Eisenmenger’s syndrome overview: Difference between revisions

Jump to navigation Jump to search
Line 14: Line 14:


== Causes ==
== Causes ==
[[Eisenmenger's syndrome]] is causes by cardiac defects that shunt blood heading to the systemic circulation back into the pulmonary circulation. These defects include [[ventricular septal defect]], [[atrial septal defect]], [[Atrioventricular canal defect (patient information)|atrioventricular canal defect]], [[patent ductus arteriosus]], and [[truncus arteriosus]].


== Differentiating Xyz from Other Diseases ==
== Differentiating Eisenmenger's syndrome from Other Diseases ==


== Epidemiology and Demographics ==
== Epidemiology and Demographics ==
The [[incidence]] and [[prevalence]] of [[Eisenmenger's syndrome]] has been decreasing gradually over the years. In the general population, the prevalence decreased from 24.6 to 11.9/million inhabitants in 2012. About 8% of patents with [[Congenital heart disease|congenital heart diseases]] develop Eisenmenger's syndrome. The [[mortality rate]] of Eisenmenger's syndrome is about 27%. The risk of [[Eisenmenger's syndrome]] increases in patients with large cardiac defects or who live in developing countries due to poor healthcare access.


== Risk Factors ==
== Risk Factors ==
The common risk factors for [[Eisenmenger's syndrome]] include genetic [[Mutation|mutations]], exposure to [[rubella]] virus, and drug and [[alcohol]] abuse during pregnancy. Less common risk factors include poor healthcare access and patients in developing countries.


== Screening ==
== Screening ==
Line 34: Line 37:


=== Laboratory Findings ===
=== Laboratory Findings ===
The laboratory findings of patients with Eisenmenger's syndrome include [[erythrocytosis]], [[Iron deficiency anemia|iron deficiency]], increased [[bleeding time]], increased blood [[uric acid]] and [[conjugated bilirubin]] concentrations, as well as mixed [[Respiratory acidosis|respiratory]] and [[metabolic acidosis]].


=== Electrocardiogram ===
=== Electrocardiogram ===


=== X-ray ===
=== X-ray ===
Chest [[X-rays|X-ray]] of patients with [[Eisenmenger's syndrome]] may show [[cardiomegaly]], right ventricular or biventricular enlargement, right atrial or biatrial enlargement, and pulmonary vascular [[plethora]].


=== Echocardiography and Ultrasound ===
=== Echocardiography and Ultrasound ===


=== CT scan ===
=== CT scan ===
[[Computed tomography]] can be helpful as a diagnostic tool in conditions where the echocardiographic findings are inconclusive. The findings on CT scan may include large main [[pulmonary artery]], [[ventricular septal defect]], and [[right ventricular hypertrophy]].


=== MRI ===
=== MRI ===
[[Magnetic resonance imaging]] can be helpful as a diagnostic tool in conditions where the [[echocardiographic]] findings are inconclusive. The following can be observed on MRI examination of [[Eisenmenger's syndrome]] patients: Magnitude and direction of the [[cardiac shunt]], reduced systolic function of the cardiac [[Ventricle|ventricles]], and brain [[diffusion]] changes on brain [[Magnetic resonance imaging|MRI]].


=== Other Imaging Findings ===
=== Other Imaging Findings ===
Line 52: Line 59:


=== Medical Therapy ===
=== Medical Therapy ===
=== Interventions ===


=== Surgery ===
=== Surgery ===

Revision as of 05:01, 20 January 2020

Eisenmenger’s syndrome Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Eisenmenger’s syndrome from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

Echocardiography and Ultrasound

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Eisenmenger’s syndrome ACC/AHA Guidelines for Evaluation of Patients

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

ACC/AHA Guidelines for Reproduction

Eisenmenger’s syndrome overview On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Eisenmenger’s 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 Eisenmenger’s syndrome overview

CDC on Eisenmenger’s syndrome overview

Eisenmenger’s syndrome overview in the news

Blogs on Eisenmenger’s syndrome overview

Directions to Hospitals Treating Type page name here

Risk calculators and risk factors for Eisenmenger’s syndrome overview

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Abdelrahman Ibrahim Abushouk, MD[2], Priyamavada Singh, MBBS [3];Kristin Feeney, B.S. [4]

Overview

Eisenmenger's syndrome or Eisenmenger's reaction is defined as the process in which a left-to-right shunt in the heart causes increased flow through the pulmonary vasculature, which leads to pulmonary hypertension, which finally causes increased pressures in the right side of the heart and reversal of the shunt into a right-to-left shunt. This right to left shunt causes the patient to become cyanotic. Thus, Eisenmenger's syndrome is said to develop when there is a pulmonary artery disease, right-to-left heart shunting and cyanosis.

Historical Perspective

Victor Eisenmenger first described the syndrome in 1897 in a patient who presented with dyspnea and cyanosis since infancy. Since then, advances in the medical treatment of pulmonary hypertension improved the survival of Eisenmenger's syndrome.

Classification

Pathophysiology

Causes

Eisenmenger's syndrome is causes by cardiac defects that shunt blood heading to the systemic circulation back into the pulmonary circulation. These defects include ventricular septal defect, atrial septal defect, atrioventricular canal defect, patent ductus arteriosus, and truncus arteriosus.

Differentiating Eisenmenger's syndrome from Other Diseases

Epidemiology and Demographics

The incidence and prevalence of Eisenmenger's syndrome has been decreasing gradually over the years. In the general population, the prevalence decreased from 24.6 to 11.9/million inhabitants in 2012. About 8% of patents with congenital heart diseases develop Eisenmenger's syndrome. The mortality rate of Eisenmenger's syndrome is about 27%. The risk of Eisenmenger's syndrome increases in patients with large cardiac defects or who live in developing countries due to poor healthcare access.

Risk Factors

The common risk factors for Eisenmenger's syndrome include genetic mutations, exposure to rubella virus, and drug and alcohol abuse during pregnancy. Less common risk factors include poor healthcare access and patients in developing countries.

Screening

Natural History, Complications, and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

The laboratory findings of patients with Eisenmenger's syndrome include erythrocytosis, iron deficiency, increased bleeding time, increased blood uric acid and conjugated bilirubin concentrations, as well as mixed respiratory and metabolic acidosis.

Electrocardiogram

X-ray

Chest X-ray of patients with Eisenmenger's syndrome may show cardiomegaly, right ventricular or biventricular enlargement, right atrial or biatrial enlargement, and pulmonary vascular plethora.

Echocardiography and Ultrasound

CT scan

Computed tomography can be helpful as a diagnostic tool in conditions where the echocardiographic findings are inconclusive. The findings on CT scan may include large main pulmonary artery, ventricular septal defect, and right ventricular hypertrophy.

MRI

Magnetic resonance imaging can be helpful as a diagnostic tool in conditions where the echocardiographic findings are inconclusive. The following can be observed on MRI examination of Eisenmenger's syndrome patients: Magnitude and direction of the cardiac shunt, reduced systolic function of the cardiac ventricles, and brain diffusion changes on brain MRI.

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

References

Template:WH Template:WS