AUA: Overactive Bladder (2019)

See Original Guidelines

Definitions

• Urgency: complaint of a sudden, compelling desire to pass urine which is difficult to defer
• Urgency urinary incontinence: involuntary leakage of urine associated with a sudden compelling desire to void
• Overactive bladder: Urinary urgency, usually accompanied by frequency and nocturia, with or without urgency urinary incontinence, in the absence of a urinary tract infection (UTI) or other obvious pathology.
• Nocturia: interruption of sleep one or more times because of the need to void

Diagnosis and Evaluation

• Clinical diagnosis
  • When urinary frequency (both daytime and night) and urgency, with or without urgency incontinence, in the absence of UTI or other obvious pathology are self-reported as bothersome, the patient may be diagnosed with OAB

Recommended Investigations

Mandatory (2)

1. History and Physical Exam
2. Urinalysis

Optional (4)

1. Urine culture
2. Post void residual
3. Bladder diaries
4. Symptom questionnaire

Not recommended in the initial workup of the uncomplicated patient

1. Urodynamics
2. Cystoscopy
3. Diagnostic renal and bladder ultrasound
4. For complicated or refractory patients, the choice of additional diagnostic tests depends on patient history, QoL and clinician judgment. Neurogenic OAB requires specific evaluation.

History

• Characterize lower urinary tract symptoms (storage and voiding/emptying), including duration of symptoms and baseline symptoms
  • Urinary frequency
    • Varies across individuals.
      • In community-dwelling healthy adults, normal frequency consists of voiding every 3-4 hours with a median of approximately 6 voids a day.
      • Traditionally, up to 7 micturition episodes during waking hours has been considered normal, but this number is highly variable based upon hours of sleep, fluid intake, comorbid medical conditions and other factors.
    • Can be reliably measured with a voiding diary.
  • Incontinence
    • Can be measured reliably with a diary.
• Degree of bother
  • If patient is not significantly bothered by his/her bladder symptoms, then there is a less compelling reason to treat the symptoms.
• Amount and type of fluid intake.
  • Excessive fluid intake can produce voiding patterns that mimic OAB symptoms.
  • Can be measured with a fluid diary
• Current medications
  • Should be reviewed to ensure that symptoms are not related to medications.
• Co-morbid conditions such as neurologic diseases and other genitourinary conditions should be considered as they directly impact bladder function.

Physical exam

1. Abdominal exam
2. Rectal/genitourinary exam
3. Assessment of lower extremities for edema.
4. Patient’s attire and ability to dress independently
   • The ability of the patient to dress independently is informative of sufficient motor skills related to toileting habits. This can provide information on the cognitive function of the patient, which is important to evaluate when considering anticholinergics

Urinalysis

• Rule out UTI and hematuria

Urine culture

• May be appropriate in certain patients given that a urinalysis may be unreliable.

Post-void Residual

• Measurement of the PVR is not necessary for patients who are receiving first-line behavioral interventions or for uncomplicated patients receiving antimuscarinic medications.
  • Anti-muscarinics should be used with caution in patients with PVR 250–300 mL.
• Indications to assess PVR (4)
  1. Presence of voiding/obstructive symptoms
  2. History of incontinence surgery or prostatic surgery
  3. Neurologic diagnoses
  4. Clinician discretion

Bladder diaries

• Diaries that document intake and voiding behavior
• May be useful, particularly for patient education and to document baseline symptoms and treatment efficacy              

Symptoms questionnaire

• Validated symptom questionnaires are useful in the quantification of bladder symptoms and bother- changes with OAB treatment.

Differential Diagnosis

1. Nocturia
2. Polydipsia and polyuria
3. Interstitial cystitis/bladder pain syndrome

Nocturia

• Often due to factors unrelated to OAB, including excessive nighttime urine production and sleep apnea.
• The differential of nocturia includes nocturnal polyuria, low nocturnal bladder capacity or both.
  • In nocturnal polyuria, nocturnal voids are frequently normal or large volume as opposed to the small volume voids commonly observed in nocturia associated with OAB.
  • Sleep disturbances, vascular and/or cardiac disease and other medical conditions are often associated with nocturnal polyuria.

Polydipsia and polyuria

• Frequency that is the result of polydipsia and resulting polyuria may mimic OAB; the two are distinguished with the use of frequency-volume charts.
• Polydipsia-related frequency is physiologically self-induced and should be managed with education and consideration of fluid management.

Interstitial cystitis/bladder pain syndrome

• Clinical presentation of interstitial cystitis/bladder pain syndrome shares the symptoms of OAB
• Bladder and/or pelvic pain, including dyspareunia, is a crucial component of its presentation in contradistinction to OAB.

Management

OAB may compromise QoL but generally does not affect survival. A treatment plan, therefore, should carefully weigh the patient’s potential benefit of a particular treatment against that treatment’s risk for, severity and reversibility of AEs.

Treatment failure occurs when the patient with reasonable expectations does not have the anticipated symptom improvement or is unable to tolerate the treatment due to AEs; lack of efficacy and the presence of intolerable AEs reduce compliance provide education to patients regarding normal lower urinary tract function, what is known about OAB, the benefits vs. risks/burdens of the available treatment alternatives and the fact that acceptable symptom control may require trials of multiple therapeutic options before it is achieved.

that OAB has a variable and chronic course likely requiring multiple management strategies over time with no single ideal treatment and understands that treatments vary in invasiveness, risk of AEs and reversibility.

Most OAB treatments improve patient symptoms but are unlikely to eliminate all symptoms

Options

• Observation
• Lifestyle changes
• Medications
• Other

Observation

OAB is not a disease; it is a symptom complex that generally is not a life-threatening condition.

After assessment has been performed to exclude conditions requiring treatment and counseling, no treatment is an acceptable choice made by some patients and caregivers.

Lifestyle changes

bladder control strategies, pelvic floor muscle training, fluid management) as first-line therapy to all patients with OAB

Behavioral treatments are a group of risk-free tailorable therapies, which improve individual symptoms by changing patient behavior or the patient’s environment.

They are first-line treatments because they are as effective in reducing symptom levels as are antimuscarinic medications. There are two fundamental approaches to behavioral treatment. One modifies bladder symptoms by changing voiding habits, as with bladder training and delayed voiding. The other focuses on pelvic floor muscle training to improve control and techniques for urge suppression.

While most patients do not experience complete symptom relief, most patients experience significant reductions in symptoms and improvements in QoL.

The literature supports the positive effects of weight loss on incontinence specifically

Fluid management with a 25% reduction in fluid intake reduced frequency and urgency

randomized trials indicates that behavioral treatments are generally either equivalent to16–18 or superior to12,19,20 medications in terms of reducing incontinence episodes, improving frequency and nocturia and improving QoL.

Behavioral therapies may be combined with anti-muscarinic therapies.

Medications

Anticholinergics

• Options
  1. Darifenacin
  2. Fesoterodine
  3. Oxybutynin
  4. Solifenacin
  5. Tolterodine
  6. Trospium

no compelling evidence for differential efficacy across medications

Patients with more severe symptoms, on average, experienced greater symptom reductions. Only patients with relatively low baseline symptom levels

are likely to experience complete symptom relief

As similar efficacy was observed for all oral antimuscarinic medications, the choice of medication is patient dependent; however, AE profiles for dry

mouth and constipation vary with medications

If an immediate release (IR) and an extended release (ER) formulation are available, then ER formulations should preferentially be prescribed over IR formulations because of lower rates of dry mouth.

ER formulations of oxybutynin and tolterodine resulted in statistically significantly fewer patient reports of dry mouth than the IR formulations of either medication.

Optimizing medication tolerability is critical to obtaining patient compliance in the treatment of this chronic condition. Compliance with a once daily dosing is greater than with medications taken more than once a day.

Transdermal (TDS) oxybutynin (patch or gel) may be offered

If a patient experiences inadequate symptom control and/or unacceptable adverse drug events with one anti-muscarinic medication, then a dose modification or a different anti-muscarinic medication may be tried.

Clinicians should not use anti-muscarinics in patients with narrow angle glaucoma unless approved by the treating ophthalmologist and should use anti-muscarinics with extreme caution in patients with impaired gastric emptying or a history of urinary retention

Prior to initiation of anti-muscarinics, a patient at risk for gastric emptying problems or for urinary retention should receive clearance from a gastroenterologist

or urologist, respectively. A PVR may be useful in any patient suspected of a higher risk of urinary retention. Anti-muscarinics are also contraindicated in patients using solid oral forms of potassium chloride, as the reduced gastric emptying potentially caused by the anti-muscarinics may increase the potassium absorption of these agents.

Anti-muscarinic therapy may be used with caution with alternative forms of potassium chloride.

Clinicians should manage constipation and dry mouth before abandoning effective anti-muscarinic therapy. Management may include bowel management, fluid management, dose modification or alternative anti-muscarinics.

Patients should be educated about the possible AEs of these medications on bowel function, the roles of adequate dietary fiber and fluid, psylliumbased fiber supplements, regular exercise and normal bowel habits. Treatment advice regarding possible dry mouth could include oral lubricants, avoiding mouthwashes with alcohol, small sips of water, sucking on sugar-free hard candies and chewing sugar-free gum. In older patients who may metabolize drugs differently, it is advisable to start

with a minimal dose and titrate as tolerated.

use caution in prescribing

anti-muscarinics in patients who are using

other medications with anti-cholinergic properties.

Medications with anti-cholinergic properties include

tricyclic antidepressants, acetylcholinesterase

inhibitors and medications for Parkinsonism, other

extra-pyramidal diseases and Alzheimer’s disease.

Certain anti-nausea medications and those with atropine-

like properties may also potentiate AEs.

use caution in prescribing

anti-muscarinics in the frail OAB patient.

OAB medication trials generally are not conducted

in the frail elderly, resulting in a lack of efficacy

and AE data in this group. Additional AEs are

reported in this group, including impaired thermoregulation

with dangerous core temperature elevation.

Clinicians should begin with the lowest possible dose

and titrate slowly while carefully assessing for the

balance between symptom control and AEs.

While newer agents (eg, darifenacin) are reported

to be less likely to produce cognitive deficits in elderly

patients, the literature is limited; the twoweek

drug administration period in these studies is

not long enough to yield definitive conclusions.31,32

Patients may not recognize that memory deterioration

has occurred, making it essential for monitoring

by the clinician, family members and caregivers.

Polypharmacy is common in frail communitydwelling

patients,33 placing them at higher risk for AEs, including impaired cognition. In dementia patients,

anti-muscarinics may be contraindicated entirely

depending on the level of cognitive impairment.

Patients who are refractory to behavioral

and medical therapy should be evaluated

by an appropriate specialist if they desire additional

Other

Before a patient is

exposed to third-line therapies with increased risk compared to behavioral or medical therapy, the patient’s

realistic desire for further treatment should be ascertained,

and a comprehensive evaluation should

be conducted to confirm the diagnosis of OAB and

not another disease process

Neuromodulation or onabotulinumtoxinA therapy

may be offered to the carefully selected patient who

has failed behavioral and anti-muscarinic therapy

or who is not a candidate for these therapies and

continues to have bothersome symptoms after appropriate

counseling. Neuromodulation therapies

are FDA-approved for OAB treatment; however, the

use of onabotulinumtoxinA in non-neurogenic OAB

patients is not FDA-approved.

Neuromodulation