Intestinal obstruction after lung transplantation in children with cystic fibrosis

R. K. Minkes, J. C. Langer, M. A. Skinner, R. P. Foglia, A. O'Hagan, A. H. Cohen, G. B. Mallory, C. B. Huddleston, E. N. Mendeloff

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31 Scopus citations

Abstract

Background/Purpose: Distal intestinal obstruction syndrome (DIOS) occurs in 15% of patients with cystic fibrosis (CF). The authors reviewed their experience to determine the incidence, risk factors, and natural history of adhesive intestinal obstruction and DIOS after lung transplantation. Methods: Eighty-three bilateral transplants were performed in 70 CF patients between January 1990 and September 1998. All were on pancreatic enzymes preoperatively, and none had preoperative bowel preparation. Fifty-six patients (80%) had prior gastrostomy (n = 54) or jejunostomy (n = 2). Eighteen patients (25.7%) had a previous laparotomy for meconium ileus (n = 8), fundoplication (n = 4), liver transplant (n = 1), jejunal atresia (n = 1), Janeway gastrostomy takedown (n = 1), pyloromyotomy (n = 1), free air (n = 1), or appendectomy (n = 1). Results: After lung transplantation, 7 patients (10%) required laparotomy for bowel obstruction (6 during the same hospitalization, and 1 during a subsequent hospitalization). The causes of obstruction were adhesions only (n = 1), DIOS only (n = 2), and a combination of DIOS and adhesions (n = 4). Adhesiolysis was performed in the 5 patients with adhesions, and a small bowel resection was also performed in 1 patient. DIOS was treated by milking secretions distally without an enterotomy (n = 3) with an enterotomy and primary closure (n = 1) or with an end ileostomy and mucus fistula (n = 2). Five had recurrent DIOS early postoperatively. One resolved with intestinal lavage, 2 were treated successfully with hypaque disimpaction, and 2 underwent reoperation; 1 required an ileostomy. The most important risk factor for posttransplant obstruction was a previous major abdominal operation. Obstruction occurred in 7 of 18 (39%) who had undergone a prior laparotomy versus 0 of 52 who had not (P < .001, X2). Conclusions: (1) The incidence of intestinal obstruction is high after lung transplantation in children with CF. (2) Previous laparotomy is a significant risk factor. (3) Recurrent obstruction after surgery for this condition is common. (4) Preventive measures such as pretransplant bowel preparation and early postoperative bowel lavage may be beneficial in these patients.

Original languageEnglish (US)
Pages (from-to)1489-1493
Number of pages5
JournalJournal of Pediatric Surgery
Volume34
Issue number10
DOIs
StatePublished - Oct 1999

Keywords

  • Cystic fibrosis
  • Distal intestinal obstruction syndrome
  • Intestinal lavage
  • Lung transplantation

ASJC Scopus subject areas

  • Surgery
  • Pediatrics, Perinatology, and Child Health

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    Minkes, R. K., Langer, J. C., Skinner, M. A., Foglia, R. P., O'Hagan, A., Cohen, A. H., Mallory, G. B., Huddleston, C. B., & Mendeloff, E. N. (1999). Intestinal obstruction after lung transplantation in children with cystic fibrosis. Journal of Pediatric Surgery, 34(10), 1489-1493. https://doi.org/10.1016/S0022-3468(99)90110-0