eMedicine Specialties > Pediatrics: Surgery > General Surgery
Duodenal Atresia and Stenosis: Surgical Perspective: Follow-up
Updated: Oct 1, 2008
Outcome and Prognosis
Current survival rates for infants with duodenal atresia or stenosis are 90-95%. Higher mortality rates are associated with prematurity and multiple congenital abnormalities.
Postoperative complications are reported in 14-18% of patients; some require reoperation.2 Possible indications for reoperation include anastomotic leak, functional duodenal obstruction, adhesions, and missed atresias.
Long-term follow-up of these patients reveals that most of these patients are asymptomatic with a normal nutritional status. In a 1988 study, Kokkonen et al found a poor correlation between symptoms and radiologic and endoscopic findings; the megaduodenum failed to return to normal caliber, and duodenogastric reflux and duodenal dysmotility persisted decades after the initial surgery in asymptomatic patients.21 Approximately 12% of patients develop late complications. Late deaths occur in approximately 6% of patients, and 50% of these are related to complex cardiac conditions. Less than 10% of patients require fundoplication for gastroesophageal reflux, and less than 10% require revision of the initial repair.23
Dysmotility disorders associated with megaduodenum can be managed with an antimesenteric tapering duodenoplasty or duodenal plication.
Future and Controversies
Duodenal webs can be diagnosed and excised by an expert surgical endoscopist. This is feasible in patients who present after the neonatal period with duodenal stenosis. The morbidity and complications associated with a megaduodenum may require further surgical intervention.
Transanastomotic feeding tubes or gastrostomies were used in the past but have been demonstrated to offer no clear advantage and, instead, result in a delay in establishing oral feedings and an increase in the duration of hospitalization.24,3,25
More on Duodenal Atresia and Stenosis: Surgical Perspective |
| Overview: Duodenal Atresia and Stenosis: Surgical Perspective |
| Workup: Duodenal Atresia and Stenosis: Surgical Perspective |
| Treatment: Duodenal Atresia and Stenosis: Surgical Perspective |
Follow-up: Duodenal Atresia and Stenosis: Surgical Perspective |
| Multimedia: Duodenal Atresia and Stenosis: Surgical Perspective |
| References |
| « Previous Page | Next Page » |
References
Fonkalsrud EW, DeLorimier AA, Hays DM. Congenital atresia and stenosis of the duodenum. A review compiled from the members of the Surgical Section of the American Academy of Pediatrics. Pediatrics. Jan 1969;43(1):79-83. [Medline].
Bailey PV, Tracy TF Jr, Connors RH, et al. Congenital duodenal obstruction: a 32-year review. J Pediatr Surg. Jan 1993;28(1):92-5. [Medline].
Mooney D, Lewis JE, Connors RH, Weber TR. Newborn duodenal atresia: an improving outlook. Am J Surg. Apr 1987;153(4):347-9. [Medline].
Kimura K, Mukohara N, Nishijima E, et al. Diamond-shaped anastomosis for duodenal atresia: an experience with 44 patients over 15 years. J Pediatr Surg. Sep 1990;25(9):977-9. [Medline].
Mishalany HG, Der Kaloustian VM, Ghandour MH. Familial congenital duodenal atresia. Pediatrics. Mar 1971;47(3):633-4. [Medline].
Boyden EA, Cope JG, Bill AH Jr. Anatomy and embryology of congenital intrinsic obstruction of the duodenum. Am J Surg. Aug 1967;114(2):190-202. [Medline].
Grosfeld JL, Rescorla FJ. Duodenal atresia and stenosis: reassessment of treatment and outcome based on antenatal diagnosis, pathologic variance, and long-term follow-up. World J Surg. May-Jun 1993;17(3):301-9. [Medline].
Harberg FJ, Pokorny WJ, Hahn H. Congenital duodenal obstruction. A review of 65 cases. Am J Surg. Dec 1979;138(6):825-8. [Medline].
Kimble RM, Harding J, Kolbe A. Additional congenital anomalies in babies with gut atresia or stenosis: when to investigate, and which investigation. Pediatr Surg Int. 1997;12(8):565-70. [Medline].
Spitz L, Ali M, Brereton RJ. Combined esophageal and duodenal atresia: experience of 18 patients. J Pediatr Surg. Feb 1981;16(1):4-7. [Medline].
Hancock BJ, Wiseman NE. Congenital duodenal obstruction: the impact of an antenatal diagnosis. J Pediatr Surg. Oct 1989;24(10):1027-31. [Medline].
Feingold M, Hall BP, Lacassie Y, Martinez-Frias ML. Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay. American Journal of medical genetics. 1997;69(3):[Medline].
Phelps S, Fisher R, Partington A, et al. Prenatal ultrasound diagnosis of gastrointestinal malformations. J Pediatr Surg. Mar 1997;32(3):438-40. [Medline].
al-Salem AH, Khwaja S, Grant C, Dawodu A. Congenital intrinsic duodenal obstruction: problems in the diagnosis and management. J Pediatr Surg. Dec 1989;24(12):1247-9. [Medline].
Reid IS. Biliary tract abnormalities associated with duodenal atresia. Arch Dis Child. Dec 1973;48(12):952-7. [Medline].
Britton JR, Britton HL. Gastric aspirate volume at birth as an indicator of congenital intestinal obstruction. Acta Paediatr. Aug 1995;84(8):945-6. [Medline].
Stringer MD, Brereton RJ, Drake DP, Wright VM. Double duodenal atresia/stenosis: a report of four cases. J Pediatr Surg. May 1992;27(5):576-80. [Medline].
Keckler SJ, St Peter SD, Spilde TL, Ostlie DJ, Snyder CL. The influence of trisomy 21 on the incidence and severity of congenital heart defects in patients with duodenal atresia. Pediatr Surg Int. Aug 2008;24(8):921-3. [Medline].
Tashjian DB, Moriarty KP. Duodenal atresia with anomalous bile duct masquerading as midgut volvulus. Journal of Pediatric Surgery. 2001;36(6):956-957. [Medline].
Ein SH, Kim PC, Miller HA. The late nonfunctioning duodenal atresia repair--a second look. J Pediatr Surg. May 2000;35(5):690-1. [Medline].
Kokkonen ML, Kalima T, Jaaskelainen J, Louhimo I. Duodenal atresia: late follow-up. J Pediatr Surg. Mar 1988;23(3):216-20. [Medline].
Spigland N, Yazbeck S. Complications associated with surgical treatment of congenital intrinsic duodenal obstruction. J Pediatr Surg. Nov 1990;25(11):1127-30. [Medline].
Escobar MA, Ladd AP, Grosfeld JL, et al. Duodenal atresia and stenosis: long-term follow-up over 30 years. J Pediatr Surg. Jun 2004;39(6):867-71; discussion 867-71. [Medline].
Berger D, Roulet M. Early postoperative enteral feeding through a needle catheter jejunostomy. Z Kinderchir. Oct 1984;39(5):328-31. [Medline].
Upadhyay V, Sakalkale R, Parashar K, et al. Duodenal atresia: a comparision of three modes of treatment. European Journal of Pediatric Surgery. 1996;6(2):75-77. [Medline].
Cordes L. Congenital occlusions of the duodenum. Arch Pediatr. 1901;18:401-424.
Cragan JD, Martin ML, Moore CA, Khoury M. Descriptive epidemiology of small intestinal atresia, Atlanta, Georgia. Teratology. Nov 1993;48(5):441-50. [Medline].
Takahashi A, Tomomasa T, Suzuki N, et al. The relationship between disturbed transit and dilated bowel, and manometric findings of dilated bowel in patients with duodenal atresia and stenosis. J Pediatr Surg. Aug 1997;32(8):1157-60. [Medline].
Further Reading
Keywords
duodenal atresia, stenosis, congenital duodenal obstruction, gastrojejunostomy, duodenojejunostomy, duodenoduodenostomy, duodenoplasty, intrinsic duodenal obstruction, high intestinal obstruction, upper intestinal obstruction, sustained vomiting, bilious vomiting, nonbilious vomiting, loss of fluid, loss of electrolytes, hyperalimentation, Down syndrome, esophageal atresia, malrotation, anterior portal vein, second distal web, anorectal anomalies, intestinal atresias, cloacal anomalies, renal tract anomalies, polyhydramnios, choledochal cyst, failure to thrive
Follow-up: Duodenal Atresia and Stenosis: Surgical Perspective