NORCET-7 Mains-2024
Child Health Nursing (Pediatrics)
Easy

Swenson and Duhamel procedure used to correction of?

Appeared in: NORCET-7 Mains-2024

Explanation

  • Hirschsprung's disease is a congenital condition characterized by the absence of ganglion nerve cells in a segment of the colon, leading to a functional obstruction.
  • The Swenson and Duhamel procedures are definitive surgical treatments for this condition.
  • Both are 'pull-through' techniques that involve removing the defective (aganglionic) bowel and connecting the healthy (ganglionated) bowel to the anus to restore normal function.
  • The Swenson procedure involves a direct end-to-end anastomosis, while the Duhamel procedure creates a side-to-side anastomosis behind the rectum.

Why Other Options Were Wrong

  • Option A: Diverticulitis is an acquired inflammatory condition, not a congenital defect of nerve cells. Its surgical management involves resecting the inflamed colon segment, often with a temporary or permanent colostomy (Hartmann's procedure), which is fundamentally different from a pull-through procedure.
  • Option B: Intussusception is a telescoping of the bowel. The primary treatment is non-surgical reduction using a therapeutic enema. Surgery is only indicated if this fails or if there is bowel perforation or necrosis.
  • Option D: Volvulus is the twisting of the bowel. It is a surgical emergency requiring immediate detorsion (untwisting). If caused by malrotation, a Ladd procedure is performed to prevent recurrence. This is different from the resection and pull-through technique of the Swenson/Duhamel procedures.

Related Visual

An illustration comparing the three main surgical procedures for Hirschsprungs disease: Swenson end-to-end anastomosis, Duhamel side-to-side retrorectal anastomosis, and So...
Clinical Relevance
  • Nursing practice connection: This is primarily an exam-oriented knowledge point with limited direct bedside application, so retain Surgical management of congenital gastrointestinal disorders as background academic context rather than a clinical decision trigger.
  • Nurses play a critical role in the pre- and post-operative care of infants with Hirschsprung's disease. Pre-operatively, this includes managing constipation with saline enemas (never tap water, to avoid water intoxication) and monitoring for signs of enterocolitis.
  • Post-operatively, care focuses on monitoring for complications like anastomotic leak or stricture, managing pain, providing meticulous perineal care to prevent skin breakdown, and educating parents on long-term bowel management and signs of complications.
  • What if? If a newborn fails to pass meconium within the first 24-48 hours and develops abdominal distention and bilious vomiting, the nurse should have a high index of suspicion for Hirschsprung's disease and escalate to the physician for further evaluation, such as a contrast enema or rectal biopsy.
How to Approach the Question
  • First, identify the keywords in the question stem: 'Swenson' and 'Duhamel procedure'. Recognize these as specific, named surgical techniques.
  • This is a factual recall question. The task is to match the named procedures to the correct medical condition.
  • Evaluate the options. All are gastrointestinal disorders.
  • Recall or deduce that Swenson and Duhamel are classic 'pull-through' procedures developed for a congenital defect of the colon.
  • Match this knowledge to the options. Hirschsprung's disease is the congenital aganglionic megacolon, which fits the description of the pathology corrected by these surgeries.
  • Eliminate the other options by recalling their standard treatments: Diverticulitis (medical/resection), Intussusception (enema reduction), and Volvulus (detorsion).
Concept Tested & Keywords
  • Concept Tested: Surgical management of congenital gastrointestinal disorders.
  • Stem keywords: Swenson, Duhamel procedure, correction
  • Lead-in keywords: used to correction of

Question ID

QIamDNbOqvxrAlFssfLnFL

Reference Book

E6 Nelson Textbook of Pediatrics(2024) — Volume 2 pp. 64-66, 65-67

E6 Medicine Harrison 22e Part 2 p. 486-488

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