Initial Management of Superior Mesenteric Artery (SMA) Syndrome
The initial management for a patient diagnosed with Superior Mesenteric Artery (SMA) syndrome should be conservative treatment, including postural changes, gastroduodenal decompression, and nutritional support, which has a 70-80% success rate. 1
Pathophysiology and Clinical Presentation
SMA syndrome (also known as Wilkie's syndrome, cast syndrome, or aorto-mesenteric compass syndrome) is characterized by:
- Compression of the third part of the duodenum between the SMA and the aorta
- Reduced aorto-mesenteric angle (<20° compared to normal 38-65°)
- Loss of retroperitoneal fat padding between these vessels
Common presenting symptoms include:
- Postprandial abdominal pain
- Nausea and vomiting (often bilious)
- Early satiety
- Anorexia
- Weight loss
Diagnostic Confirmation
Before initiating treatment, confirm diagnosis with:
- CT angiography (gold standard) - to measure the aorto-mesenteric angle and distance
- Upper GI series with barium/gastrografin - showing duodenal dilation and abrupt cutoff
- Endoscopy - to rule out other causes of obstruction
Initial Conservative Management Algorithm
Positional Therapy
- Left lateral decubitus position or prone positioning after meals
- Knee-chest position to reduce duodenal compression
Gastroduodenal Decompression
- Nasogastric tube placement for symptomatic relief
- Decompression to prevent vomiting and aspiration
Nutritional Support
- Small, frequent meals if tolerated
- Hyperalimentation through:
- Nasojejunal feeding tube (placed beyond obstruction)
- Parenteral nutrition if enteral feeding not tolerated
Fluid and Electrolyte Management
- Correction of dehydration
- Monitoring and replacement of electrolytes
Weight Gain Promotion
- Nutritional consultation
- High-calorie supplements
- Goal: Restore retroperitoneal fat pad
Monitoring Response
- Daily weight measurements
- Symptom assessment
- Tolerance to oral intake
- Radiological reassessment if symptoms persist
When to Consider Surgical Intervention
If conservative management fails after 4-6 weeks, or in cases of:
- Severe malnutrition
- Refractory symptoms
- Duodenal compromise
- Gastric pneumatosis or portal venous gas
Surgical options include:
- Laparoscopic duodenojejunostomy (preferred, 80-100% success rate) 1, 2
- Laparoscopic dissection of the ligament of Treitz 3
- Strong-type duodenojejunostomy
Common Pitfalls to Avoid
- Misdiagnosis: SMA syndrome shares symptoms with many other conditions including anorexia nervosa and functional dyspepsia 1
- Delayed diagnosis: Can lead to aspiration pneumonia or respiratory depression via metabolic alkalosis 1
- Premature surgery: Conservative management should be given adequate trial before proceeding to surgery
- Inadequate nutritional support: Insufficient caloric intake will perpetuate the syndrome
- Failure to address underlying causes: Any predisposing factors (rapid weight loss, prolonged bed rest, body casting) should be identified and addressed
Special Considerations
- Multidisciplinary approach involving gastroenterology, nutrition, and surgery
- Psychological support may be needed, especially in cases associated with eating disorders
- Long-term follow-up to prevent recurrence through maintenance of adequate weight
By following this systematic approach to management, most patients with SMA syndrome can achieve symptomatic relief and avoid surgical intervention.