Duodenal atresia natural history, complications and prognosis: Difference between revisions
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===Prognosis=== | ===Prognosis=== | ||
*Prognosis is generally | *Prognosis is generally good, and the survival rate of patients with duodenal atresia is approximately 90%.<ref name="pmid15185215">{{cite journal| author=Escobar MA, Ladd AP, Grosfeld JL, West KW, Rescorla FJ, Scherer LR et al.| title=Duodenal atresia and stenosis: long-term follow-up over 30 years. | journal=J Pediatr Surg | year= 2004 | volume= 39 | issue= 6 | pages= 867-71; discussion 867-71 | pmid=15185215 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15185215 }} </ref> | ||
==References== | ==References== | ||
Revision as of 12:38, 27 December 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
If left untreated, [#]% of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].
OR
Common complications of [disease name] include [complication 1], [complication 2], and [complication 3].
OR
Prognosis is generally excellent/good/poor, and the 1/5/10-year mortality/survival rate of patients with [disease name] is approximately [#]%.
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
- 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%.[2]
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.
- ↑ 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.