Intermediate - Cardiac Abnormalities: Difference between revisions

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{{Template:Intermediate Cardiac menu}}
{{Intermediate Cardiac menu}}




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{{Cardiac_modules}}


[[File:Intermediate Heart Development Timeline.jpg|center|850px]]


Congenital Heart Disease (CHD) is a broad term for a variety of cardiac and vasculature pre-natal defects.  They affect about 8-10 of every 1 000 births in the United States.  Heart and vascular abnormalities make up around 20% of all congenital malformations.  Some of the more common abnormalities are outlined in the table below, in order of frequency.
 
Congenital Heart Disease (CHD) is a broad term for a variety of cardiac and vasculature prenatal defects.  They affect about 8-10 of every 1,000 births in the United States.  Heart and vascular abnormalities make up around 20% of all congenital malformations.  Some of the more common abnormalities are outlined in the table below in order of frequency.




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!Description
!Description
|-
|-
|[[Image:HeartILP_draft_vsd.jpg|thumb|x100px|VSD]]
|[[File:Ventricular Septal Defect.jpg|100px]]
|'''Ventricular Septal Defect'''
|'''Ventricular Septal Defect'''
|25% of CHD; more frequent in males
|25% of CHD; more frequent in males
|Growth failure of the membranous IV septum or endocardial cushions resulting in a lack of closure of the IV foramen. 30-50% close spontaneously; large VSDs result in dyspnoea and cardiac failure in infancy.
|Growth failure of the membranous IV septum or endocardial cushions, resulting in a lack of closure of the IV foramen. 30-50% close spontaneously; large VSDs result in dyspnoea and cardiac failure in infancy.
|-style="background:lightsteelblue"
|-style="background:lightsteelblue"
|[[Image:HeartILP_draft_tetralogyoffallot.jpg|thumb|x100px|Tetralogy of Fallot]]
|[[File:Tetralogy of Fallot.jpg|100px]]
|'''Tetralogy of Fallot'''
|'''Tetralogy of Fallot'''
|9-14% of CHD
|9-14% of CHD
|Classic group of defects: pulmonary stenosis, VSD, dextroposition of aorta, RV hypertrophy.  Results in cyanosis.
|Classic group of defects: pulmonary stenosis, VSD, dextroposition of aorta, RV hypertrophy.  Results in cyanosis.
|-
|-
|[[Image:HeartILP_draft_transposition.jpg|thumb|x100px|Transposition of the Great Vessels]]
|[[File:Transposition of the Great Vessels.jpg|100px]]
|'''Transposition of the Great Vessels'''
|'''Transposition of the Great Vessels'''
|10-11% of CHD
|10-11% of CHD
|Aorta arises from the RV with the pulmonary trunk arising from the left.  Most common cause of cyanotic heart disease in newborns; surgically corrected.
|Aorta arises from the RV with the pulmonary trunk arising from the left.  Most common cause of cyanotic heart disease in newborns; surgically corrected.
|-style="background:lightsteelblue"
|-style="background:lightsteelblue"
|[[Image:HeartILP_draft_asd.jpg|thumb|x100px|ASD]]
|[[File:Atrial Septal Defect.jpg|100px]]
|'''Atrial Septal Defect'''
|'''Atrial Septal Defect'''
|6-10% of CHD; more common in females
|6-10% of CHD; more common in females
|Most commonly patent foramen ovale; can also be an ostium secundum defect, and endocardial cushion defect with ostium primum defect, sinus venosus defect, common atrium.  Results in cyanosis due to right-to-left shunt.
|Most commonly patent foramen ovale; can also be an ostium secundum defect, an endocardial cushion defect with ostium primum defect, sinus venosus defect, common atrium.  Results in cyanosis due to right-to-left shunt.
|-
|-
|[[Image:HeartILP_draft_pulmonaryatresia.jpg|thumb|x100px|Pulmonary Atresia]][[Image:HeartILP_draft_pulmonarystenosis.jpg|thumb|x100px|Pulmonary Stenosis]]
|[[File:Pulmonary Atresia.jpg|100px]][[Image:Pulmonary Stenosis.jpg|100px]]
|'''Pulmonary Atresia & Pulmonary Stenosis'''
|'''Pulmonary Atresia & Pulmonary Stenosis'''
|10% of CHD
|10% of CHD
|Unequal division of trunks causes cusps to fuse to form a dome with a narrow/non existent lumen.  Heart-lung transplantation may be the only therapy
|Unequal division of trunks causes cusps to fuse to form a dome with a narrow/non-existent lumen.  Heart-lung transplantation may be the only therapy.
|-style="background:lightsteelblue"
|-style="background:lightsteelblue"
|[[Image:HeartILP_draft_patentda.jpg|thumb|x100px|Patent Ductus Arteriosus]]
|[[File:Patent Ductus Arteriosus.jpg|100px]]
|'''Patent Ductus Arteriosus'''
|'''Patent Ductus Arteriosus'''
|6-8% of CHD; 2-3 times more common in females; common in preterm newborns
|6-8% of CHD; 2-3 times more common in females; common in preterm newborns
|Failure of contraction of the muscular wall of the DA.  Spontaneous or surgical closure.
|Failure of contraction of the muscular wall of the DA.  Spontaneous or surgical closure.
|-
|-
|[[Image:HeartILP_draft_aorticstenosis.jpg|thumb|x100px|Aortic Stenosis]]
|[[File:Aortic Stenosis.jpg|100px]]
|'''Aortic Stenosis'''
|'''Aortic Stenosis'''
|7% of CHD
|7% of CHD
|Persistence of tissue that normally degenerates.  Results in LV hypertrophy, heart murmurs.
|Persistence of tissue that normally degenerates.  Results in LV hypertrophy, heart murmurs.
|-style="background:lightsteelblue"
|-style="background:lightsteelblue"
|[[Image:HeartILP_draft_hlh.jpg|thumb|x100px|Hypoplastic Left Heart]]
|[[File:Hypoplastic Left Heart.jpg|100px]][[Image:Functional Hypoplastic Left Heart.jpg|100px]]
[[Image:HeartILP_draft_funchlh.jpg|thumb|x100px|Functional Hypoplastic Left Heart]]
|'''Hypoplastic Left Heart Syndrome'''
|'''Hypoplastic Left Heart Syndrome'''
|4-8% of CHD
|4-8% of CHD
|RV maintains both pulmonary and systemic circulations aided by an ASD.  Infants usually die within weeks.
|RV maintains both pulmonary and systemic circulations aided by an ASD.  Infants usually die within weeks.
|-
|-
|[[Image:HeartILP_draft_coarctationoftheaorta.jpg|thumb|x100px|Coarctation of the Aorta]]
|[[File:Coarctation of the Aorta.jpg|100px]]
|'''Coarctation of the Aorta'''
|'''Coarctation of the Aorta'''
|5-7% of CHD
|5-7% of CHD
|Aortic constriction.  Treatment aims at maintaining the ductus arteriosus via prostaglandins.
|Aortic constriction.  Treatment aims at maintaining the ductus arteriosus via prostaglandins.
|-style="background:lightsteelblue"
|-style="background:lightsteelblue"
|[[Image:HeartILP_draft_papvd.jpg|thumb|x100px|PAPVD]][[Image:HeartILP_draft_tapvc.jpg|thumb|x100px|TAPVC]]
|[[File:Partial Anomalous Pulmonary Venous Drainage.jpg|100px]][[Image:Total Anomalous Pulmonary Venous Connection.jpg|100px]]
|'''Partial/Total Anomalous Pulmonary Venous Connection'''
|'''Partial/Total Anomalous Pulmonary Venous Connection'''
|<4% of CHD; more common in females
|<4% of CHD; more common in females
|Total or partial lack of connection of the pulmonary veins with LA.  They open into RA, one of the systemic veins or both.  The overloaded pulmonary circuit leads to cyanosis, tachypnoea and dyspnoea.  Treatment is via surgical redirection
|Total or partial lack of connection of the pulmonary veins with LA.  They open into RA, one of the systemic veins or both.  The overloaded pulmonary circuit leads to cyanosis, tachypnoea and dyspnoea.  Treatment is via surgical redirection
|-
|-
|[[Image:HeartILP_draft_tricuspidatresia.jpg|thumb|x100px|Tricuspid Atresia]]
|[[File:Tricuspid Atresia.jpg|100px]]
|'''Tricuspid Atresia'''
|'''Tricuspid Atresia'''
|1-3% of CHD
|1-3% of CHD
|Complete lack of formation of the tricuspid valve with absence of direct connection between the right atrium and right ventricle.  Results in cyanosis.
|Complete lack of formation of the tricuspid valve with absence of direct connection between the right atrium and right ventricle.  Results in cyanosis.
|-style="background:lightsteelblue"
|-style="background:lightsteelblue"
|[[Image:HeartILP_draft_dorv.jpg|thumb|x100px|DORV]]
|[[File:Double Outlet Right Ventricle.jpg|100px]]
|'''Double Outlet Right Ventricle'''
|'''Double Outlet Right Ventricle'''
|1-1.5% of CHD
|1-1.5% of CHD
|Both great arteries arise wholly or in large part from the right ventricle. Arrangement of the atrioventricular valves and the ventriculoarterial connections are variable.  Clinical manifestations variable.
|Both large arteries arise wholly or mainly from the right ventricle. Arrangement of the atrioventricular valves and the ventriculoarterial connections are variable.  Clinical manifestations variable.
|-
|-
|[[Image:HeartILP_draft_interruptaorticarch.jpg|thumb|x100px|Interrupted Aortic Arch]]
|[[File:Interrupted Aortic Arch.jpg|100px]]
|'''Interrupted Aortic Arch'''
|'''Interrupted Aortic Arch'''
|Very rare
|Very rare
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|bgcolor="firebrick" align="right"|<big>'''[[Advanced_-_Abnormalities|Go to this section in the advanced level]]'''</big>
|bgcolor="#FF6666" align="right"|<big>'''[[Advanced_-_Abnormalities|Go to this section in the advanced level]]'''</big>
|}
|}
{{Glossary}}
[[Template:Heart terms|Heart terms]]
'''Atresia:''' Abnormal closure or absence of a body vessel or orifice.
'''Congenital heart disease:''' Abnormal structure or function of the heart due to a developmental defect arising prior to birth.
'''Cyanosis:''' Blue colouration of the skin and mucous membrane due to poor oxygenation of the blood.
'''Dyspnoea:''' Shortness of breath.
'''Heart murmur:''' Extra heart sounds appearing upon auscultation due to turbulent blood flow.
'''Hypertrophy:''' Increase in size of an organ or tissue due to enlargement of component cells.
'''Pulmonary circulation:''' Carries blood between the heart and lungs.
'''Stenosis:''' Abnormal narrowing of a blood vessel or orifice.
'''Systemic circulation:''' Carries oxygenated blood away from the heart to the other body organs and returns to the heart deoxygenated.
'''Tachypnoea:''' Abnormally rapid breathing rate.
[[Category:Heart]] [[Category:Abnormal Development‏‎]]

Latest revision as of 12:05, 26 May 2016

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Begin Intermediate: Primordial Heart Tube  Heart Tube Looping  Atrial Ventricular Septation  Outflow Tract  Heart Valves  Cardiac Abnormalities  Vascular Overview


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Intermediate Heart Development Timeline.jpg


Congenital Heart Disease (CHD) is a broad term for a variety of cardiac and vasculature prenatal defects. They affect about 8-10 of every 1,000 births in the United States. Heart and vascular abnormalities make up around 20% of all congenital malformations. Some of the more common abnormalities are outlined in the table below in order of frequency.


Diagram Abnormality Epidemiology Description
Ventricular Septal Defect.jpg Ventricular Septal Defect 25% of CHD; more frequent in males Growth failure of the membranous IV septum or endocardial cushions, resulting in a lack of closure of the IV foramen. 30-50% close spontaneously; large VSDs result in dyspnoea and cardiac failure in infancy.
Tetralogy of Fallot.jpg Tetralogy of Fallot 9-14% of CHD Classic group of defects: pulmonary stenosis, VSD, dextroposition of aorta, RV hypertrophy. Results in cyanosis.
Transposition of the Great Vessels.jpg Transposition of the Great Vessels 10-11% of CHD Aorta arises from the RV with the pulmonary trunk arising from the left. Most common cause of cyanotic heart disease in newborns; surgically corrected.
Atrial Septal Defect.jpg Atrial Septal Defect 6-10% of CHD; more common in females Most commonly patent foramen ovale; can also be an ostium secundum defect, an endocardial cushion defect with ostium primum defect, sinus venosus defect, common atrium. Results in cyanosis due to right-to-left shunt.
Pulmonary Atresia.jpgPulmonary Stenosis.jpg Pulmonary Atresia & Pulmonary Stenosis 10% of CHD Unequal division of trunks causes cusps to fuse to form a dome with a narrow/non-existent lumen. Heart-lung transplantation may be the only therapy.
Patent Ductus Arteriosus.jpg Patent Ductus Arteriosus 6-8% of CHD; 2-3 times more common in females; common in preterm newborns Failure of contraction of the muscular wall of the DA. Spontaneous or surgical closure.
Aortic Stenosis.jpg Aortic Stenosis 7% of CHD Persistence of tissue that normally degenerates. Results in LV hypertrophy, heart murmurs.
Hypoplastic Left Heart.jpgFunctional Hypoplastic Left Heart.jpg Hypoplastic Left Heart Syndrome 4-8% of CHD RV maintains both pulmonary and systemic circulations aided by an ASD. Infants usually die within weeks.
Coarctation of the Aorta.jpg Coarctation of the Aorta 5-7% of CHD Aortic constriction. Treatment aims at maintaining the ductus arteriosus via prostaglandins.
Partial Anomalous Pulmonary Venous Drainage.jpgTotal Anomalous Pulmonary Venous Connection.jpg Partial/Total Anomalous Pulmonary Venous Connection <4% of CHD; more common in females Total or partial lack of connection of the pulmonary veins with LA. They open into RA, one of the systemic veins or both. The overloaded pulmonary circuit leads to cyanosis, tachypnoea and dyspnoea. Treatment is via surgical redirection
Tricuspid Atresia.jpg Tricuspid Atresia 1-3% of CHD Complete lack of formation of the tricuspid valve with absence of direct connection between the right atrium and right ventricle. Results in cyanosis.
Double Outlet Right Ventricle.jpg Double Outlet Right Ventricle 1-1.5% of CHD Both large arteries arise wholly or mainly from the right ventricle. Arrangement of the atrioventricular valves and the ventriculoarterial connections are variable. Clinical manifestations variable.
Interrupted Aortic Arch.jpg Interrupted Aortic Arch Very rare Gap in ascending and descending thoracic aorta. Treated with prostaglandin to maintain ductus arteriosus followed by surgery.
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Heart terms

Atresia: Abnormal closure or absence of a body vessel or orifice.

Congenital heart disease: Abnormal structure or function of the heart due to a developmental defect arising prior to birth.

Cyanosis: Blue colouration of the skin and mucous membrane due to poor oxygenation of the blood.

Dyspnoea: Shortness of breath.

Heart murmur: Extra heart sounds appearing upon auscultation due to turbulent blood flow.

Hypertrophy: Increase in size of an organ or tissue due to enlargement of component cells.

Pulmonary circulation: Carries blood between the heart and lungs.

Stenosis: Abnormal narrowing of a blood vessel or orifice.

Systemic circulation: Carries oxygenated blood away from the heart to the other body organs and returns to the heart deoxygenated.

Tachypnoea: Abnormally rapid breathing rate.