Anesthesia+CHD+Non+Cardiac+Surgery

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    Anesthesia for noncardiac surgery in

    children with congenital heart disease

    Sheila Espina-Bertoso MD, DPBA

    University of the Philippines-PGH

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    Introduction

    Decades of advancement in diagnostic and interventional

    cardiology, surgical techniques, cardiopulmonary bypass,

    anesthetic management, and critical care have dramatically

    altered the natural history of congenital heart disease(CHD).

    This resulted to a decrease in morbidity and mortality inaffected children and improved quality of life.

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    Introduction

    Anesthesiologists will encounter children with CHD for

    elective non-cardiac surgery at one of three stages:

    Unpalliated

    Partially palliated

    Completely palliated

    ASD and PDA only congenital lesions

    that can be truly corrected

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    Increase in life expectancy leads to increased survival

    rates

    In some cases, children may require noncardiac surgery

    before undergoing procedures to repair their cardiovascular

    pathology.

    Introduction

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    Objective

    Review general principles of anesthetic practice with afocus on preoperative assessment, intraoperative

    management, and postoperative care for children with CHD

    having noncardiac surgery.

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    Pre-operative Assessment

    50% Dx by 1st week of life; rest by 5 years

    Childs diagnosis & current medical condition will determinepreoperative evaluation

    Understand the anatomic and hemodynamic function ofchilds heart

    Discuss case with pediatrician and cardiologist

    Review diagnostic & therapeutic interventions

    Above will estimate disease severity and help formulateanesthetic plan

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    Preoperative Assessment

    Gather information regarding the nature of the

    cardiovascular disease and prior therapeutic interventions.

    Determine functional status.

    The history and physical examination, in addition to the

    laboratory data and ancillary tests provide complementaryinformation.

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    Preoperative Assessment

    Based on this clinical assessment and consideration of the

    major pathophysiologic consequences, a systematic,

    detailed, organized plan should be formulated for

    anesthetic and perioperative management.

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    History and Physical Examination

    History should focus on the status of the cardiovascular

    system.

    Relevant information includes

    the type of CVD and comorbid conditions

    medications

    allergies

    prior hospitalizations, surgeries, anesthetic

    experiences, and complications elective cases.

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    History and Physical Examination

    Symptomatology

    tachypnea, dyspnea, tachycardia, dysrhythmias, and

    fatigue should be sought.

    feeding difficulties and diaphoresis may represent

    significant symptoms in infants

    decreased activity level orexercise intolerance may be

    of concern in older children palpitations, chest pain, and syncope should be

    characterized.

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    History and Physical Examination

    Should include an assessment of growth and development

    History ofrecent illnesses such as respiratory infections orpulmonary disease

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    Physical Examination

    Physical Examination

    weight and height

    vital signs: HR, RR, O2 sat, BP.ex1: In general, children who have undergone definitive procedures

    should be expected to have normal to near-normal SpO2(95%).After

    palliative interventions, SpO2 values typically range between 75% and

    85%.

    ex2: For those aortic arch obstruction or has had any systemic-to-

    pulmonary shunt, upper and lower extremity as well as right and left

    upper extremity blood pressure and palpation of the quality of pulses

    should be documented.

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    Physical Examination

    Airway

    General appearance

    - child's level of activity- breathing pattern

    - level of distress and presence of cyanosis

    Respiratory evaluation

    - quality of the breath sounds

    - the presence or absence of labored breathing,

    - intercostal retractions, wheezing, rales, or rhonchi..

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    Physical Examination

    Cardiac Examination

    assessment of heart sounds, pathologic murmurs, and

    gallop rhythms

    presence of a thrill, representing a palpable murmur,

    should be noted

    GI Examination- Hepatosplenomegaly

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    Physical Examination

    Extremities should include examination of pulses, overall

    perfusion, capillary refill, cyanosis, clubbing, and edema.

    Noncardiac anomalies or pathology that may affect

    anesthetic care (e.g., a specific syndrome complex, a

    potentially difficult airway, gastroesophageal reflux) should

    be noted.

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    Ancillary Studies and Laboratory Data

    In cyanotic children, CBC provides the determination of

    polycythemia, microcytic anemia, and thrombocytopenia.

    Prothrombin time, partial thromboplastin times, and

    international normalized ratio (INR) provide an indication of

    clotting ability

    In those receiving diuretic therapy, digoxin, or angiotensin-

    converting enzyme inhibitors, the determination of serum

    electrolytes may be useful.

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    Ancillary Studies and Laboratory Data

    Blood typing and crossmatching

    A recent ECG should be reviewed for changes from priorstudies.

    Exercise tolerance test or treadmill study

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    Ancillary Studies and Laboratory Data

    Review of a recent chest Xray, including a lateral view,

    provides information regarding cardiac size, chamber

    enlargement, and pulmonary vascularity.

    Recent echocardiogram, cardiac catheterizations,

    electrophysiologic procedures, and magnetic resonance

    imaging should be reviewed.

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    Goal of Pre-operative Evaluation

    The goals of the preoperative evaluation is to obtain the

    most diagnostic information with the fewest tests and theleast risk, discomfort, and expense to the child.

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    Intraoperative Management

    Premedication

    Should be routine.

    This facilitates parental separation, entry into the operating

    room, placement of monitors, and induction of anesthesia.

    Commonly used premedications include oral or intravenous

    benzodiazepines, opioids, and small amounts of hypnotic

    agents.

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    Premedication

    a) Omit for infants < six months of age

    b) Administer under direct supervision of Anesthesiologist inpreoperative facility

    c) Oxygen, ventilation bag, mask and pulse oximetryimmediately available

    d) Oral Premedication

    Midazolam 0.25 -1.0 mg/kg

    Ketamine 2 - 4 mg/kg

    Atropine 0.02 mg/kg

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    Premedication

    e) IV Premedication

    Midazolam 0.02 - 0.05 mg/kg titrated in small

    increments

    f) IM Premedication

    Uncooperative or unable to take orally

    Ketamine 1-2 mg/kg

    Midazolam 0.2 mg/kg

    Glycopyrrolate or Atropine 0.02 mg/kg

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    Intravenous Access

    To secure a good intravenous access is mandatory for administration

    of fluids and medications during anesthetic care.

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    Intravenous Access

    Regarding:

    Size of the intravenous catheter

    Central venous access

    Air in the intravenous infusion tubing.

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    Emergency Drugs

    In view of the potential for hemodynamic instability in some

    children with CHD that may occur at any time, drugs for

    emergency situations should be prepared or immediately

    available to the anesthesiologist.

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    Monitoring

    Basic monitoring involves observation of the child, including

    skin color, capillary refill, respiration, pulse palpation,

    events on the surgical field, and color of shed blood.

    Standard noninvasive monitors

    blood pressure

    electrocardiography (5-lead) pulse oximetry

    capnography

    temperature monitoring

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    Monitoring

    Electrocardiography

    An ECG is used to monitor heart rate, cardiac rhythm, and

    ST-segment analysis. Usually one or multiple leads are

    displayed.

    Most systems use two leads: standard lead II and lead V5.

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    Monitoring

    Pulse Oximetry

    Placement is often well tolerated

    One of the earliest monitors applied during anestheticinduction.

    Indicate the adequacy of peripheral perfusion and cardiac

    output.[

    http://www.expertconsultbook.com/expertconsult/b/linkTo?type=bookPage&isbn=978-1-4160-3134-5&eid=4-u1.0-B978-1-4160-3134-5..50025-1--bib61&appID=NGEhttp://www.expertconsultbook.com/expertconsult/b/linkTo?type=bookPage&isbn=978-1-4160-3134-5&eid=4-u1.0-B978-1-4160-3134-5..50025-1--bib61&appID=NGE
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    Monitoring

    Capnography

    To confirm proper placement of the ETT

    To assess adequacy of ventilation

    To recognize certain pathologic conditions such as

    bronchospasm, airway obstruction, and malignant

    hyperthermia.

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    Monitoring

    Temperature Monitoring

    Watch out for hypothermia

    This may influence oxygen delivery (increased oxygen

    consumption) and emergence from anesthesia, cause

    detrimental changes in hemodynamics, and affect

    hemostasis.

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    Monitoring

    Urinary Output Measurements

    Useful index of the adequacy of renal perfusion and cardiac

    output esp during cases involving major fluid shifts or bloodloss, or long surgical procedures.

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    Monitoring

    Precordial stethoscope can be extremely helpful to

    monitor for changes in heart tones that may suggest

    early hemodynamic compromise.

    Invasive monitoring (A-line) may be needed depending

    on the level of monitoring required is influenced by the

    child's cardiovascular pathology, clinical condition andfunctional status, and the complexity and duration of the

    surgery or procedure being performed.

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    Monitoring

    PDA

    Pulse oximetry right hand to measure pre-ductal

    oxygenation

    2nd probe on toe to measure post-ductal oxygenation

    COARCTATION OF AORTA

    Pulse oximeter on right upper limb

    Pre and post - coarctation blood pressure cuffs should

    be placed

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    Anesthetic Technique

    No specific formula or recipe.

    The anesthetic techniques and agents used for a particular

    situation should be selected in consideration of the

    procedure to be performed

    the child's disease process and functional status

    factors such as age, physical characteristics, and

    preferences of the anesthesiologist must be taken intoconsideration.

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    Anesthetic Technique

    The primary goals of anesthetic management with respect

    to the cardiovascular system are

    to optimize systemic oxygen delivery

    maintain ventricular function within expected parameters

    for the individual patient

    ensure the adequacy of cardiac output.

    always keep in mind a potential decreasedcardiovascular reserve and reduced tolerance for

    perioperative stress.

    to do a carefully titrated anesthetic, regardless of the

    specific agents.

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    Anesthetic technique

    General Anesthesia

    Advantage

    widely accepted

    ease of application

    certainty of effect

    the appropriate choice for most children undergoing

    noncardiac surgery

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    General Anesthesia

    DISADVANTAGES

    - a greater potential for wide fluctuations in the

    hemodynamics

    - prolonged recovery period.

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    Regional Anesthesia

    Demonstrated to be safe and effective in children with CHD

    ADVANTAGES

    effect is limited to the surgical site

    decreased number of systemic medications

    potentially shorter overall recovery period

    a more pleasant experience for the child.

    may be used for post-op pain mangement

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    Regional Anesthesia

    DISADVANTAGE

    Its use is limited in small children and may not always be

    effective.

    There is also the potential for hemodynamic compromise,

    particularly in hypovolemic children or those with a fixed cardiac

    output, and is contraindicated in those with coagulation defects.

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    Inhalational Agents

    Halothane was considered for many decades the primary

    agent for inhalation induction in children in combination with

    oxygen and nitrous oxide.

    However, with the introduction of sevoflurane in the mid

    1990s, it has replaced halothane for induction of anesthesia

    in many centers.

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    Inhalational Agents

    The safety and efficacy of halothane vs sevoflurane in

    infants and children with CHD during cardiac surgery.

    Sevoflurane provides better hemodynamic stability

    minimal impact on myocardial performance

    advocated as the preferred anesthetic for children withheart disease.

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    Inhalational Agents

    NITROUS OXIDE

    Enlarge intravascular air emboli

    May cause microbubbles and macrobubbles to expand

    obstruction to blood flow in arteries and capillaries

    In shunts, potential for bubbles to be shunted into systemic

    circulation

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    IM & IV ANESTHETICS

    KETAMINE No change in PVR in children when airway maintained &

    ventilation supported

    Sympathomimetic effects help maintain HR, SVR, MAPand contractility

    Greater hemodynamic stability in hypovolemic patients

    Increases SVR, not recommended for L-R shunt CHD

    Copious secretions laryngospasm atropine orglycopyrrolate

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    IM & IV ANESTHETICS

    KETAMINE

    Relative contraindications may be coronary insufficiencycaused by:

    anomalous coronary artery severe critical AS

    hypoplastic left heart syndrome with aortic atresia

    hypoplasia of the ascending aorta Above patients prone to VF d/t coronary insufficiency d/tcatecholamine release from ketamine

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    IM & IV ANESTHETICS

    IM Induction with Ketamine:

    Ketamine 5 mg/kg

    Succinylcholine 5 mg/kg or Rocuronium 1.5 2.0 mg/kg

    Atropine or Glycopyrrolate 0.02 mg/kgIV Induction with Ketamine:

    Ketamine 1-2 mg/kg

    Succinylcholine 1-2 mg/kg or Rocuronium 0.6-1.2 mg/kg

    Atropine or Glycopyrrolate 0.01 mg/kg

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    IM & IV ANESTHETICS

    OPIOIDS & BENZODIAZEPINE

    Excellent induction agents in very sick children

    Blunt the stress response in the pulmonary circulation

    elicited by airway manipulations and at the same timeprovide sedation and amnesia.

    No cardiodepressant effects if bradycardia avoided

    Fentanyl 25-100 g/kg IV

    Midazolam 0.05-0.1 mg/kg

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    IM & IV ANESTHETICS

    ETOMIDATE

    CV stability

    0.3 mg/kg IV

    Pain on injection & myoclonic movements

    THIOPENTAL & PROPOFOL

    Not recommended in patients with severe cardiac

    defects In moderate cardiac defects:

    Thiopental 1-2 mg/kg IV or Propofol 1-1.5 mg/kg IV

    Patient euvolemic

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    Induction of Anesthesia

    Techniques:

    1. Intravenous: preferred technique because of greater

    margin of safety

    2. Inhalational: should be carefully titrated, but generally safe

    even with patients with moderate hemodynamic issues

    3. IM: Ketamine: uncooperative, devt delayed px

    4. Intranasal, Rectal and Subcutaneous: less common

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    Anesthetic Management

    ANESTHESIA INDUCTION

    Myocardial function preserved IV or inhalational

    techniques suitable

    Severe cardiac defects IV induction

    Modify dosages in patients with severe failure

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    Maintenance of Anesthesia

    Inhalation or intravenous technique.

    A combination of inhalational and intravenous anesthetics

    (opioid and muscle relaxant) is frequently used.

    The same inhalational agent administered for induction

    may be continued or a different anesthetic or technique

    may be selected for maintenance.

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    Emergence

    Most children undergoing noncardiac surgical interventions

    are expected to awaken immediately at the completion of

    the procedure .

    This usually involves reducing and then discontinuing

    intravenous or inhalational anesthetics, antagonizing

    neuromuscular blockade, and removing the endotrachealtube, if present.

    l f f

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    Classification of CHD

    A. L-R shunt

    B. R-L Shunt

    C. Complex Shunts

    D. Obstructive Lesions

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    A. L-R Shunts

    L - R SHUNTS INCLUDE :

    ASD 7.5% of CHD

    VSD COMMONEST CHD 25%

    PDA 7.5% of CHD

    Common in premature infants

    ENDOCARDIAL CUSHION DEFECT - 3%

    Often seen with trisomy 21

    AORTOPULMONARY WINDOW

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    L-R Shunts

    L R SHUNTS

    Defects connecting arterial & venous circulation

    SVR > PVR PBF

    pulmonary blood flow pulmonary congestion

    CHF

    Long standing L-R shunts PHT

    PVR > SVR R-L shunt Eisenmengers syndrome

    V

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    SVR?

    Systemic Vascular Resistance

    Systemic vascular resistance (SVR) refers to the resistance

    to blood flow offered by allof the systemic vasculature,

    excluding the pulmonary vasculature.

    SVR = (MAP - CVP) CO

    http://www.cvphysiology.com/Blood%20Pressure/BP019.htmhttp://www.cvphysiology.com/Blood%20Pressure/BP019.htm
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    VENTRICULAR SEPTAL DEFECT

    h d

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    Anesthetic Considerations:

    L - R SHUNTS :

    Continuous dilution in pulmonary circulation

    may onset time of IV agents

    Speed of induction with inhalation agents

    not affected unless CO is significantly

    reduced

    Degree of RV overload and/or failureunderappreciated careful induction

    h d

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    Anesthetic Considerations

    L-R SHUNTS :

    GOAL = SVR and PVR L-R shunt

    PPV & PEEP increases PVR Ketamine increases SVR

    Inhalation agents decrease SVR

    h

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    B. R-L Shunts

    Defect between R and L heart

    PVR> SVR

    Resistance to pulmonary blood flow PBF

    hypoxemia and cyanosis

    Goal: Increase SVR

    A h i id i

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    Anesthetic Considerations

    R-L SHUNTS :

    GOAL : PBF by SVR and PVR

    PVR & SVR PBF

    Hypoxemia/atelectasis/PEEP

    Acidosis/hypercapnia

    HCT

    Sympathetic stimulation & surgical stimulation

    Vasodilators & inhalation agents SVR

    B R L Sh

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    B. R-L Shunt

    TOF 10% of CHD, commonest R-L shunt

    PULMONARY ATRESIA

    TRICUSPID ATRESIA

    EBSTEINS ANOMALY

    T l f F ll

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    Tetralogy of Fallot

    10% of all CHD

    Most common R L shunt

    4 anomalies:

    RVOT obstruction ( infundibular, pulmonic or

    supravalvular stenosis )

    Subaortic VSD

    Overriding aorta

    RVH

    T t l f F ll t

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    Tetralogy of Fallot

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    T t S ll (h ti i d )

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    Tet Spells (hypercyanotic episodes)

    Result from decreased pulmonary blood flow in children

    with significant dynamic right ventricular outflow tract

    obstruction.

    Relatively rare during noncardiac surgery, probablybecause GA attenuates the triggers.

    Factors that decrease systemic blood pressure and

    systemic vascular resistance such as hypovolemia andextreme vasodilation should be avoided.

    T t S ll

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    Tet Spells

    MANAGEMENT

    1. Increasing blood volume

    2. Increase inspired oxygen concentrations

    3. Increase systemic vascular resistance, often with

    phenylephrine

    4. Lower inspiratory ventilatory pressures may also lead to

    clinical improvement.5. Increase the level of sedation or anesthetic depth and -

    adrenergic blockade.

    T t l f F ll t

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    Tetralogy of Fallot

    Treatment of Hypercyanotic Spells

    High FiO2 pulmonary vasodilator PVR

    Hydration (fluid bolus) opens RVOT

    Morphine (0.1mg/kg/dose) sedation, PVR

    Ketamine SVR, sedation, analgesia PBF

    Phenylephrine (1mcg/kg/dose) SVR

    -blockers (Esmolol 100-200mcg/kg/min)

    HR,-ve inotropy improves flow across obstructed

    valve & infundibular spasm

    A th ti C id ti

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    Anesthetic Considerations

    PVR & SVR PBF

    Hyperoxia/Normal FRC

    Alkalosis/hypocapnia

    Low HCT

    Low mean airway pressure

    Blunted stress response

    Nitric oxide/ pulmonary vasodilators

    A th ti C id ti

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    Anesthetic Considerations

    RL SHUNTS :

    Adequate hydration esp. if HCT > 50%

    Inhalation induction prolonged by limited pulmonary

    blood flow

    IV induction times are more rapid d/t bypassing

    pulmonary circulation dilution

    Avoid PEEP and PPV increase PVR

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    Complex Shunts

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    Complex Shunts

    COMPLEX SHUNTS INCLUDE :

    TRUNCUS ARTERIOSUS

    TRANSPOSITION OF GREAT VESSELS 5%

    Arterial switch procedure > 95% survival TOTAL ANOMALOUS PV RETURN

    DOUBLE OUTLET RIGHT VENTRICLE

    HYPOPLASTIC LEFT HEART SYNDROME

    Most common CHD presenting 1st week of life

    Most common cause of death in 1st month of life

    T tal A al P l ar V R t r

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    Total Anomalous Pulmonary Venous Return

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    Hupoplastic Left Heart Syndrome

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    Hupoplastic Left Heart Syndrome

    Transposition of Great Vessels

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    Transposition of Great Vessels

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    Double Outlet Right Ventricle

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    Double Outlet Right Ventricle

    Fontan Procedure

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    Fontan Procedure

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    Jantene Procedure

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    Jantene Procedure

    Anesthetic Considerations

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    Anesthetic Considerations

    COMPLEX SHUNTS : Manipulating PVR or SVR to PBF will:

    Not improve oxygenation

    Worsen biventricular failure

    Steal circulation from aorta and cause

    coronary ischemia

    Maintain status quo with high dose opioidsthat do not significantly affect heart rate,

    contractibility, or resistance is recommended

    Anesthetic Considerations

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    Anesthetic Considerations

    COMPLEX SHUNTS :

    Short procedures :slow gradual induction with low dose

    Sevoflurane has least effect on +ve chronotropy & SVR

    Nitrous Oxide limits FiO2 & helps prevent coronary steal& sevoflurane requirements

    D Obstuctive Lesions

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    D. Obstuctive Lesions

    OBSTRUCTIVE LESIONS

    Either valvular stenosis or vascular bands

    perfusion & pressure overload of corresponding

    ventricle CHF common

    Right sided obstructions PBF hypoxemia andcyanosis

    Left sided obstructions systemic blood flow tissue hypoperfusion, metabolic acidosis and shock

    Classification of CHD

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    Classification of CHD

    OBSTRUCTIVE LESIONS INCLUDE : AORTIC STENOSIS

    MITRAL STENOSIS

    PULMONIC STENOSIS COARCTATION OF AORTA 8% of CHD

    80% have bicuspid aortic valve

    COR TRIATRIATUM INTERRUPTED AORTIC ARCH

    Coarctation of Aorta

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    Coarctation of Aorta

    Interuption of Aortic Arch

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    Interuption of Aortic Arch

    Cor Triatiatium

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    Cor Triatiatium

    Anesthetic Considerations

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    Anesthetic Considerations

    OBSTRUCTIVE LESIONS

    Lesions with > 50 mmHg pressure gradient + CHF

    opioid technique

    Optimize preload improves flow beyond lesion

    Avoid tachycardia myocardial demand & flow

    beyond obstruction

    Inhalation agents -ve inotropy & decrease SVRworsens gradient & flow past obstruction

    Classification of CHD

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    Classification of CHD

    Classification of CHD

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    Classification of CHD

    Postoperative Management

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    Postoperative Management

    Children with CHD are very susceptible to:

    i. Deleterious effects of hypoventilation

    ii. Mild decreases in oxyhemoglobin saturation

    Therefore, give supplemental O2 and maintain patent

    airway

    In patients with single ventricle titrate SaO2 to 85%.

    Higher oxygen saturations can PVR PBFsystemic blood flow

    Postoperative Management

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    Avoid significant hypoventilation during this time because

    this may negatively affect pulmonary vascular tone and

    overall hemodynamics in vulnerable children.

    Analgesia is very important postoperatively Pain catecholamines which can affect vascular

    resistance and shunt direction

    Pain

    infundibular spasm in TOF

    RVOT obstruction cyanosis, hypoxia, syncope, seizures, acidosis and

    death

    Anticipate conduction disturbances in septal defects

    Postoperative Management

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    Thank You!

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