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Pediatric Physiology. Presented by- Dr Kamal Prakash Sharma Moderator-Prof. Dr Surinder Singh. Aspects of the pediatric Physiology. The neonatal oxygen consumption is approximately 6-7 ml/kg/min versus 3-4 ml/kg/min in the adult
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Pediatric Physiology Presented by- Dr Kamal Prakash Sharma Moderator-Prof. Dr Surinder Singh
Aspects of the pediatric Physiology • The neonatal oxygen consumption is approximately 6-7 ml/kg/min versus 3-4 ml/kg/min in the adult • Even under normal circumstances the immature cardiac and respiratory systems must function near maximum to support this metabolic demand.
Respiratory Physiology • The respiratory system is not fully developed at birth and continues through early childhood. • Airways fully developed at 16 wks of gestation • Alveolarize at 24-28 wks with complete maturation at 8 - 10 yrs.
Respiratory Physiology (cont’d) • Control of respiration matures rapidly in neonatal period • Ventilatory response to raised CO2 increases with postnatal age. • Response to hypoxemia is somewhat more complex during first 3 weeks as compared to CO2 & depends upon temperature.
Respiratory Physiology (cont’d) • In normothermia, hypoxemia causes transient hyperventilation(via peripheral chemoreceptors) followed by decrease in ventilation. • In hypothermia, hypoxemia decreases ventilation. • By the end of 1st month hypoxemia causes hyperventilation irrespective of temperature.
Respiratory Physiology (cont’d) Differences in airway anatomy • Head is relatively large with prominent occiput, retrognathic chin in neonate. • Nasal passages are relatively narrow, predisposing them to obstruction • Infants are obligate nasal breathers. Almost all infants can easily convert to oral breathing by 5 months of age. • Most infants can convert to oral breathing if the obstruction lasts longer than 15 seconds.
Respiratory Physiology (cont’d) Differences in airway anatomy • Relatively large size of the infant's tongue in relation to the oropharynx increases the likelihood of airway obstruction and technical difficulties during laryngoscopy • Short neck & Larynx is located higher (more cephalic) in the neck
Respiratory Physiology (cont’d) • Larynx is located higher (more cephalic) in the neck at C3-4 level as compared to C5-6 level in adults. • Epiglottis is shaped differently, long, floppy & omega shaped & angled over laryngeal inlet; control with laryngoscope blade is more difficult
Respiratory Physiology (cont’d) • Vocal cords are Bow shaped being cephalad ant. & rostralposteriorly, so a “blindly” passed endotracheal tube may easily lodge in the anterior commissure rather than slide into the trachea • Infant larynx is funnel shaped, the narrowest portion (3-5 mm) occurring at the cricoid cartilage & is covered with loose pseudo-stratified columnar epithelium.
Respiratory Physiology (cont’d) • Small diameter of the airways increases resistance to airflow; resistance is inversely proportional to the radius raised to the fourth power for laminar flow and to the fifth power for turbulent flow. • The airway of infants is highly compliant and poorly supported by surrounding structures. • Interstitium in neonates contains less elastin than in adult, leads to greater lung compliance, greater closing capacity.
Respiratory Physiology (cont’d) • The diaphragm(primary respiratory muscle) has fewer (type-1) high-oxidative muscle fibers which are more resistant to fatigue, until child is of 2 years age. • Mechanical efficiency of diaphragm is decreased in neonates. • Intercostal muscles are poorly developed, has fewer high-oxidative muscle (type-1) fibers.
Respiratory Physiology (cont’d) • Tidal volume & Dead space ventilation per kg body weight is proportionally similar to that in adults. • FRC per kg body weight is similar to those in adults. • Total alveolar surface area is 50 fold less in neonate as compared to adults • Spontaneous resp. rate decreases from 35-40/min to adult values (12-16 b/min) with increasing age.
Respiratory Physiology (cont’d) • Alveolar ventilation decreases as age increases from 100-150 ml/kg/min to 60 ml/kg/min • Periodic breathing with central apnea (of 5-15 seconds)may be present in preterm neonates • Apnea of duration >15 seconds are associated with desaturation episodes and bradycardia • Resolves at 50-55 weeks of postconceptual age.
Respiratory Physiology (cont’d) • Chest wall development • Ribs oriented parallel and unable to effectively increase the thoracic volume during inspiration • At 2 years of age ribs are oriented oblique • Highly compliant chest wall, ribs provide little support for the lungs; that is, negative intrathoracic pressure is poorly maintained. • Thus, each breath is accompanied by functional airway closure.
Cardiovascular Physiology • Fetal circulation – high pulmonary vascular resistance, low systemic resistance (placenta) and right to left shunt via PFO and DA. • Soon after birth aeration of the lungs – decrease pulmonary vascular resistance, mediated by NO, increase systemic resistance by placenta removal • PVR in neonate is less than that in fetus & is 82-240 dynes.sec/cm5 and in case of adults is 30-120 dynes.sec/cm5 • SVR in neonate is around 800 dynes.sec/cm5
Cardiovascular Physiology (cont’d) • Factors required for transition from fetal to neonatal circultaion are Oxygen, Nor-epinephrine, epinephrine, Acetylcholine, Braykinin. • Functional closure of FO occurs immediately after birth & of DA within few hours • Anatomical closure of FO is complete at 1 year & of DA at age of 3 months • Hypoxemia, hypercarbia, acidosis can cause pulmonary vasoconstriction and opening of the FO/DA.
Cardiovascular Physiology (cont’d) • During this critical period, the infant readily reverts from the adult to a fetal type of circulation; this state is called transitional circulation. • When such a “flip-flop” occurs, PAP increases to systemic levels, blood is shunted past the lungs via the PFO, and the DA may reopen and allow blood to shunt. • A rapid downhill course may occur & lead to severe hypoxemia, which explains why hypoxemic events in infants are often prolonged despite adequate ventilation with 100% O2
Cardiovascular Physiology (cont’d) • Risk factors increasing the likelihood of prolonged transitional circulation include prematurity, infection, acidosis, pulmonary disease resulting in hypercapnia or hypoxemia, acidosis, hypothermia & congenital heart disease. • Care must be directed to keeping the infant warm, maintaining normal PaO2,PaCo2 and minimizing anesthetic-induced myocardial depression.
Cardiovascular Physiology (cont’d) • Neonatal myocardium contains immature contractile elements & more connective tissue & is less compliant than the adult myocardium • This developmental immaturity of myocardial structures accounts for the tendency toward biventricular failure, sensitivity to volume loading, Poor tolerance of increased afterload, and Heart rate–dependent cardiac output
Cardiovascular Physiology (cont’d) • At birth autonomic innervation of heart & peripheral vasculature is primarily parasympathetic • Balance of autonomic innervation matures as child matures, with increasing innervation by sympathetic nervous system.
Cardiovascular Physiology (cont’d) • The infant cardiovascular system maintains lower catecholamine stores and displays a blunted response to exogenous catecholamines. • The vascular tree is less able to respond to hypovolemia with vasoconstriction d/t immaturity of baroreceptor reflex. • The hallmark of intravascular fluid depletion in neonates and infants is therefore hypotension without tachycardia.
Cardiovascular Physiology (cont’d) • Cardiac calcium stores are reduced because of immaturity of the sarcoplasmic reticulum • consequently, neonates have a greater dependence on exogenous (ionized) calcium and probably increased susceptibility to myocardial depression by potent inhaled agents that have calcium channel blocking activity
Cardiovascular Physiology (cont’d) • To meet increased metabolic demand, the Cardiac output relative to body weight is twice that of the adult. • CO is 200ml/kg/min in newborns, 150 ml/kg/min at 2 months of age • Resting Stroke volume remains fairly constant at about 1ml/kg, increased CO is achieved mainly by increase in Heart rate( average HR at birth140 b/min)
Central Nervous System • Soft & pliable cranium, non-fused sutures, two open fontanels. • Brain is structuraly complete but incompletely myelinated until 2 years of age, cerebral cortex that is poorly developed. • In neonate, predominant constituent of brain is water. • During infancy and childhood fraction of water decrease steadily and fraction of myelin, protein increases
Central Nervous System • Decreasing fraction of water is reflected in inverse changes in partition coefficients that is increase in coeff. with increasing age. • Blood-brain barrier is immature after birth, facilitate passage of lipid soluble drugs (anaesthetics) into brain.
Central Nervous System • One third of total CO perfuses brain as compared to one seventh in adults. • Cerebrovascular responses to changes in Co2 & O2 are attenuated in neonate. • CBF autoregulation is present in healthy neonate & less developed in preterm neonate. • Neuroendocrine axis is well developed even in preterm neonates • Spinal cord ends at L3/L4 • Dural sac ends at the level of S3 .
Hematologyc Physiology • Blood vol in preterm neonate is greatest 90-100 ml/kg, in term neonate 80 ml/kg, in adult 70 ml/kg. • Hb conc. at birth is between 14-20 gm% in term neonate, conc. decreases during infancy reaches nidus of 10 gm% at 10-15 wk & adult conc. at end of infancy. • At birth 80% is HbF type and only 5% remains at age of 6 months & rest is HbA
Renal Physiology • Renal function is immature in neonates because of low perfusion pressure and low glomerular filtration rate and poor tubular function • Poor concentrating ability • Complete maturation of renal function takes place by about 2 years of age. • Ability to handle free water and solute loads may be impaired in neonates • Half-life of medications excreted by means of glomerular filtration will be prolonged.
Electrolyte • Sodium conc is similar to adults in fullterm neonate. • Potassium conc may be as high as 7.5 meq/l, decreases after birth, reaching adult level during infancy. • Hypocalcemia may be present, particularly in preterm.
Thermoregulation • The thermoregulatory range is the ambient temperature range within, an unclothed subject can maintain normal body temperature • The lower limit of the thermoregulatory range is 10C for an adult, 230C and 280C for the full term and premature infant, respectively.
Thermoregulation • Enhanced heat loss due to: • relatively larger surface area to body weight ratio 2:1 (Body wt is 1/10 of adult & surface area is 1/5 of adult) • thinner layer of insulation(skin) • limited capability of heat production • Thermogenesis in brown fat is mediated by the sympathetic system and stimulated by norepinephrine, resulting in triglyceride hydrolysis.
Thermoregulation • It is very important to address all aspects of possible heat loss during anesthesia, as well as during transport to and from the operating room. • Placing the baby on a warming mattress and warming the operating room (=/>27°C) reduce heat lost by conduction. • Keeping the infant in an incubator, covered with blankets, minimizes heat lost through convection. The head should also be covered.
Thermoregulation • Heat lost from radiation is decreased with the use of a double-shelled Isolette during transport. • Heat lost through evaporation is lessened by humidification of inspired gases, the use of plastic wrap to decrease water loss through the skin and warming of skin disinfectant solutions.
Thermoregulation • Hot air blankets are the most effective means of warming children. • Anesthetic agents can alter many thermoregulatory mechanisms, particularly nonshivering thermogenesis in neonates.
Gastrointestinal System • At birth, gastric pH is alkalotic; by the second day of life, pH is in the normal physiologic range for older children. • Ability to coordinate swallowing with respiration not fully mature till infants is 4 to 5 months of age • high incidence of gastro-esophageal reflux in newborns (common in preterm infants).
Changes in Body Composition Reproduced from - R. S. Litman: Pediatric Anesthesia – The Requisites in Anesthesiology, Elsevier Mosby 2004
Hepatic Physiology • Hepatic functions are immature at birth • Hepatic synthesis of vitamin K dependent clotting factors in term neonate is between 20-60% of adult values, less in preterm. • Activity of phase-1 cytochrome P450-dependent mixed function oxidaes is immature in neonate but matures to adult values by 6 months of age.
Hepatic Physiology • Activity of phase-2 reactions, primarily conjugative immature at birth & matures gradually. • Based on above considerations, elimination half life of drugs dependent on hepatic biotransformation may be prolonged in neonate. • Albumin and alpha-1acid glycoprotein are low in neonate, so free fraction of protein bound drugs(opioids) also increase
Glucose Homeostasis • Neonates have low glycogen stores that predispose them to hypoglycemia. Impaired glucose excretion by the kidneys may partially offset this tendency. • Neonates at greatest risk for hypoglycemia are premature or small for gestational age, have been receiving hyperalimentation, and were born to diabetic mothers.
Glucose Homeostasis • Hypoglycemia is defined as <30 mg/dl in term neonate & <20 mg/dl in preterm neonate during first 3 days and <40 mg/dl after 3 days. • To maintain euglycemia 3-5 mg/kg/min of glucose in term neonate & 5-6 mg/kg/min in preterm neonate is required. • Basal energy requirement of neonate is very high about 120 kcal/kg/d as compared to 35-50 kcal/kg/d in adults.