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APPLIED ANATOMY AND PHYSIOLOGY OF PAEDIATRIC ANAESTHESIA Dr. KHAIRUNNISA BINTI AZMAN Anaethesiology department TGH

Applied anatomy and physiology of paediatric anaesthesia

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Page 1: Applied anatomy and physiology of paediatric anaesthesia

APPLIED ANATOMY AND

PHYSIOLOGY OF

PAEDIATRIC

ANAESTHESIA

Dr. KHAIRUNNISA BINTI AZMAN

Anaethesiology department TGH

Page 2: Applied anatomy and physiology of paediatric anaesthesia

What Makes Pediatric Anesthesia Different?

Airway!! Airway!!! Airway!!!

• HYPOXIA is the most common cause of pediatric perioperative cardiac arrest. – INFANTS TURN BLUE FAST. UPPER AIRWAY OBSTRUCTION

during anesthesia (particularly at induction and emergence) is a fairly common phenomenon.

• Complete and/or Partial LARYNGOSPASM is a fairly common problem

• Infants and young children ARE NOT SMALL ADULTS. "One size fits all" DOES NOT APPLY.

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Difference between adult VS Paediatric airway

Tongue Larger in propotion to the oral cavity than in adult

Epiglottis Narrower, U-Shaped, flops posteriorly

Larynx High & anterior. Level of C3-C4. (C5-C6 in adult)

Cricoid More conically shaped in infants, narrowest at cricoid ring whereas in adult it is at level of vocal cords

Trachea Deviated posteriorly & downwards Become anatomically similar to adult between 8-10 yo

Head large head, short neck & prominent occiput

Sniffing position will not help bag mask ventilation or to visualise the glottis Head needs to be in neutral position

AIRWAY & RESPIRATORY SYSTEM

Page 6: Applied anatomy and physiology of paediatric anaesthesia

• Neonates preferentially breathe through their nose – Narrow nasal passage easily blocked by

secretions & may be damaged by NG tube/ Nasal ETT

– 50% Airway resistance is from nasal passages

• The airway is funnel shaped & narrowest at level of cricoid cartilage – The epithelium is loosely bound to underlying

tissue

– Trauma to the airway easily results in oedema

– 1mm of oedema can narrow a baby’s airway by 60%

Page 7: Applied anatomy and physiology of paediatric anaesthesia

• Narrowest at cricoid rather than vocal cords

• Tube may be small enough to pass through cords but not cricoid

• Larynx is funnel shaped, so secretions accumulate in retropharangeal space

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Ideal maneuvre is combination of jaw thrust & chin lift, keeping the mouth open

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• It is suggested that a leak present around the ETT to prevent trauma resulting in subglottic oedema & subsequent post-extubation stridor

• Neonates& infant have limited respiratory reserve:

– Horizontal ribs prevent the “buckle-handle” action seen in adult breathing and limit an increase in TV

– Ventilation is primarily diaphragmatic

– Bulky abdominal organ/ stomach filled with gases from poor bag mask ventilation impinge chest content & splint diaghragm inadequate ventilation

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• The ribs are cartilaginous & perpendicular relative to the vertebral column (Horizontal), reducing the movement of the rib cage

• The infant chest wall is remarkably compliant & compliance decrease with increasing age • Subsequently the functional residual capacity (FRC) is

relatively low. • FRC ↓ with apnoea & anaesthesia causing lung collapse

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• The closing volume is larger than FRC until 6-8 yrs of age

– Increase tendency for airway closure at end of expiration

– Thus, neonates & infant generally need IPPV during anaesthesia & would benefit from a higher RR & the use of PEEP (High RR to maintain FRC)

– CPAP during spontaneus ventilation improves oxygenation & decreases the work of breathing

• Work of respiration may be 15% of O2 Consumption

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• Muscle of ventilation are easily subject to fatigue d/t low percentage of Type I muscle fibres in diaphragm. – The num ↑ to adult level over 1st year of life

• The alveoli are thick walled at birth: – There is only 10% of the total number of alveoli

found in adults

– The alveoli clusters develop over the first 8 yrs of life

• Apneas are common post-operatively in premature infants – Significant if last longer than 15 sec & are

associated with desaturation & bradycardia.

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NEONATAL CARDIAC PHYSIOLOGY • The transformation to neonatal circulation occurs with

the first few breaths, involes 2 major changes: • A marked increase in systemic resistance • A marked decrease in pulmonary resistance

• Remnats:Patent Foramen Ovale & Ductus Arteriosus

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• The patent ductus contracts in the first few days of life & will fibrose within 2-4 wks

• Closure of foramen ovale is pressure dependant & closes in the 1st day of life but may reopen within the next 5 years

• Neonatal pulmonary vasculature reacts to the rise in PaO2 & pH & the fall in PaCO2 at birth

• However, alterations in pressure & in response to hypoxia & acidosis, reversion to the transitional circulation may occur in first few weeks after birth.

Page 17: Applied anatomy and physiology of paediatric anaesthesia

CARDIOVASCULAR SYSTEM

• In neonates Myocardium less contractile causing the ventricles to be less compliant & less able to generate tension during contraction

– Limits the size of stroke volume

– Cardiac output therefore rate dependant

– Infant behaves as with fixed cardiac output state

• Cardiac output

– 300-400 ml/kg/min at birth

– 200 ml/kg/min within few months

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• Vagal parasymphathetic tone is most dominant which makes neonates & infants more prone to bradycardias

• Bradycardia:

– Assc with reduced cardiac output

– If assc with hypoxia, should be treated with O2 & Ventilation initially

– Cardiac compression will be required in neonate with HR 60 or less OR 60-80bpm with adequate ventilation

• sinus arrythmia is common in children, other irregular rhythm are abnormal

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• BP is low at birth (approx. 80/50) secondary to a low SVR, d/t large propotion of vessels-rich tissue in children

• BP increases within the 1st month to approx. 90/60

• Reach adult levels at approx. 16 y.o • Neonates have a reactive pulmonary vasculature

– Reversion to transitional circulation may occur during 1st few weeks of life, precipitated by an increase in PVR (Eg: acidosis, hypoxia, hypercapnia) & decrease in SVR (eg: most anaesthetics)

CARDIOVASCULAR SYSTEM

Page 22: Applied anatomy and physiology of paediatric anaesthesia

Infant kidneys : Immature at birth, thus:

• ↓ GFR/ Renal blood flow

– Till 2yo, d/t high renal vascular resistance

• ↓ Concentrating capacity

– U/O 1-2mls/kg/hr

• ↓ Na reabsorption

– Tubular function is immature until 8 months, so infants are unable to excrete a large sodium load

• ↓HCO3/H exchange

RENAL SYSTEM

Page 23: Applied anatomy and physiology of paediatric anaesthesia

• Dehydration:

– Poorly tolerated

– Premature infants have increased insensible losses as they have large surface area relative to weight

– There is larger proportion of ECF in children (40% BW as compared to 20% in adult)

• Conclusion:

– Newborn kidneys has limited capacity to compensate for Volume EXCESS or Volume DEPLETION

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HEPATIC SYSTEM

• Liver fx is initially immature with decreased function of hepatic enzymes

• Barbiturates & opiods for example have a longer duration of action d/t slower metabolism

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GLUCOSE METABOLISM

• Hypoglycaemia is common in stressed neonate glucose level should be monitored regularly

• Glycogen stores are located in the liver & myocardium

• Neurological damage may result from hypoglycaemia – Prevention: IVI D10%

• Infants & older children maintain blood glucose better

• Hyperglycaemia is usually iatrogenic

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HAEMATOLOGY

• 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.

• O2 dissociation curve shifts to the right as the level of HbA & 2,3-DPG rise.

• Vit K dependant clotting factor (II, VII, IX, X) & PLT fx are deficient in first few months

• Transfusion recommended when 15% of the circulating volume has been lost.

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Temperature control

• Poorly developed shivering, sweating & vasoconstriction mechanism d/t: – Large surface area to weight ratio

– Minimal subcutaneous fat

• Heat loss during anaesthesia d/t: – Conduction

– Convection & evaporation

• Optimal ambient temp to prevent heat loss: – Premature infant: 34⁰C

– Neonates: 32⁰C

– Adults: 28⁰C

Page 28: Applied anatomy and physiology of paediatric anaesthesia

• The fetus floats in warm amniotic fluid that is maintained at a temperature of approximately 98.6°F with very little fluctuation.

• Birth exposes newborns to a cooler environment in which they have to regulate their own body temperature.

• Newborns have a higher ratio of surface area to volume than adults. - This means that their body has less volume

throughout which to produce heat, and more surface area from which to lose heat.

- As a result, newborns produce heat more slowly and lose it more quickly.

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• Effect of low body temp:

– Causes respiratory depression

– Acidosis

– Decreaswd cardiac output

– Increases duration of action of drugs

– Decrease platelet function

– Increases risk of infection

Temperature control

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CENTRAL NERVOUS SYSTEM

• 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 IVH

– Risk increased with hypoxia, hypercarbia, hypernatraemia, low HCT, Awake airway manipulation, rapid bicarb administration, & fluctuation in BP & CBF

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Different Anatomy

Different Physiology Different Pharmacology

Different psychology ↓↓↓↓↓

Different approach & preparation

CONCLUSIONS ???

Page 32: Applied anatomy and physiology of paediatric anaesthesia

Be aware of:

• Sudden changes in hemodynamics

• Unexpected responses

• Unknown congenital problem

Most of the complications that arise are

attributable to a lack of understanding of these

special considerations prior to induction of

anesthesia

Page 33: Applied anatomy and physiology of paediatric anaesthesia

THANK YOU

Page 34: Applied anatomy and physiology of paediatric anaesthesia

PRACTICALITIES FOR ANAESTHETISING CHILDREN

Page 35: Applied anatomy and physiology of paediatric anaesthesia

PRE-OPERATIVE VISIT

• Evaluates: – Medical conditions of the child – The needs of planned surgical procedure – Physiological makeup of patient & family

• Weight; all drugs must be calculated according to weight • Investigations may occasionally be necessary:

– HB: Large expected blood loss, premature infant, systemic disorder, congenital heart disease

– Electrolytes: Renal or metabolic disease, IV Fluid, dehydration – CXR: Active respiratory disease, scoliosis, congenital heart

disease

• Discuss regarding post OP pain Mx – If suppository medications to be used Explain & get consent

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Page 37: Applied anatomy and physiology of paediatric anaesthesia

PRE-OPERATIVE FASTING

Solids 6 Hours

Formula milk 4-6 hours

Breast milk 3-4 hours

Clear fluids 2 hours

PREMEDICATIONS

Sedations Analgesics

Midazolam Chloral hydrate

Ketamine Clonidine

Paracetamol Ibuprofen

Codeine phosphate EMLA Cream

Page 38: Applied anatomy and physiology of paediatric anaesthesia

BASIC SET UP

TABLE & WARMER

MACHINE/ CIRCUIT

MONITOR

SUCTION & AIRWAY

EQUIPMENT IV ACCESS DRUGS

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Breathing Systems and Circuits

• The Pediatric Breathing Circuit is extendable up to 60 inches, and comes with a 1L (default) latex free reservoir bag.

• The Neonatal Breathing Circuit is a fixed length circuit which commands very low compliance loss volume.

• The neonatal circuit comes with a 0.5L (default) reservoir bag. The Y connector is designed to minimize anatomical dead space.

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INTUBATION & INDUCTION

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Page 46: Applied anatomy and physiology of paediatric anaesthesia

Greater alveolar to FRC ratio

High cardiac output to vessels

rich organ (eg: Brain)

Reduced tissue blood solubility

EFFECT OF FAST INDUCTION

INDUCTION: 1. IV Induction

2. Gas induction

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FLUIDS MANAGEMENT

• Perioperative fluid management is divided into three phases

– Maintenance, deficit and replacement of losses.

• Administration: Volumetric chambers/ Microdrip/Infusion Pump

• Warm fluid/blood/blood product

• Include dextrose in maintainance hydration fluid if needed

– Risk of hypoglycaemia higher in premature babies

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DAY 1 OL 50MLS/KG/HR D10%

DAY 2 OL 100MLS/KG/HR D10% ½ NS

> DAY 7 OL 150MLS/KG/HR D5-D10% ¼ NS

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3RD SPACE FLUID LOSS

Intra-abdominal surgery 6-10 mls/kh/hr

Intra-thoracic surgery 4-7 mls/kg/hr

Eye surgery 1-2 mls/kg/hr

Neurosurgery

Superficial surgery

Fluid deficits: • Calculated and replaced based on duration of fasting, presence

of associated conditions like • Fever, • Vomiting,diahorrea, sweating • Particular disease state or surgical problem likely to affect

fluid status (bowel obstruction, peritonitis etc). INTRAOPERATIVE FLUID LOSS 3RD Space fluid loss & blood loss

Page 55: Applied anatomy and physiology of paediatric anaesthesia

ESTIMATED BLOOD VOLUME (EBV)

Premature Neonate 90-100mls/kg

Term neonate 80-90mls/kg

3mo – 1yr 75-80mls/kg

3-6 yrs 70-75mls/kg

>6 yrs 65-70 mls/kg

Allowable blood loss

ABL = WEIGHT x EBV X (H₀ - H₁)/Hₐ

H₀ = Starting Hematocrit

H₁ = Lowest acceptable hematocrit

Hₐ = average hematocrit

Intraoperative blood loss replacement is done with Ringer’s lactate 3 ml per 1ml of blood loss, 1 ml of colloid solution for each ml of blood loss and 0.5 ml of red cell concentrates for each ml of blood loss.

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PAIN MANAGEMENT

• Regional:

– Caudal block

– Ilioinguinal block

• Local anaesthesia

• Post operative analgesia (Syp/Supp)

Page 57: Applied anatomy and physiology of paediatric anaesthesia

THANK YOU AGAIN

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REFERENCES:

• Dr. M.N.Chidananda Swamy, Dr. D. Mallikarjun. Applied aspect of anatomy and physiology relevance to apaediatric anaesthesia. Indian J Anaesth 2004

• Sue clark. The differences of anaesthetic care in paediatrics compared to adult. The association of paediatric practice 2010

• F. Macfarlane. Paediatric anatomy & physiology and the basic of paediatric anaesthesia. Anaethesia tutorial of the week

• Paediatric anaesthesia digital book

• Ahmad A.L. Paediatric anaethesia basic and beyond presentation