PEDIATRIC ANESTHETIC CONSIDERATIONS KIDS ARE NOT SMALL ADULTS

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PEDIATRIC ANESTHETIC CONSIDERATIONS

PEDIATRIC ANESTHETIC CONSIDERATIONS

KIDS ARE NOT SMALL ADULTS

KIDS ARE NOT SMALL ADULTS

Respiratory System Anatomy… Tongue relatively large n Larynx more cephalic and anterior u C

Respiratory System Anatomy… Tongue relatively large n Larynx more cephalic and anterior u C 3 -4 in child u C 4 -5 in adult u Epiglottis long and stiff t Protrudes posterior at 45 o n

Respiratory System Anatomy… Narrowest diameter upper airway at cricoid ring (glottis in adult) u

Respiratory System Anatomy… Narrowest diameter upper airway at cricoid ring (glottis in adult) u Susceptible to airway obstruction n Trachea short— 4 -5. 7 cm vs. 6 -8 cm n Equidistant bronchi from trachea— increased chance of endobronchial intubation n Lung alveoli— 20 mil at birth, 300 mil age 8 n

Respiratory Physiology… Alveolar ventilation: O 2 requirement u Infant: 100 -150 cc/kg/min u Adult:

Respiratory Physiology… Alveolar ventilation: O 2 requirement u Infant: 100 -150 cc/kg/min u Adult: 60 cc/kg/min n Increase in Va 2 o increased metabolic rate in infant n FRC (functional residual capacity) exp. reserve vol. + residual vol. n

Respiratory Physiology… FRC— u acts as a buffer to maintain Pa. O 2 during

Respiratory Physiology… FRC— u acts as a buffer to maintain Pa. O 2 during inspiration and expiration u smaller reserve u less O 2 during apnea n Va/FRC (adult) = 1. 5/1 n Va/FRC (infant) = 5/1 n

Respiratory Physiology… n n Lung mechanics u Increased resistance 2 o narrow nasal passage

Respiratory Physiology… n n Lung mechanics u Increased resistance 2 o narrow nasal passage u Resp. rate increased (24 -30 vs. 20) Oxygen transport (left shift) u Incr. affinity of hemoglobin for O 2 u Favors uptake not unload u Less O 2 available to tissues, therefore increased HR and CO necessary

Cardiovascular Anatomy & Physiology… n n Ventricle in infant u Right > Left (size

Cardiovascular Anatomy & Physiology… n n Ventricle in infant u Right > Left (size and thickness) u Less compliant Pulse rate is the major determinant of CO in infant u New born— 130; adult— 77 Sinus dysrhythmia common BP; infant— 70/43, adult— 122/80

Cardiovascular Anatomy & Physiology… n Response to hypoxia u Metab. demand for O 2

Cardiovascular Anatomy & Physiology… n Response to hypoxia u Metab. demand for O 2 - 60% > adult u Va/FRC is high (5: 1) u Hypoxemia can develop rapidly u Bradycardia is always initial response to hypoxia u Treat unexplained bradycardia immediately with O 2

Pediatric Pharmacology… n n n Brain, heart, liver, and kidneys = 18% of body

Pediatric Pharmacology… n n n Brain, heart, liver, and kidneys = 18% of body weight in infant vs. 5% adult u Larger fraction of drug distributed to these organs vs. muscle and fat Infants have less plasma protein conc. More perm. BBB Hepatic enzymes—inactive/immature GF less in infant—slower elimination of drugs and metabolites

Pediatric Sedation… n n n ASA status—I’s and II’s Risk factors for pediatric sedation

Pediatric Sedation… n n n ASA status—I’s and II’s Risk factors for pediatric sedation u Age—the younger the patient the greater the risk u Respiratory arrest is the greatest liability Rule of thumb “adults will have a cardiac arrest, children will have a respiratory arrest”

Evaluation of Physical Risks During Sedation… n History u Syndrome associated with difficult airway?

Evaluation of Physical Risks During Sedation… n History u Syndrome associated with difficult airway? u Does the child snore at night? t Most crucial question in history t Accurate predictor of obstruction t Most common etiology is hypertrophy of adenoids and tonsils • Problems with emergency airway

Evaluation of Physical Risks During Sedation… n n History u Previous surgeries and anesthetics

Evaluation of Physical Risks During Sedation… n n History u Previous surgeries and anesthetics t Very good indicator of success/failure Physical exam u Differences in child’s airway t Kids are smaller • Smaller mouths • Mallampati evaluation

Evaluation of Physical Risks During Sedation… n Physical exam u Disproportionate sized features t

Evaluation of Physical Risks During Sedation… n Physical exam u Disproportionate sized features t Relatively large epiglottis t Floppier epiglottis t Narrowest part of airway is subglottic t Glottis is prone to laryngospasm during sedation t Thyromental distance

Evaluation of Physical Risks During Sedation… n Physical exam u URI t Most children

Evaluation of Physical Risks During Sedation… n Physical exam u URI t Most children have 2 -10 viral respiratory tract infections per year • Is a snotty nose just a cold or day 1 of a viral infection? t More prone to laryngospasm, bronchospasm, coughing, mucus plugging

Factors Influencing the Outcome of Sedation n n The best success rate with children

Factors Influencing the Outcome of Sedation n n The best success rate with children is (20 -40% failure) Age Cognitive development Degree of expression of fear u Flight response of crying/screaming Child temperament 60 -80 %

SEDATION PHARMACOLOGY Sedative Hypnotics n Phenothiazines/Antihistamines n Benzodiazepines n Narcotics n Barbiturates n Reversal

SEDATION PHARMACOLOGY Sedative Hypnotics n Phenothiazines/Antihistamines n Benzodiazepines n Narcotics n Barbiturates n Reversal Agents n

SEDATIVE HYPNOTICS CHLORAL HYDRATE

SEDATIVE HYPNOTICS CHLORAL HYDRATE

CHLORAL HYDRATE “Classic” pediatric sedative n Moderately effective sedative/hypnotic n Mild depressant of the

CHLORAL HYDRATE “Classic” pediatric sedative n Moderately effective sedative/hypnotic n Mild depressant of the central nervous system n Trichloroethanol is the active metabolite n

CHLORAL HYDRATE Often combined with other agents n No analgesic properties n No reversal

CHLORAL HYDRATE Often combined with other agents n No analgesic properties n No reversal agent n May cause GI irritation, respiratory depression, hypotension and paradoxical excitement n Hepatic elimination n

CHLORAL HYDRATE n Side effects: u Nausea u Vomiting u Diarrhea u Flatulence u

CHLORAL HYDRATE n Side effects: u Nausea u Vomiting u Diarrhea u Flatulence u disorientation u excitement u rash

CHLORAL HYDRATE DOSE u 50 -75 mg/kg PO n ONSET u 30 - 60

CHLORAL HYDRATE DOSE u 50 -75 mg/kg PO n ONSET u 30 - 60 minutes PO n PEAK EFFECT u 1 -2 hours PO n

CHLORAL HYDRATE n n WORKING TIME u 45 -60 minutes DURATION u 7 -10

CHLORAL HYDRATE n n WORKING TIME u 45 -60 minutes DURATION u 7 -10 hours

ANTIHISTAMINES DIPHENHDRAMINE HYDROXYZINE

ANTIHISTAMINES DIPHENHDRAMINE HYDROXYZINE

DIPHENHYDRAMINE Trade name: Benadryl n H 1 receptor antagonist with anticholinergic and sedative effects

DIPHENHYDRAMINE Trade name: Benadryl n H 1 receptor antagonist with anticholinergic and sedative effects n Partially inhibits vasodilator effect of histamine on peripheral vascular smooth muscle n

DIPHENHYDRAMINE n USES: u Antiemetic u Antivertigo u Treatment of allergic reactions u Treatment

DIPHENHYDRAMINE n USES: u Antiemetic u Antivertigo u Treatment of allergic reactions u Treatment of extrapyramidal reactions

DIPHENHYDRAMINE DOSE: u 0. 5 to 1 mg/kg q 6 h (25 -50 mg)

DIPHENHYDRAMINE DOSE: u 0. 5 to 1 mg/kg q 6 h (25 -50 mg) PO u maximum 300 mg/day n ONSET: u <15 minutes PO n

DIPHENHYDRAMINE PEAK EFFECT: u 2 hours PO n DURATION: u < 7 hours PO

DIPHENHYDRAMINE PEAK EFFECT: u 2 hours PO n DURATION: u < 7 hours PO n

DIPHENHYDRAMINE Children are at an increased risk of paradoxic CNS stimulant effects such as

DIPHENHYDRAMINE Children are at an increased risk of paradoxic CNS stimulant effects such as restlessness, insomnia, tremors, euphoria and seizures

HYDROXYZINE Vistaril/Atarax n Antihistamine n Anxiolytic n Sedative n Hepatic elimination n

HYDROXYZINE Vistaril/Atarax n Antihistamine n Anxiolytic n Sedative n Hepatic elimination n

HYDROXYZINE n n DOSE: u. 6 - 1 mg/kg PO ONSET: u 15 -30

HYDROXYZINE n n DOSE: u. 6 - 1 mg/kg PO ONSET: u 15 -30 minutes PO PEAK EFFECT: u 30 - 60 minutes PO DURATION: u 2 - 4 hours

PHENOTHIAZINES PROMETHAZINE

PHENOTHIAZINES PROMETHAZINE

PROMETHAZINE Phenothiazine derivative n H 1 receptor antagonist with good sedative, antiemetic, anticholinergic and

PROMETHAZINE Phenothiazine derivative n H 1 receptor antagonist with good sedative, antiemetic, anticholinergic and antimotion sickness effects n Hepatic elimination n

PROMETHAZINE n Uses: u Antiemetic u Adjunct to other sedatives (antiemetic and co-sedative) u

PROMETHAZINE n Uses: u Antiemetic u Adjunct to other sedatives (antiemetic and co-sedative) u Used alone for mild sedation or to control gagging

PROMETHAZINE n n DOSE: u 1 mg/kg PO ONSET: u 15 - 30 minutes

PROMETHAZINE n n DOSE: u 1 mg/kg PO ONSET: u 15 - 30 minutes PO PEAK EFFECT: u <2 hours PO DURATION: u 2 -8 hours PO

PROMETHAZINE n n Extrapyramidal reactions Use with caution in children with severe cardiovascular or

PROMETHAZINE n n Extrapyramidal reactions Use with caution in children with severe cardiovascular or liver disease

BENZODIAZEPINES DIAZEPAM MIDAZOLAM

BENZODIAZEPINES DIAZEPAM MIDAZOLAM

DIAZEPAM n n DOSE: u 0. 25 - 0. 5 mg/kg PO ONSET: u

DIAZEPAM n n DOSE: u 0. 25 - 0. 5 mg/kg PO ONSET: u 30 minutes to 1 hour PO PEAK EFFECT: u 1 hour PO DURATION: u 2 - 6 hours PO

MIDAZOLAM Trade name: Versed n Short acting n Water soluble n Greater amnesia than

MIDAZOLAM Trade name: Versed n Short acting n Water soluble n Greater amnesia than with diazepam n Dose dependent respiratory and circulatory depression n Four times more potent than diazepam n

MIDAZOLAM n n DOSE: u 0. 5 mg/kg PO ONSET: u 20 -30 minutes

MIDAZOLAM n n DOSE: u 0. 5 mg/kg PO ONSET: u 20 -30 minutes PO PEAK EFFECT: u 30 minutes PO DURATION: u 2 -6 hours PO

MIDAZOLAM - INTRANASAL Not permitted with Level 1 n Burning of the nasal mucosa

MIDAZOLAM - INTRANASAL Not permitted with Level 1 n Burning of the nasal mucosa is a major drawback n Need to make sure that the drug is absorbed through the nasal mucosa and not swallowed n

FLUMAZENIL Trade Name: Romazicon n Competes with benzodiazepines for the GABA/benzodiazepine receptor n Has

FLUMAZENIL Trade Name: Romazicon n Competes with benzodiazepines for the GABA/benzodiazepine receptor n Has a much shorter duration of action than most of the benzodiazepines n Used as a reversal agent for benzodiazepine agonists n

FLUMAZENIL DOSE: u IV/IM 0. 1 mg or 3 mcg/kg (max dose is 1

FLUMAZENIL DOSE: u IV/IM 0. 1 mg or 3 mcg/kg (max dose is 1 mg) n ONSET: u 1 - 2 minutes IV n PEAK EFFECT: u 2 - 10 minutes IV n DURATION: n

FLUMAZENIL n Precautions u May be associated with seizures in high risk patients. u

FLUMAZENIL n Precautions u May be associated with seizures in high risk patients. u Patient may become re-sedated so need to monitor patient. u Can cause confusion and agitation

NARCOTICS MEPERIDINE

NARCOTICS MEPERIDINE

MEPERIDINE DOSE: u 1 -2 mg/kg PO n ONSET: u 10 - 30 minutes

MEPERIDINE DOSE: u 1 -2 mg/kg PO n ONSET: u 10 - 30 minutes PO n PEAK EFFECT u <1 hour PO n DURATION u 2 - 4 hours PO n

MEPERIDINE Do not use in patients taking MAO inhibitors n Can cause abnormal behavior

MEPERIDINE Do not use in patients taking MAO inhibitors n Can cause abnormal behavior or dysphoria n Use with caution in patients who are high risk or hypovolemic n

NALOXONE Trade Name: Narcan n Pure opioid antagonist n Competitively inhibits opiates at the

NALOXONE Trade Name: Narcan n Pure opioid antagonist n Competitively inhibits opiates at the mu, delta, and kappa receptor sites n Reverses respiratory depression, sedation, hypotension and analgesia n No pharmacologic effects in absence of narcotics n

NALOXONE n DOSE: u n 0. 01 mg/kg IV/IM/SC (titrate to response) ONSET: 1

NALOXONE n DOSE: u n 0. 01 mg/kg IV/IM/SC (titrate to response) ONSET: 1 - 2 minutes IV, u 2 - 5 minutes IM/SC u n PEAK EFFECT: u n 5 - 10 minutes IV/IM/SC DURATION: u 1 - 4 hours IV/IM/SC

NALOXONE Abrupt reversal may cause nausea, vomiting, diaphoresis, tachycardia, hypertension, pulmonary edema n Careful

NALOXONE Abrupt reversal may cause nausea, vomiting, diaphoresis, tachycardia, hypertension, pulmonary edema n Careful monitoring needed because duration of action of opiates may be longer than that of naloxone n