Duodenal atresia: Difference between revisions
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*During weeks 6 and 7 of gestation, the GI tract becomes occluded then recanalizes during weeks 8 to 10 | *During weeks 6 and 7 of gestation, the GI tract becomes occluded then recanalizes during weeks 8 to 10 | ||
*Duodenal atresia is thought to result from failure of recanalization | *Duodenal atresia is thought to result from failure of recanalization | ||
*Often associated with other malformations such as biliary atresia or gallbladder agenesis | *Often associated with other malformations such as biliary atresia or gallbladder agenesis | ||
*May also be associated with cardiac, renal, or vertebral abnormalities | *May also be associated with cardiac, renal, or vertebral abnormalities | ||
*About a quarter of patients born with duodenal atresia have Downs syndrome | *About a quarter of patients born with duodenal atresia have Downs syndrome | ||
==Clinical Features== | |||
''Presentation is very early in the postnatal period'' | |||
===History=== | |||
* | *Abdominal distention and vomiting | ||
===Physical Exam=== | |||
*Dry mucus membranes, poor skin turgor, and sunken fontanelle | |||
* | *Signs of other congenital anomalies | ||
*The abdomen is often markedly distended with visible or palpable loops of bowel | |||
*Examine perineum and assess for patency of the anus | |||
==Differential Diagnosis== | ==Differential Diagnosis== | ||
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**NG tube to suction | **NG tube to suction | ||
**Correct fluid and electrolyte abnormalities | **Correct fluid and electrolyte abnormalities | ||
**Ampicillin and gentamicin (to prevent post-op infection) | **[[Ampicillin]] and [[gentamicin]] (to prevent post-op infection) | ||
**Surgery | **Surgery | ||
Revision as of 11:54, 7 February 2016
Background
- During weeks 6 and 7 of gestation, the GI tract becomes occluded then recanalizes during weeks 8 to 10
- Duodenal atresia is thought to result from failure of recanalization
- Often associated with other malformations such as biliary atresia or gallbladder agenesis
- May also be associated with cardiac, renal, or vertebral abnormalities
- About a quarter of patients born with duodenal atresia have Downs syndrome
Clinical Features
Presentation is very early in the postnatal period
History
- Abdominal distention and vomiting
Physical Exam
- Dry mucus membranes, poor skin turgor, and sunken fontanelle
- Signs of other congenital anomalies
- The abdomen is often markedly distended with visible or palpable loops of bowel
- Examine perineum and assess for patency of the anus
Differential Diagnosis
- Malrotation with volvulus
- Hirschsprung disease
- Meconium ileus
- Intestinal atresia
Nausea and vomiting (newborn)
| Newborn | ' |
| Obstructive intestinal anomalies |
|
| Neurologic |
|
| Renal |
|
| Infectious | |
| Metabolic/endocrine | |
| Miscellaneous |
|
Diagnosis
- Imaging
- AP, lateral, and cross table XR should be obtained on all infants with concern for obstruction
- Classic double bubble sign due to dilation of the stomach and proximal duodenum
- Absent distal gas
Management
- NPO
- NG tube to suction
- Correct fluid and electrolyte abnormalities
- Ampicillin and gentamicin (to prevent post-op infection)
- Surgery
Disposition
- Admission
