CONGENITAL HEART DEFECTS Flashcards

1
Q

What does cyanosis mean?

A

blue-purple discolouration of skin and mucous membranes caused by an elevated blood conc. of deoxygenated Hb.

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2
Q

How does cyanosis occur in congenital heart disease?

A

cyanosis results from defects that allow poorly oxygenated blood from right side of heart to be shunted to the left side of the heart, bypassing the lungs

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3
Q

What causes acyanosis?

A

defects that result in left to right shunting

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4
Q

What is the result of large left to right shunts at atrial, septal or great vessel level?

A

Cause pulmonary artery volume and pressure to increase and can be associated with later development of pulmonary arteriolar hypertrophy and increased resistance to flow
Overtime the elevated pulmonary resistance may cause the shunt to reverse direction –> hypoxemia and cyanosis e.g. seen in Eisenmenger syndrome

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5
Q

Give examples of congential heart diseases which are acyanotic.

A

ASD, VSD, PDA
Obstructive lesions: aortic stenosis (hypoplasia), pulmonary stenosis (valve, outflow branch), coarctation of the aorta, mitral stenosis

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6
Q

give examples of cyanotic congenital HD

A

Tetralogy of Fallot
Transposition of great arteries
univentricular heart

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7
Q

Discuss Atrial septal defects (ASD).

A

ASD is a persistent opening in the interatrial septum after birth.
ASDs relatively common (1 in 1500 live births)

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8
Q

What is the most common site of an ASD?

A

region of the foramen ovale - known as ostium secundum ASD. Defect arises from inadequate formation of the septum secundum, excessive resorption of the septum primum or both

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9
Q

What is a less common site for an ASD?

A

in the inferior portion of the interatrial septum - adjacent to AV valves
called the ostium primum defect. abnormality results from failure of septum primum to fuse with endocardial cushions

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10
Q

What are the haemodynamic effects of an ASD?

A

increased pulmonary blood flow
RV volume overload
pulmonary hypertension is rare
eventual right heart failure

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11
Q

What is a sinus venosus defect?

A

a type of atrial septal abnormality.
an ‘unroofing’ defect with absence of normal tissue between right pulmonary vein(s) and RA but often atrial septum is actually intact.
Sinus venosus defects often large and result in flow from right pulmonary veins and LA into right atrium –> similar pathophysiology of ASD

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12
Q

What is PFO?

A

patent foramen ovale
found in around 20% of population
normally permanently seals by age of 6 months via fusion of atrial septa
PFP remains when fusion fails to occur

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13
Q

Why is a PFO usually clinically silent?

A

because the one way valve, though not sealed remains functionally closed as LA pressure is greater than RA pressure
PFO takes significance if RA pressure becomes elevated e.g. in states of pulmonary hypertension or right heart failure, resulting in right to left intracardiac shunting
In this case deoxygenated blood passes directly into arterial circulation

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14
Q

Why is the link between a PFO and a systemic embolism?

A

Patient suffering from a systemic embolism is likely to have a PFO
situation = paradoxical embolism
occurs when thrombus in systemic vein breaks loose, travels to RA, passes across PFO to LA (if right heart pressures are elevated, at least transiently e.g. a cough) –> systemic arterial circulation

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15
Q

Discuss the pathophysiology of an uncomplicated ASD.

A

oxygenated blood from LA shunted to RA.
results in volume overload and enlargement of RA and RV
if RV compliance decreases over time due to excess load, the left to right shunt may lessen
if severe pulmonary vascular disease develops e.g. Eisenmenger syndrome, the shunt may reverse –> cyanosis

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16
Q

What is a VSD?

A

Ventricular septal defect is an abnormal opening in the interventricular septum

17
Q

Where are VSDs located - give the most common location and others?

A

Most often located in membranous (70%) and muscular (20%) portions of septum
rare VSDs occur just below aortic valve or adjacent to AV valves

18
Q

Discuss the haemodynamic changes that accompany VSDs.

A
  1. Left to right shunt
  2. LV volume overload
  3. pulmonary venous congestion
  4. eventual pulmonary hypertension
    shunting from LV –> RV causes increased pressure and volume in pulmonary artery –> pulmonary circulation, LA and LV experience volume overload
    initially increased blood return to LV –> increased SV via Frank Starling mechanism
    eventually increased volume overload –> chamber dilatation, systolic dysfunction, and HF
19
Q

VSD leads to eventual pulmonary hypertension. What can this lead to?

A

augmented circulation through the pulmonary vasculature can cause pulmonary vascular disease as early as 2 years old.
As pulmonary vascular resistance increases –> intracardiac shunt may reverse its direction (Eisenmenger syndrome) –> cyanosis

20
Q

What are atrioventricular septal defects?

A

defects that arise from faulty development of embryonic endocardial tissues

21
Q

What is a PDA?

A

Patent ductus arteriosus
the ductus arteriosus is the vessel that connects the left pulmonary artery to the descending aorta during fetal life.
PDA results when ductus fails to close after birth –> persistent connection between the great vessels

22
Q

What causes the ductus arteriosus to constrict after birth?

A

smooth muscle of the ductus arteriosus usually constricts due to sudden rise in blood oxygen tension and a reduction in level of circulating PGs. Over next few weeks intimal prolif. and fibrosis –> permanent closure

23
Q

Discuss the pathophysiology of PDA.

A

As pulmonary resistance drops postnatally, the shunt reverse direction and blood flows from aorta into pulmonary circulation instead.
Due to Left to R shunt, the pulmonary circulation, LA and LV become volume overloaded
can lead to LV dilatation and left sided heart failure
Eisenmenger syndrome can develop causing reverse shunting

24
Q

What is congenital aortic stenosis and how is it caused?

A

most often caused by abnormal structural development of the valve leaflets
most common abnormality is coarctation of the aorta
The aortic valve in congenital AS usual have a bicuspid leaflet structure instead of a tricuspid leaflet config, causing an eccentric stenotic opening through which blood is ejected
bicuspid valves often become progressively stenotic over many years as the leaflets progressively fibrose and calcify –> common cause of AS in adults

25
Q

discuss the pathophysiology in congenital aortic stenosis

A

as the valvular orifice is significantly narrowed, LV systolic pressure must increase to pump blood across the valve into the aorta
in response to increased pressure load –> LV hypertrophies
the high velocity jet of blood that passes through the stenotic valve may impact the proximal aortic wall and contribute to dilatation of the vessel

26
Q

What is coarctation of the aorta?

A

consists of a discrete narrowing of the aortic lumen
most common associated cardiac abnormality is a bicuspid aortic valve
aortic coarctation often occurs in patients with Turner syndryme (45,XO)
majority of coarctations are next to the ductus arteriosus

27
Q

Discuss the pathophysiology of coarctation of the aorta.

A

due to aortic narrowing in coarctation, the LV faces an increased afterload
blood flow to head and upper extremities is preserved because the vessels supplying these areas usually branch off the aorta proximal to the obstruction but blow to descending aorta and lower extremities may be diminished

28
Q

What are possible compensatory alterations that can occur if aortic coarctation is not corrected?

A
  1. development of LV hypertrophy
  2. dilatation of collateral blood vessels from the intercostal arteries that bypass the coarctation and provide blood to more distal descending aorta
    eventually collateral vessels enlarge and can erode undersurface of ribs
29
Q

What are the two main categories of congenital heart lesions?

A

cyanotic and acyanotic