First-Line and Second-Line Medications for Overactive Bladder
Behavioral therapies should be offered as first-line treatment for all patients with overactive bladder, followed by antimuscarinic medications or beta-3 adrenergic agonists as second-line therapy when behavioral interventions are insufficient. 1, 2
First-Line Treatment: Behavioral Therapies
- Bladder training, bladder control strategies, and pelvic floor muscle training should be offered to all patients with OAB as initial management 1
- Fluid management with reduction in fluid intake can reduce frequency and urgency 1
- Weight loss in obese patients can reduce incontinence episodes by up to 47% 1
- Behavioral treatments are as effective as antimuscarinic medications in reducing symptom levels 1
Second-Line Treatment: Pharmacologic Options
Antimuscarinic Medications (alphabetical order)
- Darifenacin - selective M3 receptor antagonist with lower risk of cognitive effects 1, 3
- Fesoterodine - non-selective muscarinic receptor antagonist 1
- Oxybutynin - available in oral and transdermal formulations; highest risk of discontinuation due to adverse effects 1, 2
- Solifenacin - indicated for OAB with symptoms of urge urinary incontinence, urgency, and frequency; better tolerability profile 4, 5
- Tolterodine - similar efficacy to oxybutynin but with lower incidence of dry mouth 6, 3
- Trospium - quaternary amine structure limits CNS penetration 3, 5
Beta-3 Adrenergic Agonists
- Mirabegron - indicated for OAB in adults with symptoms of urge urinary incontinence, urgency, and urinary frequency 7
- Starting dose is 25 mg once daily, may increase to 50 mg once daily after 4-8 weeks if needed 7
- Better tolerated than antimuscarinics with lower incidence of dry mouth and constipation 1
Special Considerations
Antimuscarinic Side Effects and Precautions
- Dry mouth is the most common side effect of antimuscarinic medications 1, 6
- Antimuscarinics should be used with extreme caution in patients with:
- Potential risk for developing dementia and cognitive impairment with antimuscarinic medications, which may be cumulative and dose-dependent 1
- Beta-3 agonists are typically preferred before antimuscarinic medications due to cognitive risk concerns 1
Dosage Adjustments
- For patients with renal impairment (eGFR 15-29 mL/min/1.73m²), mirabegron should be limited to 25 mg once daily 7
- For patients with moderate hepatic impairment (Child-Pugh Class B), mirabegron should be limited to 25 mg once daily 7
Treatment Algorithm
Start with behavioral therapies for all patients with OAB 1, 2
- Bladder training
- Pelvic floor muscle training
- Fluid management
- Weight loss (if applicable)
If behavioral therapies are insufficient, add pharmacotherapy 1
If first medication is ineffective or causes intolerable side effects 1
- Try dose modification
- Switch to a different antimuscarinic medication
- Switch to a beta-3 agonist
- Consider combination therapy with an antimuscarinic and beta-3 agonist for refractory cases 1
For patients who fail pharmacotherapy or have intolerable side effects 1
- Consider minimally invasive procedures:
- Sacral neuromodulation
- Tibial nerve stimulation
- Intradetrusor botulinum toxin injection
- Consider minimally invasive procedures:
Common Pitfalls
- Failing to optimize behavioral therapies before starting medications 1, 2
- Not considering cognitive risks when prescribing antimuscarinics, especially in elderly patients 1
- Abandoning antimuscarinic therapy after failure of one medication instead of trying another agent or a beta-3 agonist 1
- Not adjusting medication doses for patients with renal or hepatic impairment 7
- Using antimuscarinics in patients with contraindications such as narrow-angle glaucoma, impaired gastric emptying, or history of urinary retention 1