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The continuum of anesthesia includes varying degrees of sedation (i.e., mild, moderate, or deep) and general anesthesia. All forms of sedation are characterized by some preservation of purposeful movement (see Chapter 75 ), whereas general anesthesia is defined by the complete loss of consciousness. Potent pharmacologic agents are required to suppress the perception and physiologic response to noxious stimuli. Perioperatively, the anesthesiologist is responsible for providing analgesia while preserving physiologic and metabolic stability ( Table 74.1 ). This responsibility begins with the performance of a comprehensive preanesthesia history ( Table 74.2 ). Although anesthetic risk has greatly decreased with advancements in pharmacology and monitoring technology, the persistent risk of perioperative morbidity and mortality demands vigilance. The risk is elevated in certain disease states ( Table 74.3 ).
Analgesia
Amnesia
Hypnosis
Akinesia
Maintenance of physiologic homeostasis
Vigilance
Child's previous anesthetic and surgical procedures:
Review previous anesthetic records:
Ease of mask ventilation
Grade of laryngoscopy; type and size of laryngoscope; endotracheal tube size
Issues during emergence (awakening) from anesthesia (postoperative vomiting, emergence delirium)
History of hyperthermia or acidosis in the child or family members.
Perinatal problems (especially for infants):
Prematurity
Need for supplemental oxygen or intubation and ventilation
History of apnea and bradycardia
History of cardiovascular compromise
Other major illnesses and hospitalizations
Family history of anesthetic complications, malignant hyperthermia, or pseudocholinesterase deficiency
Respiratory problems:
Long-term exposure to environmental tobacco smoke
Obstructive breathing score
STBUR (snoring, trouble breathing, un-refreshed)
Cyanosis (especially in infants <6 mo of age)
Recurrent respiratory infections
Recent lower respiratory tract infection
Previous laryngotracheitis (croup) or laryngomalacia
Reactive airway disease
Airway abnormalities, facial anomalies, mucopolysaccharidosis
Cardiac problems:
Murmur or history of congenital heart disease
Dysrhythmia
Exercise intolerance
Syncope
Cyanosis
Gastrointestinal problems:
Reflux and vomiting
Feeding difficulties
Failure to thrive
Liver disease
Exposure to infectious pathogens
Neuromuscular problems:
Neuromuscular diseases
Developmental delay
Myopathy
Seizure disorder
Hematologic problems:
Anemia
Bleeding diathesis
Tumor
Immunocompromise
Prior blood transfusions and reactions
Renal problems:
Renal insufficiency, oliguria, anuria
Fluid and electrolyte abnormalities
Psychosocial considerations:
Drug abuse, use of cigarettes or alcohol
Physical or sexual abuse
Family dysfunction
Previous traumatic medical or surgical experience
Psychosis, anxiety, depression
Gynecologic considerations:
Sexual history (sexually transmitted infections)
Possibility of pregnancy
Current medications:
Prior administration of corticosteroids
Allergies:
Drugs
Iodine
Latex products
Surgical tape
Food (especially soya and egg albumin)
Dental condition (loose or cracked teeth)
When and what the child last ate (especially in emergency procedures)
DISEASE | IMPLICATIONS |
---|---|
RESPIRATORY SYSTEM | |
Asthma | Intraoperative bronchospasm that may be life threatening |
Pneumothorax or atelectasis | |
Optimal preoperative medical management is essential. | |
Difficult airway | Special equipment and personnel may be required. |
Should be anticipated with dysmorphic features or storage diseases | |
Patients with trisomy 21 may require atlantooccipital joint evaluation. | |
Increased risk with acute airway obstruction, epiglottitis, laryngotracheobronchitis, or airway foreign body | |
Bronchopulmonary dysplasia | Barotrauma with positive pressure ventilation |
Oxygen toxicity, pneumothorax a risk | |
Cystic fibrosis | Airway reactivity, bronchorrhea, increased intraoperative pulmonary shunt and hypoxia |
Risk of pneumothorax, pulmonary hemorrhage | |
Atelectasis, risk of prolonged postoperative ventilation | |
Patient should be assessed for cor pulmonale. | |
Sleep apnea | Pulmonary hypertension and cor pulmonale must be excluded. |
Careful postoperative observation for obstruction required | |
CARDIAC | |
Bacterial endocarditis prophylaxis as indicated | |
Use of air filters; careful purging of air from the intravenous equipment | |
Physician must understand the effects of various anesthetics on the hemodynamics of specific lesions. | |
Possible need for preoperative evaluation of myocardial function and pulmonary vascular resistance | |
Provide information about pacemaker function and ventricular device function. | |
HEMATOLOGIC | |
Sickle cell disease | Possible need for simple or exchange transfusion based on preoperative hemoglobin concentration and percentage of hemoglobin S |
Avoid hypoxemia, hypothermia, dehydration, and hyperviscosity states. | |
Oncology | Pulmonary evaluation of patients who have received bleomycin, bis -chloroethyl-nitrosourea, chloroethyl-cyclohexyl-nitrosourea, methotrexate, or radiation to the chest |
Avoidance of high oxygen concentration | |
Cardiac evaluation of patients who have received anthracyclines; risk of severe myocardial depression with volatile agents | |
Potential for coagulopathy | |
RHEUMATOLOGIC | |
Limited mobility of the temporomandibular joint, cervical spine, arytenoid cartilages | |
Careful preoperative evaluation required | |
Possible difficult airway | |
GASTROINTESTINAL | |
Esophageal, gastric | Potential for reflux and aspiration |
Liver | Altered metabolism of many anesthetic drugs |
Potential for coagulopathy and uncontrollable intraoperative bleeding | |
RENAL | |
Altered electrolyte and acid-base status | |
Altered clearance of many anesthetic drugs | |
Need for preoperative dialysis in selected cases | |
Succinylcholine to be used with extreme caution and only when the serum potassium level has recently been shown to be normal | |
NEUROLOGIC | |
Seizure disorder | Avoidance of anesthetics that may lower the seizure threshold |
Optimal control ascertained preoperatively | |
Preoperative serum anticonvulsant measurements | |
Increased intracranial pressure | Avoidance of agents that increase cerebral blood flow |
Maintain cerebral perfusion pressure. | |
Neuromuscular disease | Avoidance of depolarizing relaxants; at risk for hyperkalemia |
Patient may be at risk for malignant hyperthermia; avoid volatile anesthetics in myopathies. | |
Developmental delay | Patient may be uncooperative during induction and emergence. |
Psychiatric | Monoamine oxidase inhibitor (or cocaine) may interact with meperidine, resulting in hyperthermia and seizures. |
Selective serotonin reuptake inhibitors may induce or inhibit various hepatic enzymes that may alter anesthetic drug clearance. | |
Illicit drugs may have adverse effects on cardiorespiratory homeostasis and may potentiate the action of anesthetics. | |
ENDOCRINE | |
Diabetes | Greatest risk is unrecognized intraoperative hypoglycemia; intraoperative blood glucose level monitoring needed especially when insulin is administered. |
SKIN | |
Burns | Difficult airway |
Fluid shifts | |
Bleeding | |
Risk of rhabdomyolysis and hyperkalemia from succinylcholine following burns for many months | |
IMMUNOLOGIC | |
Retroviral drugs may inhibit benzodiazepine clearance. | |
Immunodeficiency requires careful infection control practices. | |
Cytomegalovirus-negative blood products, irradiation, or leukofiltration may be required. | |
METABOLIC | |
Careful assessment of glucose homeostasis in infants |
All children presenting for surgery should undergo a preanesthetic history and multiorgan system assessment with assignment of American Society of Anesthesiologists Physical Status (ASA-PS) ( Table 74.4 ). Children of ASA-PS I-II generally require a brief history, notation of medical allergies, and physical examination focusing on the neurologic and cardiorespiratory systems, with no additional testing. Patients with complex medical history of ASA-PS ≥III require a more comprehensive preanesthetic assessment often with ancillary preoperative testing. Children should be screened for anesthetic risks, including drug allergies, previous reactions to anesthetics, and family history of problems with anesthesia (e.g., sudden perioperative death, hyperthermia after surgery), which may indicate risk of malignant hyperthermia.
Class 1: Healthy patient, no systemic disease
Class 2: Mild systemic disease with no functional limitations (mild chronic renal failure, iron-deficiency anemia, mild asthma)
Class 3: Severe systemic disease with functional limitations (hypertension, poorly controlled asthma or diabetes, congenital heart disease, cystic fibrosis)
Class 4: Severe systemic disease that is a constant threat to life (critically and/or acutely ill patients with major systemic disease)
Class 5: Moribund patients not expected to survive 24 hr, with or without surgery
Additional classification: “E”—emergency surgery
Recent respiratory tract infections should be noted. Clear rhinorrhea without fever is not associated with increased anesthetic risk. Respiratory illnesses associated with fever, mucopurulent nasal discharge, productive cough, or lower respiratory symptoms (wheezing, rales) are associated with increased airway reactivity and anesthetic complications for up to 6 wk thereafter. There may also be increased risk of perioperative laryngospasm and bronchospasm, reduced mucociliary clearance, atelectasis, and hypoxemia. It is recommended that elective procedures requiring general anesthesia be postponed 4-6 wk in this setting.
Children with reactive airway disease require a thorough preanesthetic assessment. Acute, potentially fatal bronchospasm can occur during induction of anesthesia and endotracheal intubation for routine, minor surgery in children with asthma. Children at increased risk for anesthetic complications have experienced asthma exacerbations requiring (1) hospital admission within the previous year; (2) emergency department (ED) care within the last 6 mo; (3) previous intensive care unit (ICU) admission; or (4) previous parenteral systemic corticosteroids. Ideally, children should be free of wheezing for least several days before surgery, even if this necessitates increased controller medication administration (β-adrenergic agonist and corticosteroids). Active wheezing is an indication for delaying elective surgery. Chronic respiratory conditions such as bronchopulmonary dysplasia and cystic fibrosis are also associated with significant intraoperative risks. Every effort should be made to ensure that children with such disorders achieve optimal respiratory status before surgery.
Induction of general anesthesia is associated with reduced spontaneous ventilation and airway reflexes. Prediction of difficult bag-mask ventilation and/or intubation before anesthesia is critical. Congenital anomalies associated with airway compromise include micrognathia, macroglossia, and thoracic anomalies ( Table 74.5 ). Conditions that impair mouth opening (e.g., temporomandibular joint disease) should also be noted. A history of wheezing or stridor may indicate postoperative airway complications and difficult intraoperative airway management. It is also essential to ask about a history of sleep-disordered breathing using the STBUR (snoring, trouble breathing, un-refreshed) index, which may be predictive of perioperative respiratory complications.
Achondroplasia
Airway tumors, hemangiomas
Apert syndrome
Beckwith-Wiedemann syndrome
Choanal atresia
Cornelia de Lange syndrome
Cystic hygroma/teratoma
DiGeorge syndrome
Fractured mandible
Goldenhar syndrome
Juvenile rheumatoid arthritis
Mucopolysaccharidosis
Pierre Robin syndrome
Smith-Lemli-Opitz syndrome
Treacher-Collins syndrome
Trisomy 21
Turner syndrome
Most anesthetic agents possess myocardial depressant properties. All patients should be screened for the presence of heart disease. Important cardiovascular considerations include history of congenital heart disease (CHD), cyanosis, arrhythmias, or cardiomyopathy. Room-air pulse oximetry should be performed as part of the preanesthetic evaluation. Accurate diagnosis of cardiac murmurs in neonates is essential. A history of cardiac dysrhythmias should be investigated because inhalational anesthetics may be arrhythmogenic. A pediatric cardiologist should evaluate children with known CHD undergoing surgery. Preoperative ancillary studies may include electrocardiogram (ECG), echocardiogram, or cardiac catheterization. Lesions associated with increased anesthetic risk include single-ventricle heart disease, fixed obstructive outflow tract lesions (aortic valve and pulmonary valve stenosis), and cardiomyopathy. Children with these conditions should be cared for by a cardiac anesthesia service . Antibiotic prophylaxis for the prevention of bacterial endocarditis may also be indicated, and the American Heart Association (AHA) guidelines should be followed.
Evidence of coagulopathy should be sought. Easy bruising, familial bleeding disorders, and anticoagulant (e.g., aspirin, heparin, warfarin) use should be discussed. Preoperative adequacy of hemostatic function (e.g., platelet count, fibrinogen, prothrombin time, partial thromboplastin time) and correction of coagulopathic disorders may be indicated for complex procedures associated with significant risk of perioperative hemorrhage. In neonates, assurance of vitamin K prophylaxis and adequate coagulation status is critical before any major surgery. Although anemia may be well tolerated in healthy children, anesthesia and surgery increase oxygen consumption. Preoperative anemia should be corrected in the setting of reduced oxygen delivery or expected blood loss. In the patient with life threatening hemorrhage (trauma), massive transfusion protocols of 1 : 1:1 replacement of packed red blood cells:fresh-frozen plasma:platelets should be used.
A history of neurologic and neuromuscular disorders should be sought. Preoperative developmental assessments may be helpful in interpreting age-dependent variation in the response to pain. Maintenance of appropriate perioperative anticonvulsant therapy is essential in children with seizure disorders because the seizure threshold may be lowered perioperatively. Children with obstructive hydrocephalus typically require ventriculoperitoneal (VP) shunt insertion to divert cerebrospinal fluid (CSF) and to prevent intracranial hypertension (ICH). Repeated shunt malfunction is common, and these children my present for shunt revision with signs of ICH (vomiting, altered mentation, sundowning). Similarly, shunt patency and function should be ensured preoperatively in children with VP shunts presenting for nonneurosurgical procedures.
Surgery and painful medical procedures are psychologically traumatic events for children and families. Children who require anesthesia may experience fear and anxiety. They may also sense stressful signals from parents and caregivers. Many children undergoing surgery have new-onset negative behavioral changes postoperatively. These maladaptive behavioral responses may include enuresis, separation anxiety, temper tantrums, and nighttime crying, as well as fear of strangers, doctors, and hospitals. Sleep quality may be altered postoperatively, resulting in further behavioral compromise. Risk factors for postoperative behavioral changes include preoperative anxiety and emergence excitation. Need for recurrent procedures is another risk factor. Preoperative psychological preparation programs decrease the incidence of postoperative behavioral changes. Parental presence during induction (PPI) has not been shown to improve postoperative behavior (see later). Oral midazolam (0.5 mg/kg) may decrease negative behavioral changes after surgery. Midazolam has the benefit of providing rapid-onset anxiolysis and amnesia.
Children with genetic conditions may have syndrome-specific anesthetic considerations. For example, children with trisomy 21 may have cardiac anomalies, macroglossia, upper airway obstruction, and hypothyroidism (see Chapter 98.2 ). Atlantoaxial instability, common in trisomy 21, has been linked to cervical dislocation and spinal cord trauma with neck extension during intubation. Some anesthesiologists recommend extension and flexion lateral neck films to detect instability before surgery. For children with other known genetic disorders it is essential to review specific anesthetic considerations.
Preoperative fasting guidelines have been developed to reduce the incidence of aspiration of gastric contents during anesthesia. Aspiration may lead to laryngospasm, bronchospasm, and postoperative pneumonitis. Aspiration of gastric contents may be a potentially lethal complication in children with chronic lung disease or critical illness. Table 74.6 lists preoperative fasting guidelines (e.g., nothing by mouth, or nil per os [NPO] status). Clear, sweet liquids (e.g., Pedialyte, 5% dextrose in water [D5W]) facilitate gastric emptying, prevent hypoglycemia, and may be given up to 2 hr before anesthesia. Breast milk may be given to infants up to 4 hr before surgery. Solids should be avoided for 6-8 hr before surgery. Many conditions delay gastric emptying and may require prolonged periods of fasting.
TIME BEFORE SURGERY (hr) | ORAL INTAKE |
---|---|
2 | Clear, sweet liquids |
4 | Breast milk |
6 | Infant formula, fruit juices, gelatin |
8 | Solid food |
* These are general guidelines and may differ among hospitals.
Gastric emptying may be delayed for up to 96 hr after an acute episode of trauma or surgical illness. Because of the serious complications of aspiration of gastric contents, it is desirable to secure the airway as rapidly as possible during induction of anesthesia in patients at risk for having a full stomach. Under these circumstances, rapid sequence induction of anesthesia is indicated ( rapid sequence induction ; see Chapter 89 ).
Parents may expect to be with their child during the induction of anesthesia. Removing a fearful child from the comforting arms of a parent is stressful for the child, parents, and caregivers. When parental separation cannot be achieved comfortably with premedication and behavioral modification (patient education and desensitization to the operative environment), there may be a need to defer parent–child separation until general anesthesia is induced. Premedication with the oral benzodiazepine midazolam more frequently provides calm, smooth induction conditions than PPI without pharmacologic preparation. Although PPI in the hands of a confident, competent anesthesia practitioner may replace the need for preoperative medication, it does not reliably predict smooth induction. PPI has not been shown to decrease emergence delirium or postoperative behavioral changes, and it does not appear to be superior to premedication with oral midazolam.
Pediatric anesthesiologists are responsible for providing analgesia to children for procedures within operating room (OR) and non-OR settings ( Table 74.7 ). Multimodal techniques exist to provide pain relief during operative procedures for children of all ages, including critically ill infants. Effective analgesia is essential to blunt physiologic responses to painful stimuli (surgery) and modulate the deleterious physiologic and metabolic consequences. The response to painful and stressful stimuli may provoke systemic inflammatory response syndrome (SIRS) , which has been linked to increased catabolism, physiologic instability, and mortality (see Chapter 88 ).
A designated anesthesia service in which an anesthesiologist has been requested to participate in the care of a patient undergoing a diagnostic or therapeutic procedure.
Monitored anesthesia care includes all aspects of anesthesia care: a preprocedure assessment, intraprocedure care, and postprocedure anesthesia management.
During monitored anesthesia care, the anesthesiologist or a member of the anesthesia care team provides a number of specific services, which may include but are not limited to the following:
Discussing anesthesia care with the family and child, obtaining consent for anesthesia, allaying anxiety and answering questions—family-centered anesthesia care.
Monitoring of vital signs, maintenance of the patient's airway, and continual evaluation of vital functions.
Diagnosing and treating clinical problems that occur during the procedure.
Administering sedatives, analgesics, hypnotics, anesthetic agents, or other medications as necessary to ensure patient safety and comfort.
Providing other medical services as needed to accomplish the safe completion of the procedure.
Anesthesia care often includes the administration of medications for which the loss of normal protective reflexes or loss of consciousness is likely.
Monitored anesthesia care refers to those clinical situations in which the patient remains able to protect the airway for the majority of the procedure.
If the patient is rendered unconscious and/or loses normal protective reflexes for an extended period, this is considered a general anesthetic.
Administration of anxiolysis or analgesia that obtunds consciousness but does not obtund normal protective reflexes (cough, gag, swallow, hemodynamic), or spontaneous ventilation.
Sedation that obtunds consciousness and normal protective reflexes or possesses a significant risk of blunting normal protective reflexes (cough, gag, swallow, hemodynamic), hemodynamic and respiratory insufficiency may occur.
Administration of hypnosis, sedation, and analgesia that results in the loss of normal protective reflexes.
Induction of neural blockade (either central, neuraxial, epidural, or spinal; or peripheral nerve block, e.g., digital nerve block, brachial plexus block), which provides analgesia and is associated with regional motor blockade.
Consciousness is not obtunded.
Special expertise is required.
Frequently, in children, anxiolysis and sedation are also necessary for this technique to be successful.
Regional anesthesia (e.g., caudal epidural blockade) is used to supplement general anesthesia and provide postoperative analgesia.
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