Duodenal atresia natural history, complications and prognosis: Difference between revisions
Hamid Qazi (talk | contribs) No edit summary |
Hamid Qazi (talk | contribs) |
||
Line 16: | Line 16: | ||
===Complications=== | ===Complications=== | ||
The complications of duodenal atresia are as follows:<ref name="pmid2273425">{{cite journal| author=Spigland N, Yazbeck S| title=Complications associated with surgical treatment of congenital intrinsic duodenal obstruction. | journal=J Pediatr Surg | year= 1990 | volume= 25 | issue= 11 | pages= 1127-30 | pmid=2273425 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2273425 }} </ref><ref name="pmid3357136">{{cite journal| author=Kokkonen ML, Kalima T, Jääskeläinen J, Louhimo I| title=Duodenal atresia: late follow-up. | journal=J Pediatr Surg | year= 1988 | volume= 23 | issue= 3 | pages= 216-20 | pmid=3357136 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3357136 }} </ref> | |||
*There are no complications associated with duodenal atresia, however post surgical complications may occur. | *There are no complications associated with duodenal atresia, however post surgical complications may occur. | ||
*Post surgical complications include: | |||
**Adhesions | |||
**Duodenal dysmotility | |||
**Megaduodenum with blind loop syndrome | |||
**Duodenogastric reflux and gastritis | |||
**Peptic ulcer disease | |||
**Gastroesophageal reflux | |||
**Cholelithiasis | |||
**Cholecystitis | |||
===Prognosis=== | ===Prognosis=== |
Revision as of 16:34, 2 January 2018
Duodenal Atresia Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Duodenal atresia natural history, complications and prognosis On the Web |
American Roentgen Ray Society Images of Duodenal atresia natural history, complications and prognosis |
FDA on Duodenal atresia natural history, complications and prognosis |
CDC on Duodenal atresia natural history, complications and prognosis |
Duodenal atresia natural history, complications and prognosis in the news |
Blogs on Duodenal atresia natural history, complications and prognosis |
Risk calculators and risk factors for Duodenal atresia natural history, complications and prognosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [2]
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
- The symptoms of duodenal atresia usually develop in the first 48 hours of life, and start with symptoms such as vomiting.[1]
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.
- Post surgical complications include:
- Adhesions
- Duodenal dysmotility
- Megaduodenum with blind loop syndrome
- Duodenogastric reflux and gastritis
- Peptic ulcer disease
- Gastroesophageal reflux
- Cholelithiasis
- Cholecystitis
Prognosis
- Prognosis is generally good, and the survival rate of patients with duodenal atresia is approximately 90%.[4]
References
- ↑ 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. ISSN 0378-3782.
- ↑ Spigland N, Yazbeck S (1990). "Complications associated with surgical treatment of congenital intrinsic duodenal obstruction". J Pediatr Surg. 25 (11): 1127–30. PMID 2273425.
- ↑ Kokkonen ML, Kalima T, Jääskeläinen J, Louhimo I (1988). "Duodenal atresia: late follow-up". J Pediatr Surg. 23 (3): 216–20. PMID 3357136.
- ↑ 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. PMID 15185215.