HEART
TRANSPLANTATION
SURGERY
DR. MUHAMMED SHIBLY
DEFINITION
CARDIAC TRANSPLANTATION IS A THERAPEUTIC
PROCEDURE WHERE BY THE HEART OF A SUITABLE
DONOR IS IMPLANTED TO A RECIPIENT
INDICATIONS
 Cardiogenic shock requires mechanical assistance
 Refractory heart failure with continuous inotropic infusion
 Progressive symptoms with maximal therapy
 Severe symptomatic hypertrophic or restrictive cardiomyopathy
 Medically refractory angina with unsuitable anatomy for revascularisation
 life-threatening ventricular arrhythmias despite aggressive medical and
device intervention
 Cardiac tumours with low likelihood of metastasis
 Hypoplastic left heart and complex congenital heart disease
 Patient should receive max medical therapy before being
considered for transplantation i.e. they should be considered for
the alternative surgical therapies including CABG valve replacement /
repair cardiac septalplasty
 Peak VO2 (VO2 MAX) less than 10mL/kg/min
CONTRA-INDICATION
ABSOLUTE
 Systemic illness that will limits survival
despite heart transplantation
1. Neoplasm other than skin
2. HIV/AIDS
3. SLE/SARCOID that has multistage
involvement or is still active
4. Any systemic process that has high
probability of recurring in
transplanted heart
RELATIVE
 Age over 65 yrs
 PVD not amenable to surgical /
percutaneous therapy
 Ankle brachial index <0.7 or
substantial risk of limb loss with
diminished perfusion
 Asymptomatic carotid stenosis >75%
or symptomatic carotid stenosis of
less severity
 DM with end organ damage
E.g.:- nephropathy, neuropathy
ABSOLUTE
 Fixed pulmonary hypertension
1. Pulmonary vascular resistance >5
wood units
2. Trans-pulmonary gradient >15mmHg
 Age >70 years
Relative
 Severe lung disease
 Uncorrected abdominal aortic
aneurysm >4-6cm
 Systemic infection causing immune
suppression risk
1. HIV
2. Hep.B
3. CMV (+ve donor to –ve recipient )
 Psychological impairment that
jeopardizes the transplanted heart
EVALUATION OF CARDIAC
TRANSPLANTATION RECIPIENT
 Right and Left heart catheterization
 Cardiopulmonary testing
 Labs including BMP, CBC, LFT, UA, coags, TSH, UDS, ETOH level, HIV,
Hepatitis panel, PPD, CMV IgG, RPR/VDRL, PRA(panel reactive antibodies)
ABO and Rh blood type, lipid
 CXR, PFT’s including DLCO, ECG
 Substance abuse history and evidence of abstinence for at least 6 month
and enrolment in formal rehab.
 Mental health evaluation
 Financial support
 Weight no more than 140% of ideal body weight
Cardiac Donor
 Brain death is necessary for any cadaveric organ donation. This is
defined as absent cerebral function and brainstem reflexes with
apnoea during hypercapnea in the absence of any CNS
depression
 There should not be any hypothermia , hypotension , metabolic
abnormality, or drug intoxication
 If brain death is uncertain confirmation test using EEG, cerebral
flow imaging or cerebral angiography are indicated
Cardiac Donor – Exclusion Criteria
 Age older than 55 yrs .
 Serologic test positive for HIV, Hep.B/C
 Systemic infection
 Malignant tumours with metastatic potential
 Systemic comorbidity (DM, collagen vascular disease)
 Cardiac disease
 CAD
 Allograft ischemic time estimated to be >than 4-5 hrs
 Left ventricular hypertrophy or left ventricular dysfunction on echo.
 Death of carbon monoxide poisoning
 IV drug abuse
Matching Donor & Recipient
 Because of ischemic time during cardiac transplantation is crucial
DONOR – RECIPIENT MATCHING is based primarily not on HLA typing
but on the
1. Severity of illness
2. ABO typing
3. Response to PRA
4. Donor wt. to recipient ratio (must be 75%-125%)
5. Geographic location of donor
SURGICAL TRANSPLANTATION
TECH.
ORTHOTOPIC IMPLANTATION
 IT IS THE MOST COMMON
 IT INVOLVES COMPLETE
EXPLANTATION OF THE
NATIVE HEART
HETEROTOPIC IMPLANTATION
 IT IS AN ALTERNATIVE
TECH. IN WHICH THE
DONOR HEART
FUNCTIONS IN PARALLEL
WITH THE RECIPIENT
Orthotopic heart transplantation
 the recipient’s diseased heart is removed
 the donor allograft is inserted anatomically in its place
 After the sternotomy,
 The ascending aorta is cannulated close to the aortic arch, venous return
cannulae are inserted into both the superior and inferior cavae, and the
patient is placed on CPB.
 The cavae are encircled with tourniquets to isolate all of the venous
return from the heart, the ascending aorta is clamped close to the aortic
arch, and the recipient heart is then excised. There are two techniques of
orthotopic heart transplantation
 the classic or biatrial method and the bicaval method. In the classic
method, the recipient’s right atrium is divided through the body, leaving
its posterior aspect in situ
 In the bicaval method, the recipient’s entire right atrium is removed by
dividing both the inferior and superior vena cavae proximal to the atrium
 the bicaval technique may result in fewer postoperative rhythm problems
and less tricuspid regurgitation. The left atrium is divided, leaving its
posterior aspect and the pulmonary veins of the recipient in situ and the
recipient heart is removed.
 The donor heart is then placed in the pericardial well and attached to the
recipient with left atrial and right atrial (or bicaval) suture lines, and then
the donor pulmonary artery and donor ascending aorta are
anastomosed end-to-end to the recipient’s artery and aorta. When the
aortic anastomosis is completed, the aortic cross clamp is removed from
the recipient aorta, ending the ischemic time of the donor heart.
Heterotopic heart transplantation
 Heterotopic heart transplantation is a rarely performed procedure in
which the recipient’s heart remains in place, and the donor heart is
attached to its right side so that the flow in each is in parallel, permitting
the recipient’s heart to continue to pump blood, particularly through the
lungs . This procedure is
 primarily reserved for patients with pulmonary hypertension as a strategy
to avoid acute right heart failure in the unconditioned donor heart and in
cases in which there is a marked difference in size of the donor and
recipient
PHYSIOLOGICAL CINCERNS
 Biatrial connection means less atrial contribution to stroke vol.
 Resting HR is faster (95-110 bpm) and acceleration of HR is slower during
exercise bcoz. Of denervation
 Diurnal changes in BP are abolished
 Diastolic dysfunction is very common bcoz. the myocardium is stiff from
some degree of rejection and possibly from denervation
POST OPERATIVE COMPLICATION
SURGICAL
 Aortic pseudo aneurysm or rupture
at cannulation site
 Haemorrhagic pericardial effusion
due to bleeding or coagulopathy
MEDICAL
 Severe tricuspid regurgitation
 RV. Failure
1. Pulmonary artery compression
2. Pulmonary HNT
 LV. Failure
1. Ischemia
2. Operative injury
3. Acute rejection
RHYTHM DISTURBANCES
 Asystole
 Complete heart block
 Sinus node dysfunction with
bradyarrythmias
 Atrial fibrillation
 Ventricular tachycardia
RESP. FAILURE
 Cardiogenic pulmonary oedema
 Non cardiogenic pulmonary oedema
 infection
 COAGULOPATHY INDUCED BY CARDIOPULMONARY BYPASS
 RENAL OR HEPATIC INSUFFICIENCY (drugs , CHF )
POST OPERATIVE MANAGEMENT
 INITIATION OF MEDICATION, PERTICULARLY IMMUNOSUPRESSIVE
AGENTS BEGINS ON THE DAY OF OPERATION
1. CYCLOSPORINE
2. AZATHIOPRINE
3. SOLUMEDROL
4. +/- MUROMONAB-CD3 (OKT3)
 PNEUMOCYSTIS CARINII PROPHYLAXIS IS STARTED WITHIN THE FIRST
WEEK AFTER TRANSPLANTATION
 IF PATIENT / DONOR IS CMV +VE THEN GANCICLOVIR IS STRATED
 ANTICOAGULANT IS STARTED IF HETEROTOPIC TECH. HAS BEEN
PERFORMED
 ECG ARE OBTAINED IN EVERY DAY
LONG-TERM MANAGEMENT
 Cyclosporine levels are checked periodically by individual centre
protocols
 Echo. Is useful periodically and as an adjunct to endocardial biopsy
 Cardiac catheterization is performed annually for early detection of
allograft vasculopathy
 There is no need of routine exercise or nuclear stress testing.
HEART TRANSPLANTATION SUGERY
HEART TRANSPLANTATION SUGERY

HEART TRANSPLANTATION SUGERY

  • 1.
  • 5.
    DEFINITION CARDIAC TRANSPLANTATION ISA THERAPEUTIC PROCEDURE WHERE BY THE HEART OF A SUITABLE DONOR IS IMPLANTED TO A RECIPIENT
  • 6.
    INDICATIONS  Cardiogenic shockrequires mechanical assistance  Refractory heart failure with continuous inotropic infusion  Progressive symptoms with maximal therapy  Severe symptomatic hypertrophic or restrictive cardiomyopathy  Medically refractory angina with unsuitable anatomy for revascularisation  life-threatening ventricular arrhythmias despite aggressive medical and device intervention  Cardiac tumours with low likelihood of metastasis
  • 7.
     Hypoplastic leftheart and complex congenital heart disease  Patient should receive max medical therapy before being considered for transplantation i.e. they should be considered for the alternative surgical therapies including CABG valve replacement / repair cardiac septalplasty  Peak VO2 (VO2 MAX) less than 10mL/kg/min
  • 8.
    CONTRA-INDICATION ABSOLUTE  Systemic illnessthat will limits survival despite heart transplantation 1. Neoplasm other than skin 2. HIV/AIDS 3. SLE/SARCOID that has multistage involvement or is still active 4. Any systemic process that has high probability of recurring in transplanted heart RELATIVE  Age over 65 yrs  PVD not amenable to surgical / percutaneous therapy  Ankle brachial index <0.7 or substantial risk of limb loss with diminished perfusion  Asymptomatic carotid stenosis >75% or symptomatic carotid stenosis of less severity  DM with end organ damage E.g.:- nephropathy, neuropathy
  • 9.
    ABSOLUTE  Fixed pulmonaryhypertension 1. Pulmonary vascular resistance >5 wood units 2. Trans-pulmonary gradient >15mmHg  Age >70 years Relative  Severe lung disease  Uncorrected abdominal aortic aneurysm >4-6cm  Systemic infection causing immune suppression risk 1. HIV 2. Hep.B 3. CMV (+ve donor to –ve recipient )  Psychological impairment that jeopardizes the transplanted heart
  • 10.
    EVALUATION OF CARDIAC TRANSPLANTATIONRECIPIENT  Right and Left heart catheterization  Cardiopulmonary testing  Labs including BMP, CBC, LFT, UA, coags, TSH, UDS, ETOH level, HIV, Hepatitis panel, PPD, CMV IgG, RPR/VDRL, PRA(panel reactive antibodies) ABO and Rh blood type, lipid  CXR, PFT’s including DLCO, ECG  Substance abuse history and evidence of abstinence for at least 6 month and enrolment in formal rehab.  Mental health evaluation  Financial support  Weight no more than 140% of ideal body weight
  • 11.
    Cardiac Donor  Braindeath is necessary for any cadaveric organ donation. This is defined as absent cerebral function and brainstem reflexes with apnoea during hypercapnea in the absence of any CNS depression  There should not be any hypothermia , hypotension , metabolic abnormality, or drug intoxication  If brain death is uncertain confirmation test using EEG, cerebral flow imaging or cerebral angiography are indicated
  • 12.
    Cardiac Donor –Exclusion Criteria  Age older than 55 yrs .  Serologic test positive for HIV, Hep.B/C  Systemic infection  Malignant tumours with metastatic potential  Systemic comorbidity (DM, collagen vascular disease)  Cardiac disease  CAD  Allograft ischemic time estimated to be >than 4-5 hrs  Left ventricular hypertrophy or left ventricular dysfunction on echo.  Death of carbon monoxide poisoning  IV drug abuse
  • 13.
    Matching Donor &Recipient  Because of ischemic time during cardiac transplantation is crucial DONOR – RECIPIENT MATCHING is based primarily not on HLA typing but on the 1. Severity of illness 2. ABO typing 3. Response to PRA 4. Donor wt. to recipient ratio (must be 75%-125%) 5. Geographic location of donor
  • 14.
    SURGICAL TRANSPLANTATION TECH. ORTHOTOPIC IMPLANTATION IT IS THE MOST COMMON  IT INVOLVES COMPLETE EXPLANTATION OF THE NATIVE HEART HETEROTOPIC IMPLANTATION  IT IS AN ALTERNATIVE TECH. IN WHICH THE DONOR HEART FUNCTIONS IN PARALLEL WITH THE RECIPIENT
  • 15.
    Orthotopic heart transplantation the recipient’s diseased heart is removed  the donor allograft is inserted anatomically in its place  After the sternotomy,  The ascending aorta is cannulated close to the aortic arch, venous return cannulae are inserted into both the superior and inferior cavae, and the patient is placed on CPB.  The cavae are encircled with tourniquets to isolate all of the venous return from the heart, the ascending aorta is clamped close to the aortic arch, and the recipient heart is then excised. There are two techniques of orthotopic heart transplantation
  • 16.
     the classicor biatrial method and the bicaval method. In the classic method, the recipient’s right atrium is divided through the body, leaving its posterior aspect in situ  In the bicaval method, the recipient’s entire right atrium is removed by dividing both the inferior and superior vena cavae proximal to the atrium  the bicaval technique may result in fewer postoperative rhythm problems and less tricuspid regurgitation. The left atrium is divided, leaving its posterior aspect and the pulmonary veins of the recipient in situ and the recipient heart is removed.
  • 17.
     The donorheart is then placed in the pericardial well and attached to the recipient with left atrial and right atrial (or bicaval) suture lines, and then the donor pulmonary artery and donor ascending aorta are anastomosed end-to-end to the recipient’s artery and aorta. When the aortic anastomosis is completed, the aortic cross clamp is removed from the recipient aorta, ending the ischemic time of the donor heart.
  • 18.
    Heterotopic heart transplantation Heterotopic heart transplantation is a rarely performed procedure in which the recipient’s heart remains in place, and the donor heart is attached to its right side so that the flow in each is in parallel, permitting the recipient’s heart to continue to pump blood, particularly through the lungs . This procedure is  primarily reserved for patients with pulmonary hypertension as a strategy to avoid acute right heart failure in the unconditioned donor heart and in cases in which there is a marked difference in size of the donor and recipient
  • 19.
    PHYSIOLOGICAL CINCERNS  Biatrialconnection means less atrial contribution to stroke vol.  Resting HR is faster (95-110 bpm) and acceleration of HR is slower during exercise bcoz. Of denervation  Diurnal changes in BP are abolished  Diastolic dysfunction is very common bcoz. the myocardium is stiff from some degree of rejection and possibly from denervation
  • 20.
    POST OPERATIVE COMPLICATION SURGICAL Aortic pseudo aneurysm or rupture at cannulation site  Haemorrhagic pericardial effusion due to bleeding or coagulopathy MEDICAL  Severe tricuspid regurgitation  RV. Failure 1. Pulmonary artery compression 2. Pulmonary HNT  LV. Failure 1. Ischemia 2. Operative injury 3. Acute rejection
  • 21.
    RHYTHM DISTURBANCES  Asystole Complete heart block  Sinus node dysfunction with bradyarrythmias  Atrial fibrillation  Ventricular tachycardia RESP. FAILURE  Cardiogenic pulmonary oedema  Non cardiogenic pulmonary oedema  infection
  • 22.
     COAGULOPATHY INDUCEDBY CARDIOPULMONARY BYPASS  RENAL OR HEPATIC INSUFFICIENCY (drugs , CHF )
  • 23.
    POST OPERATIVE MANAGEMENT INITIATION OF MEDICATION, PERTICULARLY IMMUNOSUPRESSIVE AGENTS BEGINS ON THE DAY OF OPERATION 1. CYCLOSPORINE 2. AZATHIOPRINE 3. SOLUMEDROL 4. +/- MUROMONAB-CD3 (OKT3)
  • 24.
     PNEUMOCYSTIS CARINIIPROPHYLAXIS IS STARTED WITHIN THE FIRST WEEK AFTER TRANSPLANTATION  IF PATIENT / DONOR IS CMV +VE THEN GANCICLOVIR IS STRATED  ANTICOAGULANT IS STARTED IF HETEROTOPIC TECH. HAS BEEN PERFORMED  ECG ARE OBTAINED IN EVERY DAY
  • 25.
    LONG-TERM MANAGEMENT  Cyclosporinelevels are checked periodically by individual centre protocols  Echo. Is useful periodically and as an adjunct to endocardial biopsy  Cardiac catheterization is performed annually for early detection of allograft vasculopathy  There is no need of routine exercise or nuclear stress testing.