Drugs for management of urinary incontinence
Urinary incontinence is broadly classified into disorders of storage and disorders of voiding. Storage disorders are associated with normal post-void residual volume and can be functional (e.g. urethral sphincter mechanism incompetence in dogs) or mechanical (ectopic ureters). Voiding disorders involve incomplete bladder emptying with increased post-void residual volume and may result from functional outflow obstruction or mechanical blockage. Functional causes affect the coordination of bladder contraction and urethral relaxation, while mechanical causes include anatomical abnormalities like strictures or masses. Classification helps guide appropriate diagnostic and treatment strategies. For details, please refer to textbooks and Kendall et al. (2024).
Storage phase
The bladder fills gradually under sympathetic control via the hypogastric nerve, which relaxes the detrusor muscle (beta-adrenergic effect) and contracts the internal urethral sphincter (alpha-adrenergic effect). Simultaneously, the pudendal nerve maintains tone in the external urethral sphincter (acetylcholine nicotinic receptors in the striated muscle). These mechanisms prevent urine leakage during bladder filling.
Voiding phase
Once the bladder is full, afferent signals from the bladder wall (via the pelvic nerve) reach the brainstem. When voluntary voiding is initiated, the parasympathetic system (pelvic nerve, acetylcholine muscarinic receptors) contracts the detrusor muscle while sympathetic and somatic outflow (hypogastric and pudendal nerves) are inhibited, relaxing both urethral sphincters. This coordination allows complete bladder emptying.
Detrusor muscle: acetylcholine muscarinic receptors
are activated during voiding phase and beta-adrenergic receptors are activated during storage phase.
Internal sphincter muscle (smooth muscle sphincter): alpha-adrenergic receptors are activated during storage phase and inhibited during voiding phase.
External sphincter (striated muscle sphincter): acetylcholine nicotinic receptors are activated during storage phase and inhibited during voiding phase.
TABLE: Medications to treat storage disorders
| Drug | Class and effect | Indication | Dose | Adverse effects |
|---|---|---|---|---|
|
Phenylpropanolamine
|
Alpha agonist: directly stimulates alpha and some beta receptors Effect: increases internal sphincter/urethral tone |
USMI |
Dogs and cats: 1.5–2 mg/kg p.o. q8–12h |
Hypertension, restlessness, GI effects, urine retention |
|
Estriol
|
Oestrogen: binds to oestrogen receptors within sphincter cells, resulting in increased responsiveness to norepinephrine. May also sensitize the urethral sphincter to alpha-adrenergic stimulation Effect: increases internal sphincter/urethral tone |
USMI (females) |
Dogs: 2 mg per dog p.o. q24h for 14 days, then reduce to 1 mg per dog q24h |
Attractiveness to males, mammary/vulvar swelling, behavioural changes |
|
Diethylstilbestrol
|
Oestrogen (see Estriol) |
USMI (females) |
Dogs: 0.1–1 mg per dog p.o. q24h for 3–5 days, then weekly or prn |
Myelosuppression (rare at these doses), attractiveness to males, mammary/ vulvar swelling, behavioural changes |
|
Testosterone cypionate
|
Androgen: exact mechanism unknown. Suspected to maintain tone of urethra and bladder smooth muscle. May also cause hypertrophy of the prostate, which increases urethral resistance Effect: increases internal sphincter/urethral tone |
USMI (males) |
Dogs: 2.2 mg/kg i.m. q4–8wk |
Behavioural changes, aggression, perianal adenoma, prostatic hyperplasia |
|
Methyltestosterone
|
Androgen (see Testosterone cypionate) |
USMI (males) |
Dogs: 0.5 mg/kg p.o. q24h; if effective, change to testosterone cypionate |
Behavioural changes, aggression, perianal adenoma, prostatic hyperplasia |
|
Oxybutynin
|
Muscarinic receptor antagonist Effect: decreases detrusor contractility |
Detrusor instability |
Dogs: 0.2–0.3 mg/kg q8–12h in dogs |
GI effects, urine retention, hypersalivation, sedation |
TABLE: Medications to treat voiding disorders.
| Drug | Class and effect | Indication | Dose | Adverse effects |
|---|---|---|---|---|
|
Tamsulosin hydrochloride
|
Alpha antagonist Effect: decreases internal sphincter/urethral tone |
Functional outflow obstruction |
Dogs: 0.4–0.8 mg per dog p.o. q24h Cats: 4–6 micrograms/kg p.o. q12–24h |
Hypotension |
|
Prazosin
|
Alpha antagonist Effect: decreases internal sphincter/urethral tone |
Functional outflow obstruction |
Dogs: 1 mg per dog <15 kg, 2 mg per dog >15 kg p.o. q8–12h 30 minutes before blader expression Cats: 0.25–1 mg per cat p.o. q8–12h |
Hypotension, weakness, syncope, GI upset |
|
Phenoxybenzamine
|
Alpha antagonist Effect: decreases internal sphincter/urethral tone |
Functional outflow obstruction |
Dogs and cats: 0.25–1 mg/kg p.o. q8–24h |
Hypotension, tachycardia, weakness |
|
Diazepam
|
Benzodiazepine/skeletal muscle relaxant Effect: decreases external sphincter tone |
Functional outflow obstruction |
Dogs: 0.04–0.8 mg/kg/day, p.o., divided q8–12h; recommended 30 minutes prior to a walk or bladder expression Avoid in cats |
Sedation, ataxia |
|
Dantrolene sodium
|
Calcium release inhibitor/skeletal muscle relaxant Effect: decreases external sphincter tone |
Functional outflow obstruction |
Dogs: 1–2.7 mg/kg/day, p.o., divided q8–12h Cats: 0.5–2 mg/kg/day divided q8–12h |
Sedation, weakness, hepatotoxicity |
|
Alprazolam
|
Benzodiazepine/skeletal muscle relaxant Effect: decreases external sphincter tone |
Functional outflow obstruction |
Dogs: 0.02–0.1 mg/kg, p.o. q12h Cats: 0.125–0.25 mg/kg p.o. q12h |
Sedation, increased appetite, paradoxical hyperactivity in cats |
|
Bethanechol
|
Muscarinic receptor agonist Effect: increases detrusor muscle contraction |
Detrusor atony |
Dogs: 2.5–25 mg per dog p.o. q8h Cats: 1.25–5 mg per cat p.o. q8–12h Always use in combination with sphincter relaxants |
Increased GI motility, vomiting, diarrhoea, hypersalivation, hypotension, bradycardia, dyspnoea |
|
Cisapride
|
Increases acetylcholine release |
Detrusor atony |
Dogs: 0.5 mg/kg p.o. q8h Cats: 1.25–5 mg per cat p.o. q8–12h |
Diarrhoea, abdominal pain |
|
Metoclopramide
|
Increases acetylcholine release |
Detrusor atony |
Dogs and cats: 0.2–0.5 mg/kg p.o. q8h |
Diarrhoea, abdominal pain, sedation or hyperactivity |
References
Kendall A, Byron JK, Westropp JL et al. (2024) ACVIM consensus statement on diagnosis and management of urinary incontinence in dogs. Journal of Veterinary Internal Medicine 38, 878–903
Granger N, Olby NJ, Nout-Lomas YS and the Canine Spinal Cord Injury Consortium (2020) Bladder and bowel management in dogs with spinal cord injury. Frontiers in Veterinary Science 7, 583342
Coates JR and De Decker S (2026) Tail, anal and bladder dysfunction. In: BSAVA Manual of Canine and Feline Neurology, 5th edn, ed. SR Platt, N Olby and E Beltran. BSAVA Publications, Gloucester [in production]
Mitchell WC and Venable DD (1985) Effects of metoclopramide on detrusor function. The Journal of Urology 134, 791–794