Evans syndrome natural history, complications and prognosis: Difference between revisions

Jump to navigation Jump to search
No edit summary
Line 3: Line 3:


{{CMG}}
{{CMG}}
Please help WikiDoc by adding more content here.  It's easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.


==Overview==
==Overview==
Line 16: Line 18:
==References==
==References==
{{Reflist|2}}
{{Reflist|2}}
[[Category:Needs content]]

Revision as of 14:29, 21 September 2012

Evans syndrome Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Evans syndrome from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Laboratory Findings

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

Evans 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 Evans 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 Evans syndrome natural history, complications and prognosis

CDC on Evans syndrome natural history, complications and prognosis

Evans syndrome natural history, complications and prognosis in the news

Blogs on Evans syndrome natural history, complications and prognosis

Directions to Hospitals Treating Evans syndrome

Risk calculators and risk factors for Evans syndrome natural history, complications and prognosis

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

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

Overview

Prognosis

Given the fact that the signs and symptoms of this disease are related directly to the abnormal laboratory findings, the prognosis depends on the patient’s response to treatment. Spontaneous remissions of each of the individual component conditions have been reported. If the child responds well to the treatment and the levels of platelets and red blood cells increase, the child can expect to live a normal life. Medications will be needed life long, and laboratory tests will need to be constantly monitored to detect any abnormal changes so that treatment can be adjusted.

In more serious cases it can massively reduce life span and is seriously life threatening.

Evan's Syndrome is rare, serious, and has a reported mortality rate of just under 18%.

References