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cardiac surgery: a walk on the Dark Side? Prof Rik De Decker Red - - PowerPoint PPT Presentation

The complications of cardiac surgery: a walk on the Dark Side? Prof Rik De Decker Red Cross Childrens Hospital CME Nov/Dec 2011 http://www.cmej.org.za Why should you care? You are about to leave your office after a hectic Friday, and are


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The complications of cardiac surgery: a walk on the Dark Side?

Prof Rik De Decker

Red Cross Children’s Hospital

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CME Nov/Dec 2011

http://www.cmej.org.za

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Why should you care?

You are about to leave your office after a hectic Friday, and are looking forward to a quiet weekend off. Just as you reach the door, the phone rings, and your first instinct is to ignore it. But you answer it anyway. It is a Mrs Harmse, in a panic. Then you recall: you had sent her 8-month-old son, Karl, who has tricuspid atresia, to Red Cross Hospital 6 weeks ago. Karl had become very blue when his Blalock-Taussig shunt, inserted 7 months ago, blocked. This time, she says, he has had diarrhoea for 3 days, he has become very blue again, and his face is now horribly swollen! She reads from his discharge letter from RXH, which says something about a “successful heart operation 4 weeks ago with a Glenn…”

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Do you wonder….?

Who is this Glenn bloke, and why did he make Karl’s head swell up?

Or do you suspect….?

Karl’s been dehydrated by his diarrhoea, … so his Glenn shunt has thrombosed, … causing poor flow to his branch PAs and SVC syndrome!

I’d better get him to RXH now!

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What does cardiac surgery do?

Cardiac surgery (and cath interventions) removes or palliates physiological processes that lead to morbidity or death … but it replaces them with other, more benign ones, that may not be entirely innocent.

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What are those

(less innocent) processes?

The incorrect perception by parents that The Operation has been done, and all is well...

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The life-line of a child with tricuspid atresia

ROUTINE VISITS SIGNIFICANT EVENTS

REFERRAL TO ADULT SERVICE

Antenatal/Birth Teenage years ADMISSIONS

Clinical assessment ECG Echocardiography Cardiac catheterisation CT angiogram Non-cardiac investigations Pre-op medical management Surgery Post-op TOE Post-op ICU echocardiograms Post-op catheterisation Twice daily ICU rounds Twice daily ward rounds Discharge work-up Echo ECG Bloods

CARDIAC CLINIC

ECG Echo Clinical assessment

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The unnatural history of post-op CHD

  • recoarctation
  • hypertension
  • PA distortion
  • shunt obstruction
  • LA enlargement
  • LV hypertrophy
  • PA aneurysm
  • RV failure
  • arrhythmias
  • liver failure
  • …. etc, etc
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Some common misconceptions

  • Heart surgery is corrective
  • Late post-op complications are rare
  • Parents usually know what is wrong with their

child’s heart

  • Only cardiologists need to know about heart
  • perations
  • Paediatric cardiologists hate being disturbed
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Large variety of operations

  • from “simple” to complex
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Five operative categories

  • by their longer-term outlook

1. temporary palliation for defects that cannot be repaired initially PA BAND SHUNTS 2.

  • perations for heart defects that are “fully corrected” at

the first procedure COARCTATION TAPVD TGA 1. heart defects that might require further surgery or intervention after repair TETRALOGY COARCTATION 2. heart defects that will definitely require further surgery after the initial procedure HOMOGRAFT FOR PA/VSD 1. long-term palliation of uncorrectable lesions: functionally univentricular hearts GLENN & FONTAN SHUNTS

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Temporary palliation for defects that cannot initially be repaired

  • Blalock-Taussig shunts (BTS)
  • Central shunts
  • Pulmonary artery bands (PABs)

Palliative operations provide symptomatic relief but leave the basic pathophysiology uncorrected.

  • they may create the false impression that “the operation” has

been done.

  • the patient is often lost to follow-up, and the late post-op

mortality is consequently very high.

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BT shunts (and a central shunt)

Temporary palliation for defects that cannot initially be repaired

Central shunt Left BT shunt Right BT shunt

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PA band

Aorta MPA Aorta MPA LPA

Temporary palliation for defects that cannot initially be repaired

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Operations for heart defects that are “fully corrected” at the first procedure

  • Patent ductus arteriosus (PDA)
  • Coarctation of the aorta
  • Atrial septal defect (ASD)
  • Ventricular septal defect (VSD)
  • Atrioventricular septal defect (AVSD)
  • Total anomalous pulmonary venous drainage (TAPVD)
  • Transposition of the great arteries (TGA)
  • Anomalous left coronary artery from the pulmonary artery

(ALCAPA)

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End-to-end coarctation repair

Operations for heart defects that are “fully corrected” at the first procedure

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Aortic switch operation for TGA

Operations for heart defects that are “fully corrected” at the first procedure

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Aortic switch operation for TGA

Operations for heart defects that are “fully corrected” at the first procedure

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Heart defects that might require further surgery or intervention after repair

  • Tetralogy of Fallot (TOF)

– by far the most common redo procedure in adult congenital heart surgery

  • Transposition of the great arteries (TGA)
  • Ebstein’s anomaly

Mr Tim Jones Adult CHD surgery

PV replacement for Fallot

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Heart defects that will require further surgery after the initial procedure

  • Homografts

– Pulmonary atresia with VSD (PA/VSD) – Truncus arteriosus

  • Transposition with pulmonary stenosis

(TGA/PS)

  • Congenital aortic stenosis (AS)
  • Left ventricular outflow tract obstructions

(LVOTO)

  • Permanent pacemaker (PPM)
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Homograft repair (Rastelli)

Heart defects that will require further surgery after the initial procedure

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Homografts always spell trouble!

  • They do not grow with the patient
  • Complications include

– PS and PR – aneurysm formation – branch pulmonary stenoses – calcification – endocarditis – RV failure

  • They need surgical replacement every 5-

10 years!

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Long-term palliation of uncorrectable lesions: the Fontan circulation (TCPC) for functionally univentricular hearts

  • Tricuspid atresia
  • Double inlet left or right ventricle (DILV/DIRV)
  • Univentricular heart (UVH)
  • Hypoplastic left heart syndrome (HLHS)
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The Glenn shunt

Heart defects that will require further surgery after the initial procedure

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The Fontan operation

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The 10 “commandments” for a Fontan repair

  • 1. Age > 4 years
  • 2. Sinus rhythm
  • 3. Normal systemic venous return
  • 4. Normal right atrial volume
  • 5. Mean pulmonary artery pressure <15 mm Hg
  • 6. Pulmonary arteriolar resistance <4 Wood units/m2
  • 7. Pulmonary artery–aorta ratio >0.75
  • 8. Left-ventricular ejection fraction >0.60
  • 9. Competent mitral valve
  • 10. Absence of pulmonary artery distortion

Choussat A, Fontan F, Besse P (1977) Selection criteria for the Fontan

  • procedure. In: Anderson RH, Shinebourne EA (eds) Paediatric
  • cardiology. Churchill Livingstone, Edinburgh, Scotland, pp 559–566

33 years later… “It is clear from a historic perspective that total compliance with all criteria does not necessarily portend excellent long-term survival…. I suggest the following single commandment: ‘‘Thou Shalt Be Perfect!” Fontan ‘‘Ten Commandments’’ Revisited and Revised Stern H. Pediatr Cardiol (2010) 31:1131–1134

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Post-op complications of heart surgery

  • Early: usually not your problem
  • Late

– wound sepsis – pericardial effusion – pleural effusion – obstruction – endocarditis – arrhythmias – cardiac failure – liver failure – protein losing enteropathy – etc, etc…

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Specific complications

  • Shunts

blockage, seroma

  • PA bands slippage, PR, branch PA stenosis
  • Glenn

stenosis, blockage, SVC syndrome

  • Fontan

pleural effusions, liver failure

  • Tetralogy RV failure, arrhythmias
  • PA/VSD

PA stenosis, PR, RV failure

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What scar is that?

  • median sternotomy

– all bypass cases, Glenn, Fontan

  • right lateral thoracotomy

– RMBTS

  • left lateral thoracotomy

– LMBTS, coarctation, PAB

  • mini sternotomy

– pericardial effusion

  • left subcostal

– permanent pacemaker

  • right minithoracotomy

– ASD repair

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Cardiac cath interventions

1. PDA occlusion 2. PDA stenting 3. ASD occlusion 4. VSD occlusion 5. Atrial septostomy 6. Relief of PA stenosis 7. Relief of conduit stenosis 8. Coarctation of aorta stenting 9. Aortic valvuloplasty 10. Pulmonary valvuloplasty 11. RV outflow tract stenting 12. Opening obstructed shunts 13. Recruiting disconnected PAs 14. Creating or closing Fontan fenestrations 15. Occlusion of pulmonary AVMs 16. Occlusion of PAPVD 17. Occlusion of coronary cameral fistulae 18. Occlusion of carotid-jugular fistula 19. Stenting of Takayasu aortitis 20. Myocardial biopsy 21. Renal artery stenoses 22. Retrieval of foreign bodies 23. Pericardiocentesis

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In conclusion

What is a GP to do?

  • Panic
  • Treat the symptoms and signs as best you can
  • Phone a friend

– talk to them frequently

  • Maintain “ownership” of your patient

– shared care!

  • Learn to echo!

UCT PG DIPLOMA IN PAEDIATRIC CARDIOLOGY

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Shared care?

ROUTINE VISITS SIGNIFICANT EVENTS

REFERRAL TO ADULT SERVICE

Antenatal/Birth Teenage years CARDIAC CLINIC

Clinical assessment Medication (INR, ECG, Echo) rik.dedecker@uct.ac.za

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Thank you for your attention!

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The cardiac surgeon’s idea of a waiting list..

A very cute patient