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Pediatric Anatomy &
physiology
Presented by : Dr. Kundan Kishor Ghimire
Moderator:- Dr. Pawan Puspa Baral
Objectives:
• To understand the anatomic variations in
pediatric group
• To understand the physiologic differences
between pediatric and adult group
• Anesthetic implications of the anatomic and
physiologic variations
• Preterm infants (born
before 37 weeks
gestation)
• Post mature infants (born
after 42 weeks gestation)
• Neonates (0-1 months)
• Infants (1-12 months)
• Toddlers (1-3 years)
• Small children ( 4 – 12
years)
Respiratory System
Pediatric airway
Adult Vs Pediatric airway
Structure Features
Tongue Larger in proportion to the oral cavity than in
adult.
Epiglottis Narrower, U- shaped, flops posteriorly
Larynx High and anterior. Level of C3-C4. (C5-C6 in adults)
Cricoid More conical shaped in infants, narrower at cricoid
cartilage whereas in adults it is at level of vocal
cords
Trachea Shorter (4-5cm), deviated posteriorly and
downwards
Become anatomically similar to adult between 8-
10 years
Pediatric airway
•Obligate nose breathers until 5 months
of age.
•Mouth breathing occurs only during
crying
•Obligate nose breathing is vital for
respiration during feeding
pharynx
•Completely soft tissue
•Easily collapsed by posterior
displacement of the mandible, or
external compression of the hyoid.
•Pharyngeal lumen may collapse with
negative pressure generated through
inspiratory effort.
Larynx
•Funnel shaped
•Glottis more cephalad (premature
C3, Term C4 and adults C5-6)
•Cricoid ring is complete, and is the
narrowest point of the pediatric
airway
Larynx
•Anterior and slanting vocal cords
•Epiglottis is omega or tubular shaped
• stubby base and thick and bulky
aryepiglottic fold, tip lies at C1 in close
apposition with soft palate
INFANTADULT
Figure: adult and pediatric larynx
Figure: standard tracheal tube and microcuff tracheal tube
RESPIRATORY SYSTEM
Change at birth:
• 90ml of plasma ultra-filtrate in lungs squeezed out
during delivery
• Catecholamine during labor : augment release of
surfactant from type II pneumatocytes,
• Lung expansion : increases alveolar and arterial
oxygen tension; decreases pulmonary vascular
resistance
Pediatric airway
RESPIRATORY SYSTEM
Lungs
•Maturation does not complete until 8
years.
•Alveoli grow and increase in number.
•Surfactant production begins at 20
weeks, but increases between 30-34
weeks
RESPIRATORY SYSTEM
Anatomical differences in the thorax
• compliant chest wall
• Ribs are cartilaginous, horizontally
located, limiting an increase in tidal
volume.
• Ventilation is primarily diaphragmatic.
• Diaphragm is deficient in type 1 muscle
fibers reaches adult level by 2 yrs
Figure: newborn and adult ribs type
RESPIRATORY SYSTEM
RESPIRATORY SYSTEM
• Central apnea- self limited in newborns,
approximately 5 seconds
• Apnea of prematurity – 20 seconds or associated
with desaturation episodes and bradycardia
• Resolves at 50- 55 weeks gestational age.
RESPIRATORY SYSTEM
• Pediatric airway
• Infants increase their respiratory rate in the presence of
hypercarbia
• Not as much as adults because chemoreceptors are immature
• Hypoxia-brief hyperventilation followed by hypoventilation
• Periodic breathing occurs in 78% of infants, usually during quiet
sleep
Anesthetic consideration
• Difficult airway management
• Rapid desaturation
• MAC values
• premature 20-30%, after 6mth 50%,
term to 6mths= adult level
• immature CNS,
• maternal progesterone and endorphins
and
• immature BBB
•Volatile anesthetic fast onset and
recovery
• alveolar ventilation/FRC 5:1( adults
1.5:1)
• high cardiac output goes to vessel rich
organs
• low blood gas partition coefficient for
volatile anesthetics
CARDIOVASCULAR SYSTEM
Fetal circulation
• high pulmonary vascular resistance, low
systemic resistance (placenta) and right to
left shunt via PFO and DA.
• Aeration of the lungs – decrease pulmonary
vascular resistance(3-4 days), mediated by
NO,
• Systemic vascular resistance doubles after
first breath by placenta removal
Figure: Fetal Circulation
At birth
• Placenta removal from circulation- portal
blood pressure falls- ductus venosus
closure
• Exposure of ductus arteriosus to ↑ O2
concentration- ductus arteriosus closure
• ↓ PVR- ↑ left side pressure – foramen
ovale closure
Closure of ductus arteriosus: functional
closure 10-15 hrs. after birth, anatomic
closure 2-3 wks. after (ligamentous
arteriosus)
Closure of foramen ovale: functional
closure at birth, anatomic closure at 6
wks.
Closure of ductus venosus: functional
closure 3-7 days after birth, anatomic
closure – 2-3 months of age (ligamentous
venosum)
CARDIOVASCULAR SYSTEM
• Neonatal myocardium contains immature
contractile elements (undeveloped SR)
and is less compliant
• Stroke volume is relatively fixed
• CO rate dependent
• Neonatal myocardium have high glycogen
store
CARDIOVASCULAR SYSTEM
• CO is twice that of the adult.
• CO
• 300-400ml/kg/min in newborns,
• 200ml/kg/min at 2 months of age
• Adrenergic receptors mature at birth but
incomplete sympathetic innervation.
• Impaired baroreceptor reflex activity.
CARDIOVASCULAR SYSTEM
CARDIOVASCULAR SYSTEM
• The electrocardiogram shows an axis oriented
to the right due to right dominance.
Anesthetic considerations
Transitional circulation
•Neonates have a reactive pulmonary
vasculature
•during first few weeks of life, reversion to fetal
circulation.
•Factors: hypoxia, hypercapnia, acidosis,
infection, hypothermia, prematurity
•Sudden increase in pulmonary artery pressure
causes shunting of blood past the lungs
through a patent foramen ovale or the ductus
arteriosus, which may reopen.
• Fixed CO and HR dependent (CPR if HR
<60)
•Low catecholamine store and blunted
response
• Sensitive to Ca channel blocking property
of volatile agents and opioids induced
bradycardia
CENTRAL NERVOUS SYSTEM
• CMRO2- 5ml/100g/min
• CBF- 70-110ml/min/100g
• Intact cerebral autoregulation in full term
and nonstressed infant.
• BBB is poorly formed
–Drugs (barbiturates, opioids,
antibiotics, bilirubin) cross BBB easily
cause prolong & variable duration of
action
Cerebral vessels in preterm infant
are thin walled & fragile.
• Prone to Intra Ventricular Haemorrhage
• Risk increased with hypoxia,
hypercarbia, hypernatraemia, low
HCT,
• Awake airway manipulation, rapid
bicarb administration, &
fluctuation in BP & CBF
Compartment Premature Neonate Infants Adults
ECF 50 35 30 20
ICF 30 40 40 40
Plasma 5 5 5 5
Total 85 80 75 65
Table: Distribution of water as a percentage of body weight
RENAL SYSTEM
RENAL SYSTEM
• Immature infant kidney
• Diminished renal function due to small
perfusion pressure and immature
glomerular and tubular function.
• At 20 wks. after birth- nearly complete
maturation of glomerular filtration and
tubular function.
• At 2 year- complete maturation of renal
function
• Full term infants have the same number
of nephrons as adults
• Glomeruli are much smaller than in
adults
• GFR in the newborn is 30% that of the
adult (until 2yrs)
• Tubular immaturity leads to a relative
inability to concentrate urine (mature
at 8 mths)
Anesthetic considerations
• Meticulous fluid and electrolyte
management
•Dehydration is poorly tolerated
–increased insensible losses due to
large surface area relative to weight
–larger proportion of ECF in children
(40% BW as compared to 20% in
adult)
• Increased half life of renally excreted
drugs
HEMATOLOGIC SYSTEM
•Physiologic anemia at 3 months
•Fetal hemoglobin (HbF) predominates
(70-90%) and low 2,3 DPG level
•Shifts to the adult type (HbA) by 3 to 4
months of age
•Vitamin K dependent clotting factors (II,
VII, IX, X) and platelet function are
deficient in the first few months
HEPATOBILIARY SYSTEM
•Hepatic metabolic capacity is immature at
birth.
•Some enzyme system are developed but
not induced(stimulated).
•Phase I reactions- Some CYP450 enzymes
are fully developed, whereas others are
approx. 50% of adult values.
•Phase II reactions- immature until the age
of 1 year.
•Prolonged half life of benzodiazepines,
morphine, and caffeine.
•Reduced plasma concentration of both
albumin and alpha1-acid glycoprotein
•Low plasma level-decreased protein
binding-higher free drug
GLUCOSE METABOLISM
• Reduced glycogen stores and impaired
gluconeogenesis, increased metabolic rate.
•Hypoglycaemia is common in stressed
neonate glucose level should be
monitored regularly
•Neurological damage may result
from hypoglycaemia
•Prevention: IVI D10%
•Hyperglycaemia is usually iatrogenic
TEMPERATURE REGULATION
• Greater surface area to body weight ratio
with minimal subcutaneous fat
• Poorly developed shivering, sweating and
vasoconstriction mechanisms
• Neonate produce heat by non shivering
thermogenesis.
•Severely limited in premature infants and
in sick neonates.
TEMPERATURE REGULATION
Neutral thermal environment
• 34ºC premature infant,
• 32ºC neonates and
• 28ºC in adolescents and adults
Effect of Low body temperature:
• Respiratory depression
• Acidosis
• Decreased cardiac output
•Increases the duration of action of drugs
• Decreases platelet function and
• Increases the risk of infection.
Summary
Differences(Physiological)
• HR dependent CO
• Faster HR
• Lower BP
• Faster RR
• Lower lung compliance
• Greater chest wall
compliance
• Lower FRC
• Higher ratio of body
surface area to body
weight
• Higher total body water
content
Summary
Differences(Anatomical)
• Non compliant left
ventricle
• Residual fetal
circulation
• Difficult venous &
arterial cannulation
• Large head & tongue
• Narrow nasal passage
• Ant. & cephalad larynx
• Long curled epiglottis
(omega shaped)
• Short trachea & neck
• Prominent adenoids &
tonsil
• Weak intercostal &
diaphragmatic muscle
• High resistance to
airflow
Summary
Pharmacological
• Immature hepatic biotransformation
• Decreased protein binding
• Rapid rise in FA/FI
• Rapid induction and recovery
• Increased MAC
• Larger volume of distribution of water soluble
drugs
• Immature neuromuscular junction
References
• Barash, Clinical Anesthesia 7th edition
• Morgan, Clinical Anesthesiology 6th edition
• Miller’s Anesthesia 8th edition
• Aitkenhead, Textbook of Anaesthesia 7th edition
Thanks

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Pediatric Anatomy & Physiology Overview

  • 1. Pediatric Anatomy & physiology Presented by : Dr. Kundan Kishor Ghimire Moderator:- Dr. Pawan Puspa Baral
  • 2. Objectives: • To understand the anatomic variations in pediatric group • To understand the physiologic differences between pediatric and adult group • Anesthetic implications of the anatomic and physiologic variations
  • 3. • Preterm infants (born before 37 weeks gestation) • Post mature infants (born after 42 weeks gestation) • Neonates (0-1 months) • Infants (1-12 months) • Toddlers (1-3 years) • Small children ( 4 – 12 years)
  • 5. Adult Vs Pediatric airway Structure Features Tongue Larger in proportion to the oral cavity than in adult. Epiglottis Narrower, U- shaped, flops posteriorly Larynx High and anterior. Level of C3-C4. (C5-C6 in adults) Cricoid More conical shaped in infants, narrower at cricoid cartilage whereas in adults it is at level of vocal cords Trachea Shorter (4-5cm), deviated posteriorly and downwards Become anatomically similar to adult between 8- 10 years
  • 6. Pediatric airway •Obligate nose breathers until 5 months of age. •Mouth breathing occurs only during crying •Obligate nose breathing is vital for respiration during feeding
  • 7. pharynx •Completely soft tissue •Easily collapsed by posterior displacement of the mandible, or external compression of the hyoid. •Pharyngeal lumen may collapse with negative pressure generated through inspiratory effort.
  • 8. Larynx •Funnel shaped •Glottis more cephalad (premature C3, Term C4 and adults C5-6) •Cricoid ring is complete, and is the narrowest point of the pediatric airway
  • 9. Larynx •Anterior and slanting vocal cords •Epiglottis is omega or tubular shaped • stubby base and thick and bulky aryepiglottic fold, tip lies at C1 in close apposition with soft palate
  • 10. INFANTADULT Figure: adult and pediatric larynx
  • 11. Figure: standard tracheal tube and microcuff tracheal tube
  • 12. RESPIRATORY SYSTEM Change at birth: • 90ml of plasma ultra-filtrate in lungs squeezed out during delivery • Catecholamine during labor : augment release of surfactant from type II pneumatocytes, • Lung expansion : increases alveolar and arterial oxygen tension; decreases pulmonary vascular resistance
  • 14. RESPIRATORY SYSTEM Lungs •Maturation does not complete until 8 years. •Alveoli grow and increase in number. •Surfactant production begins at 20 weeks, but increases between 30-34 weeks
  • 15. RESPIRATORY SYSTEM Anatomical differences in the thorax • compliant chest wall • Ribs are cartilaginous, horizontally located, limiting an increase in tidal volume. • Ventilation is primarily diaphragmatic. • Diaphragm is deficient in type 1 muscle fibers reaches adult level by 2 yrs
  • 16. Figure: newborn and adult ribs type
  • 18. RESPIRATORY SYSTEM • Central apnea- self limited in newborns, approximately 5 seconds • Apnea of prematurity – 20 seconds or associated with desaturation episodes and bradycardia • Resolves at 50- 55 weeks gestational age.
  • 19. RESPIRATORY SYSTEM • Pediatric airway • Infants increase their respiratory rate in the presence of hypercarbia • Not as much as adults because chemoreceptors are immature • Hypoxia-brief hyperventilation followed by hypoventilation • Periodic breathing occurs in 78% of infants, usually during quiet sleep
  • 20. Anesthetic consideration • Difficult airway management • Rapid desaturation • MAC values • premature 20-30%, after 6mth 50%, term to 6mths= adult level • immature CNS, • maternal progesterone and endorphins and • immature BBB
  • 21. •Volatile anesthetic fast onset and recovery • alveolar ventilation/FRC 5:1( adults 1.5:1) • high cardiac output goes to vessel rich organs • low blood gas partition coefficient for volatile anesthetics
  • 22. CARDIOVASCULAR SYSTEM Fetal circulation • high pulmonary vascular resistance, low systemic resistance (placenta) and right to left shunt via PFO and DA. • Aeration of the lungs – decrease pulmonary vascular resistance(3-4 days), mediated by NO, • Systemic vascular resistance doubles after first breath by placenta removal
  • 24. At birth • Placenta removal from circulation- portal blood pressure falls- ductus venosus closure • Exposure of ductus arteriosus to ↑ O2 concentration- ductus arteriosus closure • ↓ PVR- ↑ left side pressure – foramen ovale closure
  • 25. Closure of ductus arteriosus: functional closure 10-15 hrs. after birth, anatomic closure 2-3 wks. after (ligamentous arteriosus) Closure of foramen ovale: functional closure at birth, anatomic closure at 6 wks. Closure of ductus venosus: functional closure 3-7 days after birth, anatomic closure – 2-3 months of age (ligamentous venosum)
  • 26. CARDIOVASCULAR SYSTEM • Neonatal myocardium contains immature contractile elements (undeveloped SR) and is less compliant • Stroke volume is relatively fixed • CO rate dependent • Neonatal myocardium have high glycogen store
  • 27. CARDIOVASCULAR SYSTEM • CO is twice that of the adult. • CO • 300-400ml/kg/min in newborns, • 200ml/kg/min at 2 months of age • Adrenergic receptors mature at birth but incomplete sympathetic innervation. • Impaired baroreceptor reflex activity.
  • 29.
  • 30.
  • 31. CARDIOVASCULAR SYSTEM • The electrocardiogram shows an axis oriented to the right due to right dominance.
  • 32.
  • 33. Anesthetic considerations Transitional circulation •Neonates have a reactive pulmonary vasculature •during first few weeks of life, reversion to fetal circulation. •Factors: hypoxia, hypercapnia, acidosis, infection, hypothermia, prematurity •Sudden increase in pulmonary artery pressure causes shunting of blood past the lungs through a patent foramen ovale or the ductus arteriosus, which may reopen.
  • 34. • Fixed CO and HR dependent (CPR if HR <60) •Low catecholamine store and blunted response • Sensitive to Ca channel blocking property of volatile agents and opioids induced bradycardia
  • 35. CENTRAL NERVOUS SYSTEM • CMRO2- 5ml/100g/min • CBF- 70-110ml/min/100g • Intact cerebral autoregulation in full term and nonstressed infant. • BBB is poorly formed –Drugs (barbiturates, opioids, antibiotics, bilirubin) cross BBB easily cause prolong & variable duration of action
  • 36. Cerebral vessels in preterm infant are thin walled & fragile. • Prone to Intra Ventricular Haemorrhage • Risk increased with hypoxia, hypercarbia, hypernatraemia, low HCT, • Awake airway manipulation, rapid bicarb administration, & fluctuation in BP & CBF
  • 37. Compartment Premature Neonate Infants Adults ECF 50 35 30 20 ICF 30 40 40 40 Plasma 5 5 5 5 Total 85 80 75 65 Table: Distribution of water as a percentage of body weight RENAL SYSTEM
  • 38. RENAL SYSTEM • Immature infant kidney • Diminished renal function due to small perfusion pressure and immature glomerular and tubular function. • At 20 wks. after birth- nearly complete maturation of glomerular filtration and tubular function. • At 2 year- complete maturation of renal function
  • 39. • Full term infants have the same number of nephrons as adults • Glomeruli are much smaller than in adults • GFR in the newborn is 30% that of the adult (until 2yrs) • Tubular immaturity leads to a relative inability to concentrate urine (mature at 8 mths)
  • 40. Anesthetic considerations • Meticulous fluid and electrolyte management •Dehydration is poorly tolerated –increased insensible losses due to large surface area relative to weight –larger proportion of ECF in children (40% BW as compared to 20% in adult) • Increased half life of renally excreted drugs
  • 41. HEMATOLOGIC SYSTEM •Physiologic anemia at 3 months •Fetal hemoglobin (HbF) predominates (70-90%) and low 2,3 DPG level •Shifts to the adult type (HbA) by 3 to 4 months of age •Vitamin K dependent clotting factors (II, VII, IX, X) and platelet function are deficient in the first few months
  • 42. HEPATOBILIARY SYSTEM •Hepatic metabolic capacity is immature at birth. •Some enzyme system are developed but not induced(stimulated). •Phase I reactions- Some CYP450 enzymes are fully developed, whereas others are approx. 50% of adult values. •Phase II reactions- immature until the age of 1 year.
  • 43. •Prolonged half life of benzodiazepines, morphine, and caffeine. •Reduced plasma concentration of both albumin and alpha1-acid glycoprotein •Low plasma level-decreased protein binding-higher free drug
  • 44. GLUCOSE METABOLISM • Reduced glycogen stores and impaired gluconeogenesis, increased metabolic rate. •Hypoglycaemia is common in stressed neonate glucose level should be monitored regularly •Neurological damage may result from hypoglycaemia •Prevention: IVI D10% •Hyperglycaemia is usually iatrogenic
  • 45. TEMPERATURE REGULATION • Greater surface area to body weight ratio with minimal subcutaneous fat • Poorly developed shivering, sweating and vasoconstriction mechanisms • Neonate produce heat by non shivering thermogenesis. •Severely limited in premature infants and in sick neonates.
  • 46. TEMPERATURE REGULATION Neutral thermal environment • 34ÂşC premature infant, • 32ÂşC neonates and • 28ÂşC in adolescents and adults
  • 47. Effect of Low body temperature: • Respiratory depression • Acidosis • Decreased cardiac output •Increases the duration of action of drugs • Decreases platelet function and • Increases the risk of infection.
  • 48. Summary Differences(Physiological) • HR dependent CO • Faster HR • Lower BP • Faster RR • Lower lung compliance • Greater chest wall compliance • Lower FRC • Higher ratio of body surface area to body weight • Higher total body water content
  • 49. Summary Differences(Anatomical) • Non compliant left ventricle • Residual fetal circulation • Difficult venous & arterial cannulation • Large head & tongue • Narrow nasal passage • Ant. & cephalad larynx • Long curled epiglottis (omega shaped) • Short trachea & neck • Prominent adenoids & tonsil • Weak intercostal & diaphragmatic muscle • High resistance to airflow
  • 50. Summary Pharmacological • Immature hepatic biotransformation • Decreased protein binding • Rapid rise in FA/FI • Rapid induction and recovery • Increased MAC • Larger volume of distribution of water soluble drugs • Immature neuromuscular junction
  • 51. References • Barash, Clinical Anesthesia 7th edition • Morgan, Clinical Anesthesiology 6th edition • Miller’s Anesthesia 8th edition • Aitkenhead, Textbook of Anaesthesia 7th edition

Editor's Notes

  1. They have different anatomic and physiological characteristics.
  2. weak oropharyngeal muscles-nares narrow, and a significant fraction of the work of breathing is needed to overcome nasal resistance. Occlusion of the nares by bilateral choanal atresia or tenacious secretions can cause complete airway obstruction. Placement of an oral airway, a laryngeal mask airway, or an endotracheal tube may be necessary to reestablish airway patency during sedation or anesthesia
  3. Large tongue- airway obstruction Epiglottis- control with laryngoscope is difficult Larynx is high- curved blades are useful.
  4. Large tongue tends to occlude the oral cavity by pressing against the soft palate, hence the preference of neonates and young infants for nasal breathing
  5. --Almost completely soft tissue. -- pharyngeal lumen may collapse with negative pressure generated through inspiratory effort, particularly when the muscles that maintain airway structure are depressed or paralyzed
  6. Angled vocal cords- blindly passed tracheal tube may easily lodge in the anterior commissure rather than slide over trachea. Stubby base- short and thick base
  7. The narrowest part of the adult larynx and the pediatric larynx is at the level of the cricoid cartilage. The narrowing in adults is not as pronounced as it is in infants . One millimetre of oedema can narrow a baby’s airway by 60%
  8. Microcuff tracheal tube has a soft polyurethane cuff that symmetrically inflates and is located distally than standard tracheal tubes. This configuration results in more even pressure applied to the mucosa of the trachea, less potential for edema formation in the subglottic region because the cuff is located below the cricoid cartilage and a reduced risk for VAP. Expensive so reserved in anticipated prolonged intubation.
  9. --Type of 1 fibres- slow twitch, high oxidative muscle fibres, These cells are required for continuous, repeated exercise activities -- Pump handle action- to increase anterioposterior diameters of thorax Bucket-handle action- to increase transverse diameter of thorax.
  10. Adult can increase lung volumes by raising the ribs and contracting the diaphragm. In newborn, ribs are already raised and the contraction of the diaphragm results in a relatively small increase in thoracic cavity volume. Cartilagenous ribs make chest wall compliant.
  11. Pediatric airway High metabolic rate necessitates high respiratory rate Pulmonary parameters vastly different
  12. Rapid desaturation in neonates and infants. Fewer, smaller airways increase airway resistance. Fewer and smaller alveoli reduces lung compliance. Increase oxygen consumption 6-8ml/kg/min vs 3-4ml/kg/min in adults. Hypoxic and hypercapnic drive not fully developed.
  13. Basal O2 consumption in neonates and young infants is twice that of adults (6-7ml/kg/min vs 3ml/kg/min) because of the metabolic requirement of growth and temp homeostasis. To meet this need, alveolar ventilation is increased, which in turn achieved by increasing RR, as tidal volumes are relatively fixed 7-8ml/kg
  14. Oxygenated blood passes from the placenta via a single umbilical vein, passing to the IVC. A proportion bypasses the liver via the ductus venosus. Eustachean valve at a junction betn IVC and rt. Atrium stream oxygenated blood into lt. atrium via foramen ovale. Oxygen rich blood then passes via lt. ventricle to the ascending aorta. Deoxygenated blood from head and neck enters SVC and passes into rt. Atrium, rt. Ventricle and pulmonary artery. Approx 90% of the rt. Ventricular output is directed via ductus arteriosus to the descending aorta because of high PVR of the non-aerated lungs. In this way relatively oxygenated blood is conserved for developing brain and coronary circulation with less oxygenated blood delivered to the rest of the body. Deoygenated blood returns to the placenta via the paired umbilical arteries.
  15. --Limited preload and afterload reserve so stroke volume is relatively fixed. --Limited increase in CO by volume load in a normovolemic newborn --in infant atropine increase CO not only by increasing HR but also augmenting a calcium dependent force frequency response. -- Parasympathetic NS, anesthetic overdose or hypoxia can quickly trigger bradycardia and profound reduction in CO. -- sympathetic NS and baroreceptor reflexes are not fully mature. -- infant cvs has blunted response to exogenous cathecholamaine. Dependent on exogenous (blood-ionized) calcium and probably increased susceptibility to myocardial depression by volatile anesthetics that have calcium channel blocking activity.
  16. --To meet increased metabolic demand, CO is twice that of the adult. --vagal parasympathetic tone is dominant which makes neonates and infants more prone to bradycardias. ---The baroreceptor reflex activity is impaired and a 10% reduction in blood volume will cause a 15-30% decrease in MAP.
  17. True mechanical closure of ductus arteriosus by fibrosis does not occur until 2-3 weeks of age. Hyperventilation- return increased pul. Artery pressure to normal. Keep infant warm, normal arterial oxygen and CO2 tensions and minimal anesthetic induced myocardial depression.
  18. Brain occupies 10-15% of total body weight vs 2 %adult. CMRO2 in adult is 3.5ml/100/min, CBF- 50ml/min/100g
  19. Diminished renal function due to small perfusion pressure and immature glomerular and tubular function in neonates and even more in preterm infants. Decreased creatinine clearance, impaired sodium retention, impaired glucose excretion, impaired bicarbonate reabsorption, reduced diluting ability and reduced concentrating ability.
  20. Premature infants have increased insensible losses as they have large surface area relative to weight
  21. At birth, 70-90% of Hb molecules are HbF. Within 3 months, levels drop to around 5% & HbA predominates HB in newbown ~ 18-20g/dL , HCT ~ 0.6 3-6 Mo : 9-12 g/dl as the increase in circulating volume increases more Rpidly the bone marrow function HbF combines more rapidly with 02 but release less readily as there is less 2,3-DPG
  22. Cyp4503a- adult values at birth while others are absent or reduced. Long drug half-life of morphine and benzodiazepines in several days. Neonates rely on limited supply of stored fats Hepatic metabolism and clearance of drugs is reduced, and drugs cleared by this means have a longer duration of effects.
  23. A1-acid glycoprotein binds to basic drug like lidocaine. Higher proportion of free drug and increased risk of drug toxicity.
  24. Glycogen stores are located in the liver & myocardium Infants & older children maintain blood glucose better
  25. Thermal homeostasis is immature in neonates and small children, and hypothermia in a particular risk during anesthesia. --Heat lost during anaesthesia is mostly via radiation but ma y also be lost by conduction, convection and evaporation
  26. Heat lost during anaesthesia is mostly via radiation The neutral thermal environment is defined as the range of ambient temperatures at which temperature regulation is achieved by non-evaporative physical processes alone. The metabolic rate at this temperature is minimal
  27. Dunn, Clinical Anesthesia Procedures of the Massachusetts General Hospital 7th edition