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Duodenal atresia natural history, complications and prognosis

Introduction

Overview

Overview

The symptoms of duodenal atresia usually develop in the first 48 hours of life, and start with symptoms such as bilious vomiting in 80% of the cases. Prognosis is generally very good, and the survival rate of patients with duodenal atresia is approximately 90%.

Natural History, Complications, and Prognosis

Natural History, Complications, and Prognosis

Natural History

  • The symptoms of duodenal atresia usually develop in the first 48 hours of life, and start with symptoms such as vomiting.[1]
  • If duodenal atresia is left untreated it will result in death.

Complications

The complications of duodenal atresia are as follows:[2][3]

  • There are no complications associated with duodenal atresia, however post surgical complications may occur.

Prognosis

  • Prognosis is generally good, and the survival rate of patients with duodenal atresia is approximately 90% after surgery.[4]
References

References

  1. ↑ Adams, Stephen D.; Stanton, Michael P. (2014). “Malrotation and intestinal atresias”. Early Human Development. 90 (12): 921–925. doi:10.1016/j.earlhumdev.2014.09.017. ISSNΒ 0378-3782.
  2. ↑ Spigland N, Yazbeck S (1990). “Complications associated with surgical treatment of congenital intrinsic duodenal obstruction”. J Pediatr Surg. 25 (11): 1127–30. PMIDΒ 2273425.
  3. ↑ Kokkonen ML, Kalima T, JÀÀskelΓ€inen J, Louhimo I (1988). “Duodenal atresia: late follow-up”. J Pediatr Surg. 23 (3): 216–20. PMIDΒ 3357136.
  4. ↑ Escobar MA, Ladd AP, Grosfeld JL, West KW, Rescorla FJ, Scherer LR; et al. (2004). “Duodenal atresia and stenosis: long-term follow-up over 30 years”. J Pediatr Surg. 39 (6): 867–71, discussion 867-71. PMIDΒ 15185215.

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [2]