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Congenital heart disease (CHD)
Mohammad Shafiq, MD, FESC, FSCAI
1
2
• Dating since birth.
• Can continue to adulthood.
• If present search for other cardiac anomalies and
other systems congenital anomalies
• Either acyanotic or cyanotic or
Common features of acyanotic heart disease
3
• Usually discovered accidently as a murmur during early
childhood. If no murmur can be undiagnosed till elderly
• Usually survives to adulthood as age matched
populations (Simple defects).
• Anatomically: Either :
1 Left to right shunt e.g: Atrial Septal defect (ASD),
Ventricular Septal defect (VSD) or patent ductus arteriosus
(PDA)
2 Ostructive pathology e.g: Aortic Stenosis, Pulmonary
Stenosis or coarctation of aorta.
Atrial septal defect (ASD).
4
Ventricular septal defect (VSD).
5
Patent ductus arteriosus (PDA).
6
Ebstein anomaly .
7
Aortic valve stenosis (Bicuspid aortic valve)
8
Coarcatation of aorta (COA).
9
10
• Spontaneous closure of left to right shunt can occur
without intervention in majority of cases.
• Usually asymptomatic or repeated chest infections.
• Patient may develop Eisenminger syndrome (severe
pulmonary hypertension with reversal of shunt to become
right to left i.e becomes cyanotic).
• Can easily be diagnosed by echocardiography and
rarely needs other investigations
• Can be easily treated by:
• a- Percutaneous intervention (closure of the shunt by
device or balloon dilatation for obstructive lesions
• b- Surgical repair if not feasible for percutaneous
intervention.
12
Cyanotic congenital heart
disease (CCHD):
13
Common features of cyanotic heart disease
• Usually discovered during neonatorum due to cyanosis.
• Usually of aggressive course due to complex anatomy with high
mortality especially if untreated (poor prognosis).
• Anatomically : Usually there is
A- Significant right to left shunt of blood &/or
B- Markedly diminished or absent pulmonary blood flow with
subsequent necessary ASD VSD or PDA to maintain life.
• Patient may have symptoms of heart failure or complications of
cyanosis eg: hyperviscosity syndrome (haedach, blurring of
vision, fatigue or thrombosis) or pulmonary hypertension.
14
• Can be diagnosed easily by echo but usually needs other
investigations e.g multislice CT, cardiac MRI or right heart
catheterization.
• Usually needs surgical intervention at early stages with
common need for staged correction.
• Usulally of unfavorable outcomes with high mortality if
untreated and if treated most of them die at 3rd or 4th
decade.
Tetraology of fallot (TOF )
15
Transposition of great arteries (TGA): D-
TGA
16
Systemic hypertension (HTN)
17
18
1) Normal BP BP < 120 & 80.
2) Pre-HTN: BP < 140 and/or 90
3) HTN: BP ≥ 140 and/or 90 or person not talking anti-HTN medications.
- Stage 1 (Mild): BP < 160 and/or 100.
- Stage 2 (Moderate) : BP ≥ 160 and/or 100.
- Stage 3 (Severe ) : BP ≥ 180 and or 110mmhg.
Systemic HTN
- BP ≥ 140 or 90 in person not talking anti-HTN medications or
controlled BP in patient already on ttt.
19
Complications of HTN
1 Heart failure up to acute pulmonary
edema.
2 CVS: either haeomrrhagic or embolic
3 Retinal haemorrhage
4 Arrhytmias: most common AF
5 Renal failure.
6 Aortic aneurysm and / or aortic dissection
20
Treatment of HTN
A- general measures: Avoid caffeine beverges, avoid drugs e.g: NSAIDs,
alcohol or decongestants (common cold ttt) and improve life style including:
salt restriction, stop smoking, low fats diet and regular exercise.
B- Pharmaholgical therapy: includes different drugs categories:
1 Angiotensine converting enzyme (ACE ) inhibitors: e.g: captopril or enlapril
2 Angiotensin Receptors Blockers (ARBs) eg: vlasartan or olmesartan.
3 Beta blockers (BBs): eg:bisoprolol, metoprolol, nebivolol or carvidolol.
4 Calcium channel blockers (CCBs): e.g:verapamil or amlodipine.
5 Thiazide diuretics eg: hydrochlorothiazide or chlorothalidone.
6 Direct vasodialtors: eg:Hydralazine or minoxidil.
C- treatment of complications : eg treatment of cerebral haeorrage.
21
Thank You

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Congestive HD and hypertension. ppt.pptx

  • 1. Congenital heart disease (CHD) Mohammad Shafiq, MD, FESC, FSCAI 1
  • 2. 2 • Dating since birth. • Can continue to adulthood. • If present search for other cardiac anomalies and other systems congenital anomalies • Either acyanotic or cyanotic or
  • 3. Common features of acyanotic heart disease 3 • Usually discovered accidently as a murmur during early childhood. If no murmur can be undiagnosed till elderly • Usually survives to adulthood as age matched populations (Simple defects). • Anatomically: Either : 1 Left to right shunt e.g: Atrial Septal defect (ASD), Ventricular Septal defect (VSD) or patent ductus arteriosus (PDA) 2 Ostructive pathology e.g: Aortic Stenosis, Pulmonary Stenosis or coarctation of aorta.
  • 8. Aortic valve stenosis (Bicuspid aortic valve) 8
  • 10. 10 • Spontaneous closure of left to right shunt can occur without intervention in majority of cases. • Usually asymptomatic or repeated chest infections. • Patient may develop Eisenminger syndrome (severe pulmonary hypertension with reversal of shunt to become right to left i.e becomes cyanotic).
  • 11. • Can easily be diagnosed by echocardiography and rarely needs other investigations • Can be easily treated by: • a- Percutaneous intervention (closure of the shunt by device or balloon dilatation for obstructive lesions • b- Surgical repair if not feasible for percutaneous intervention.
  • 13. 13 Common features of cyanotic heart disease • Usually discovered during neonatorum due to cyanosis. • Usually of aggressive course due to complex anatomy with high mortality especially if untreated (poor prognosis). • Anatomically : Usually there is A- Significant right to left shunt of blood &/or B- Markedly diminished or absent pulmonary blood flow with subsequent necessary ASD VSD or PDA to maintain life. • Patient may have symptoms of heart failure or complications of cyanosis eg: hyperviscosity syndrome (haedach, blurring of vision, fatigue or thrombosis) or pulmonary hypertension.
  • 14. 14 • Can be diagnosed easily by echo but usually needs other investigations e.g multislice CT, cardiac MRI or right heart catheterization. • Usually needs surgical intervention at early stages with common need for staged correction. • Usulally of unfavorable outcomes with high mortality if untreated and if treated most of them die at 3rd or 4th decade.
  • 15. Tetraology of fallot (TOF ) 15
  • 16. Transposition of great arteries (TGA): D- TGA 16
  • 18. 18 1) Normal BP BP < 120 & 80. 2) Pre-HTN: BP < 140 and/or 90 3) HTN: BP ≥ 140 and/or 90 or person not talking anti-HTN medications. - Stage 1 (Mild): BP < 160 and/or 100. - Stage 2 (Moderate) : BP ≥ 160 and/or 100. - Stage 3 (Severe ) : BP ≥ 180 and or 110mmhg. Systemic HTN - BP ≥ 140 or 90 in person not talking anti-HTN medications or controlled BP in patient already on ttt.
  • 19. 19 Complications of HTN 1 Heart failure up to acute pulmonary edema. 2 CVS: either haeomrrhagic or embolic 3 Retinal haemorrhage 4 Arrhytmias: most common AF 5 Renal failure. 6 Aortic aneurysm and / or aortic dissection
  • 20. 20 Treatment of HTN A- general measures: Avoid caffeine beverges, avoid drugs e.g: NSAIDs, alcohol or decongestants (common cold ttt) and improve life style including: salt restriction, stop smoking, low fats diet and regular exercise. B- Pharmaholgical therapy: includes different drugs categories: 1 Angiotensine converting enzyme (ACE ) inhibitors: e.g: captopril or enlapril 2 Angiotensin Receptors Blockers (ARBs) eg: vlasartan or olmesartan. 3 Beta blockers (BBs): eg:bisoprolol, metoprolol, nebivolol or carvidolol. 4 Calcium channel blockers (CCBs): e.g:verapamil or amlodipine. 5 Thiazide diuretics eg: hydrochlorothiazide or chlorothalidone. 6 Direct vasodialtors: eg:Hydralazine or minoxidil. C- treatment of complications : eg treatment of cerebral haeorrage.