Budd-Chiari syndrome natural history, complications and prognosis

Revision as of 15:24, 6 November 2017 by Mazia Fatima (talk | contribs)
Jump to navigation Jump to search

Budd-Chiari syndrome Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Budd-Chiari syndrome from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X Ray

CT

MRI

Echocardiography or 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

Budd-Chiari syndrome natural history, complications and prognosis On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Budd-Chiari syndrome natural history, complications and prognosis

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Budd-Chiari syndrome natural history, complications and prognosis

CDC on Budd-Chiari syndrome natural history, complications and prognosis

Budd-Chiari syndrome natural history, complications and prognosis in the news

Blogs on Budd-Chiari syndrome natural history, complications and prognosis

Directions to Hospitals Treating Type page name here

Risk calculators and risk factors for Budd-Chiari syndrome natural history, complications and prognosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

Please help WikiDoc by adding content here. It's easy! Click here to learn about editing.

Overview

If left untreated, patients with Budd-Chiari syndrome have a high mortality rate.About 90% die within 3 years as the disease may progresss to develop intractable ascites with emaciation, gastrointestinal bleeding, and liver failure.Prognosis is generally good with treatment, and the 5 year survival rate of patients with treatment of Budd-Chiari syndrome is approximately 74 %.Poor prognostic factors include older age at diagnosis, chronic disease, severe liver failure and associated refractory ascites.

Natural History

  • The symptoms of Budd-Chiari syndrome usually develop in the third or fourth decade of life and start with symptoms such as hepatomegaly, ascites, and abdominal pain.
  • Without treatment, the patient will develop complications like hepatic encephalopathy, variceal hemorrhage, hepatorenal syndrome, portal hypertension, Complications secondary to hepatic decompensation, which will/ may eventually lead to intractable ascites with emaciation, gastrointestinal bleeding, and liver failure.

Complications

  • Complications that can develop as a result of Budd-Chiari syndrome are:
    • Portal Hypertension
    • Hepatic encephalopathy
    • Variceal hemorrhage
    • Hepatorenal syndrome
    • Hepatic decompensation
    • Bacterial peritonitis especially following paracentesis

Prognosis

  • The prognosis of Budd-Chiari syndrome is good with treatment.
  • Without treatment, Budd-Chiari syndrome will result in death as a result of progressive liver failure within 3 years from diagnosis.
  • Budd-Chiari syndrome is associated with a 10-year survival rate of 55% with treatment.Among patient with liver transplantation, the 5-year survival rate is 70%.
  • good prognostic factors include:
    • Younger age at diagnosis
    • Low Child-Pugh score
    • Absence of ascites or easily controlled ascites
    • Low serum creatinine level

Poor prognostic factors include:

    • older age at diagnosis
    • chronic disease
    • severe liver failure
    • refractory ascites.


References

Template:WS Template:WH