Ogilvie syndrome

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Acute colonic pseudo-obstruction


Ogilvie syndrome
CT scan of the abdomen showing colonic distension
Synonyms Acute colonic pseudo-obstruction
Pronounce
Field Gastroenterology, Surgery
Symptoms Abdominal distension, pain, nausea, vomiting, constipation, absent bowel movements
Complications Bowel ischemia, colonic perforation, sepsis
Onset Sudden
Duration Variable; can be acute or prolonged
Types
Causes Dysregulation of autonomic nervous system, often triggered by trauma, surgery, infection, or medications
Risks Hospitalization, trauma, major surgery, electrolyte imbalances, use of opioids or anticholinergic medications
Diagnosis Abdominal X-ray, CT scan, exclusion of mechanical obstruction
Differential diagnosis Mechanical bowel obstruction, Toxic megacolon, Volvulus
Prevention Minimize use of causative medications, early mobilization post-surgery
Treatment Bowel rest, decompression with rectal tube or colonoscopy, neostigmine in refractory cases
Medication Neostigmine (cholinesterase inhibitor)
Prognosis Generally good with timely management; risk of complications if delayed
Frequency Rare
Deaths Associated with delayed diagnosis and complications such as perforation


Ogilvie syndrome, also known as acute colonic pseudo-obstruction, is a condition characterized by the acute dilation of the colon in the absence of any mechanical obstruction. It is named after Sir William Heneage Ogilvie, who first described the syndrome in 1948.

Pathophysiology[edit | edit source]

Ogilvie syndrome is thought to result from an imbalance in the autonomic nervous system, which leads to a dysfunction in the colonic motility. The exact mechanism is not fully understood, but it is believed that there is an excessive sympathetic nervous system activity or a lack of parasympathetic activity, leading to colonic atony and dilation.

Causes[edit | edit source]

Ogilvie syndrome can occur in a variety of clinical settings. It is often associated with:

Symptoms[edit | edit source]

The symptoms of Ogilvie syndrome are similar to those of a mechanical bowel obstruction and may include:

  • Abdominal distension
  • Abdominal pain
  • Nausea and vomiting
  • Constipation or inability to pass gas

Diagnosis[edit | edit source]

The diagnosis of Ogilvie syndrome is primarily clinical, supported by imaging studies. A plain abdominal X-ray or CT scan can show colonic dilation without evidence of mechanical obstruction. It is important to rule out true mechanical obstruction, which may require surgical intervention.

Treatment[edit | edit source]

The management of Ogilvie syndrome involves both conservative and pharmacological approaches:

Conservative Management[edit | edit source]

  • Bowel rest and nasogastric decompression
  • Correction of any underlying electrolyte imbalances
  • Discontinuation of medications that may contribute to colonic atony

Pharmacological Treatment[edit | edit source]

  • Administration of neostigmine, a cholinesterase inhibitor, can stimulate colonic motility and is often effective in resolving the condition.

Surgical Intervention[edit | edit source]

In cases where conservative and pharmacological treatments fail, or if there is evidence of colonic ischemia or perforation, surgical intervention may be necessary. This can include colonoscopy for decompression or, in severe cases, surgical resection of the affected bowel segment.

Prognosis[edit | edit source]

The prognosis of Ogilvie syndrome is generally good with appropriate treatment. However, if left untreated, it can lead to serious complications such as colonic perforation, peritonitis, and sepsis.

Related pages[edit | edit source]

External links[edit | edit source]



Classification
External resources



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