›Amitriptyline (tricyclic antidepressant)
›Amitriptyline 10-25 mg nightly — start low and titrate
›Target dose 25-75 mg nightly
›Mechanism: central pain modulation, bladder anticholinergic effect
›Evidence: significant symptom improvement in randomized trials
›Adverse effects: sedation, dry mouth, constipation, urinary retention risk
›Hydroxyzine (H1 antihistamine)
›Hydroxyzine 10-25 mg nightly — start low
›Target dose 25-75 mg nightly
›Benefit in patients with allergic history or mast cell hypothesis
›Adverse effects: sedation; minimal anticholinergic effect
›Cimetidine (H2 antagonist)
›Cimetidine 400 mg twice daily
›H2-receptor blockade mechanism in bladder mucosa
›Evidence from small RCT showing symptom improvement
›Well tolerated; check for drug interactions (CYP450 inhibitor)
›Gabapentinoids
›Gabapentin 100-300 mg three times daily — titrate to effect
›Target 1800-3600 mg/day in divided doses
›Renal dose adjustment required
›Adverse effects: sedation, dizziness, peripheral edema
›Pregabalin 75 mg twice daily — alternative
›Titrate to 150-300 mg twice daily
›Renal dose adjustment required
›Pentosan polysulfate sodium (PPS)
›Pentosan polysulfate 100 mg three times daily (300 mg/day total)
›Only FDA-approved oral therapy for IC/BPS
›Mechanism: glycosaminoglycan (GAG) layer restoration
›Conflicting efficacy data — Cochrane review shows modest benefit
›Response may take 3-6 months to observe
›Ophthalmologic monitoring required
›Baseline retinal exam before initiation
›Retinal exam within 6 months of initiation and annually thereafter
›Pigmentary maculopathy: dose-dependent, potentially irreversible
›Symptoms: difficulty reading, impaired dark adaptation, blurred vision
›Cumulative dose greater than 1500 g associated with higher maculopathy risk
›Analgesics for flare management
›NSAIDs (ibuprofen 400-600 mg three times daily with food)
›Short-term flare symptom relief
›Renal function monitoring with prolonged use
›Phenazopyridine 200 mg three times daily after meals
›Urinary analgesic — symptomatic relief only
›Maximum 2 days; urine orange discoloration expected
›Not to be used as diagnostic test for UTI
Intravesical instillations
›DMSO (dimethyl sulfoxide) intravesical instillation
›DMSO 50 mL of 50% solution instilled intravesically
›Dwell time 15-20 minutes, then voided
›Series of 6 treatments every 1-2 weeks
›Often combined with heparin, lidocaine, and steroid (DMSO cocktail)
›Characteristic garlic-like odor from skin during treatment
›Heparin intravesical
›Heparin 10,000-40,000 units in 10 mL sterile water
›Self-instillation daily or 3 times weekly
›GAG layer restoration mechanism
›Frequently combined with lidocaine for immediate relief
›Lidocaine intravesical
›Alkalinized lidocaine 2% 10-20 mL with sodium bicarbonate
›Dwell time 30-60 minutes
›Enhanced absorption with alkalinization (pH 8.0 target)
›Short-term pain relief; often combined with heparin
›Hyaluronic acid or chondroitin sulfate
›Hyaluronic acid 40 mg in 40 mL weekly for 4 weeks then monthly
›GAG layer augmentation; European approval; off-label in North America
›Chondroitin sulfate intravesical — evidence emerging
›Improved sexual function reported in IC/BPS patients in 2026 RCT
›Cystoscopy with hydrodistension under anesthesia
›Distension to 80-100 cmH2O for 1-2 minutes
›Diagnostic and potentially therapeutic
›Symptomatic improvement in 30-50% short-term
›Effect typically lasts weeks to months; can be repeated
›Hunner lesion fulguration or resection
›Transurethral fulguration or laser ablation
›High responder rate (70-90%) in Hunner lesion subtype
›Lesion recurrence expected; repeat procedures often required
›Sacral neuromodulation
›InterStim device implantation
›Modulates S3 nerve root afferent signaling
›FDA-approved for urgency, frequency, and non-obstructive urinary retention
›Benefit demonstrated in refractory IC/BPS
›Two-stage procedure: test stimulation then permanent implant
›Botulinum toxin A intradetrusor injection
›OnabotulinumtoxinA 100-200 units in 20-40 injection sites
›Performed cystoscopically under sedation
›Mechanism: inhibition of sensory afferents and detrusor overactivity
›Effect duration 6-12 months; repeat injections required
›Risk of post-procedure urinary retention (up to 5-10%)
Major surgical options (refractory cases only)
›Surgical salvage for treatment-refractory IC/BPS
›Augmentation cystoplasty
›Bladder augmentation using bowel segment (typically ileum)
›Increases functional bladder capacity
›Significant surgical morbidity; life-long follow-up required
›Urinary diversion with or without cystectomy
›Considered only after all other options exhausted
›Ileal conduit or continent pouch
›Pain relief not guaranteed even after cystectomy