtained during filling cystometry.

  • 4.

    EMG is the study of electronic potentials produced by the depolarization of muscle membranes. In the case of urodynamics, EMG measurement is usually performed with patch electrodes placed in close proximity to the striated sphincter muscles of the perineum. The test is mostly used to assure appropriate coordination between the pelvic floor muscles and LUT. EMG activity is measured during both filling and voiding.

  • 5.

    Urethral pressure profilometry (UPP): This is measurement of the intraluminal pressure along the length of the urethra. The urethral pressure is defined as the fluid pressure needed to just open a closed urethra. The UPP is obtained by withdrawal of a pressure sensor catheter along the length of the urethra.

  • 6.

    Pressure-flow studies of voiding are the method by which the relationship between pressure in the bladder and urine flow rate is measured during bladder emptying. P det is measured with a simultaneous measurement of flow. The voiding phase starts when permission to void is given or when uncontrollable voiding begins and ends when the patient considers that voiding has finished.

Fig. 11.6 demonstrates a typical setup for a multichannel urodynamic assessment. The technique of performing a full urodynamic assessment in our laboratory is as follows:

  • 1.

    The patient presents with a symptomatically full bladder. She voids spontaneously in a uroflow chair. A PVR urine volume is obtained via a transurethral catheter.

  • 2.

    With the patient in the supine position on a urodynamic chair, the abdominal catheter is placed into the vagina and taped to the inside of the leg. If the patient has severe vaginal prolapse or has undergone previous vaginal surgery resulting in a narrowed vagina, the catheter is placed into the rectum. A dual microtransducer catheter with a filling port is then placed into the bladder. The patient is moved to a sitting position, and the catheter is secured to a mechanical puller (if urethral pressure studies are anticipated) or to the inside of the leg, so that the proximal transducer is near the midurethra (area of maximum urethral closure pressure).

  • 3.

    After the catheters are appropriately placed, the subtraction is checked by asking the patient to cough. Cough-induced pressure spikes should be seen on the P ves , intraabdominal pressure, and urethral pressure channels, but not on the true P det channel. If there is an inappropriate deflection on the P det channel, it is usually secondary to inaccurate placement of the vaginal (or rectal) catheter. If repositioning the catheter does not correct the problem, all connections and calibration techniques should be rechecked. demonstrates appropriate calibration and subtraction during cough spikes and Valsalva.

  • 4.

    Bladder filling is begun. First sensation, first desire to void, and strong desire to void are recorded. Throughout the filling portion of the examination, the patient is asked to perform provocative activities, such as coughing and straining. The external urethral meatus is constantly observed for any involuntary urine loss. The first set of provocative maneuvers should be performed at a volume between 150 and 250 mL. If the patient has urodynamic stress incontinence, leak point pressures can be obtained. Any abnormal rise in true P det is noted. If the patient’s symptoms are reproduced during filling, then the test can be completed in the sitting position. If they are not, the patient should be asked to stand and repeat provocative maneuvers in an attempt to reproduce her symptoms.

  • 5.

    At the completion of filling, urethral pressure and flow studies can be performed, if indicated.

Fig. 11.6, Setup for urodynamic testing. The patient is typically seated on the urodynamic chair after the catheters have been placed. Abdominal and vesical pressures are measured by catheters in the bladder and vagina or rectum. The machine automatically calculates true detrusor pressure ( P det ) by subtracting intraabdominal pressure ( P abd ) from intravesical pressure ( P ves ). Electromyography ( EMG ) activity using surface electrodes and urinary flow is also measured.

Fig. 11.7 illustrates an example of filling and voiding urethrocystometry. No urodynamic abnormalities are noted in this study.

Fig. 11.7, Normal filling and voiding subtracted cystometry. Note that provocation in the form of coughing and straining does not provoke any abnormal rise in true detrusor pressure. At maximum capacity on command, a detrusor contraction is generated, and voiding is initiated. USUI , Urodynamic stress urinary incontinence.

Interpretation of specific tests

Uroflowmetry

Uroflowmetry is noninvasive and inexpensive and is best used as a screening test for patients who may have voiding dysfunction. Many clinicians feel that uroflowmetry should routinely precede all other urodynamic studies. It is easy to perform and quickly provides data on both storage and emptying symptoms. The study should be conducted with as much privacy as possible, with patients being asked to void when they feel they have a normal desire. The addition of a PVR measurement, usually by ultrasound, adds value to this study. Normal voiding includes detrusor muscle contraction, coordinated bladder outlet relaxation, low voiding pressure, and a smooth arc-shaped flow curve ( ). It should be noted that uroflowmetry alone is insufficient to diagnose BOO, because it cannot distinguish true obstruction from poor detrusor contractility. Because small, voided volumes affect the curved shape, only voided volumes of at least 150 mL are interpretable ( Fig. 11.8 ). Because women have very short urethras with minimal outlet resistance, generally speaking the only factors influencing female outflow are the strength of the detrusor muscle, the urethral resistance, and the degree of relaxation of the sphincter mechanism. The most common conditions associated with increase in outlet resistance are previous antiincontinence surgery or significant anatomic distortion, usually from pelvic organ prolapse.

Fig. 11.8, Uroflow curve from a void of only 90 mL. Data obtained are not useful, because the voided volume was less than 150 mL.

Urine flow may be described in terms of flow rate and flow pattern and may be continuous or intermittent. Flow rate ( Q ) is defined as the volume of fluid expelled via the urethra per unit time and is expressed in milliliters per second (mL/s). Certain information is necessary in interpreting the tracing, including the volume voided, the environment and position in which the patient passed urine, whether the bladder filled naturally or by a catheter, and whether diuresis was stimulated by fluid or diuretics. If filling was by catheter, the type of fluid used should be stated; it should also be stated whether the flow study was part of another investigation. Maximum flow rate ( Q max ) is the maximum measured value of the flow rate after correction for artifacts. Voided volume is the total volume expelled via the urethra.

Flow time is the time over which measurable flow occurs. Average flow rate is voided volume divided by flow time. The average flow should be interpreted with caution if flow is interrupted or if there is a terminal dribble. Time to maximum flow is the elapsed time from onset of flow to maximum flow.

Most experts agree that a study can be considered normal if the patient voids at least 200 mL over 15 to 20 seconds and if it is recorded as a smooth single curve with a Q max greater than 20 mL/s ( Fig. 11.5 ). Q max values of less than 15 mL/s with a voided volume greater than 200 mL are generally considered abnormal. However, because flow rate is determined by the relationship between detrusor force and urethral resistance, and because these factors may vary considerably and still produce adequate bladder emptying, a precise definition of a normal or a low flow rate cannot be made. The maximum urinary flow rate (MUFR) and average urinary flow rate are the two most important uroflowmetry parameters.

The clinical usefulness of uroflowmetry has been hampered by the lack of absolute values defining normal limits. These normal limits would need to be over a wide range of voided volumes, ideally in the form of nomograms. performed uroflowmetry on 249 female volunteers between ages 16 and 63 years. Uroflowmetry was performed on each woman in a completely private environment, and a second uroflow study was obtained in 46 of those women. The MUFR and the average urinary flow rate of the first voids were compared with respective voided volumes. By using statistical formulations of both voided volumes and urine flow rates, relationships between the two variables were obtained. This allowed the construction of nomograms, which are shown in Fig. 11.9 . The previously described nomograms refer to free flowmetry voids and are not applicable to flow rates obtained during a pressure-flow study, because all urethral catheters can be expected to have the effect of decreasing urine flow rates for the equivalent voided volume. In 1999, Haylen et al. completed a further study of 250 symptomatic women who were consecutively referred for urogynecologic assessment, which included urodynamics. Flow data for these women were converted to centiles from the Liverpool nomograms. The authors noted a decreased flow rate in symptomatic women in general, and specifically in women with genital prolapse. In contrast to asymptomatic women, there is a decline in flow rates with age, and final urodynamic diagnosis shows that women with various combinations of stress incontinence, overactive bladder (OAB), or voiding dysfunction have flow rates that are significantly different than those of asymptomatic women.

Fig. 11.9, A , Liverpool maximum flow rate nomogram for women; curves are centiles. B , Liverpool average flow rate nomogram for women; curves are centiles.

Curve patterns refer to the configuration of the uroflowmetric curve. Continuous flow that shows a rapidly increasing flow rate that reaches the maximum within one-third of the total voiding time is usually considered normal ( Fig. 11.10 A). Fig. 11.10 B demonstrates what has been termed a superflow pattern, in which there is a very rapid acceleration to a high MUFR.

Fig. 11.10, Graphic representation of various uroflow patterns. A , Normal curve; voided volume of 145 mL; maximum urinary flow rate (MUFR) 23 mL/s. B , Superflow pattern; voided volume of 330 mL; MUFR 49 mL/s. C , Intermittent flow rate with multiple peak pattern. This tracing is characteristic of voluntary urethral sphincter activity. D , Intermittent flow rate with interrupted pattern. This is a characteristic pattern seen when abdominal pressure is used to expel urine. E , Reduced urine flow rate secondary to detrusor outflow obstruction.

Flow is considered intermittent when the flow rate drops and subsequently increases. Intermittent flow rates are described as multiple-peak patterns when there is a downward deflection of the flow rate that does not reach 2 mL/s ( Fig. 11.10 C). When the downward deflection of the flow rate reaches 2 mL/s or less ( Fig. 11.10 D), an interrupted pattern occurs. Obstructed voiding patterns are much less common in women than in men, and usually produce a low, flat tracing ( Fig. 11.10 E).

Abnormal uroflowmetric parameters can occur secondarily to factors that affect detrusor contractility, urethral resistance, or both. Also, inappropriate contraction of pelvic floor muscles can affect flow rates. Detrusor contractility can be affected by neuropathic lesions, pharmacologic manipulation, intrinsic detrusor muscle or bladder wall dysfunction, or psychogenic inhibition. Urethral resistance can be altered by tissue trophic changes producing atrophy or fibrosis, drug effects such as alpha-adrenergic stimulators or blockers, neuropathic striated muscle contraction, pain or fear, and urethral axis distortion secondary to severe pelvic organ prolapse. Outlet obstruction secondary to an intraurethral lesion or stricture is exceedingly rare in women. Extraurethral lesions, such as vaginal masses or cysts, or a large enterocele or rectocele may externally compress the urethra, resulting in obstructed voiding. Inability to relax pelvic floor muscles appropriately can cause prolonged flow times. This may occur after a traumatic delivery or pelvic floor reconstructive surgery, or as part of any disease state that causes vaginal pain. Detrusor-external (or striated) sphincter dyssynergia is a condition in which there is lack of coordination between the detrusor muscle and the external striated urethral sphincter. This leads to obstructed voiding and is always secondary to a neurologic lesion, most classically high spinal cord trauma. In the nervous and anxious but neurologically intact patient, the urethra may be closed by pelvic floor contracture. Urethral closure may be attributed to contraction of the intraurethral striated muscle or contraction of the pelvic floor musculature. This condition has been termed dysfunctional voiding.

If uroflow measures are normal in patients complaining of symptoms of voiding difficulty, further investigation is unnecessary, but abnormal flow rates may require further urodynamic testing. Uroflowmetry is a simple urodynamic investigation that is useful as a preliminary screening test to distinguish patients who need more extensive studies from those who do not. Uroflowmetry is also an integral part of a full urodynamic study performed for more complex problems.

Filling cystometry

Cystometry is the urodynamic study used to describe the pressure/volume relationship of the bladder. One should also collect information on bladder sensation during filling. Normal bladder sensation is usually judged at three defined points: a first sensation of bladder filling, a first desire to void, and a strong desire to void ( Fig. 11.11 ). Although specific parameters are not given for these various changes in sensation, increased bladder sensation is defined as an early first sensation of bladder filling or an early strong desire to void that occurs at what is felt to be a low bladder volume and ultimately persists, whereas reduced bladder sensation is a diminished sensation through bladder filling. P det during filling should be very low, with no involuntary contractions. Detrusor overactivity (DO) is defined as involuntary detrusor contractions during filling that may be spontaneous or provoked ( Fig. 11.12 and ). DO is classified as either neurogenic (when there is a relevant neurologic condition) or idiopathic (when there is no identifiable cause). Bladder compliance describes the relationship between the change in bladder volume and change in P det . Compliance is calculated by dividing the volume change by the change in P det during that change in bladder volume. It is expressed in mL/cm H 2 O. Although it is difficult to define what normal compliance is in terms of mL/cm H 2 O, several authors have shown that the mean values for compliance in healthy subjects range from 46 to 124 mL/cm H 2 O ( ; ; ). Because of these wide-ranging values, it is more practical from a clinical standpoint to use absolute pressure instead of a compliance number. For example, it has been shown that urine storage pressure greater than 40 cm H 2 O can be associated with harmful effects to the upper tract ( ). In general, prolonged storage at high pressures can lead to upper tract deterioration.

Fig. 11.11, Filling cystometry; first sensation, fullness, and maximum capacity are noted. Detrusor remained stable during filling, and no stress incontinence was demonstrated.

Fig. 11.12, Filling cystometry in a patient with detrusor overactivity; note that two uninhibited bladder contractions occurred during the filling portion of the test.

When there appears to be an abnormal rise in true P det , the urodynamicist must determine if this rise is caused by poor bladder compliance ( Fig. 11.13 ) or best classified as DO ( Fig. 11.14 ). Abnormal bladder compliance is going to be more common in certain subsets of patients, including women with neurogenic disease, a history of radiation or multiple bladder surgeries, multiple bladder tumor resections, a defunctionalized bladder after long-term anuria, long-term indwelling catheterization, recurrent bladder infections, or long-standing BOO. In patients with abnormal bladder compliance during filling cystometry, there will be a steep rise in P det that is usually parallel to bladder filling. Abnormal compliance is related to filling; DO is not. Most of the time, if you stop infusing fluid, the P det will plateau in cases of low compliance but continue to rise toward the peak with DO ( Fig. 11.11 and 11.12 ). With continuation of filling, assuming there is no “pop-off” effect, as noted by leakage from the urethra or vesicoureteral reflux, the P det will continue to rise in low compliance, but a detrusor contraction will usually end, resulting in a significant drop in P det ultimately returning to the baseline pressure before the DO ( and ).

Fig. 11.13, Multichannel filling cystometry in a patient with poor bladder compliance. Note steady rise in true detrusor pressure with plateaus when filling stops and increases when filling is resumed.

Fig. 11.14, Multichannel filling cystometry in a patient with detrusor overactivity. Note that detrusor pressure returns to baseline after completion of contraction.

The condition of urodynamic stress incontinence is defined as involuntary loss of urine simultaneous with a rise in abdominal pressure in the absence of any rise in true P det ( Fig. 11.15 ; ). This diagnosis is made during filling cystometry. Provocation in the form of coughing, straining, and heel bouncing in the sitting (and, if necessary, standing) position should be performed at different volumes throughout the testing session. Once the diagnosis is made, Valsalva and cough leak point pressure measurements can be obtained if felt to be clinically indicated.

Fig. 11.15, Filling cystometry demonstrating the condition of urodynamic stress incontinence. Urine leakage occurred simultaneous with a cough (rise in intraabdominal pressure) in the absence of any rise in true detrusor pressure.

Leak point pressures

There are two distinct types of leak point pressures that can be measured in an incontinent patient. The first is an abdominal leak point pressure sometimes termed either a Valsalva leak point pressure (VLPP) or cough leak point pressure; the second is a detrusor leak point pressure (DLPP). These pressures are independent of each other and conceptually measure completely different things. An abdominal leak point pressure, whether measured during cough or Valsalva, is a measure of the intrinsic sphincter strength of the urethra or its ability to resist leakage with increases in abdominal pressure. It is specifically defined as the intravesical pressure at which urine leakage occurs because of an increased abdominal pressure in the absence of a detrusor contraction. Thus, it is an objective assessment of the amount of abdominal pressure required to overcome outlet resistance and create leakage. This test is applicable to patients with urodynamic stress incontinence. Theoretically, the lower the abdominal leak point pressure, the weaker the sphincter. There is no normal abdominal leak point pressure, because patients without stress incontinence will not leak at any volume or physiologic abdominal pressure. The pressure should be a measure of the total (absolute) abdominal pressure required to cause leakage, not the change in pressure. The reading is taken from the vesicle channels, because it is usually a cleaner channel to obtain the pressure, assuming there are no involuntary contractions of the detrusor. A Valsalva effort is the most reliable method of provocation; however, if the patient cannot Valsalva on command, coughing can be used ( Figs. 11.16 and 11.17 ; ).

Fig. 11.16, A , Graphic representation of Valsalva leak point pressure measurement at bladder volumes of 150 and 300 mL. Leak point pressures tend to decrease with increased bladder volume. B , Graphic representation of cough leak point pressure at bladder volumes of 150 and 300 mL. Note the difficulty involved in isolating the cough that generates the minimal amount of abdominal pressure required to produce leakage.

Fig. 11.17, Filling cystometry. Valsalva leak point pressure of 92 cm H 2 O is noted in sitting position at a volume of 187 mL.

The second type of leak point pressure is the DLPP, which is a measure of P det in patients with decreased bladder compliance. It is defined as the lowest P det at which urine leakage occurs in the absence of either a detrusor contraction or an increase in abdominal pressure ( ). From a clinical perspective, a DLPP is most useful in patients with lower motor neuron disease causing decentralization, and rarely in nonneurogenic patients with abnormal bladder compliance, which can occur after multiple bladder surgeries, radiation therapy, tuberculosis cystitis, and other rare situations or conditions. In general, the higher the DLPP, the more likely the upper urinary tract could be damaged because of intravesical pressure being transferred to the ureters and the kidneys. showed that DLPPs greater than 40 cm H 2 O would result in hydronephrosis or vesicoureteral reflux in 85% of myelodysplastic patients.

Urethral pressure profilometry

Urethral pressure profilometry (UPP) indicates the intraluminal pressure along the length of the urethra with the bladder at rest. The maximum urethral pressure is the maximum pressure of the measured profile. The maximum urethral closure pressure is the difference between the maximum urethral pressure and the intravesical pressure ( Fig. 11.18 ). The functional urethral length (FUL) is the length of the urethra along which the urethral pressure exceeds the intravesical pressure, and the anatomic urethral length is the total length of the urethra. The pressure transmission ratio is the increment in urethral pressure on stress as a percentage of the simultaneously reported increment in vesical pressure.

Fig. 11.18, Technique of static urethral pressure profilometry with simultaneous measurement of bladder pressure. Study begins with both microtransducers in the bladder ( top ). As the catheter is mechanically withdrawn through the urethra ( middle and bottom ), urethral and bladder pressures are recorded.

UPP involves the withdrawal of a catheter through the urethra at a constant rate of speed. Pressure is measured along the entire urethral length, as well as in the bladder. UPP can be performed using open or balloon catheters perfused with liquid or gas, catheter-mounted (microtip) transducers, or fiberoptic catheters, as well as air-charged catheters ( Fig. 11.18 ).

Normal values for maximal urethral closure pressure (MUCP) and FUL vary widely among women; however, most continent women will have an FUL of approximately 3 cm and an MUCP between 40 and 60 cm H 2 O. Although many authors have used an MUCP of less than 20 cm H 2 O to define intrinsic sphincter deficiency (ISD) in women with urodynamic stress urinary incontinence (SUI), this definition has many of the same problems that hamper the definition and diagnosis of ISD.

In 2002, the ICS standardization subcommittee concluded that the clinical utility of UPP is unclear ( ), stating that there are no urethral pressure measurements that:

  • 1.

    Discriminate urethral incompetence from other disorders.

  • 2.

    Provide a measure of the severity of the condition.

  • 3.

    Provide a reliable indicator to surgical success.

Electromyography

EMG studies have become popular components of a urodynamic assessment. Muscle depolarization is detected by an electrode placed in or near a muscle. The test can be done with needle or surface electrodes; however, surface electrodes with self-adhesive skin patches that are applied over the skin of the anal sphincter are the most commonly used during a urodynamic assessment. The surface electrodes have a significant advantage over needle electrodes regarding patient convenience and comfort, as well as ease of doing the test. Although using a concentric needle electrode is a superior technique for obtaining a signal source of EMG activity of the striated external urethral sphincter muscle, the information obtained by the perianal surface electrodes will suffice in the evaluation of most women with LUT dysfunction. In a neurologically intact individual, EMG activity should increase during filling and provocation to prevent any leakage. Normal voiding requires external sphincter relaxation followed by contraction of the detrusor. Failure of the sphincter to relax or stay completely relaxed during micturition is abnormal. Thus, normally, EMG activity decreases before a voluntary bladder contraction; however, it is not abnormal for EMG activity to increase with an involuntary contraction as part of a guarding reflex to inhibit the detrusor contraction. Some question the clinical utility of routine EMG during urodynamic performance, and others argue that it remains a good objective method to assure appropriate synergistic responses during filling, voiding, and provocation.

Pressure-flow studies

Because uroflowmetry can provide only limited information, pressure-flow studies represent a natural progression. However, if uroflowmetry is normal, the information obtained in a pressure-flow study is largely unnecessary. In contrast, in those with voiding symptoms and an abnormal MUFR and/or peak flow velocity, pressure-flow studies are necessary to determine the cause. Flow rate depends on both the outlet resistance and the contractile properties of the detrusor, as well as the volume of fluid in the bladder. A low flow rate may be associated with a high voiding pressure or a below-normal voiding pressure. Similarly, the finding of a normal flow rate does not exclude BOO, because normal flow may be maintained by a high voiding pressure.

Some women have normal flow rates in the absence of a detrusor contraction. This may be because sphincteric relaxation, either alone or assisted by increased intraabdominal pressure from straining, is sufficient to produce a normal flow rate. Pressure-flow studies are essential for a complete functional classification of LUT disorders and an objective assessment of the basis of a patient’s voiding dysfunction.

These studies are usually performed after a cystometric evaluation. In most patients, it is clear when bladder filling should be stopped. However, if the patient has little sensation, it is important to use the functional bladder capacity from the frequency–volume chart as a guide to cystometric capacity. At this point, if a separate filling catheter is being used, it is removed; the intravesical catheter is left in place. An intravaginal or intrarectal catheter records intraabdominal pressure to assess whether the patient uses a Valsalva maneuver to void and to electronically derive true P det . Thus, these studies involve the monitoring of abdominal, intravesical, and true P det synchronously with flow ( Fig. 11.19 and 11.20 ). External sphincter EMG activity and urethral pressure also may be measured. To ensure that proper pressure transmission is occurring, the patient should be asked to cough before being allowed to void. With the patient in a sitting position, she is then instructed to void to completion if possible. It is important during the voiding phase to respect the patient’s privacy. Few women are able to void in the presence of others, so it may be necessary for the practitioner to leave the room for her to initiate voiding. demonstrates a voiding mechanism with an appropriate detrusor contraction, and demonstrates a voiding mechanism with significant Valsalva effort.

Fig. 11.19, Pressure-flow study in a patient who voids with urethral relaxation and bladder contraction. Note minimal Valsalva effort.

Fig. 11.20, Pressure-flow study in a patient who has voiding dysfunction after suburethral sling procedure. The study is consistent with outlet obstruction in that the flow is reduced and detrusor pressure is elevated.

Pressure-flow studies are invasive because the patient is asked to void around catheters. It is important to appreciate the limitations of pressure-flow studies, as well as the differences between the patient’s performance during urodynamic testing and her normal voiding. This is best judged by asking the patient and by comparing the noninstrumented urine flow rate with the flow rate obtained from the pressure-flow study.

Voiding in a urodynamic laboratory can be affected by a variety of factors. It is estimated that approximately 30% of women who void without problems at home are unable to void on command in the urodynamic laboratory. This is hardly surprising, because they are surrounded by complex equipment, have catheters in their bladder and vagina or rectum, and are usually being observed by strangers.

Fast filling or overfilling of the bladder may make normal voiding difficult. Studies that compared ambulatory urodynamics (natural bladder filling) with conventional urodynamics show that voiding pressures are higher with natural filling. This implies that the detrusor may be incompletely stimulated, partially inhibited, or mechanically less efficient if it is overfilled or filled too fast.

During the voiding phase, the detrusor muscle may be normal, acontractile, or underactive. Normal voiding is usually achieved by a voluntarily initiated continuous detrusor contraction that is sustained and can be suppressed. An underactive detrusor during micturition implies that the detrusor contraction is of inadequate magnitude or duration (or both) to effect bladder emptying within a normal time span.

During voiding, urethral function may be normal or abnormal. A normal urethra opens during voiding and is continuously relaxed to allow the bladder to be emptied at a normal pressure. Abnormal urethral function may be secondary to urethral overactivity or a mechanical obstruction, such as a urethral stricture or tumor. BOO, regardless of the cause, is characterized by increased P det and reduced urine flow rate, seen by observing the synchronous values of flow rate and P det during voiding ( ). In mechanical obstruction, which is rare in females, the voiding pressures are constantly elevated. If the obstruction is caused by urethral overactivity, the voiding pressures may fluctuate. Urethral overactivity is characterized by the urethra contracting during voiding or the urethra failing to relax. In detrusor external sphincter dyssynergia (DESD), the patient’s phasic contractions of the intrinsic urethral striated muscle are simultaneous with the detrusor contraction. This produces a very high voiding pressure and an interrupted flow. The urodynamic characteristic of this type of urethral overactivity is a fall in flow rate accompanied by a rising P det that then falls when the urethra relaxes, leading to a resumption of urine flow. Another form of urethral overactivity is called dysfunctional voiding. This is most commonly seen in children who are neurologically normal but complain of urinary incontinence or recurrent infections. The interrupted flow in these children is caused by pelvic floor overactivity rather than contractions of the intrinsic striated muscle.

Depending on age, menopausal status, total voided volume, and the presence or absence of LUT dysfunction, women void by any combination of a detrusor contraction, abdominal straining, and urethral relaxation.

It is difficult to ascertain whether abdominal straining that occurs during a pressure-flow study is real or artifactually induced by the surroundings and presence of indwelling catheters. The patient should always be asked to void normally and in as relaxed a way as possible. If the patient has an acontractile detrusor, voiding can be achieved only by straining. If the detrusor contracts during voiding, but the patient also strains, then the tracing is more difficult to interpret. It is also difficult to understand precisely what effect straining has on urine flow. In patients without obstruction, straining increases flow, but it does not produce the same increase in flow as that achieved by a P det rise of the same magnitude ( ).

Although pressure-flow studies are an established and accepted urodynamic modality, what constitutes a normal voiding mechanism is poorly understood, as is the normal range for P det during voiding in women. Most of the previously published literature has been derived from male subjects in whom pressures are abnormally high secondary to outflow obstruction.

Because there is no highly prevalent condition such as benign prostatic hypertrophy in women that causes female obstruction, it has been very difficult to establish nomograms. Because voiding dynamics differ in women, nomograms derived for men cannot be used in women. As mentioned, anatomic differences allow women to void by simply relaxing their pelvic floor, or by increasing abdominal pressure by straining. Small elevations in P det or decreases in flow rates, which might be considered insignificant in a male, may be consistent with BOO in a female. Thus, clinicians should always have a high index of suspicion for BOO in women with a prior history of an antiincontinence procedure, chronic cystitis, pelvic organ prolapse, or incomplete bladder emptying.

Numerous investigators have attempted to establish cutoff values for pressure and flow to diagnose outlet obstruction in women ( ; ). These studies, however, have some limitations in that obstruction was predefined clinically, and only patients with anatomic obstruction were included. A study by used normal asymptomatic women as the control group and found the highest sensitivity and specificity for predicting obstruction was obtained with Q max less than 12 mL/s and P det Q max greater than 25 cm H 2 O. created a nomogram defining voiding obstruction in women using Q max from a noninstrumented uroflow and a maximum P det from the pressure-flow study. More recently, an analysis of the urodynamic data from the Trial of Mid-Urethral Slings (TOMUS) study noted that the difference between these two values increases as voided volumes increase ( ), concluding that values from a pressure-flow study and noninstrumented uroflow cannot be used interchangeably, as has been suggested by the Blaivas–Groutz nomogram for obstruction in women.

The main clinical use of pressure-flow studies is to document the mechanism of abnormal voiding. If a patient has symptoms and signs of abnormal voiding, has low flow rates, and voids with a high P det , she is probably voiding against an obstruction. On the other hand, if a patient has low flow rates and voids with minimal or no rise in P det , then her voiding dysfunction is probably secondary to an acontractile or underactive detrusor. As previously mentioned, the limiting factor is that there is no clear cutoff between normal and abnormally high P det during voiding.

The clinical setting in which pressure-flow studies are most useful in women is in the patient who has undergone pelvic surgery and has developed postoperative voiding dysfunction. The dysfunction may be secondary to denervation, resulting in an underactive or acontractile detrusor, but more commonly the dysfunction is secondary to increased outlet resistance produced from the surgery. Voiding dysfunction or retention occurs in 3% to 20% of patients after various operations to correct stress incontinence. It is always a clinical dilemma whether urethrolysis or a takedown of the repair will restore normal voiding. Filling cystometry and pressure-flow studies may be helpful in this setting. If the patient is able to void around a catheter and is noted to have a high P det with a low flow rate ( Fig. 11.21 ), then she is obstructed, and relieving the obstruction should improve voiding ( ).

Fig. 11.21, Technique for performing pressure-flow studies. The patient must be able to void around the catheters.

Although some previous studies have shown that a preoperative pressure flow study may be predictive of postoperative voiding dysfunction after an antiincontinence procedure ( ), others have shown that the only true predictor is a preoperative elevated PVR volume ( ). Thus, at the present time it remains controversial whether there is a role for preoperative pressure-flow studies in women with SUI and/or pelvic organ prolapse as a predictor of postoperative voiding dysfunction.

Urodynamics and specific conditions

Stress urinary incontinence

The role of urodynamics in SUI in women has been recently debated. Urodynamic studies have been cited historically as being potentially beneficial for diagnosing the condition of urodynamic stress incontinence, assessing urethral function with either VLPPs or maximum urethral closure pressures, and also potentially predicting postoperative voiding dysfunction based on preoperative pressure-flow studies.

Recently, many data have questioned whether there is any beneficial role for urodynamics in women with straightforward symptoms of stress incontinence in which the sign of stress incontinence is demonstrable in an office setting. published the results of the Value of Urodynamic Evaluation (VALUE) trial, a randomized trial focused on the role of urodynamics in women with SUI. Six hundred thirty women meeting criteria for an antiincontinence procedure were randomized to preoperative urodynamics or a simple office-based evaluation. The primary outcome of the study was treatment success, defined as a 70% reduction or more from baseline to 12 months in the urogenital distress inventory and a patient global impression of improvement response of “very much better” or “much better” at 12 months. Secondary outcomes sought to determine if preoperative urodynamic findings in women with stress-predominant incontinence would affect surgical outcome, with the secondary outcomes being cost and utility of performing urodynamics. At 12 months, no significant difference was seen between the urodynamic testing group and the office evaluation–only group with respect to treatment success (76.9% and 77.2%, respectively). When secondary outcomes were examined, there was no difference between the two groups for changes in incontinence severity index or patient global impression of improvement. The study concluded that, in a woman with straightforward symptoms of SUI, urodynamics did not improve the rate of treatment success, and thus showed no benefit over a simple office evaluation in which the sign of stress incontinence was objectively demonstrated.

Based on the VALUE trial, women with symptoms of stress incontinence who meet the following criteria gain no benefit from a urodynamic evaluation before SUI surgery:

  • 1.

    Stress-predominant urinary incontinence symptoms.

  • 2.

    Positive urine stress test.

  • 3.

    PVR less than 150 mL.

  • 4.

    A mobile urethra.

  • 5.

    Stage 0 to 2 pelvic organ prolapse.

  • 6.

    No prior incontinence surgery or pelvic radiation.

A more recent follow-up study looking at the cost of preoperative urodynamics in a secondary analysis of the VALUE trial noted that $13 million to $33 million could be saved annually by not performing preoperative urodynamics studies ( ). Incorporating these data into diagnostic and treatment algorithms will significantly reduce the number of women undergoing preoperative urodynamics prior to placement of a midurethral sling ( ).

In their October 2006 document, the UK National Institute of Health and Clinical Excellence stated that urodynamics in women with pure SUI is no longer recommended. Urodynamics was indicated only in women with urinary incontinence where there was a clinical suspicion of either mixed incontinence (coexistent DO), in women who have previously undergone surgery for SUI and developed recurrent incontinence, in women who have had previous anterior compartment prolapse surgery, and in women with symptoms suggestive of significant voiding dysfunction.

In the Netherlands, the Value of Urodynamics Before Stress Incontinence Surgery study ( ) was performed to further assess this question. This multicenter randomized controlled trial examined the role of urodynamics in women with symptoms of SUI who had urodynamic findings that were discordant with history and physical findings and were then randomized to receive either a midurethral sling or individual treatment. Individual treatment included pessary, medical treatment, physiotherapy, or surgery at the discretion of the provider. The primary outcome was clinical improvement in incontinence as measured by the validated Dutch version of the long form of the Urogenital Distress Inventory, with a secondary outcome being cost. The study concluded that, in women with uncomplicated SUI, an immediate midurethral sling operation is not inferior to individually tailored treatment based on urodynamics.

Urethral function or lack thereof has been traditionally assessed with UPP and/or VLPPs. Data from the Stress Incontinence Surgical Treatment Efficacy (SISTEr) trial ( ) indicated that VLPP did not correlate with several other indices of SUI severity or with urodynamic parameters such as volume of first leakage, volume of first sensation, and presence of DO. In the TOMUS study ( ), preoperative urodynamics was performed before randomization to a retropubic midurethral sling or a transobturator midurethral sling procedure and repeated at 12 months after surgery. Patients and surgeons were blinded to the findings of the preoperative urodynamics so that they would not be influenced in their treatment decision. The study showed that VLPP did not impact surgical outcome. The supine empty bladder stress test, which indicates a low threshold for leakage in a supine position with an empty bladder, was thought to correlate with more severe forms of incontinence and lower VLPPs; however, in a study by , VLPP and urethral closure pressure showed a moderate correlation to each other but little to no correlation to the empty supine stress test. Measurement of maximum urethral closure pressure is a technically demanding test with low reproducibility. This variability in findings is evident in the numerous definitions of ISD as determined by the maximum urethral closure pressure. Urodynamics studies from the TOMUS trial would suggest a limited future for the utilization of UPPs in clinical practice.

A great deal of information is available on the potential use of urodynamics as a predictor of the development of LUT symptoms following antiincontinence procedures. As previously mentioned, based on the results of the SISTEr trial, the predictive value of a urethral function test, specifically a VLPP, was not confirmed. A similar study by also noted that there were no urodynamic predictors that could be identified as useful for predicting the development of de novo postoperative DO after an antiincontinence procedure. published their findings on the relationship between VLPP and urodynamic study findings. Voiding dysfunction was defined as the need for surgical revision to improve voiding at any point 6 weeks postoperatively. In an analysis of the 579 participants from the SISTEr trial, there were no urodynamic parameters that predicted which patients would develop voiding dysfunction following a pubovaginal sling or Burch colposuspension. attempted to predict who would develop urinary retention following a pubovaginal sling in a study of 98 women who had a cadaveric fascia lata sling procedure for SUI. In the final analysis of the 73 women who voided preoperatively without evidence of a detrusor contraction, 19% developed urinary retention postoperatively compared with 0% in those who voided with the detrusor contraction. The authors concluded that women who void with a weak or absent detrusor contraction are more likely to have postoperative urinary retention. studied clinical and urodynamic parameters in 200 women who underwent a retropubic synthetic midurethral sling procedure for SUI. In the final analysis, which included 92 patients who were directly questioned preoperatively about their incontinence, none of the questions except increased daytime frequency were predictive of the development of de novo DO postoperatively. In addition, 56% of patients with a P det greater than 15 cm H 2 O during filling cystometry developed de novo urge incontinence, compared with 21% of patients whose pressure during filling cystometry was less than 15 cm H 2 O.

In a study of 79 women undergoing tension-free vaginal tape surgery for SUI, concluded that women with normal pressure-flow studies were more likely to have a better quality of life and pad test results as compared with patients with abnormal pressure-flow studies, as determined by a Q max of less than 12 mL/s and a P det Q max of greater than 20 cm H 2 O. Although these preliminary data may suggest a role for urodynamics before an antiincontinence procedure to predict postoperative voiding dysfunction and de novo urge incontinence, more conclusive data are required to determine whether this information would truly impact the management of women with stress incontinence. Currently, a clear role for urodynamics in patients with SUI appears to be limited to those with complex symptoms, concurrent voiding dysfunction/elevated PVR, concurrent neurologic disease, and prior incontinence surgery or pelvic radiation.

Pelvic organ prolapse

The role of urodynamic testing in predicting incontinence in women undergoing surgery for pelvic organ prolapse has been debated for many years. At the present time, there is no question that symptomatic pelvic organ prolapse that causes anatomic distortion to the urethra and LUT can mask the presence of urinary incontinence and will, in a certain percentage of women, become unmasked after surgical correction of the prolapse. In 2008, the Colpopexy and Urinary Reduction Efforts (CARE) trial ( ) was published by the Pelvic Floor Disorders Network (PFDN). One goal of the CARE trial was to assess the importance of prolapse reduction in predicting SUI after sacral colpopexy. Preoperative urodynamics were performed, and clinicians were blinded to the results. At the time of sacral colpopexy, patients were randomized to receive either a Burch urethropexy or no antiincontinence procedure. The study ended early, because the Burch colposuspension group had a significantly lower rate of SUI than the no antiincontinence procedure group. In the trial, five different methods of reduction were used (pessary, manual reduction, swabs, forceps, and a half a speculum). SUI without prolapse reduction was uncommon, seen in only 3.7% of women, all of whom had advanced prolapse. Overall, there was a 19% incidence of urodynamic SUI with prolapse reduction, with speculum reduction having the highest incidence of SUI at 30% and pessary the lowest at 6%. Furthermore, women who developed SUI on prolapse reduction were more likely to report postoperative SUI at 3 months. Similarly, the PFDN’s Outcomes Following Vaginal Prolapse Repair and Midurethral Sling trial found that women with advanced prolapse without incontinence symptoms who received a prophylactic midurethral sling had significantly less de novo SUI after surgery than those who did not, and that a preoperative stress test provided little differentiation between those who would benefit from a prophylactic sling and those who would not ( ). The debate continues between those in favor of a prophylactic SUI treatment at the time of prolapse repair and others who worry about the potential risks of performing a surgical procedure that may never have been needed. Online clinical risk prediction models exist that provide a more accurate prediction of who will develop de novo stress incontinence for an individual than do complex urodynamics or a simple bladder stress test ( ). Although the incorporation of a bladder stress test result into this prediction model improves its accuracy, there is no evidence that a full urodynamic evaluation is beneficial in these patients ( ). Given the current data, a reasonable approach to these patients would be to perform a basic reduction maneuver as part of an office bladder stress test to help guide counseling around prophylactic antiincontinence surgery at the time of prolapse repair. Electronic multichannel urodynamic testing is not necessarily required. This is assuming that the patients with symptomatic prolapse have no LUT symptoms. In patients who do have LUT symptoms in conjunction with their prolapse, or who have evidence of voiding difficulty or outlet obstruction as denoted by high PVR, a more precise evaluation that could include a formal urodynamic assessment should be considered.

Overactive bladder

In women with OAB, it is common practice to initiate nonsurgical management in the form of behavioral therapy, timed voiding, and pharmacologic therapy without a urodynamic diagnosis. Before considering a urodynamic evaluation for failure of drug therapy, the reason for failure should be explored, because many times better patient compliance or increasing drug dosage may be warranted. Urodynamic evaluation should be considered when conservative and drug therapy fail to adequately improve symptoms in a patient who is considering more invasive therapeutic interventions. Whether to discontinue antimuscarinic therapy before a urodynamic assessment is controversial. Stopping the drugs increases the likelihood of observing DO if present, whereas continuing them allows evaluation of the mechanism underlying residual refractory symptoms.

The two main urodynamic diagnoses associated with OAB are DO and increased sensation during filling. It must be emphasized that many women with OAB and urge incontinence may not have demonstrable DO on filling cystometry ( ). In some patients with OAB symptoms, the ultimate urodynamic diagnosis turns out to be stress incontinence. Additional diagnoses that can be relevant to managing OAB include BOO and inefficient bladder emptying.

During filling cystometry, ideally the patient should be seated or standing, because OAB symptoms are more commonly experienced in an upright position. However, if there is severe DO at low volumes, it may be difficult to ascertain if urinary stress incontinence is also present. Sometimes a second filling in the supine position will make the DO less overt ( ), allowing an increase in bladder capacity to sufficiently test for the possibility of coexistent stress incontinence. The urodynamic report should clearly state whether the OAB symptoms were reproduced during the testing session.

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