Anesthesia In Children With Congenital Heart Disease For Non-cardiac Surgery Regarding investigations of CHD patients for non-cardiac surgery: A- Chest X – Ray has no rule B- Cardiac Catheterization is the first choice for diagnosis of CHD C- Echocardiography non invasive method for diagnosis of CHD D- MRI has no rule IM Premedication for CHD patients presenting for non-cardiac suergery: A- Cooperative child who able to take orally B- Ketamine 1mg/kg C- Midazolam 5 mg/kg D -Glycopyrrolate or Atropine 0.02 mg/kg Procedural antibiotic prophylaxis is required in patients with A- Aortic valve replacement B- Mitral valve prolapse with regurge C- Previous history of infective endocarditis D- Ostium secundum ASD AHA guideline for antibiotic prophylaxis for genitourinary procedures: A- High risk adult patient: Ampicillin 1 g & gentamicin 1.5mg/kg i.m or i.v B- High risk Child patient: Ampicillin 5 mg/kg &gentamicin 1.5 mg/kg i.m or i.v C- Moderate risk child allergic to penicillin: Vancomycin 20 mg/kg i.v bolus D- High risk Adults allergic to penicillin: Vancomycin 1g/kg i.v over 1-2 hr Regarding using Succinylcholine in pediatric patients with CHD: A- Succinylcholine in pediatric is routine B- If used should be with atropine, to avoid tachycardia or sinus arrest C- If used with potent narcotic atropine should be used to avoid sever bradycardia in childern with Decreased cardiac reserve Postoperative Anesthetic Management of CHD patients: A- No need for supplemental O2 and maintain patent airway B- Pain decrease catech. which can affect VR and shunt direction C- Pain infundibular spasm in TOF RVOT obstruction cyanosis, hypoxia, syncope, seizures, acidosis and death D- No conduction disturbances in septal defects INTRODUCTION Due to advances in diagnosis, medical, critical and surgical care for CHD Therefore, it is common for patients with CHD to present for non-cardiac surgery, and even in patient with corrected CHD significant residual problems (arrhythmias, ventricular dysfunction, shunts, valvular stenosis, and PH) may be exist. CLASSIFICATION OF CHD I- Acyanotic congenital heart disease: 1- ASD 2- VSD 3- PDA II- Cyanotic congenital heart disease: 1- Tetralogy of Fallot, with severe right ventricular outflow obstruction 2- TGA 3- Pulmonary atresia or severe stenosis 4- Tricuspid atresia with pulmonary stenosis 5- Truncus Arteriosus ANESTHETIC MANAGEMENT Perioperative management requires a team approach CHD is polymorphic and may clinically manifest across a broad clinical spectrum The plane of Anesthetic Management includes the following: A - Preoperative Management B - Intraoperative Management C - Postoperative Management Preoperative Anesthetic Management: A- History B- physical examination C- Investigations D- Premedications E- Fasting Guidelines HISTORY & PHYSICAL EXAMINATION Assess functional status - daily activities - exercise tolerance ↓ cardiac reserve - cyanosis - respiratory distress during feeding Cyanosis Dyspnea Fainting attack Fatigue Palpitations chest pain Syncope Abdominal fullness Leg swelling Medications Vital signs Airway abnormality Associated extracardiac congenital anomalies Tachypnea, dyspnea, cyanosis Squatting Clubbing of digits Heart murmur (s) CHF: - Jugular venous distention. - Hepatomegally - Ascitis - Peripheral edema MRI Laboratory Evaluation 12 Lead ECG INVESTIGATIONS chest X – Ray Echocardiography Cardiac Catheterization Premedication Oral Premedication: - Midazolam 0.25 -1.0 mg/kg - Ketamine 2 - 4 mg/kg - Atropine 0.02 mg/kg IV Premedication: - Midazolam 0.02 - 0.05 mg/kg titrated in small increments - Ketamine 1-2 mg/kg IM Premedication: - Uncooperative or unable to take orally - Ketamine 5 – 10 mg/kg - Midazolam 0.2 mg/kg - Glycopyrrolate or Atropine 0.02 mg/kg Fasting Guidelines AHA guidelines for bacterial endocarditis Prophylaxis in patients with cardiac conditions Endocarditis prophylaxis recommended Endocarditis prophylaxis not recommended High-risk category - Complex cyanotic congenital heart disease : Transposition of the great vessels Tetralogy of Fallot - Surgically created systemic-to-pulmonary shuntsor conduits - Prosthetic, Bioprosthetic, Homograft valves - Previous bacterial endocarditis Negligible-risk category - Physiologic, or functional heart murmurs Moderate-risk category - Other congenital cardiac anomalies - Acquired valvular dysfunction - Hypertrophic cardiomyopathies - Mitral valve prolapse with valvar- Regurg - Surgical repair without residua beyond 6 months : ASD, PDA,VSD - Cardiac pacemaker or - implanted defibrillator - Isolated secundum atrial septal defect - Mitral valve prolapse without reg. - Previous coronary artery bypass surgery - Previous rheumatic heart disease without valvular dysfunction AHA guidelines for antibiotic prophylaxis: dental, oral, Respiratory tract and esophageal procedures Standard prophylaxis Amoxicillin 1 h before procedure -Children: 50 mg/kg p.o. -.Adults: 2.0 g p.o Unable to take oral medications Ampicillin within 30 min before procedure - Children: 50 mg/ kg i.m. or i.v. -.Adults: 2.0 g i.m. or i.v Allergic to penicillin Clindamycin 1 h before procedure Children: 20 mg/kg p.o. Adults: 600 mg p.o. OR Azithromycin or clarithromycin 1 h before procedure -Children: 15 mg/kg p.o. - .Adults: 500 mg p.o Unable to take oral medications AND allergic to penicillin Clindamycin within 30 min before procedur -Children: 20 mg/ kg i.v - .-Adult: 600 mg i.v. AHA guidelines for antibiotic prophylaxis: genitourinary and gastrointestinal procedures High risk patients - within 30 min before procedure - Children: Ampicillin 50 mg/ kg .and gentaicin 1.5 mg/kg i.m or i.v - Adults: Ampicillin 2.0 g and gentamicin 1.5 mg/kg i.m or i.v High risk patients Allergic to penicillin - Complete infusion 30 min before procedure - Children: Vancomycin 20 mg/kg i.v over 1-2 hr gentamicin 1.5 mg/kg i.m or i.v -Adults: Vancomycin 1g/kg i.v over 1-2 hr gentamicin 1.5 mg/kg i.m or i.v Moderate risk patients - Ampicillin within 30 min before procedure - Children: 50 mg/ kg i.m. or .iv - Adults: 2.0 g i.m or i.v Moderate risk patients AND allergic to penicillin - Complete infusion 30 min before procedure - Children: Vancomycin 20 mg/kg i.v over 1-2 hr -Adults: Vancomycin 1g/kg i.v over 1-2 hr Preoperative Anesthetic Considerations 1234- Complete history and physical examin. Review all investigations Hydration should be maintained All cardiac medication except possibly digitalis should be continued until surgery 5- Premedication should be give particularly to patients at risk for right to left shunt 6- Antibiotic prophylaxis against endocarditis must be given Anesthetic Management A - Preoperative Management B - Intraoperative Management : 1- Monitoring 2- Choice of anesthetic agent 3- Maintenance of anesthesia 4- Emergence from anesthesia Monitoring Non-invasive - Clinical observation - ECG - NIBP - Pulse oximetry on two different limbs - Precordial stethoscope - Continuous airway manometry - Multiple site temperatur measurement Invasive - Volumetric urine collection - Art. catheterization - CVP - PAC - TEE Choice of anesthetic Regimen Development of anesthetic regimen is based on various factors such as presence and direction of shunts , arrhythmia , pulmonary HF, circulation, and lowering or maintenance of PVR ● Choice of Anesthetic Agent Intravenous anesthetics Volatile anesthetics Muscle relaxants Barbiturates : Not recommended in patients with severe cardiac reserve : No in PVR in children when airway maintained & ventilation supported -Ketamine Halothane change PBF not affecting PVR, Depresses myocardial function, alters sinus node function, Sympathomimetic effects help HR, SVR,,MAP contractility sensitizes myocardium tomaintain catecholamines MAPand , HR , CI , EF Greater hemodynamic stability in hypovolemic patients Copious secretions (laryngospasm) • Desflurane Pungent , PAP and PVR, Less myocardial depression than Halothane HR , SVR Etomidate : Induction of 0.3mg/kg no change mean pulmonary artery pressure and PVR •Isoflurane Pungentdose , PAP not affecting PVR, Less in myocardial depression than Halothane, Vasodilatation leads to SVR → MAP , HR which can lead to Propofol : decrease in SBP and SVR, and increase in SBF in all patients, CI whereas HR ,PAP, PBF remained unchanged • Sevoflurane Less myocardial depression than Halothane, more in PAP compared OPIOD: Excellent induction agents in very sick children with isoflurane, No HR,avoided Mild SVR, Can produce diastolic dysfunction No cardiodepressant effects if bradycardia Fentanyl 15-25 µg/kg IV , Sufentanil 5-20 µg/kg IV • Nitrous oxide At 50% concentration does not affect PVR and PAP in children Neuromuscular Blocking Drugs Depolarizing - Succinylcholine in pediatric controversial is - If used should be with atropine, to avoid associated bradycardia or sinus arrest - also if used with potent narcotic atropine should be used avoid sever to bradycardia in children with Nondepolarizing - Atracuruim and vecronium: have few cardiovascular side effects in children when given in recommended doses. - Pancuronuim if given slowly doesn't produce HR or BP changes. if given as bolus doses it can produce tachycardia , ↑BP (through sympathomimetic effect ) -Cisatracuruim and Rocuroinuim: safe REGIONAL ANESTHESIA &ANALGESIA • Considerations : - Coarctation of aorta considerations - Childern with chronic cyanosis risk of coagulation abnormality - VD : which can: 1- be hazardous in patients with significant AS or left-sided obstructive lesions 2- Cause oxyhemoglobin saturation in R-L shunts Anesthetic Management A - Preoperative Management B - Intraoperative Management C - Postoperative Management Postoperative Anesthetic Management Supplemental O2 and maintain patent airway. In patients with single ventricle titrate SaO2 to 85%. Higher oxygen sat. can PVR PBF SBF Pain catech. which can affect VR and shunt direction Pain infundibular spasm in TOF RVOT obstruction cyanosis, hypoxia, syncope, seizures, acidosis and death Anticipate conduction disturbances in septal defects SUMMARY Familiarity with the CHD pathophysiology, adequate preoperative preparation, choice of monitors, induction, maintenance , emergence from anesthesia, and plans for the postoperative period to avoid major problems in anesthetic management A wide variety of anesthetic regimens is used for patients with congenital heart disease (CHD) undergoing cardiac or non-cardiac surgery, or other diagnostic or therapeutic procures. The goal of all of these regimens is to produce anesthesia or adequate sedation, while preserving systemic cardiac output and oxygen delivery Regarding investigations of CHD patients for non-cardiac surgery: A- Chest X – Ray has no rule B- Cardiac Catheterization is the first choice for diagnosis of CHD C- Echocardiography non invasive method for diagnosis of CHD D- MRI cannot give us idea about pulmonary veins IM Premedication for CHD patients presenting for non-cardiac suergery: A- Cooperative or unable to take orally B- Ketamine 1mg/kg C- Midazolam 5 mg/kg D -Glycopyrrolate or Atropine 0.02 mg/kg Procedural antibiotic prophylaxis is required in patients with A- Aortic valve replacement B- Mitral valve prolapse with regurge C- Previous history of infective endocarditis D- Ostium secundum ASD AHA guideline for antibiotic prophylaxis for genitourinary procedures: A- High risk adult patient: Ampicillin 1 g & gentamicin 1.5mg/kg i.m or i.v B- High risk Child patient: Ampicillin 5 mg/kg &gentamicin 1.5 mg/kg i.m or i.v C- Moderate risk child allergic to penicillin: Vancomycin 20 mg/kg i.v bolus D- High risk Adults allergic to penicillin: Vancomycin 1g/kg i.v over 1-2 hr Regarding using Succinylcholine in pediatric patients with CHD: A- Succinylcholine in pediatric is routine B- If used should be with atropine, to avoid tachycardia or sinus arrest C- If used with potent narcotic atropine should be used to avoid sever bradycardia in children with Decreased cardiac reserve Postoperative Anesthetic Management of CHD patients: A- No need for supplemental O2 and maintain patent airway B- Pain decrease catech. which can affect VR and shunt direction C- Pain infundibular spasm in TOF RVOT obstruction cyanosis, hypoxia, syncope, seizures, acidosis and death D- No conduction disturbances in septal defects