Duodenal atresia laboratory findings: Difference between revisions
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Revision as of 20:51, 28 December 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [2]
Overview
Laboratory findings consistent with the diagnosis of duodenal atresia include polyhydramnios on prenatal ultrasound, hypokalemia, and hyperchloremia.
Laboratory Findings
The lab findings are as follows:[1][2][3]
- Laboratory findings consistent with the diagnosis of duodenal atresia include:
- Polyhydramnios on prenatal ultrasound
- Complete blood count and differential
- Total, and direct bilirubin
- Serum electrolyte concentrations
- Hypokalemia
- Hyperchloremia
- Blood urea nitrogen (BUN), and creatinine
- Blood culture for sepsis
- Blood type and antibody screen
- Coagulation studies
References
- ↑ Morris, Grant; Kennedy, Alfred; Cochran, William (2016). "Small Bowel Congenital Anomalies: a Review and Update". Current Gastroenterology Reports. 18 (4). doi:10.1007/s11894-016-0490-4. ISSN 1522-8037.
- ↑ 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.
- ↑ {{Lloyd DA, Kenny SE. anomalies including hernias. In: Kleinman R, Sanderson I, Goulet O, Sherman P, Mieli-Vergani G, Shneider B, editors. Walker’s pediatric gastrointestinal disease. 5th ed. Hamilton, Ontario: B.C. Decker Inc; 2008. http://www.r2library.com/Resource/detail/1550093649/ch0013s0509}}