Augmentation Cystoplasty
- Author: Pravin K Rao, MD; Chief Editor: Bradley Fields Schwartz, DO, FACS more...
Background
Bladder augmentation, also called augmentation cystoplasty (AC), is a surgical procedure used in adults and children who lack adequate bladder capacity or detrusor compliance. Decreased bladder capacity or abnormal compliance may manifest as debilitating urgency, frequency, incontinence, recurrent urinary tract infections (UTIs), pyelonephritis, or progressive renal insufficiency. For many patients, augmentation cystoplasty can provide a safe functional reservoir that allows for urinary continence and prevention of upper tract deterioration.
History of the Procedure
Augmentation cystoplasty with a segment of native tissue (usually an intestinal segment), was first performed in the late 1880s in animals and in the 1890s in humans. The original indication for the procedure was a small contracted bladder caused by tuberculous cystitis. Since that time, advances in surgical technique, perioperative care, and antibiotics have greatly improved outcomes.
Because the augmented bladder typically empties poorly, the introduction of clean intermittent catheterization by Lapides et al in the early 1970s was pivotal in allowing the widespread use of augmentation cystoplasty.[1] This allowed convenient, controlled bladder emptying of a safe, functional reservoir.
In 2005, 162 augmentation cystoplasty procedures were logged among Medicare patients.
Etiology
Both neuropathic and non-neuropathic causes for severe bladder dysfunction exist in pediatric and adult populations.
Neuropathic causes include the following:
- Spinal cord injury
- Tethered spinal cord
Non-neuropathic causes include the following:
- Detrusor instability
- Chronic cystitis, including tuberculosis and schistosomiasis
- Defunctionalized bladder in a patient who is on dialysis
Presentation
Decreased bladder capacity or abnormal compliance may manifest as debilitating urgency, frequency, incontinence, recurrent UTIs, pyelonephritis, or progressive renal insufficiency.
Various studies used to evaluate such symptoms may reveal severe dysfunction.
- Urodynamics demonstrate a low-volume, poorly compliant reservoir, placing the kidneys at risk from high-pressure urinary storage.
- Simultaneous fluoroscopic videourodynamics may reveal vesicoureteral reflux.
- Renal ultrasonography or other imaging modalities may show renal scarring or impaired renal growth due to high-pressure urinary storage.
Indications
Any patient with marked reduction in bladder capacity or compliance may be a candidate for augmentation cystoplasty. Conservative management for these patients usually consists of intermittent self-catheterization and anticholinergic medications. Augmentation cystoplasty is considered when bothersome symptoms impair a patient’s lifestyle despite medical treatment or when high-pressure urinary storage places the upper urinary tracts at risk.
Neurogenic bladder in the pediatric population is often associated with congenital anomalies, including the following:
- Prune belly syndrome (Eagle-Barrett syndrome)
- Bladder exstrophy
- Cloacal exstrophy
Patients with these conditions most commonly undergo augmentation cystoplasty when, despite behavioral and medical management, they experience continued incontinence, debilitating urgency, enuresis, complicated UTIs, vesicoureteral reflux, or impaired renal growth.
Some adult patients who underwent urinary diversion for an embryologic urinary defect as a child seek a healthier cosmetic and functional state. In other cases, adults have an acquired cause for bladder dysfunction, including some of those discussed in Etiology. Adults may present with symptoms very similar to those of children with congenital abnormalities. Again, surgery is indicated for adults with refractory symptoms and those with risk or progression of upper tract deterioration.
Relevant Anatomy
The anatomy of the bladder forms an extraperitoneal muscular urine reservoir that lies behind the pubic symphysis in the pelvis. A normal bladder functions through a complex coordination of musculoskeletal, neurologic, and psychological functions that allow filling and emptying of the bladder contents. The prime effector of continence is the synergic relaxation of detrusor muscles and contraction of the bladder neck and pelvic floor muscles.
The normal adult bladder accommodates 300-600 mL of urine; a central nervous system (CNS) response is usually triggered when the volume reaches 400 mL. However, urination can be prevented by cortical suppression of the peripheral nervous system or by voluntary contraction of the external urethral sphincter.
See Bladder Anatomy for more information.
See Intraoperative details for a discussion of relevant anatomy.
Contraindications
Patients who are unable or unwilling to perform life-long intermittent catheterization should not undergo augmentation cystoplasty because of the high likelihood of ultimately requiring catheterization.In addition, patients with inflammatory bowel disease (especially Crohn disease), short or irradiated bowel, bladder tumors, severe radiation cystitis, or severe renal insufficiency should not undergo augmentation cystoplasty.
Poor surgical candidates and patients with a short life expectancy should consider alternatives such as continued medical management or creation of a less complex, temporizing form of urinary drainage.
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| Tissue Segment | Advantages | Disadvantages |
| Stomach | Decreases mucus, infection, and stones; better for short gut and acidosis/azotemia | Hemolytic dysuria syndrome |
| Jejunum | None (used only if other segments are contraindicated/unavailable) | Electrolyte disturbances; malabsorption |
| Ileum | Usually available, well-tolerated | Electrolyte disturbances; mucus |
| Large intestine | Usually available, well-tolerated | Electrolyte disturbances; mucus; sigmoid: strong contractions |
| Ureter | Minimizes mucus, infection, stones and electrolyte effects | Rarely available |
| Intestinal Segment | Acid-Base Effect | K+ | Cl+ | Notes |
| Stomach | Alkalosis | ↓ | ↓ | Respiratory insufficiency, seizure, arrhythmia |
| Jejunum | Acidosis | ↑ | ↓ | Hyponatremia, azotemia, malabsorption |
| Ileum/colon | Acidosis | ↓ | ↑ | Diarrhea with loss of colon, ileocecal valve |

