Journals / Şişli Etfal Hastanesi Tıp Bülteni / 2021 / Cilt: 55 - Sayı: 4

The Effects of Bladder Diverticulum on the Pathophysiology of Bladder Outlet Obstruction: An Experimental Study in Guinea Pigs

Pages
[560]–564
DOI
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

Conclusion: Physiological and histopathological changes in the bladder with BD combined with BOO are more evident than with BOO alone.

📌 3 Key Takeaways

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Objective & Hypothesis:Objectives: This study is the first to urodynamically and histopathologically evaluates the effects of bladder diverticulum (BD) secondary to bladder outlet obstruction (BOO).
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Key Findings & Data:Methods: Guinea pigs (n=32) weighing 900–1,000 g were divided randomly into four groups: Sham, BD, BOO, and BD combined with BOO.
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Conclusion & Impact:Conclusion: Physiological and histopathological changes in the bladder with BD combined with BOO are more evident than with BOO alone.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Objectives: This study is the first to urodynamically and histopathologically evaluates the effects of bladder diverticulum (BD) secondary to bladder outlet obstruction (BOO). Methods: Guinea pigs (n=32) weighing 900–1,000 g were divided randomly into four groups: Sham, BD, BOO, and BD combined with BOO. All guinea pigs in the four groups underwent urodynamic evaluation preoperatively and at 1 month postoperatively. The bladders were removed and examined histopathologically. Results: The post-operative filling detrusor pressure was lower in the Sham group (7.1±1.6 cm H2O) than in the BD (21.4±5.6 cm H2O) and BD with BOO groups (23.6±9.3 cm H2O) (p<0.05). There was no difference between the Sham and BOO (9.5±4.0) groups. Post-operative bladder compliance was better in the Sham group (2.3±0.8 ml/cm H2O) than in the BD (0.9±0.22 ml/cm H2O) and BD with BOO groups (0.6±0.3 ml/cm H2O) (p<0.05). Involuntary detrusor contraction was not observed in the Sham or BOO groups, but was observed in 37.5% of subjects in the BD and BD with BOO groups. On histological examination, the bladder wall was thicker (3.75±0.68 mm) (p=0.601), and the connective tissue volume was significant increased (p=0.046), in the bladder muscularis mucosa in the BD groups compared to the BOO group. Conclusion: Physiological and histopathological changes in the bladder with BD combined with BOO are more evident than with BOO alone.

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Cite This Article

KARADAG, A., ÇELEBİ, S., SOYSAL, F. G., ÖZAYDIN, İ. Y., KESKİN, E. (2021). The Effects of Bladder Diverticulum on the Pathophysiology of Bladder Outlet Obstruction: An Experimental Study in Guinea Pigs. Şişli Etfal Hastanesi Tıp Bülteni, Cilt: 55 - Sayı: 4, [560]–564. https://ajindex.com/articles/399596

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References (14)

  1. Levin RM, Haugaard N, O'Connor L, Buttyan R, Das A, Dixon JS, et al. Obstructive response of human bladder to BPH vs. rabbit bladder response to partial outlet obstruction: a direct comparison. Neurourol Urodyn 2000;19:609–29
  2. Levin RM, Hudson AP. The molecular genetic basis of mitochondrial malfunction in bladder tissue following outlet obstruction. J Urol 2004;172:438–47
  3. Nevéus T, von Gontard A, Hoebeke P, Hjälmås K, Bauer S, Bower W, et al. The standardization of terminology of lower urinary tract function in children and adolescents: report from the Standardisation Committee of the International Children's Continence Society. J Urol 2006;176:314–24
  4. Levin RM, Longhurst PA, Monson FC, Haugaard N, Wein AJ. Experimental studies on bladder outlet obstruction. In: Lepor H, Lawson RK, editors. Prostate diseases. Philadelphia: WB Saunders; 1993. p. 119–30
  5. Çelebi S, Kuzdan Ö, Özaydın S, Başdaş CB, Özaydın İ, Erdoğan C, et al. A bladder diverticulum model in rabbits. J Pediatr Urol 2016;12:311.e1-311.e6
  6. Celebi S, Sander S, Kuzdan O, Özaydın S, Beşik Beştaş C, Yavuz S, et al. Current diagnosis and management of primary isolated bladder diverticula in children. J Pediatr Urol 2015;11:61.e1–5
  7. Levin RM, Longhurst PA, Monson FC, Kato K, Wein AJ. Effect of bladder outlet obstruction on the morphology, physiology, and pharmacology of the bladder. Prostate Suppl 1990;3:9–26
  8. Lu SH, Chang LS, Yang AH, Lin AT, Chen KK, Wei YH. Mitochondrial DNA deletion of the human detrusor after partial bladder outlet obstruction-correlation with urodynamic analysis. Urology 2000;55:603–7
  9. Mirone V, Imbimbo C, Sessa G, Palmieri A, Longo N, Granata AM, et al. Correlation between detrusor collagen content and urinary symptoms in patients with prostatic obstruction. J Urol 2004;172:1386–9
  10. Hakenberg OW, Linne C, Manseck A, Wirth MP. Bladder wall thickness in normal adults and men with mild lower urinary tract symptoms and benign prostatic enlargement. Neurourol Urodyn 2000;19:585–93
  11. Rovner ES. Bladder and urethral diverticula. In: Wein AJ, Kavoussi LR, Novick AC, Partin AW, Peters CA, editors. Campbell-Walsh urology. Philadelphia: Saunders; 2007. p. 2361–90
  12. Psutka SP, Cendron M. Bladder diverticula in children. J Pediatr Urol 2013;9:129–38
  13. Hutch JA. Saccule formation at the ureterovesical junction in smooth walled bladders. J Urol 1961;86:390–9
  14. Alla S, Sullivan M, Resnick N. Update on detrusor hyperactivity with impaired contractility