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PEDIATRIC AIRWAY EVALUTAION & MANAGEMENT
Why so important?
80%
10%
10%respi-ratory
cardiac
shock
Majority < 1 year old
Upper airway obstruction:- infectious disease (90%), viral croup
(80%) Epiglottitis (5%) 5% - F.B, external trauma &
congenital anomaly
Airway – passage through which air passes during respiration
pediatric airway ×mini adult airway
Nasal & oral cavity
Pharynx & larynx
Trachea & large bronchi
large occiputObligate nasal breathersLarge tongueHigher placed larynxAnteriorly angulated
vocal cords
Anatomical features of pediatric airway
• Differently shaped epiglottis
• Funnel shaped larynx
• Narrowest part is cricoid
• 4-5.5mm
Work of breathing for each kg BW is same in infant& adult O2 consumption 6l/kg/min in children and 3ml/kg/min in
adult Greater O2 consumption- inc RR Tidal volume is relatively fixed ( 6-7ml/kg/min) MAV is more dependent on RR then tidal volume
(130ml/kg/min) MAV/ FRC is double , so during hypoxia ,apnea &
anesthesia , desaturation occurs rapidly Poiseuille,s law
EvaluationAge :- laryngomalacia( birth) ALTB ( <3yrs) F.B ( <15ys) Epiglottitis ( 2-6 yrs), retropharyngeal abscess ( 1-4 yr)
Presenting c/o : dyspnoeaNoisy breathing – onset
ProgressionVariabilityAssociation with sleep, crying, feedingOther aggravating & relieving factors
Associated or preceding URI, fever.h/o chocking episode, Fb intakeCOUGH:- nature
OnsetProgressionAggravating & reliving factors
VOICE changeDifficult feedingCyanosisNeck swellingh/o asthma & repeated pneumoniah/o intubation, birth trauma
General appearance of child with careful attention:Level of consciousness:- Decrease interactionIrritabilityRestlessAnxious Diaphoresis
Examination
Air hunger and hypoxemia
Increase work of breathing:Respiratory rateNasal flaringChest retractionsAccessory muscle useHead bobbingGruntingTripod position
Nose – mucus , swellingTongue, craniofacial anomalyVomitus, bleeding, Secretions in mouthAbnormal airway sounds:- stridor
StertorWheezeGrunting
Inspiratory or expiratoryCirculation:- pallor, cyanosis , skin temperature & auscultatton.
Local examination
Craniofacial anomalies
Pierre Robin S.
Treacher Collins S.
Down S.Cruzon syndrome
suctioning, positioning & supportive care are the key elements.
Stabilization of airway is primary importance during initial resuscitation.
Goal of airway management :- relieve anatomical obstruction. prevent aspiration Promote adequate gas exchange
MANAGEMENT
ACUTE AIRWAY MANAGEMENT:-
Suction nose & nasopharynx
Positioning:- reposition/ allow child to assume position of comfort
Head tilt, chin lift/ jaw thrust position
Oxygen therapy:- reduces the ventilatory requirement of oxygen.
cardiac & respiratory arrest. Hypoxemia Metabolic acidosis Respiratory distressBlood pressure, O2 saturation .
Nebulization with adrenaline (1:3) or bronchodilators.
Humidification/ steroidHeliox mixture:- 79% He and 21% O2Oropharyngeal/ bag and mask ventilatioEmergency airway access:-Intubation/
tracheostomy
Oropharyngeal airway
Bag and mask ventilation
Endotracheal tube
Tracheostomy tube
Imp laboratory test is ABGPaO2- 80-100 mm hgPaCo2- 40±5 mm hgpH- 7.40± 0.05O2 sat- >95%CBC, SE
RADIOLOGICAL - not done routinely
Xray STN lateral viewXray chest AP viewXray chest lateral oblique viewCT scan- choanal atresia
Investigations
Acute airway conditions:-Epiglottitis:- stabilize the childAvoid taking blood sample/ chest x rayAnesthetic induction-sitting positionEndotracheal intubationTracheostomy.Laryngotracheobronchitis:- O2 therapy Humidification nebulization with adrenaline Steroid/ antibiotics intubation
RETOPHARYNGEAL ABSCESS:-Maintaining airwayAntibioticsIncision & drainage
Foreign Body airwayBronchoscopy and removal
Endoscopic evaluation:-Nasopharyngolaryngoscopy
Laryngotracheoscopy
Microlaryngoscopy- gold standard
bronchoscopy
Sub acute conditions
Access nares/ choana, adenoid , lingual tonsilDynamic study access laryngeal structuresCan be used under LA & bedsideThick tongue base, overhanging epiglottis &
laryngeal scarsHigh cost & less manipulation.Less compliance
Flexible laryngoscopes
Doesn’t require GAMainly diagnostic purposeLimited interventionCan be used for intubationLimited airway control
Flexible bronchoscopy
Requires GABetter airway controlEasier interventionLaryngoscopeVentilating bronchoscopeHopkins rod telescopeOperating microscope
Micro-laryngo-bronchoscopy
MICROLARYNGOSCOPY
Spontaneous resolution 18months- 2yearsSurgical intervention:- late onset >2 yrs10% severe laryngomalacia – failure to
thrive,hypoxemia, osa, pulmonary hypertension.
supraglottoplasty or laser epiglotopexy
laryngomalacia
Glottic web: anterior or posteriorEndoscopic laser , scissors followed by stent
palcement
Vocal cord palsy:- U/L palsy – observationRarely intubation
B/L vocal cord palsy:- tracheostomy
At least for 2 years- spontaneous recovery in half of the Patients
Vocal cord lateralization
. Congenital Subglottic stenosis: lumen diameter <4mm in term & <3mm in preterm
resolves spontaneously with growth
Tracheostomy with decannulation at 3-4 years
Laser ablation if thickness <5mm
Laryngotracheoplasty- severe cases
Acquired subglottic stenosis: Initially- steroidsMild glanular stenosis- serial endoscopic
dilatation with or without steroid injectionCO2 laser- circumferential soft stenosisOpen surgical resection – grade III & IVLaryngotracheoplastyLaaryngotracheal reconstructionstenting
THANK YOU