Pediatric Surgery for Bladder Anomalies Follow-up

  • Chief Editor: Marc Cendron, MD   more...
 
Updated: Jan 25, 2010
 

Further Outpatient Care

  • Bladder diverticula: No follow-up care is required after surgical removal. Small diverticula that are treated by observation alone may be annually monitored with renal and bladder ultrasonography.
  • Urachal sinus: No follow-up care is required after surgical removal.
  • Urachal cyst: perform yearly ultrasonographic studies if small cysts are to be monitored. No follow-up is necessary after surgical removal.
  • Patent urachus: No follow-up care is necessary after surgical removal.
  • Vesicourachal diverticulum: No follow-up care is necessary.
  • Bladder ears: No follow-up care is necessary.
  • Bladder agenesis: Frequent outpatient follow-up visits are necessary after urinary diversion. Initially, outpatient follow-up care may occur as often as monthly. Once stable, follow-up visits usually are annual. Serial renal ultrasonographic evaluation is used to assess renal growth and the presence or absence of hydronephrosis. Conduit ultrasonography can detect the presence of stones. Serum electrolytes and creatinine help detect metabolic disturbances and renal insufficiency.
  • Megacystitis: Yearly renal and bladder ultrasonographic evaluation may be appropriate until just after the toilet training period to monitor the upper tracts and ensure adequate bladder emptying.
  • Bladder duplication: Yearly renal and bladder ultrasonographic evaluation may be appropriate, as described for megacystitis.
  • Bladder septation: Yearly renal and bladder ultrasonographic evaluation may be appropriate, as described for megacystitis.
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Deterrence/Prevention

  • These conditions are congenital. The timing of altered embryogenesis leading to these conditions has been a matter of speculation, and the embryologic cause of these lesions is unknown.
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Complications

  • Complications are related to persistent obstruction or recurrent urinary tract infections, namely renal insufficiency or failure. If the obstruction is corrected and urinary drainage is unimpeded, long-term complications are minimal. In the case of bladder agenesis, the long-term complications are related to those specific to urinary diversion, continent reservoir, or both. These include ureteral stricture at the junction of the ureter and reservoir, reservoir stones, recurrent urinary tract infection, stomal stenosis of the catheterizable segment, and metabolic disturbances relative to the intestinal segment used.
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Prognosis

  • Bladder diverticula - Excellent
  • Urachal sinus - Excellent
  • Urachal cyst - Excellent
  • Patent urachus - Excellent
  • Vesicourachal diverticulum - Excellent
  • Bladder ears - Excellent
  • Bladder agenesis - Guarded
  • Megacystitis - Good
  • Bladder duplication - Good to excellent
  • Bladder septation - Variable, guarded to good depending on anatomy and degree of renal dysfunction
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Patient Education

  • In all these conditions, an element of voiding dysfunction may exist. Educate parents regarding frequent and complete bladder emptying after the toilet training period to guard against infrequent and dysfunctional voiding patterns. In general, children should void approximately 5-6 times per day, which equates to voiding every 3 hours. Infrequent and dysfunctional voiding in the presence of an anatomic abnormality may place the child at increased risk for febrile urinary tract infections and renal damage.
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Contributor Information and Disclosures
Coauthor(s)

Bartley G Cilento, Jr, MD  Instructor, Department of Surgery, Division of Urology, Children's Hospital of Boston and Harvard Medical School

Bartley G Cilento, Jr, MD is a member of the following medical societies: American Academy of Pediatrics, American Urological Association, and Massachusetts Medical Society

Disclosure: Nothing to disclose.

Specialty Editor Board

Martin David Bomalaski, MD, FAAP  Pediatric Urologist, Alpine Urology

Martin David Bomalaski, MD, FAAP is a member of the following medical societies: Alpha Omega Alpha, American Academy of Pediatrics, and American Urological Association

Disclosure: Nothing to disclose.

Mary L Windle, PharmD  Adjunct Associate Professor, University of Nebraska Medical Center College of Pharmacy; Pharmacy Editor, eMedicine

Disclosure: Nothing to disclose.

Harry P Koo, MD  Chairman of Urology Division and Director of Pediatric Urology, Virginia Commonwealth University; Professor of Surgery, VCU School of Medicine, Medical College of Virginia; Director of Urology, Children's Hospital of Richmond

Harry P Koo, MD is a member of the following medical societies: American Academy of Pediatrics, American College of Surgeons, and American Urological Association

Disclosure: Nothing to disclose.

Paul D Petry, DO, FACOP, FAAP  Consulting Staff, Freeman Pediatric Care, Freeman Health System

Paul D Petry, DO, FACOP, FAAP is a member of the following medical societies: American Academy of Osteopathy, American Academy of Pediatrics, American College of Osteopathic Pediatricians, and American Osteopathic Association

Disclosure: Nothing to disclose.

Chief Editor

Marc Cendron, MD  Associate Professor of Surgery, Harvard School of Medicine; Consulting Staff, Department of Urological Surgery, Children's Hospital Boston

Marc Cendron, MD is a member of the following medical societies: American Academy of Pediatrics, American Urological Association, European Society for Paediatric Urology, Johns Hopkins Medical and Surgical Association, New Hampshire Medical Society, Society for Fetal Urology, and Society for Pediatric Urology

Disclosure: Nothing to disclose.

References
  1. Caldamone AA. Anomalies of the bladder and cloaca. In: Gillenwater JY, Grayhack JT, Howards SS, et al, eds. Adult and Pediatric Urology. 2nd ed. St. Louis, Mo: Mosby Year Book; 1987:2023.

  2. Cilento BG, Nguyen HT. Bladder diverticula, urachal anomalies, and other uncommon anomalies of the bladder. In: Gearhart JP, Rink RC, Mouriquand P, eds. Pediatric Urology. Philadelphia, Pa: WB Saunders; 2001.

  3. Tacciuoli M, Laurenti C, Racheli T. Double bladder with complete sagittal septum: diagnosis and treatment. Br J Urol. Dec 1975;47(6):645-9. [Medline].

  4. Coker AM, Allshouse MJ, Koyle MA. Complete duplication of bladder and urethra in a sagittal plane in a male infant: case report and literature review. J Pediatr Urol. Aug 2008;4(4):255-9. [Medline].

  5. Blane CE, Serin JM, Bloom DA. Bladder diverticula in children. Radiology. 1194;190:695. [Medline].

  6. Stephens FD. The vesicoureteral hiatus and paraureteral diverticula. J Urol. Jun 1979;121(6):786-91. [Medline].

  7. Pieretti RV, Pieretti-Vanmarcke RV. Congenital bladder diverticula in children. Journal of Pediatric Surgery. 1999;34:468. [Medline].

  8. Verghese M, Belman AB. Urinary retention secondary to congenital bladder diverticula in infants. J Urol. Dec 1984;132(6):1186-8. [Medline].

  9. Barrett DM, Malek RS. Observations on vesical diverticulum in childhood. Journal of Urology. 1976;116:234. [Medline].

  10. Burbige KA, Lebowitz RL, Colodny AH. The megacystis-megaureter syndrome. J Urol. Jun 1984;131(6):1133-6. [Medline].

  11. Levard G, Aigrain Y, Ferkadji L. Urinary bladder diverticula and the Ehlers-Danlos syndrome in children. J Pediatr Surg. Nov 1989;24(11):1184-6. [Medline].

  12. Burns E, Cummins H, Hyman J. Incomplete reduplication of the bladder. Journal of Urology. 1947;57:257.

  13. Shokeir AA, Ashamallah A, Abol-Enein H. Incomplete bladder duplication. Br J Urol. Jan 1995;75(1):106-7. [Medline].

  14. Cilento BG Jr, Bauer SB, Retik AB. Urachal anomalies: defining the best diagnostic modality. Urology. Jul 1998;52(1):120-2. [Medline].

  15. Powell CR, Kreder KJ. Treatment of bladder diverticula, impaired detrusor contractility, and low bladder compliance. Urol Clin North Am. Nov 2009;36(4):511-25, vii. [Medline].

  16. Yohannes P, Bruno T, Pathan M, Baltaro R. Laparoscopic radical excision of urachal sinus. J Endourol. Sep 2003;17(7):475-9; discussion 479. [Medline].

  17. Castillo OA, Vitagliano G, Olivares R, Sanchez-Salas R. Complete excision of urachal cyst by laparoscopic means: a new approach to an uncommon disorder. Arch Esp Urol. Jun 2007;60(5):607-11. [Medline].

  18. Chiarenza SF, Scarpa MG, D'Agostino S, Fabbro MA, Novek SJ, Musi L. Laparoscopic excision of urachal cyst in pediatric age: report of three cases and review of the literature. J Laparoendosc Adv Surg Tech A. Apr 2009;19 Suppl 1:S183-6. [Medline].

  19. Hutch JA. Saccule formation at the ureterovesical junction in smooth-walled bladders. Journal of Urology. 1961;86:390.

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Voiding cystourethrogram showing a bladder diverticulum arising from the posterior aspect of the bladder.
Voiding cystourethrogram showing 2 posteriorly placed bladder diverticula.
Bladder ultrasound showing 2 posteriorly placed bladder diverticula.
Duplicated bladder with a urethral catheter placed into each bladder.
Voiding cystourethrogram demonstrating a duplicated bladder.
Intravenous pyelogram demonstrating a duplicated bladder. Notice how each ureter drains into the ipsilateral bladder.
Urachal cyst at the level of the umbilicus.
Bladder anomalies. Ultrasound demonstrating urachal cyst. Ultrasound cursors mark the extent of the cyst.
Voiding cystourethrogram showing megacystitis. Bilateral vesicoureteral reflux is also observed (grade 3 on the right, grade 2 on the left).
 
 
 
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