Pediatric Anesthesia Practice

Pediatric Anesthesia Practice

by Ronald Litman
ISBN-10:
0521709377
ISBN-13:
9780521709378
Pub. Date:
07/30/2007
Publisher:
Cambridge University Press
ISBN-10:
0521709377
ISBN-13:
9780521709378
Pub. Date:
07/30/2007
Publisher:
Cambridge University Press
Pediatric Anesthesia Practice

Pediatric Anesthesia Practice

by Ronald Litman

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Overview

Cambridge Pocket Clinician / Pediatric Anesthesia is designed to be a vital point-of-care guide to aid the clinician in the care of children in the perianesthetic period. It is a condensed and practical approach to the patient management, showcasing consistent standards that have been tested at the leading children’s hospitals world-wide. It is divided into three main sections: surgical procedures, co-existing diseases, and regional anesthesia

Product Details

ISBN-13: 9780521709378
Publisher: Cambridge University Press
Publication date: 07/30/2007
Series: Cambridge Pocket Clinicians
Pages: 230
Product dimensions: 4.92(w) x 7.01(h) x 0.39(d)

Read an Excerpt

Pediatric anesthesia practice
Cambridge University Press
978-0-521-70937-8 - Pediatric Anesthesia Practice - Edited by Ronald S. Litman, DO. and FAAP
Excerpt



PART ONE

Coexisting Diseases





ANTERIOR MEDIASTINAL MASS

PAUL STRICKER, MD

BACKGROUND

■  Most common cause: lymphoma

■  Suspect in pts presenting for cervical mass biopsy.

■  Other dxs: neuroblastoma, teratoma, germ cell tumor, bronchogenic cyst, foregut cyst, lymphangioma, mesenchymal tumor

■  Symptoms due to compression of anatomic structures

■  Symptoms worse when supine

■  Symptoms may be relieved by lateral or upright position.

■  Clinical: cough, hoarseness, dyspnea, wheezing, orthopnea, stridor, chest pain, syncope, SVC syndrome, tracheal deviation, retractions

■  Asymptomatic or nonspecific: fever, fatigue, weight loss


PREOPERATIVE ASSESSMENT

■  Preoperative radiation tx may interfere with accuratehistologic dx & optimal tx regimens.

■  Physical exam: orthopnea, tracheal deviation, jugular venous distention, wheezing, retractions, unilateral decreased breath sounds

■  CXR: tracheal deviation, tracheal compression, abnormal cardiothymic silhouette

■  Echo: direct compression of cardiac chambers and/or great vessels, pericardial effusion

■  CT: assess severity & location of tracheal compression

■  Preop sedation: avoid or give in monitored setting

■  Antisialagogue (e.g., glycopyrrolate) useful

■  Obtain Ⅳ access prior to OR, ideally in lower extremity.

■  Correct preexisting dehydration or hypovolemia.


INTRAOPERATIVE MANAGEMENT

■  Potential catastrophic airway or cardiovascular collapse during induction of anesthesia

■  Monitors: std; A-line for great vessel or cardiac compression

■  All sized endotracheal tubes and rigid bronch immed avail in OR

■  For severe cases, ECMO or CPB stand-by

■  Liberal fluid administration if great vessel/cardiac compression

■  Position: semi-recumbent, sitting, or lateral

■  Local anesthesia without sedation is safest strategy, but not feasible for small children.

■  Most important to avoid airway/CV collapse: MAINTAIN SPONTANEOUS VENTILATION

■  Mask or LMA OK

■  Ketamine allows spontaneous ventilation & provides sympathetic stimulation.

■  Sevoflurane or Ⅳ agents OK if titrated to avoid apnea

■  Paralysis & controlled ventilation OK for mild cases, but no way to predict safety

■  Tx of airway obstruction: positive pressure, change position to lateral, sitting or prone if CV arrest

■  Rigid bronch may bypass airway obstruction.

■  ECMO or CPB as lifesaving measure


POSTOPERATIVE CONCERNS

■  Airway obstruction may occur postop during recovery.

■  Recover in lateral or semi-recumbent position.

■  Titrate opioids: avoid apnea.


ASTHMA

SANJAY M. BHANANKER, MD, FRCA

BACKGROUND

■  Incidence: 7–19%

■  Cause: chronic inflammation & mucus hypersecretion of lower airways

■  Symptoms: airway hyperreactivity with variable degrees of airflow obstruction

■  Strong association with atopy and allergy


PREOPERATIVE ASSESSMENT

■  Note severity and frequency of acute exacerbations, precipitating factors.

■  Elicit history of drug therapy, especially systemic steroids, to gauge severity.

■  If acute exacerbation or URI within 6 wks, consider postponing elective surgery.

■  Premed: inhaled beta-2 agonist, steroids (daily meds)

■  Anxiolysis with oral midazolam; fear, stress, excitement, or hyperventilation can provoke acute attack


INTRAOPERATIVE MANAGEMENT

■  Mask induction with sevoflurane or IV induction with propofol or ketamine

■  Minimize airway manipulation.

■  Face mask or LMA preferred

■  Avoid histamine-releasing drugs: thiopental, morphine, mivacurium, succinylcholine.

■  All volatile anesthetic drugs, propofol and ketamine are bronchodilators.

■  Administer stress dose of Ⅳ hydrocortisone if pt on oral prednisone.

■  If intraoperative wheezing occurs:

   i. Rule out kinked ET tube or bronchial intubation

   ii. Give 100% oxygen, deepen anesthesia with propofol, ketamine, or volatile agents

   iii. IV lidocaine 0.5–1 mg/kg bolus

   iv. Use low respiratory rate and long expiratory time to avoid intrinsic PEEP

   v. Nebulized beta-2 agonist such as albuterol via ET tube or LMA


POSTOPERATIVE CONCERNS

■  Deep extubation for pts with uncomplicated airway avoids risk of bronchospasm during emergence.

■  If awake extubation planned, nebulized prophylactic beta-2 agonist, IV lidocaine

■  Humidify supplemental oxygen, ensure adequate systemic hydration: dry anesthetic gases and O2 are potential triggers for asthma.


ATRIAL SEPTAL DEFECT (ASD)

LUIS M. ZABALA, MD

DISEASE CHARACTERISTICS

■  Definition: opening in the atrial septum except patent foramen ovale (PFO)

■  7–10% of all CHD

■  Incidence of PFO in adults: 25%

■  Pathophys: extra load on right side of the heart (L to R shunt)

■  Magnitude of shunt relates to size of defect, ventricular compliance, & pulmonary artery pressures.

■  L to R shunt: RA & RV enlargement

■  Pulmonary vascular changes develop from long-standing volume overload.

■  Majority of pts are asymptomatic during childhood.

■  In adulthood, extra load on RV leads to CHF, failure to thrive, recurrent respiratory infections, & symptomatic supraventricular dysrhythmias.

■  Pulm htn in up to 13% of nonoperated pts


PREOPERATIVE ASSESSMENT

■  CXR: RA & RV enlargement.

■  ECG: right or left axis deviation possible; incomplete RBBB from stretch in right bundle of His

■  Echo: secundum or primum defect; mitral regurg from anterior leaflet cleft.

■  Ventricular dysfunction possible from long-standing volume overload

■  Cardiology consultation for symptomatic pts

■  Premed: PO midazolam (0.5 mg/kg) or PO pentobarbital (4 mg/kg)

■  Caution with oversedation & hypoventilation: can worsen PVR & RV fn


INTRAOPERATIVE MANAGEMENT

■  Std monitors during noncardiac surgery or transcatheter closure of ASD

■  Symptomatic or complicated pts may require additional monitoring.

■  Intracardiac surgical repair requires extracorporeal circulation and arterial invasive monitoring.

■  Central venous monitoring at discretion of anesthesiologist

■  Transesophageal echo helpful to assess de-airing of left heart & adequacy of surgical repair

■  Inhalation induction generally safe

■  Inhalation agents, narcotics, muscle relaxants, and/or re-gional anesthesia usually well tolerated

■  De-bubble all Ⅳ lines.

■  Atrial dysrhythmias common in adult unrepaired pt


POSTOPERATIVE CONCERNS

■  Immediate or early tracheal extubation possible following uncomplicated surgical repair of ASD

■  Pts with good ventricular function prior to repair do not require inotropic support.

■  Dopamine 3–5 mcg/kg/min usually sufficient for ventricular dysfunction

■  Pulm htn may occur in older pts after ASD repair; use aggressive ventilation & milrinone.

■  Pts with unrepaired ASD undergoing noncardiac surgery should be monitored closely for CHF due to volume overload or atrial dysrhythmias.

■  Titrate analgesia to pain control without vent depression.


CEREBRAL PALSY

NATHALIA JIMENEZ, MD, MPH

BACKGROUND

■  Definition: static motor encephalopathy

■  Secondary to perinatal or early childhood (<2 yr) CNS injury

■  Incidence 2.4 per 1,000 live births

■  4 categories: spastic (quadriplegia, diplegia, hemiplegia), dyskinetic (dystonia, athetosis, chorea), ataxic (tremor, loss of balance, speech involvement), mixed

■  Assoc with developmental delay, visual & cognitive abnormalities, & motor problems possible with normal cognitive function

■  Require multiple surgeries: mainly orthopedic (spinal fusion and release of limb contractures)

■  Bulbar motor dysfunction predisposes to GE reflux, swallowing disorders & loss of airway protective mechanisms leading to chronic aspiration, recurrent pneumonia, hyperactive airways

■  Seizures in 30%: continue anticonvulsant on day of surgery & reinstitute early in postop period

■  Baclofen used for muscle spasms, can cause urinary retention & leg weakness

■  Abrupt baclofen withdrawal may cause seizures; overdose assoc with decreased consciousness & hypotension


PREOPERATIVE ASSESSMENT

■  Premedication tolerated in most pts; reduce dose or avoid if hypotonic

■  Anticholinergic will decrease secretions in pts with bulbar dysfunction.


INTRAOPERATIVE MANAGEMENT

■  Contractures make positioning and Ⅳ access difficult.

■  Impaired temp regulation due to hypothalamic dysfunction

■  Monitor temperature and use warming measures.

■  Inhalation induction safe unless severe reflux

■  Increased sensitivity of succinylcholine: use only in emergency situations

■  Decreased sensitivity to non-depolarizing muscle relaxants: requires higher doses

■  Increased sensitivity to inhaled anesthetics and opioids: use lower doses

■  Awake extubation in OR


POSTOPERATIVE CONCERNS

■  Pain assessment difficult due to inability to communicate: use modified behavioral pain scales

■  Regional techniques for postop analgesia recommended

■  Low-dose benzodiazepines (diazepam) to prevent/treat muscle spasms


COARCTATION OF THE AORTA

SCOTT D. MARKOWITZ, MD

BACKGROUND

■  Prevalence: 8% of pts with CHD

■  Coexisting bicuspid aortic valve, arch hypoplasia, other heart defects

■  Hypertension is usually present pre-repair and may persist postop.

■  May be repaired with balloon dilation or surgical correction end-to-end anastomosis or subclavian flap arterioplasty

■  Residual or recurrent coarct may occur early or late: eval by right arm vs. leg BP & Doppler echo.


PREOPERATIVE ASSESSMENT

■  ECG & echo: ventricular hypertrophy/dysfunction, valve dysfunction, residual coarct

■  BP measurements in all extremities, identification of previous recurrent laryngeal nerve injury

■  Antihypertensive regimen assessed and instructions for day of surgery medication administration given


INTRAOPERATIVE MANAGEMENT

■  SBE prophylaxis even after repair

■  If pre-repair: BP monitoring on pre-coarct artery (usually right arm except in cases of aberrant subclavian artery)

■  If post-repair: monitors accurate in any extremity, except if residual coarct

■  Left arm BP unreliable after subclavian flap repair

■  Caution with intercostal blocks if intercostal arteries dilated


POSTOPERATIVE CONSIDERATIONS

■  Std pain management: opioids & NSAIDs

■  Monitor for arrhythmias; resume antihypertensive therapy as appropriate.


CRANIOFACIAL SYNDROMES

SALLY E. RAMPERSAD, MB FRCA

BACKGROUND

■  Premature fusion of one or more skull sutures

■  Major component of several congenital syndromes: Crouzon, Saethe-Chotzen, Pfeiffer, Carpenter, Aperts


PREOPERATIVE ASSESSMENT

■  Previous anesthetic records: airway issues & management

■  Examine for obstructing mass (cystic hygroma, large tongue in Beckwith-Wiedemann syndrome; micrognathia/retrognathia in Pierre Robin); limited mouth opening, limited neck mobility, facial asymmetry (Goldenhars).

■  Abnl ear form & position indicate other facial anomalies.

■  Inform family of potential airway complications.

■  Snoring, daytime somnolence, or hx of stridor may indicate significant airway obstruction.

■  Cleft lip/palate are part of other syndromes (eg, CHARGE, trisomy 18, velocardiofacial syndrome).

■  Associated anomalies: ear, renal, CV

■  Avoid pre-op sedation in pts with potential airway obstruction, or administer with anesthesiologist present.

■  PO or Ⅳ atropine (0.02 mg/kg) as antisialagogue/vagolytic

■  Prepare different sizes of facemasks (air-filled cushion for asymmetric face), LMAs, oral & naso-pharyngeal airways, endotracheal tubes, fiberoptic bronchoscopes, stylets.





© Cambridge University Press

Table of Contents

Part I. Co-Existing Diseases: Preface; 1. Anterior mediastinal mass; 2. Asthma; 3. Atrial septal defect (ASD); 4. Cerebral palsy; 5. Coarctation of the aorta; 6. Craniofacial syndromes; 7. Cystic fibrosis; 8. Emergence agitation; 9. Endocardial cushion defects: atrioventricular septal defects (AVSD) Ex-premature infant; 10. Hemophilia; 11. Mitochondrial myopathy; 12. Mucopolysaccharidoses; 13. Muscular dystrophy; 14. Neurofibromatosis; 15. Obstructive sleep apnea; 16. Oncological disease; 17. Patent ductus arteriosus; 18. Post operative nausea and vomiting (PONV) postoperative apnea; 19. Premature infant; 20. Seizure disorders; 21. Sickle cell disease; 22. Single ventricle physiology; 23. Tetralogy of fallot; 24. Thalassemia; 25. Transposition of great arteries (d-TGA); 26. Trisomy 21 (Down Syndrome); 27. Ventricular Septal Defect (VSD); 28. von Willebrand disease; Part II. Surgical Procedures: 29. Anterior spinal fusion; 30. Arterial switch procedure for transposition of the great arteries; 31. Atrial septal defect repair; 32. Awake craniotomy for seizures; 33. Bidirectional Glenn or Hemi-Fontan procedure; 34. Brachial cleft cyst excision; 35. Burn debridement; 36. Cardiac catheterization; 37. Cervical node biopsy/excision; 38. Choledochal cyst excision; 39. Circumcision; 40. Cleft lip repair; 41. Cleft palate repair; 42. Cloacal extrophy repair; 43. Club foot repair; 44. CNS tumor excision; 45. Coarctation of the aorta repair; 46. Colonoscopy; 47. Congenital cystic adenomatoid malformation (CCAM) excision; 48. Congenital diaphragmatic hernia repair (CDH); 49. Congenital lobar emphysema; 50. Craniosynostosis repair; 51. Craniotomy for head trauma; 52. CT Scans; 53. Cystic hygroma (Lymphatic Malformation) excision; 54. Dental extractions and rehabilitation; 55. Dorsal rhizotomy; 56. Endoscopy - EGD (Esophagogastroduodenoscopy); 57. Epiglottitis; 58. Esophageal dilatation; 59. Exploratory laparotomy for abdominal trauma; 60. Fontan procedure; 61. Foreign body in the trachea or bronchus; 62. Gastroschisis repair; 63. Gastrostomy tube placement; 64. Heel cord lengthening; 65. Hypospadias repair; 66. Imperforate anus repair (pena procedure or posterior sagittal anorectoplasty); 67. Inguinal hernia repair; 68. Intussusception repair; 69. Kasai procedure for biliary atresia; 70. Kidney transplant; 71. Lacrimal duct probing and irrigation; 72. Laparoscopy; 73. Laser removal of port wine stain; 74. Liver transplant; 75. Lower extremity fracture; 76. Mediastinoscopy; 77. MRI; 78. Myelomeningocele repair; 79. Myringotomy and tubes insertion; 80. Norwood stage 1 procedure; 81. Omphalocele repair; 82. Open globe injury repair; 83. Orchidopexy (undescended testicle repair); 84. Otoplasty; 85. Patent ductus arteriosus (PDA) ligation; 86. Pectus carinatum repair; 87. Pectus excavatum repair; 88. Pelvic osteotomy; 89. Posterior spinal fusion; 90. Posterior urethral valve repair; 91. Pull-throughs for hirschsprung's; 92. Pulmonary sequestration; 93. Pyloromyotomy; 94. Radiotherapy; 95. Retropharyngeal abscess; 96. Slipped capital femoral epiphysis (SCFE) repair; 97. Splenectomy; 98. Strabismus repair; 99. Syndactyly repair; 100. Testicular torsion repair; 101. Tetralogy of fallot repair; 102. Thyroglossal duct cyst; 103. Total anomalous pulmonary venous return (TAPVR) repair; 104. Tracheoesophageal fistula and esophageal atresia repair; 105. Tracheostomy; 106. Umbilical hernia repair; 107. Ureteral reimplant; 108. Vascular ring repair; 109. Ventricular septal defect repair; 110. Video-assisted thoracoscopic surgery (VATS); 111. Volvulus (malrotation); 112. Wilms' tumor excision; Part III. Regional Anesthesia: 113. Epidural analgesia; 114. Spinal anesthesia.
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