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Intestinal obstruction after lung transplantation in children with cystic fibrosis

R K Minkes1, J C Langer, M A Skinner

  • 1Department of Surgery, Washington University School of Medicine, St Louis, Missouri, USA.

Insights

Intestinal obstruction is common after lung transplantation in cystic fibrosis patients, with prior abdominal surgery being a key risk factor. Preventive measures like bowel preparation may reduce obstruction rates.

Area of Science:

  • Gastroenterology
  • Pulmonary Medicine
  • Transplant Surgery

Background:

  • Distal intestinal obstruction syndrome (DIOS) affects 15% of cystic fibrosis (CF) patients.
  • Lung transplantation in CF patients carries a risk of intestinal obstruction.
  • This study investigates adhesive intestinal obstruction and DIOS post-lung transplant.

Observation:

  • 70 CF patients underwent 83 bilateral lung transplants.
  • 80% had prior gastrostomy or jejunostomy.
  • 25.7% had a history of laparotomy for various conditions, including meconium ileus.

Findings:

  • 10% of patients experienced bowel obstruction post-transplant.
  • Previous major abdominal surgery significantly increased obstruction risk (39% vs. 0%).
  • Adhesions and DIOS were the primary causes, with a high rate of recurrence.

Implications:

  • Intestinal obstruction is a significant complication following lung transplantation in CF.
  • History of laparotomy is a critical risk factor for post-transplant obstruction.
  • Pretransplant bowel preparation and early postoperative lavage may mitigate obstruction risk.
Abstract

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