Difference between revisions of "Congenital heart disease"
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==Ventricular septal defect== | ==Ventricular septal defect== | ||
*Most common congenital | *Common serious congenital heart defect. | ||
**Most common congenital defect = bicuspid aortic valve.<ref name=pmid20579534>{{cite journal |author=Siu SC, Silversides CK |title=Bicuspid aortic valve disease |journal=J. Am. Coll. Cardiol. |volume=55 |issue=25 |pages=2789–800 |year=2010 |month=June |pmid=20579534 |doi=10.1016/j.jacc.2009.12.068 |url=}}</ref> | |||
==Tetralogy of Fallot (TOF)== | ==Tetralogy of Fallot (TOF)== | ||
Revision as of 05:00, 14 November 2010
Congenital heart disease is a niche area of a niche area.
Ventricular septal defect
- Common serious congenital heart defect.
- Most common congenital defect = bicuspid aortic valve.[1]
Tetralogy of Fallot (TOF)
General
- Most common cause of a blue baby.
Etiology
- Abnormal septation of the truncus arteriosus.
Definition
Features:[2]
- Right ventricular hypertrophy.
- Right ventricular outflow tract obstruction.
- Overriding aorta.
- VSD (ventricular septal defect).
Notes:
- Overriding aorta = aorta has a biventricular connection --takes blood from the right ventricle.
- Right ventricular outflow tract obstruction is usually subpulmonic stenosis.
Atrial septal defect
- May be seen in adults.
Clinical
- Fixed S2 split.
Classification
Types:[3]
- Ostium secundum (most common) - between SVC and IVC.
- Ostium primum - between SVC and IVC closer to RV.
- Upper sinus venosus defect - at SVC.
- Lower sinus venosus defect - at IVC.
- Coronary sinus defect.
The ostium secundum are the most common and usually found in isolation, i.e. there are not other associated abnormalities.
Left hypoplastic heart syndrome
Defintion:[4]
- Physiologically inadequate left ventricle.
Key characteristic:[5]
- Atrial septal defect (ASD) -- left-to-right shunt.
Causality:
- Mitral stenosis.
- Left ventricular hypoplasia.
Associations:[5]
- Turner syndrome.
- Noonan syndrome - sometimes called "male version of Turner syndrome".
- Smith-Lemli-Opitz syndrome.
- Holt-Oram syndrome.[6]
Transposition of great vessels
- Aorta and pulmonary trunk hooked-up to the wrong ventricle.
- Survivable after birth only if there is a functional shunt, e.g. (persistent) patent ductus arteriosus and/or atrial septal defect.
- When the ductus arteriosus closes they are in trouble.
Splenic abnormalities
Asplenia is associated with cardiac abnormalities:[7]
- Aspenia = Boys, Bad congenital malformations (transposition of great vessels, pulmonary atresia/stenosis, totally anomalous pulmonary return).
- Interesting is that these are all right-to-left shunts.
For completeness... polyspenia associations:[7]
- Polyspenia = Girls, Good prognosis, Gastrointestinal situs inversus.
Eisenmenger syndrome
- Pulmonary arterial hypertension with a
- Right-to-left shunt (that was initially left-to-right), and
- Cyanosis.
Note: Eisenmenger syndrome, by definition in some sources, is (only) due to a VSD.
Causes:
- ASD - rarely causes Eisenmenger syndrome.
- VSD.
- Extra-cardiac shunt.
- End-stage disease often characterized by fibrinoid necrosis of small pulmonary arterial vessels (arterioles & small arteries).[10]
Cor pulmonale
Pulmonary hypertension due to heart disease.
Pulmonary hypertension
Main article: Pulmonary hypertension
Pressure - definition:[8]
- Mean pulm. arterial pressure >25 mmHg at rest.
See also
References
- ↑ Siu SC, Silversides CK (June 2010). "Bicuspid aortic valve disease". J. Am. Coll. Cardiol. 55 (25): 2789–800. doi:10.1016/j.jacc.2009.12.068. PMID 20579534.
- ↑ Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease (7th ed.). St. Louis, Mo: Elsevier Saunders. pp. 568. ISBN 0-7216-0187-1.
- ↑ http://en.wikipedia.org/wiki/File:ASD.png
- ↑ Moore. TDH. P.361
- ↑ 5.0 5.1 http://emedicine.medscape.com/article/890196-overview
- ↑ Ekure EN, Okoromah CN, Briggs E, Ajenifuja OA (September 2004). "Holt-Oram syndrome with hypoplastic left heart syndrome in an African child". Niger Postgrad Med J 11 (3): 190–2. PMID 15505648.
- ↑ 7.0 7.1 Rose V, Izukawa T, Moes CA (August 1975). "Syndromes of asplenia and polysplenia. A review of cardiac and non-cardiac malformations in 60 cases withspecial reference to diagnosis and prognosis". Br Heart J 37 (8): 840-52. PMC 482884. PMID 1191445. http://www.pubmedcentral.nih.gov/pagerender.fcgi?artid=482884&pageindex=1#page.
- ↑ 8.0 8.1 Jensen AS, Iversen K, Vejlstrup NG, Hansen PB, Sondergaard L (April 2009). "[Eisenmenger syndrome]" (in Danish). Ugeskr. Laeg. 171 (15): 1270-5. PMID 19416617.
- ↑ [1]
- ↑ Daliento L, Rebellato L, Angelini A, et al. (2002). "Fatal outcome in Eisenmenger syndrome". Cardiovasc. Pathol. 11 (4): 221-8. PMID 12140128.
