Aortic coarctation classification: Difference between revisions

Jump to navigation Jump to search
m (Robot: Changing Category:Disease state to Category:Disease)
m (Bot: Adding CME Category::Cardiology)
 
(17 intermediate revisions by 5 users not shown)
Line 1: Line 1:
__NOTOC__
{{Aortic coarctation}}
{{Aortic coarctation}}
{{CMG}}; '''Associate Editor(s)-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.B.B.S.]][mailto:psingh@perfuse.org], {{CZ}}; '''Assistant Editor(s)-In-Chief:''' [[Kristin Feeney|Kristin Feeney, B.S.]][mailto:kfeeney@perfuse.org]
{{CMG}}; '''Associate Editor(s)-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.B.B.S.]][mailto:psingh13579@gmail.com], {{CZ}}; '''Assistant Editor(s)-In-Chief:''' [[Kristin Feeney|Kristin Feeney, B.S.]][mailto:kfeeney@elon.edu]


==Overview==
==Overview==
An aortic coarctation can be classified in three ways depending on the anatomical configuration. These include: preductal coarctation, ductal coarctation, and postductal coarctation. All classifications involve narrowings of the aorta that directly impact the aortic hemodynamics.
Aortic coarctation can be classified as preductal coarctation, ductal coarctation, and postductal coarctation depending upon the coarctation's anatomic relationship to the [[ductus arteriosus]]. All classifications involve narrowings of the aorta that directly impact the [[aortic]] [[hemodynamics]].


==Classification==
==Classification==
There are three types:<ref>Valdes-Cruz LM, Cayre RO: ''Echocardiographic diagnosis of congenital heart disease.'' Philadelphia, 1998.</ref>
[[Image: 220px-Coarctation_and_PDA.png‎|center]]
# Preductal coarctation: The narrowing is proximal to the ductus arteriosus. If severe, blood flow to the aorta distal (to lower body) to the narrowing is dependent on a patent ductus arteriosus, and hence its closure can be life-threatening. Preductal coarctation results when an intracardiac anomaly during fetal life decreases blood flow through the left side of the heart, leading to hypoplastic development of the aorta.  
 
# Ductal coarctation: The narrowing occurs at the insertion of the ductus arteriosus. This kind usually appears when the ductus arteriosus closes.
Schematic drawing of alternative locations of a coarctation of the aorta, relative to the ductus arteriosus. A: Ductal coarctation, B: Preductal coarctation, C: Postductal coarctation. 1: Aorta ascendens, 2: Arteria pulmonalis, 3: Ductus arteriosus, 4: Aorta descendens, 5: Truncus brachiocephalicus, 6: Arteria carotis communis sinistra, 7: Arteria subclavia sinistra<ref>Valdes-Cruz LM, Cayre RO: ''Echocardiographic diagnosis of congenital heart disease.'' Philadelphia, 1998.</ref>
# Postductal coarctation: The narrowing is distal to the insertion of the ductus arteriosus. Even with an open ductus arteriosus blood flow to the lower body can be impaired. Newborns with this  type of coarctation may be critically sick from the birth. This type is most common in adults. It is associated with notching of the ribs, hypertension in the upper extremities, and weak pulses in the lower extremities. Postductal coarctation is most likely the result of muscular ductal (ductus arteriosis) extends into the aorta during fetal life.
 
There are three variations of coarctation of the aorta:
 
===Preductal Coarctation===
The narrowing is proximal to the [[ductus arteriosus]]. If severe, [[blood flow]] to the [[aorta]] distal (to lower body) to the narrowing is dependent on a [[patent ductus arteriosus]], and hence its closure can be life-threatening. Preductal coarctation results when an intracardiac anomaly during fetal life decreases [[blood flow]] through the left side of the [[heart]], leading to hypoplastic development of the [[aorta]].  
===Ductal Coarctation===
The narrowing occurs at the insertion of the [[ductus arteriosus]]. This kind usually appears when the [[ductus arteriosus]] closes.
===Postductal Coarctation===
The narrowing is distal to the insertion of the [[ductus arteriosus]]. Even with an open [[ductus arteriosus]] [[blood flow]] to the lower body can be impaired. [[Newborns]] with this  type of coarctation may be critically sick from [[birth]]. This type is most common in adults. It is associated with notching of the [[ribs]], [[hypertension]] in the [[upper extremities]], and weak [[pulses]] in the [[lower extremities]]. Postductal coarctation is most likely the result of muscular ductal ([[ductus arteriosis]]) extension into the [[aorta]] during [[fetal]] life.


==References==
==References==
Line 16: Line 25:


{{WS}}
{{WS}}
[[CME Category::Cardiology]]


[[Category:Cardiology]]
[[Category:Cardiology]]
[[Category:Pediatrics]]
[[Category:Pediatrics]]
[[Category:Disease]]
[[Category:Disease]]
[[Category:Mature chapter]]
[[Category:Congenital heart disease]]
[[Category:Congenital heart disease]]

Latest revision as of 22:13, 14 March 2016

Aortic coarctation Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Aortic Coarctation from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Electrocardiogram

Chest X-Ray

CT

MRI

Angiography

Echocardiography

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Aortic coarctation classification On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Aortic coarctation classification

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Aortic coarctation classification

CDC on Aortic coarctation classification

Aortic coarctation classification in the news

Blogs on Aortic coarctation classification

Directions to Hospitals Treating Aortic coarctation

Risk calculators and risk factors for Aortic coarctation classification

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Priyamvada Singh, M.B.B.S.[2], Cafer Zorkun, M.D., Ph.D. [3]; Assistant Editor(s)-In-Chief: Kristin Feeney, B.S.[4]

Overview

Aortic coarctation can be classified as preductal coarctation, ductal coarctation, and postductal coarctation depending upon the coarctation's anatomic relationship to the ductus arteriosus. All classifications involve narrowings of the aorta that directly impact the aortic hemodynamics.

Classification

Schematic drawing of alternative locations of a coarctation of the aorta, relative to the ductus arteriosus. A: Ductal coarctation, B: Preductal coarctation, C: Postductal coarctation. 1: Aorta ascendens, 2: Arteria pulmonalis, 3: Ductus arteriosus, 4: Aorta descendens, 5: Truncus brachiocephalicus, 6: Arteria carotis communis sinistra, 7: Arteria subclavia sinistra[1]

There are three variations of coarctation of the aorta:

Preductal Coarctation

The narrowing is proximal to the ductus arteriosus. If severe, blood flow to the aorta distal (to lower body) to the narrowing is dependent on a patent ductus arteriosus, and hence its closure can be life-threatening. Preductal coarctation results when an intracardiac anomaly during fetal life decreases blood flow through the left side of the heart, leading to hypoplastic development of the aorta.

Ductal Coarctation

The narrowing occurs at the insertion of the ductus arteriosus. This kind usually appears when the ductus arteriosus closes.

Postductal Coarctation

The narrowing is distal to the insertion of the ductus arteriosus. Even with an open ductus arteriosus blood flow to the lower body can be impaired. Newborns with this type of coarctation may be critically sick from birth. This type is most common in adults. It is associated with notching of the ribs, hypertension in the upper extremities, and weak pulses in the lower extremities. Postductal coarctation is most likely the result of muscular ductal (ductus arteriosis) extension into the aorta during fetal life.

References

  1. Valdes-Cruz LM, Cayre RO: Echocardiographic diagnosis of congenital heart disease. Philadelphia, 1998.

Template:WH

Template:WS CME Category::Cardiology