Newer Agents for the Management of Overactive Bladder

BENJAMIN J. EPSTEIN; JOHN G. GUMS; EMERSON MOLINA

BENJAMIN J. EPSTEIN, PHARM.D., B.C.P.S., JOHN G. GUMS, PHARM.D., AND EMERSON MOLINA, PHARM.D.

Am Fam Physician. 2006;74(12):2061-2068

Author disclosure: Nothing to disclose.

The anticholinergics tolterodine and oxybutynin are well established in the management of overactive bladder. However, their activity at muscarinic receptors distant from the target site (i.e., bladder) produces anticholinergic side effects leading to poor tolerability. In 2004, trospium, solifenacin, and darifenacin were approved by the U.S. Food and Drug Administration for the treatment of overactive bladder. Trospium is water soluble and therefore is less likely to enter the central nervous system, and solifenacin and darifenacin are more selective for the bladder than older agents. Although these attributes could improve tolerability, clinical trials comparing relevant agents to validate this are lacking. Trials have shown that these newer agents decrease the frequency of incontinence episodes, the number of voids per day, and the number and severity of urgency episodes compared with placebo. These agents also have been shown to improve quality of life in women with overactive bladder and urinary incontinence. Head-to-head studies of the newer agents and immediate-release oxybutynin and tolterodine have suggested similar effectiveness across the class, although the newer agents are better tolerated. Trospium and darifenacin have not been compared with extended-release formulations of tolterodine or oxybutynin, which are better tolerated than the immediate-release versions. In one study, solifenacin produced a somewhat greater decrease in the number of incontinence episodes than extended-release tolterodine, with no difference in tolerability. In general, the newer agents appear to be at least as effective as their predecessors, although it is unclear whether they are better tolerated. Important pharmacokinetic differences among the agents (e.g., route of elimination) allow for selection of an appropriate agent based on individual factors such as cost and tolerability.

Overactive bladder is a clinical syndrome characterized by one or more symptoms of urgency (a difficult-to-defer need to urinate), frequency (greater than eight urinations per 24 hours), nocturia, and incontinence. In persons without overactive bladder, the need to empty the bladder becomes progressively more demanding; in overactive bladder, urgency is characterized by unheralded messages of an immediate need to empty the bladder. These signals are difficult (and sometimes impossible) to delay. The inability to delay urination results in episodes of incontinence in up to 40 percent of patients with overactive bladder.

Clinical recommendation	Evidence rating	References
Nonpharmacologic therapy is recommended for all patients with overactive bladder.	A	^17–19
All available anticholinergic agents effectively decrease the frequency of urgency and incontinence episodes; one should be offered to patients who remain symptomatic despite nonpharmacologic therapy.	A	^26,31
Anticholinergics should be selected on the basis of cost and tolerability.	C	^19,22,26,31
Extended-release formulations of oxybutynin (Ditropan) and tolterodine (Detrol) are better tolerated than immediate-release versions.	A	^23–31
The lowest effective dose of anticholinergics should be prescribed to avoid dose-dependent adverse effects.	C	^26,31

At present, the only class of drugs with widely accepted clinical effectiveness for the treatment of overactive bladder is the anticholinergics, typified by tolterodine (Detrol; Detrol LA) and oxybutynin (Ditropan; Ditropan XL). However, because these drugs create widespread blockade of cholinergic activity, they may cause anticholinergic adverse effects such as blurred vision, dry mouth, urinary retention, constipation, and central nervous system (CNS) effects such as somnolence and confusion. These effects are dose dependent but often occur at therapeutic doses. In 2004, three new anticholinergic drugs were approved by the U.S. Food and Drug Administration for the management of overactive bladder: trospium (Sanctura), solifenacin (Vesicare), and darifenacin (Enablex). Table 1^1–9 provides an overview of all five agents; key clinical trials of the newer agents are summarized in Table 2.^10–16

Drug	Availability	Dose	Frequency	Cost per month (generic)*	Uroselective?	Route of elimination	Comments
Darifenacin (Enablex)	ER tablet: 7.5, 15 mg	7.5 to 15 mg	Once daily without regard for meals	$96	Yes	Hepatic (CYP 3A4)	Dose should be decreased in patients with moderate hepatic impairment; not recommended for use in patients with severe hepatic impairment.
Oxybutynin (Ditropan; Ditropan XL)	IR tablet: 5 mg	2.5 to 5 mg	Two to four times daily	(13 to 30)	No	Hepatic (CYP 3A4)	No formal recommendations exist for dosing in patients with hepatic impairment, but extensive hepatic elimination warrants caution in this setting .
	IR syrup: 5 mg per 5 mL	2.5 to 5 mg	Two to four times daily	75 to 113 (24 to 36)
	ER tablet: 5, 10, 15 mg	5 to 30 mg	Once daily	100 to 112
Oxybutynin patch (Oxytrol)	Transdermal patch: 36 mg	1 patch	Every three to four days	93
Solifenacin (Vesicare)	Tablet: 5, 10 mg	5 to 10 mg	Once daily	101	Yes	Hepatic (CYP 3A4)/Renal	Dose should be decreased in patients with moderate hepatic or severe renal impairment; not recommended for use in patients with severe hepatic impairment. Approximately 15 percent is eliminated unchanged in the urine.
Tolterodine (Detrol; Detrol LA)	IR tablet: 1, 2 mg	1 to 2 mg	Twice daily	112 to 115	No	Hepatic (CYP 2D6/3A4)	Lowest dose should be used in patients with severe hepatic or renal impairment who are taking CYP 3A4 inhibitors. Tolterodine has a lesser effect at the salivary gland than oxybutynin.
Tolterodine (Detrol; Detrol LA)	ER capsule: 2, 4 mg	2 to 4 mg	Once daily	97 to 100	No	Hepatic (CYP 2D6/3A4)
Trospium (Sanctura)	Tablet: 20 mg	20 mg	Twice daily at least one hour before meals or on an empty stomach	89	No	Renal	May have functional selectivity Administer once daily in patients with severe renal impairment.

Pathophysiology

Normally, during bladder filling the detrusor wall relaxes and the urethral sphincter contracts, promoting urine storage. During the normal voiding process, when threshold bladder volume has been reached, a decrease in urethral pressure and relaxation of the urethral sphincter precedes contraction of the detrusor muscle. At the same time, the pelvic floor muscles relax and the bladder neck forms a funnel. Parasympathetic stimulation of the detrusor muscle, mediated by the interaction between acetylcholine and muscarinic receptors, causes it to contract, and the flow of urine begins. Overactive bladder occurs when the detrusor muscle contracts in the face of submaximal bladder volumes. Anticholinergic drugs suppress such contractions by interfering with the interaction between acetylcholine and muscarinic receptors.

Nonpharmacologic Therapies

Nonpharmacologic intervention is the foundation of treatment for overactive bladder. Pelvic floor muscle training and bladder training have been proven to be effective strategies,¹⁷ and in motivated patients can be more effective than medication.¹⁸ Traditional nonpharmacologic tools and lifestyle modification should be provided consistently as part of a balanced program for improving target symptom control. Reviews of appropriate behavioral methods and pelvic floor training are available.¹⁹

Older Anticholinergics

Tolterodine and oxybutynin are muscarinic receptor antagonists. Oxybutynin also displays antispasmodic activity in smooth muscle. These agents are recommended for patients with overactive bladder who remain symptomatic despite nonpharmacologic therapy.^20–22 The introduction of extended-release formulations has improved tolerability without substantively impairing the effectiveness of these drugs.^23–27 Completion rates in long-term studies approach 70 percent with extended-release tolterodine, but are as low as 18 percent with immediate-release oxybutynin.^28–30 On average, anticholinergic therapy reduces weekly urge-incontinence episodes by 70 percent. Dry mouth is the most common adverse event, affecting 20 to 30 percent of patients administered these agents.^28–30

A Cochrane review of randomized controlled trials comparing anticholinergic drugs with placebo or no treatment in patients with overactive bladder showed that patients treated with anticholinergics were more likely to report cure or improvement in their symptoms than those receiving placebo (60 versus 45 percent;P < .05, number needed to treat = 7).³¹ Maximal cystometric capacity increased 54 mL in patients receiving anticholinergics compared with those receiving placebo. Dry mouth was reported significantly more often in the active medication group (32 versus 14 percent; P < .05, number needed to harm = 5); however, similar numbers of patients withdrew because of adverse events. Drug therapy resulted in approximately one less episode of leakage and one less void per 48 hours compared with placebo. Because the placebo-adjusted effectiveness of these agents is marginal, the clinical impact must be weighed against the risk of adverse events.

Newer Agents

Head-to-head studies comparing the three newer agents—trospium, solifenacin, and darifenacin—with immediate-release oxybutynin and tolterodine have suggested similar effectiveness across the class.^10–14,16 Although the attributes of these newer agents in theory could improve tolerability, clinical trials comparing relevant agents to validate this are lacking (Table 2).^10–16

Study	Agent(s)	Design (no. of participants)	Outcomes	Adverse effects
Placebo-controlled studies
Chapple, et al., 2005¹⁰	Darifenacin (Enablex) 7.5 to 15 mg per day versus placebo	Pooled analysis of three RCTs (1,059)	Decrease in incontinence episodes per day: −1.25 (7.5 mg), −1.5 (15 mg) versus −0.99 placebo (P < .004) Decreases in frequency and severity of urgency, leakage, voids per day, and nocturnal awakenings	Dry mouth: 20.2 to 35.3% versus 8.2% placebo (P < .05)
				Constipation: 14.8 to 21.3% versus 6.2% placebo (P < .05)
				Dyspepsia: 2.7 to 8.4% versus 2.6% placebo (P < .05)
Cardozo, et al., 2004¹¹	Solifenacin (Vesicare) 5 to 10 mg per day versus placebo	RCT (911)	Decrease in incontinence episodes per day: −1.63 (5 mg), −1.57 (10 mg) versus −1.25 placebo (P = .002) Decreases in voids per day, urgency episodes, and nocturia; increase in bladder capacity	Dry mouth: 7.7% (5 mg), 23.1% (10 mg), 2.3% placebo
				Constipation: 3.7% (5 mg), 9.1% (10 mg), 2.0% placebo
				Blurred vision: 4.0% (5 mg), 5.9% (10 mg), 2.3% placebo
Zinner, et al., 2004¹²	Trospium (Sanctura) 40 mg per day versus placebo	RCT (523)	Decrease in incontinence episodes per day: −2.0 versus −1.3 placebo (P < .001) Complete dryness in 21% versus 11% placebo Decreases in frequency and severity of urgency, leakage, voids per day, and nocturnal awakenings	Dry mouth: 21.8% versus 6.5% placebo (P < .05)
				Constipation: 9.5% versus 3.8% placebo (P < .05)
				Abdominal pain: 3.1% versus 1.1% placebo
Active-comparator studies
Zinner, et al., 2005¹³	Darifenacin 15 to 30 mg per day versus oxybutynin IR (Ditropan) 5 mg per day or placebo	RCT crossover (76)	Incontinence episodes per week: 10.9 (15 mg), 8.8 (30 mg) versus 9.5 oxybutynin, 14.6 placebo (P < .05)	Dry mouth: 13.1% (15 mg), 34.4% (30 mg) versus 36.1% oxybutynin, 4.9% placebo
Zinner, et al., 2005¹³		RCT crossover (76)		Constipation: 9.8% (15 mg), 21.3% (30 mg) versus 8.2% oxybutynin, 3.3% placebo
Chapple, et al., 2004¹⁴	Solifenacin 5 to 10 mg per day versus tolterodine IR (Detrol) 2 mg per day or placebo	RCT (1,081)	Decrease in incontinence episodes per day: −1.42 (5 mg), −1.45 (10 mg) versus −1.14 tolterodine, −0.76 placebo Decreases in voids per day and urgency episodes; increase in bladder capacity	Early discontinuation: 10.0% (5 mg), 7.1% (10 mg) versus 9.9% tolterodine, 12.0% placebo
				Dry mouth: 14.0% (5 mg), 21.3% (10 mg) versus 18.6% tolterodine, 4.9% placebo
				Constipation: 7.2% (5 mg), 7.8% (10 mg) versus 2.6% tolterodine, 1.9% placebo
				Blurred vision: 3.6% (5 mg), 5.6% (10 mg) versus 1.5% tolterodine, 2.6% placebo
Chapple, et al., 2005¹⁵	Solifenacin 5 to 10 mg per day versus tolterodine ER (Detrol LA) 4 mg per day	RCT (1,177)	Decrease in incontinence episodes per day: −1.60 (10 mg) versus −1.11 tolterodine (P < .0001) Significant decrease in urgency episodes with solifenacin (P < .05)	Early discontinuation: 3.5% versus 3.0% tolterodine
				Dry mouth: 30.0% versus 24.0% tolterodine
				Constipation: 6.4% versus 2.5% tolterodine
				Blurred vision: 0.7% versus 1.7% tolterodine
Halaska, et al., 2003¹⁶	Trospium 40 mg per day versus oxybutynin IR 10 mg per day	RCT (358); unblinded	Similar changes in urodynamic parameters	Early discontinuation (< 52 weeks): 25.0% versus 26.7% oxybutynin
				Dry mouth: 33.0% versus 50.0% oxybutynin
				Constipation: 7.0% versus 4.0% oxybutynin

TROSPIUM

Trospium, a nonselective anticholinergic agent with antispasmodic properties, is approved for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, or frequency. It has been in use in Europe for more than 20 years. Unlike other anticholinergics, trospium is water soluble and crosses the blood-brain barrier poorly.⁹ Although it has been suggested that this feature might minimize centrally mediated events such as drowsiness, nervousness, dizziness, and cognitive impairment, the limited clinical trial data do not support this.

In a prospective, randomized, controlled trial comparing trospium with immediate-release oxybutynin in patients with detrusor instability, there were fewer overall adverse events with trospium (mainly because of a lower incidence of dry mouth).¹⁶ However, there was no difference in CNS adverse effects. Another study evaluated the impact of trospium on somnolence and daytime sleepiness. Trospium did not increase sleepiness or produce other CNS adverse effects; however, the lack of an active comparator arm hinders interpretation of this study.³²

In one placebo-controlled study that enrolled patients experiencing approximately 30 episodes of urinary incontinence per week, trospium significantly reduced the number of voids and episodes of urge urinary incontinence compared with placebo (Table 2^10–16).¹² After 12 weeks, patients treated with trospium experienced between 1.5 and 4.0 fewer incontinence episodes per week than those treated with placebo and had a greater improvement in quality of life. However, these modest results were tempered by an increased incidence of anticholinergic adverse events. In addition, patients enrolled in this study were highly symptomatic, and thus a favorable effect on quality of life is not surprising.¹² Whether these results can be extrapolated to other populations is debatable.

Trospium was compared with immediate-release oxybutynin in several randomized, double-blind clinical trials.^16,33,34 These studies reported similar improvements in detrusor contractions, maximal cystometric bladder capacity, and bladder volume at first sensation with both agents. However, trospium was better tolerated because of fewer reports of dry mouth.

Collectively, these data suggest that trospium effectively reduces symptoms of overactive bladder and is better tolerated than immediate-release oxybutynin.^16,33,34 Trospium has not been compared with extended-release forms of oxybutynin or tolterodine.

SOLIFENACIN

Solifenacin is a selective M₃ muscarinic receptor antagonist approved for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, or frequency. Selectivity for the M₃ receptor may confer improved tolerability given the preferential location of this receptor subtype on the detrusor wall. However, M₃ receptors also are present on smooth muscles in the gastrointestinal tract, salivary glands, eyes, and brain. For this reason, common adverse effects include constipation, dry mouth, blurred vision, fatigue, and cognitive impairment.⁵

Results from several 12-week, double-blind, placebo-controlled studies involving patients with approximately 20 urinary incontinence episodes per week showed that solifenacin reduced urinary frequency by approximately two voids per day compared with a decrease of approximately one void per day with placebo (Table 2^10–16).^5,11,35 Solifenacin also significantly improved urgency, nocturia, and bladder emptying. Compared with immediate-release tolterodine, solifenacin resulted in greater decreases in urgency and incontinence episodes but produced anti-cholinergic side effects at a similar frequency.^14,36 One possible explanation for these findings is that trials of solifenacin used doses up to the maximum of 10 mg, whereas the dose of tolterodine was capped at 2 mg. Solifenacin improved health-related quality of life in patients with overactive bladder and urinary incontinence.³⁶

Another study compared 5 to 10 mg of solifenacin daily with 4 mg of extended-release tolterodine daily.¹⁵ In this study, patients treated with solifenacin had better symptom control but experienced more adverse events. Again, however, the dosing strategy may explain these findings: patients treated with solifenacin initially were given 5 mg daily and could request an increase in dosage after four weeks; 48 percent of patients requested such increase and subsequently were treated with 10 mg daily. In the tolterodine arm, 51 percent of patients requested a dosage increase, but they already were receiving the maximal dosage.

DARIFENACIN

Similar to solifenacin, darifenacin is a muscarinic receptor antagonist with enhanced specificity for theM₃ receptor subtype. It is approved for the management of overactive bladder, and improves overactive bladder symptomatology to an extent similar to that of other agents (Table 2).^10–16 One unique parameter that has been examined with darifenacin is “warning time”: the time from the first sensation of urgency to the time of voluntary urination or incontinence.³⁷ An increase in this duration may permit more patients to experience or maintain continence. Darifenacin increased warning time by 4.3 minutes compared with placebo (P = .003), and 47 percent of patients treated with darifenacin experienced a 30 percent or greater increase in mean warning time compared with only 20 percent of patients treated with placebo (P = .009).³⁷

In a crossover study with immediate-release oxybutynin, the incidence of dry mouth was significantly lower with darifenacin 15 mg than with oxybutynin (13 versus 36 percent, respectively; P < .05) but not with darifenacin 30 mg (34 versus 36 percent).¹³ Constipation was more common in patients given darifenacin 30 mg (21 versus 8 percent with oxybutynin; P < .05) but not in those given 15 mg (10 percent). Effectiveness was similar for patients receiving either dose of darifenacin and those receiving oxybutynin. Comparisons of darifenacin with extended-release oxybutynin or tolterodine are lacking.

Selecting Pharmacologic Agents for Overactive Bladder

The availability of three newer anticholinergic drugs increases the pharmacologic armamentarium for the treatment of overactive bladder. Caution is required with each of these agents, particularly in patients with contraindications to anticholinergic therapy (e.g., untreated open-angle glaucoma, constipation, urinary retention, gastrointestinal disease). A careful evaluation of the balance between benefits and harms, with special attention paid to quality of life, is warranted when considering use of these agents. Appropriately conducted trials are needed to determine the clinical value of functional, structural, and pharmacokinetic nuances. The pharmacokinetic differences among anticholinegic agents allow for the selection of agents based on individual factors (Table 3).^{2,5,9,15,16,22,27,31,35} In the absence of definitive comparative data, a reasonable strategy is to select a therapy according to the individual patient and to try alternative agents if the first is not effective or cannot be tolerated.

Factor	Agent to consider	Comments	References
Anticholinergic adverse effects	Darifenacin (Enablex), solifenacin (Vesicare), tolterodine ER (Detrol LA), oxybutynin ER (Ditropan XL)	ER products and drugs with uroselectivity may offer enhanced tolerability.	^15,27,31
CNS adverse effects	Trospium (Sanctura)	Trospium may be less likely to cross the blood-brain barrier (unproven benefit).	³¹
Cost	Oxybutynin IR	ER and newer agents may be more expensive; generics are available for oxybutynin IR.	²²
Drug-drug interactions	Trospium	Agents other than trospium are metabolized by CYP 3A4 or 2D6, which are responsible for elimination of hepatically metabolized drugs.*	⁹
Effectiveness	Oxybutynin	Nonselectivity may offer more complete suppression of detrusor overactivity. Head-to-head studies of tolterodine and oxybutynin have suggested improved efficacy with oxybutynin.	²⁷
Pregnancy	Oxybutynin	Oxybutynin is pregnancy risk category B whereas all other agents are class C.	²
Severe hepatic impairment	Trospium	Trospium is eliminated renally whereas all other agents undergo extensive hepatic metabolism.*	^5,16,22,35
Severe renal impairment	Oxybutynin, tolterodine, darifenacin, solifenacin	Avoid trospium because it is eliminated renally.	⁹

Enablex (darifenacin) [Prescribing information]. Stein, Switzerland: Novartis, 2005.

Ditropan (oxybutynin chloride) [Prescribing information]. Raritan, N.J.: Ortho McNeill Pharmaceutical, 2003.

Ditropan XL (oxybutynin chloride) [Package insert]. Mountain View, Calif.: ALZA, 2003.

Oxytrol (oxybutynin transdermal system) [Package insert]. Corona, Calif.: Watson Pharma, 2003.

Vesicare (solifenacin succinate) [Package insert]. Paramus, N.J.: Yamanouchi Pharma America, 2004.

Detrol (tolterodine tartrate) [Package insert]. New York, N.Y.: Pfizer, 2005.

Detrol LA (tolterodine tartrate) [Package insert]. New York, N.Y.: Pfizer, 2004.

Nilvebrant L, Andersson KE, Gillberg PG, Stahl M, Sparf B. Tolterodine—a new bladder-selective antimuscarinic agent. Eur J Pharmacol. 1997;327:195-207.

Sanctura (trospium chloride) [Prescribing information]. Hanover, N.J.: Odyssey Pharmaceuticals, 2004.

Chapple CR, Steers W, Norton P, Millard R, Kralidis G, Glavind K, et al. A pooled analysis of three phase III studies to investigate the efficacy, tolerability and safety of darifenacin, a muscarinic M₃ selective receptor antagonist, in the treatment of overactive bladder. BJU Int. 2005;95:993-1001.

Cardozo L, Lisec M, Millard R, van Vierssen Trip O, Kuzmin I, Drogendijk TE, et al. Randomized, double-blind placebo controlled trial of the once daily antimuscarinic agent solifenacin succinate in patients with overactive bladder. J Urol. 2004;172(5 pt 1):1919-24.

Zinner N, Gittelman M, Harris R, Susset J, Kanelos A, Auerbach S for the Trospium Study Group. Trospium chloride improves overactive bladder symptoms: a multicenter phase III trial. J Urol. 2004;171(6 pt 1):2311-5.

Zinner N, Tuttle J, Marks L. Efficacy and tolerability of darifenacin, a muscarinic M₃ selective receptor antagonist (M₃ SRA), compared with oxybutynin in the treatment of patients with overactive bladder. World J Urol. 2005;23:248-52.

Chapple CR, Rechberger T, Al-Shukri S, Meffan P, Everaert K, Huang M, et al.; for the YM-905 Study Group. Randomized double-blind placebo-and tolterodine-controlled trial of the once-daily antimuscarinic agent solifenacin in patients with symptomatic overactive bladder. BJU Int. 2004;93:303-10.

Chapple CR, Martinez-Garcia R, Selvaggi L, Toozs-Hobson P, Warnack W, Drogendijk T, et al. A comparison of the efficacy and tolerability of solifenacin succinate and extended release tolterodine at treating overactive bladder syndrome: results of the STAR trial. Eur Urol. 2005;48:464-70.

Halaska M, Ralph G, Wiedemann A, Primus G, Ballering-Bruhl B, Hofner K, et al. Controlled, double-blind, multicentre clinical trial to investigate long-term tolerability and efficacy of trospium chloride in patients with detrusor instability. World J Urol. 2003;20:392-9.

Burgio KL, Locher JL, Goode PS, Hardin JM, McDowell BJ, Dombrowski M, et al. Behavioral vs. drug treatment for urge urinary incontinence in older women: a randomized controlled trial. JAMA. 1998;280:1995-2000.

Bo K, Talseth T, Holme I. Single blind, randomised controlled trial of pelvic floor exercises, electrical stimulation, vaginal cones, and no treatment in management of genuine stress incontinence in women. BMJ. 1999;318:487-93.

Holroyd-Leduc JM, Straus SE. Management of urinary incontinence in women: scientific review. JAMA. 2004;291:986-95.

Andersson KE, Appell R, Awad S, Chapple C, Drutz H, Finkbeiner A, et al. Pharmacological treatment of urinary incontinence. In Abrams P, Cardozo L, Khoury S, Wein AJ. Incontinence. 2nd ed. Plymouth, UK: Plymbridge Distributors, 2002:479–513.

Andersson KE. Antimuscarinics for treatment of overactive bladder. Lancet Neurol. 2004;3:46-53.

Hashim H, Abrams P. Drug treatment of overactive bladder: efficacy, cost and quality-of-life considerations. Drugs. 2004;64:1643-56.

Kreder K, Mayne C, Jonas U. Long-term safety, tolerability and efficacy of extended-release tolterodine in the treatment of overactive bladder. Eur Urol. 2002;41:588-95.

Abrams P, Malone-Lee J, Jacquetin B, Wyndaele JJ, Tammela T, Jonas U, et al. Twelve-month treatment of overactive bladder: efficacy and tolerability of tolterodine. Drugs Aging. 2001;18:551-60.

Diokno A, Sand P, Labasky R, Sieber P, Antoci J, Leach G, et al. Long-term safety of extended-release oxybutynin chloride in a community-dwelling population of participants with overactive bladder: a one-year study. Int Urol Nephrol. 2002;34:43-9.

Hay-Smith J, Herbison P, Ellis G, Morris A. Which anticholinergic drug for overactive bladder symptoms in adults. Cochrane Database Syst Rev. 2005;3:CD005429.

Diokno AC, Apell RA, Sand PK, Dmochowski RR, Gburek BM, Klimberg IW, et al. Prospective, randomized, double-blind study of the efficacy and tolerability of the extended-release formulations of oxybutynin and tolterodine for overactive bladder: results of the OPERA trial. Mayo Clin Proc. 2003;78:687-95.

Kelleher CJ, Cardozo LD, Khullar V, Salvatore S. A medium-term analysis of the subjective efficacy of treatment for women with detrusor instability and low bladder compliance. Br J Obstet Gynaecol. 1997;104:988-93.

Van Kerrebroeck PHEV for the Tolterodine study group. Long-term tolerability and efficacy of once-daily (OD) tolterodine in the treatment of overactive bladder (OAB). Int Urogynecol J. 2001;12(suppl 3):549.

Lawrence M, Guay DR, Benson SR, Anderson MJ. Immediate-release oxybutynin versus tolterodine in detrusor overactivity: a population analysis. Pharmacotherapy. 2000;20:470-5.

Hay-Smith J, Herbison P, Ellis G, Moore K. Anticholinergic drugs versus placebo for overactive bladder syndrome in adults. Cochrane Database Syst Rev. 2002;3:CD003781.

Staskin DR, Harnett MD. Effect of trospium chloride on somnolence and sleepiness in patients with overactive bladder. Curr Urol Rep. 2004;5:423-6.

Osca-Garcia JM, Martinez-Aguilo E, Conejero-Sugranes J, Jimenez-Cruz JF. A comparison of trospium chloride and oxybutynin in the treatment of hyperactive bladder: a randomized double-blind study. Urod A. 1997;10:40-4.

Madersbacher H, Stohrer M, Richter R, Burgdorfer H, Hachen HJ, Murtz G. Trospium chloride versus oxybutynin: a randomized, double-blind, multicentre trial in the treatment of detrusor hyper-reflexia. Br J Urol. 1995;75:452-6.

Haab F, Halasaka M, Klaver M, for the Solifenacin Study Group. Favorable efficacy and tolerability with long-term solifenacin treatment support high patient persistence. Poster 272. Paper presented at: Annual Meeting of the International Continence Society; August 25–27, 2004; Paris, France.

Chapple CR, Arano P, Bosch JL, De Ridder D, Kramer AE, Ridder AM. Solifenacin appears effective and well tolerated in patients with symptomatic idiopathic detrusor overactivity in a placebo- and tolterodine-controlled phase 2 dose-finding study [Published correction appears in BJU Int 2004;93:1135]. BJU Int. 2004;93:71-7.

Cardozo L, Dixon A. Increased warning time with darifenacin: a new concept in the management of urinary urgency. J Urol. 2005;173:1214-8.