Ogilvie syndrome overview: Difference between revisions

Jump to navigation Jump to search
Line 20: Line 20:


==Epidemiology and Demographics==
==Epidemiology and Demographics==
The incidence of Ogilvie's syndrome is 100 per 100,000 individuals. Ogilvie's syndrome commonly affects patients more than 60years and it is more prevelant int he men more than women.


==Risk Factors==
==Risk Factors==
Common risk factors of Ogilvie's syndrome include having neurologic disorders, taking narcotic medications, and trauma. Other risk factors include systemic lupus erythematosus, alcoholism, and multiple myeloma.


==Screening==
==Screening==
There is insufficient evidence to recommend routine screening for Ogilvie's syndrome.


==Natural History, Complications, and Prognosis==
==Natural History, Complications, and Prognosis==

Revision as of 15:17, 7 February 2018

Ogilvie syndrome Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Ogilvie syndrome from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Laboratory Findings

X Ray

CT

MRI

Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Ogilvie syndrome overview On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Ogilvie syndrome overview

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Ogilvie syndrome overview

CDC on Ogilvie syndrome overview

Ogilvie syndrome overview in the news

Blogs on Ogilvie syndrome overview

Directions to Hospitals Treating Ogilvie syndrome

Risk calculators and risk factors for Ogilvie syndrome overview

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Historical Perspective

Acute intestinal pseudo-obstruction was first reported by Dr. William Heneage Ogilvie in 1948 and the syndrome was named on him after that.

Classification

Ogilvie's syndrome can be classified based on the duration of the disease into acute or chronic.

Pathophysiology

The colonic pseudo-obstruction pathogenesis is believed to be due to impairment of the autonomic nervous system. The autonomic imapairment may involve the parasympathetic fibers of S2-S4 which is responsible for innervation of the distal colon and may lead to atonic colon and proximal obstruction. In few cases, Ogilvie's syndrome (colonic pseudo-obstruction) may show atrophic myopathy with thinned colonic wall and intact myenteric plexus

Causes

Common causes of Ogilvie's syndrome include trauma, gynecological surgeries, major surgeries as hip replacement, and myocardial infarction. Other causes include causes of non mechanical bowel obstruction as acid base imbalance, acute pancreatitis, apoplexy, and cancers.

Differentiating Hereditary pancreatitis from Other Diseases

The colonic pseudo-obstruction pathogenesis is believed to be due to impairment of the autonomic nervous system. The autonomic imapairment may involve the parasympathetic fibers of S2-S4 which is responsible for innervation of the distal colon and may lead to atonic colon and proximal obstruction. In few cases, Ogilvie's syndrome (colonic pseudo-obstruction) may show atrophic myopathy with thinned colonic wall and intact myenteric plexus

Epidemiology and Demographics

The incidence of Ogilvie's syndrome is 100 per 100,000 individuals. Ogilvie's syndrome commonly affects patients more than 60years and it is more prevelant int he men more than women.

Risk Factors

Common risk factors of Ogilvie's syndrome include having neurologic disorders, taking narcotic medications, and trauma. Other risk factors include systemic lupus erythematosus, alcoholism, and multiple myeloma.

Screening

There is insufficient evidence to recommend routine screening for Ogilvie's syndrome.

Natural History, Complications, and Prognosis

Diagnosis

Diagnostic Criteria

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

Ultrasound

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

References


Template:WikiDoc Sources