The effect of rectourogenital fistula in high imperforate anus.

Saudi J Kidney Dis Transpl

Department of Pediatrics, King Hussein Medical Center, Amman, Jordan.

Published: June 2007

To determine the incidence of rectourogenital fistulae and the possible role of fistulae on the mechanism of defecation in patients with high imperforate anus, we retrospectively studied 42 children, 38 males and four females, all with high imperforate anus presenting in the period from 1982 to 1995. All children underwent radiological evaluation, to determine the level of the rectal pouch 18-24 hours after birth and to study the bony spine. A preliminary colostomy was performed in all patients after the diagnosis shortly after birth. Ultrasonography was performed in all the cases to assess the kidneys and ureters. All patients but one was operated on via a posterior sagittal anorectoplasty. Bowel control was assessed clinically regarding the presence of voluntary bowel movement, fecal soiling, incontinence and constipation. Eighteen (42.8%) patients were found to have recto-urogenital fistulae; 15 rectourethral, two rectovaginal and one rectovesical. Outcomes were known for 36 out of 42 patients; 15(41.6 %) had voluntary bowel movements, nine (25 %) had soiling, six (16.6%) had constipation and six (16.6 %) had incontinence. In conclusion, the presence of rectourogenital fistula in patients with high imperforate anus is another new prognostic factor for anorectal function which needs further clarification.

Download full-text PDF

Source

Publication Analysis

Top Keywords

high imperforate
16
imperforate anus
16
rectourogenital fistula
8
patients high
8
voluntary bowel
8
patients
6
high
4
fistula high
4
imperforate
4
anus
4

Similar Publications

Objective: While the association of a syrinx with a tethered spinal cord in the context of VACTERL (vertebral defects [V], imperforate anus or anal atresia [A], cardiac malformations [C], tracheoesophageal defects [T] with or without esophageal atresia [E], renal anomalies [R], and limb defects [L]) association is known, the incidence of idiopathic syrinxes among these patients has not previously been reported. The authors aimed to characterize the incidence of syrinxes and the pattern of congenital anomalies in pediatric patients with VACTERL association, with a specific focus on the presence of idiopathic syrinxes in this population.

Methods: An institutional database was retrospectively queried for all pediatric patients with VACTERL association.

View Article and Find Full Text PDF
Article Synopsis
  • - VACTERL association is a rare congenital disorder characterized by a combination of birth defects, including vertebral, anorectal, cardiac, tracheoesophageal, renal, and limb anomalies, requiring a clinical diagnosis of at least three of these defects.
  • - A case study highlights the anesthetic management of a newborn with VACTERL undergoing surgical repair of a tracheoesophageal fistula (TEF) and a colostomy, demonstrating the use of regional anesthesia to maintain spontaneous ventilation and minimize risks.
  • - The surgical procedure involved ketamine and dexmedetomidine for sedation, an ultrasound-guided caudal block for effective pain management, and dopamine for hemodynamic support, allowing the newborn to recover and progress
View Article and Find Full Text PDF
Article Synopsis
  • This research assessed the effectiveness of new ultrasound features in detecting fetal anal atresia and investigated its perinatal incidence across a large sample of 94,701 pregnancies.
  • The study used routine neonatal examinations as the gold standard for diagnosis and calculated the annual incidence of anal atresia, revealing rates between 0.57‰ and 1.29‰ from 2019 to 2023.
  • Results indicated that the new ultrasound approach outperformed traditional methods in key diagnostic metrics, confirming its high validity and clinical value for fetal anal atresia detection.
View Article and Find Full Text PDF

Global Strategies for Postoperative Care and Bowel Management in Patients With Anorectal Malformations: Varied Practices and Barriers.

J Pediatr Surg

December 2024

Comprehensive Colorectal Center, Section of Colorectal and Pelvic Reconstructive Surgery, Department of Pediatric Surgery, Children's Mercy Kansas City, Kansas City, MO, 64108, USA; Department of Surgery, University of Missouri-Kansas City, Kansas City, MO 64108, USA. Electronic address:

Background: Anorectal malformations (ARMs) commonly result in constipation and fecal incontinence following primary surgical reconstruction. This study investigates global variations in postoperative care and resources.

Methods: A survey was distributed via the International Pediatric Endosurgery Group (IPEG) and snowball sampling.

View Article and Find Full Text PDF
Article Synopsis
  • - Hydrocolpos is a rare condition where the vagina becomes cystically dilated, often due to issues like an imperforate hymen or vaginal atresia, and can also relate to genetic disorders like Bardet-Biedl syndrome (BBS).
  • - A specific case involving neonatal hydrocolpos linked to BBS was studied, revealing a novel mutation in the BBS10 gene, highlighting the need for genetic testing in similar cases.
  • - It’s crucial for pediatric urologists to consider genetic conditions like BBS in neonates with hydrocolpos, as these can lead to serious complications like kidney issues and obesity.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!