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ANAESTHETIC CHALLENGES
IN
NEONATAL
EMERGENCIES
Dr Sourav Dash
MKCG MRDICAL COLLEGE
BERHAMPUR, ODISHA
AIRWAY CHALLENGES
 Neonatal intubations are difficult (Large tongue, Large occiput,
floppy epiglottis, higher and anterior larynx)
AIRWAY :
Obligatory nose breather
Differences from adult airway:
Supraglottic part:
• Short neck.
• Large tongue
• Larynx is more anterior &
cephalad
• Long, thin u-shaped epiglottis - needs to be
lifted with straight blade
• Vocal cords angled slightly anterior - ETT stops
at glottic opening
UNDER NEURO-
MUSCULAR
BLOCKADE
•Cricoid cartilage
is the narrowest
portion of the
pediatric airway
Without NMB
•The vocal cords
are the narrowest
part
RESPIRATORY PHYSIOLOGY AND CHALLENGES
• O2 CONSUMPTION 5-8 ML/KG/MIN ( V5 ADULT 2-3ml/ kg /MIN)
• Increased RR in neonate - Enhanced CO2 elimination
• ALVEOLAR VENTILATION 130ml/ kg/MIN ( CAUSE OF HIGH RR) VS 60
ML/KG/MIN IN ADULTS
- Induction and emergence from inhalational anaesthesia is rapid
• Alveolar ventilation / FRC - 5:1 (1.5 : 1 in adults)
• TV 7 - 10ml/kg
• ODC IN NEONATE SHIFTED TO LEFT (BECAUSE FETAL Hb HAS HIGH 02 AFFINITY)
• Ribs are horizontal (vs vertical in adults)
• Rib cartilages more pliable
• Chest wall collapses with increased negative intrathoracic pressure
• Atelectasis risk is more because of low FRC and less no. of alveoli
Upto 20% OF
PREMATURE
INFANTS MAY NEED
ELECTIVE POST OP
VENTILATION
MORE
PRONE TO
APNOEA
1.IMMATURI
TY OF
RESPIRATORY
CENTERS
1.PROLONG
ED ACTION
OF
ANESTHETIC
S (NMB)
FATIGUE
OF
RESPIRATO
RY
MUSCLES
1.OBSTR
UCTIVE
APNEA
HYPOTHERMIA
HYPOGLYCAEMI
A HYPOXIA
SEPSIS
AND
HYPOCAL
CEMIA
CARDIOVASCULAR CONCERNS
• Cardiac output is rate dependent
INHALED ANESTHETICS
• Their negative inotropic and chronotropic effects are poorly tolerated
• Baroreceptor reflexes are blunted or obliterated by these agents
• Reflex tachycardia, which is vital in supporting blood pressure and cardiac output, may not
occur
ATROPINE
• Atropine requirements in newborns (0.03
0.05mg/kg intravenous [IV]) are almost three times greater than in adults
• Total doses of less than 0.1 to 0.15 mg may produce paradoxical
bradycardia, further contributing to hypotension
RENAL PHYSIOLOGY
↓GFR UPTO 2YRS
↓CONCENTRATING CAPACITY – prone to dehydration and hypothermia
↓Na+ REABSORPTION
↓HCO3- / H+ EXCHANGE
↓FREE H2O CLEARANCE
↓URINARY LOSS OF K, Cl
↓ ABILITY TO EXCRETE VOLUME LOADS - RISK OF FLUID OVERLOAD
Neonates are born with excess Na+
• No Na REQUIRED IN FIRST 72HRS
• Maintenance fluid should be only of hypotonic glucose solution (prevent hypoglycemia)
• Replacement of insensible third space loss and small blood vol. loss - give isotonic fluid
• If more blood loss - PRBC
• MAXIMUM ALLLOWABLE BLOOD LOSS (MABL) = EBV(STARTING HCT – TARGET
HCT)/STARTING HCT
TEMPERATURE
 Brown fat metabolism
 MAINTAIN BODY HEAT
 NON SHIVERING THERMOGENESIS
•- INCREASED BODY
SURFACE AREA
•- LOWER HEAT
RESERVES, LESS
INSULATING FAT
•- INABILITY TO SHIVER
•- DECREASED
KERATINISATION OF SKIN
• RADIANT WARMERS,
FLUID WARMERS
• WARMED SURGICAL
SOLUTIONS
• PLASTIC WRAP TO
PREVENT SKIN FROM
GETTING WET
• COVERING HEAD & OTHER
AREAS BY PADDING
VULNERABLE
TO
HYPOTHERMIA
PREVENTION
&
MANAGEMENT
 Brown fat
 Differentiate at 26 – 30wks POG
 Not present sufficiently in preterm
 So more risk of hypothermia
NERVOUS SYSTEM
• Increased chances of intra-ventricular hemorrhage
• Pain– neurological, physiological, hormonal and metabolic stress response
is present
NOCICEPTIVE SYSTEM AND STRESS RESPONSE
• Transduction of pain functionally matures by 24 wks POG
• Spinal cord transmission & supraspinal processing and integration mature at 30wks
• But NT which modulate pain do not appear in descending pathway till 1st month of life
• So results in
• Increased intensity of pain
• Increased duration
• Hyperalgesia of injured tissue decrease pain threshold by 30-35%
• Amounts to
• Permanent structural and behavioral changes in neonates’ nervous system and
somatic complaints later on
REGIONAL ANAESTHESIA:
 Distal end of spinal cord ends between L2 – L3.
 They have more spinal fluid per body weight, hence require
larger dose , duration of block is short.
 Most common approach for epidural anaesthesia is caudally.
Neonatal Pharmacology
• Hepatic function immature.
• Renal tubular function immature.
• Less protein (albumin) ↓PPB & ↑Vd
• Increased volume of distribution (Vd) – larger initial dosage of water soluble drugs
(eg- Sch, antibiotics)
• ↓Fat - slower redistribution in fat - ↑ duration of action eg: Thiopentone
• Fentanyl ; redistributes to muscle ; ↑ duration of action
Induction agents
Propofol Moderate-to-severe hypotension, no effect on PVR
Thiopentone Due to high Vd high doses required
Inhalational agents
Sevoflourane Has less effect on hemodynamics
Desflurane Emergence is faster and beneficial in neonates in whom extubation is planned.
Muscle relaxants
Succinylcholine Newborns require higher dose of (2 mg/kg)
Mivacurium, Rocuronium Predictable duration of action, provided the infant is normothermic and no significant
cardiovascular side effects
Opioids
Fentanyl Minimal cardiovascular depression, used in critically ill neonates
Local anaesthetics
Bupivacaine Caudal/epidural-associated with higher blood level in neonates
Chlorprocaine Can be used with greater safety in the newborns.
 History - significant events at birth (asphyxia,
meconium aspiration, Apgar score), review NICU care
and ventilatory support
 Examination
 Investigations – CBC, RFT, electrolytes, ECHO, Chest X
ray, blood gases
 Counseling parents and consent
Preoperative considerations
Monitoring
 ECG
 Pulse oximeter – pre ductal and post ductal
 Capnograph
 Noninvasive blood pressure
 Precordial stethoscope
 Temperature probe
 Urine output , invasive arterial pressure, central venous pressure in
major surgeries
 CVP catheters in right IJV – monitor CVP & secure iv line in
anticipated blood loss or fluid shift
 PICC line can give fluid but no CVP monitoring
• Immediate postoperative extubation
• Post anaesthetic apnoea is high in neonates <40 weeks
• Fluid, electrolytes, glucose monitoring
• Total parenteral nutrition
• Continued NICU care and ventilation
Postoperative considerations
SURGICAL EMERGENCIES
• Almost all surgical emergencies in neonates are urgencies & not
emergencies
• Can afford to wait for 24-48 hrs while baby is stabilised & allows for
better foetal to neonatal transition
• Maternal & Perinatal history which could provide important clues to
diagnosis.
• Rule out any associated anomalies especially congenital heart disease.
FIRST WEEK OF LIFE :
INTESTINAL
OBSTRUCTION
CONGENITAL
DIAPHRAGMATIC
HERNIA(CDH)
TRACHEO-OESOPHAGEAL
FISTULA(TOF)
OMPHALOCELE &
GASTROCHISIS
MENINGOMYELOCELE
SECOND WEEK OF
LIFE:
Hernia
Necrotising
enterocolitis(NEC)
THIRD TO SIXTH
WEEK OF LIFE :
Pyloric stenosis
TRACHEO-OESOPHAGEAL FISTULA(TOF)
Incidence: 1: 3000 live births.
• 50% associated with congenital anomalies.
Associated anomalies:
VATER –
 Vertebral anomalies or ventricular septal defect
 Anal atresia
 TOF
 Oesophageal atresia
 Radial aplasia & renal anomalies
VACTERL
• Also includes Cardiac and limb anomalies.
Type: 5 major varieties present
MOST COMMON TYPE - TYPE C ( upper end blind with lower end
communicating)
 Fistula commonly occurs in posterior muscular part of trachea,
just above carina.
Embryology:
Division of foregut occurs at 4th & 5th week of development.
Incomplete division leads to FISTULA.
Diagnosis:
• Antenatally: maternal polyhydramnios & absence of
stomach bubble on USG.
• Postnatally: presents with 3 C’s of oesophageal atresia
• choking
• Coughing
• cyanosis
• Passage of NG tube meets with obstruction
Clinical presentation:
DEHYDRATION: proximal oesophagus doesn’t
communicate with stomach.
Aspiration pneumonia: reflux of stomach
contents through distal oesophagus into
trachea.
Investigations:
 Chest Xray – coiled catheter in blind
proximal pouch
PRE OPERATIVE STABILISATION:
• NPO
• IV access
• Head up position
• Treat dehydration : hydrate
adequately, correct electrolyte
imbalance
• ASPIRATION PNEUMONIA : If reflux
is high , gastrostomy is planned to
protect pulmonary system
• Fistula repair is taken up if neonate
is in good health
ANAESTHETIC MANAGEMENT
INTRAOPERATIVE:
AVOID EXCESSIVE POSITIVE PRESSURE
VENTILATION
INDUCTION & TRACHEAL INTUBATION:
 UNSTABLE PT
• Awake intubation with local
anaesthesia and mild sedation
 STABLE PT
• Rapid sequence IV induction with
muscle paralysis or
• Inhalational induction with
spontaneous ventilation without
muscle relaxant
ASSESSMENT OF ETT POSITION :
• Goal: ETT just above the carina & just below the fistula (so that less
gastric insufflation through the fistula)
• Right main stem intubation & withdraw ETT until bilateral breath
sounds.
• Avoid positive pressure ventilation to decrease stomach distension via fistula
• If fistula is too close to carina- selective endobronchial intubation till fistula ligation
• ETT above fistula with spontaneous or gentle assisted ventilation
• If fistula large and PPV needed - do gastrostomy to avoid gastric rupture
• Stethoscope over axilla detects accidental rt. mainstem bronchial ETT
advancement
Patient position:
• Lateral decubitus position
• Posterolateral thoracotomy
MAINTAINENCE:
• O2 : N2O , Inhalational agent & spontaneous ventilation are used.
• Maintain PaO2 50 – 70 mmHg or SaO2 87 – 92% to avoid
retinopathy of prematurity.
•Spontaneous ventilation
with inhalational agents
before doing
the repair
•controlled ventilation &
muscle relaxant
after doing
the repair
POST OPERATIVE:
• Pharynx suctioned with a soft catheter & it must not reach
anastomotic site.
• Prolonged intensive respiratory Care.
• Postop analgesia: epidural catheter, IV narcotics.
•EXTUBATED
Child with a clear
chest who is awake &
moving vigorously
•continue controlled
ventilation
If pulmonary
complication present
Congenital diaphragmatic hernia
• Incidence
1:4000-5000, M:F-
2:1
• M/C - POSTEROLAT
- BOCHDALEK TYPE
(90%)
• THROUGH
FORAMEN OF
MORGAGNI – 10%
PATHOGENESIS
Herniation of
viscera During
branching of
bronchi and
PAs
Interference with
lung development
Decreased
bronchiolar
branching
Loss of lung mass:
HYPOPLASIA
Dysfunctional
surfactant
system
ATELECTASIS
AND
RESPIRATORY
DISTRESS
Associated anomalies
CVS Ductus arteriosus, septal defects, A-V valve defects, aortic
arch hypoplasia,
50%
CNS Neural tube defects, microcephaly 20%
GIT Malrotation & atresia 10%
Genito-
urinary
Hypospadias, renal dysplasia 10%
Musculoskel
etal
Polydactyly, talipes 10%
DELAYED CLOSURE OF PLEURO-PERITONEAL CANALS OR EARLY MIDGUT MIGRATION
OR RESULTS IN CDH
Pathophysiology
Visceral herniation
Abnormal lung
development
Abnormal pulmonary
vasculature
Atelectasis of the lung
Systemic hypotension
H
Y
P
O
X
A
E
M
I
A
Pulmonary hypoplasia
Persistent pulmonary
hypertension (PPHN)
DIAGNOSIS
USG
• Polyhydramnios on prenatal USG
• Intrathoracic gastric bubble
• Mediastinal shift away from hernia
CLINICAL FEATURES
• ↑HR, ↑RR , CYANOSIS
• Scaphoid (concave) abdomen clause
of herniation
Auscultation - no breath sounds bowel
sounds in chest
X ray - bowel loops in chest (m/c Lt. side)
• NGT in stomach in chest
• Initial stabilization with delayed surgery
• Tracheal intubation and mechanical ventilation
• Avoid hypothermia which causes ↑rt→lt shunt ↑ pvr ↑ o2 consumption
• Decompress stomach by ngt
• Avoid bag and mask ventilation (contraindicated)
• Lung protective ventilatory strategy
Low TV, RR high
PIP≤ 25cm H2O
PaCO245-60mm Hg - permissive hypercapina
pH >7.3 (avoid acidosis - pulmonary vasoconstriction and decreases SPO2)
Preductal SpO2 85%-95%
AVOID rt→lt shunt
PRE OP MANAGEMENT
• Laboratory studies: CBC, RBS, serum
electrolytes, cross matching, ABG
• CXR: Air filled viscera in the chest,
mediastinal shift
• ECHO : Assessment of myocardial
function, pulmonary hypertension,
concurrent heart defects, R-L
shunting
INVESTIGATIONS
Adequate venous access
Gastric decompression
Monitoring
 Pre induction –Standard monitors, preductal & postductal pulse
oximeter, precordial stethoscope
 Post induction - Temperature, capnography, urine output, ±
right radial arterial line, ± central venous access
INTRAOPERATIVE MANAGEMENT
• Choice of anaesthesia – Rapid sequence induction with
succinylcholine/rocuronium or awake intubation
• Maintenance- Isoflurane + O2+ air. Avoid N2O
• Volume/ Pressure control ventilation – PIP<30cm H2O,
RR 30-60/min
• Analgesia- IV opioids, epidural
• Active warming measures
INTRAOPERATIVE MANAGEMENT
Intraoperative complications
• Acute desaturation- suspect pneumothorax on
unaffected side
• Sudden hypotension - RV failure, kinking of major
blood vessels, abdominal compartment syndrome
• Hypothermia
• Hypoglycemia
• Post operative ventilation in large hernia
• Do not hyperventilate
• Aim to maintain PaO2 >150 mmHg with least FiO2
• Slow weaning from oxygen over 48-72 hours
• Abdominal compartment syndrome
• Beware of Honeymoon phenomenon
POSTOPERATIVE MANAGEMENT
UPPER GIT LOWER GIT
COMPRISES STOMACH , DUODENUM ,
PROXIMAL ILEUM
TERMINAL ILEUM ,
COLON , RECTUM ,
ANUS
CAUSES 1.Duodenal or ileal atresia.
2.Malrotation of midgut
volvulus.
3.Peritoneal bands.
4.Intra abdominal hernia.
1.Meconium ileus.
2.Intussusception.
3.Imperporate anus
INTESTINAL OBSTRUCTION
Incidence: 1 : 1500 live births
UPPER GIT LOWER GIT
CLINICAL
FEATURES
 24 hrs of birth.
Vomiting with initiation of
feeding.
Tender abdomen.
Persistent vomiting leads to
sodium loss, hypochloraemia,
metabolic alkalosis.
 bowel ischaemia – acidosis ,
bloody stools
 2 – 7 days of birth.
Increased
abdominal distention.
No passage of
faeces.
Vomiting is delayed.
Anaesthetic management:
• Aggressive correction with fluid & electrolytes, blood products
• Sodium bicarbonate only in severe acidosis (Ph < 7.20)
• Nasogastric tube suctioning and left open
• Rapid sequence intubation is preferred to prevent aspiration
• Procedure: combined general + caudal .
• Advantages : light level of anaesthesia , muscle relaxation & early extubation.
• Post operative ventilation in sick patients till condition stabilises.
Abdominal wall defects
• Most common are gastroschisis &
omphalocoele
• Although these conditions are embryologically
unique anaesthetic management is essentially
same
Gastroschisis Omphalocoele
Incidence 1:10000 1:4000-7000
Patho-physiology Interruption of
ompalomescentric
artery
Non return of bowel from
extra embryonic coelom
Defect Open with inflamed,
eodematous bowel
Amnion cover outside,
peritoneum inside
Astd anomalies Rare High
Defect size 2-5 cm, lateral 2-15 cm, midline
Umbilical cord Adjacent to defect Apex of sac
Surgical management
• Primary closure- for small defects with not much
viscero- abdominal disproportion
• Staged repair- if complete reduction is not possible
• Delayed closure- over weeks to months in very large
omphalocoele
Intraoperative management
• Choice of anaesthesia – Modified rapid sequence induction with succinylcholine
/rocuronium, maintenance- isoflurane+O2 + air. Avoid N2O
• Adequate neuromuscular blockade to facilitate
abdominal closure
• Fluid - 10-20ml/kg boluses
• Analgesia- IV opioids, regional techniques
• Active warming
 Intragastric <20mm Hg
Intravesical pressures <20mm Hg
PIP prior to abdominal closure < 35 cm H2O
End tidal CO2<50mm Hg
Urine output >0.5ml /kg/hr
Criteria for safe abdominal
closure
Complications
• Abdominal compartment syndrome
• Dehydration & electrolyte imbalance
• Hypothermia
• Hypoglycaemia
• B/L lower lobe atelectasis
Post operative care
• Continuation of mechanical ventilation for 24-48 hours
• Judicious fluid therapy
• Good analgesia
• Initiating TPN
THANK YOU

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Anaesthesia challenges in neonatal emergencies-1.pptx

  • 1. ANAESTHETIC CHALLENGES IN NEONATAL EMERGENCIES Dr Sourav Dash MKCG MRDICAL COLLEGE BERHAMPUR, ODISHA
  • 2. AIRWAY CHALLENGES  Neonatal intubations are difficult (Large tongue, Large occiput, floppy epiglottis, higher and anterior larynx)
  • 3. AIRWAY : Obligatory nose breather Differences from adult airway: Supraglottic part: • Short neck. • Large tongue • Larynx is more anterior & cephalad
  • 4.
  • 5. • Long, thin u-shaped epiglottis - needs to be lifted with straight blade • Vocal cords angled slightly anterior - ETT stops at glottic opening UNDER NEURO- MUSCULAR BLOCKADE •Cricoid cartilage is the narrowest portion of the pediatric airway Without NMB •The vocal cords are the narrowest part
  • 6. RESPIRATORY PHYSIOLOGY AND CHALLENGES • O2 CONSUMPTION 5-8 ML/KG/MIN ( V5 ADULT 2-3ml/ kg /MIN) • Increased RR in neonate - Enhanced CO2 elimination • ALVEOLAR VENTILATION 130ml/ kg/MIN ( CAUSE OF HIGH RR) VS 60 ML/KG/MIN IN ADULTS - Induction and emergence from inhalational anaesthesia is rapid • Alveolar ventilation / FRC - 5:1 (1.5 : 1 in adults) • TV 7 - 10ml/kg • ODC IN NEONATE SHIFTED TO LEFT (BECAUSE FETAL Hb HAS HIGH 02 AFFINITY)
  • 7. • Ribs are horizontal (vs vertical in adults) • Rib cartilages more pliable • Chest wall collapses with increased negative intrathoracic pressure • Atelectasis risk is more because of low FRC and less no. of alveoli
  • 8. Upto 20% OF PREMATURE INFANTS MAY NEED ELECTIVE POST OP VENTILATION MORE PRONE TO APNOEA 1.IMMATURI TY OF RESPIRATORY CENTERS 1.PROLONG ED ACTION OF ANESTHETIC S (NMB) FATIGUE OF RESPIRATO RY MUSCLES 1.OBSTR UCTIVE APNEA HYPOTHERMIA HYPOGLYCAEMI A HYPOXIA SEPSIS AND HYPOCAL CEMIA
  • 9. CARDIOVASCULAR CONCERNS • Cardiac output is rate dependent INHALED ANESTHETICS • Their negative inotropic and chronotropic effects are poorly tolerated • Baroreceptor reflexes are blunted or obliterated by these agents • Reflex tachycardia, which is vital in supporting blood pressure and cardiac output, may not occur ATROPINE • Atropine requirements in newborns (0.03 0.05mg/kg intravenous [IV]) are almost three times greater than in adults • Total doses of less than 0.1 to 0.15 mg may produce paradoxical bradycardia, further contributing to hypotension
  • 10. RENAL PHYSIOLOGY ↓GFR UPTO 2YRS ↓CONCENTRATING CAPACITY – prone to dehydration and hypothermia ↓Na+ REABSORPTION ↓HCO3- / H+ EXCHANGE ↓FREE H2O CLEARANCE ↓URINARY LOSS OF K, Cl ↓ ABILITY TO EXCRETE VOLUME LOADS - RISK OF FLUID OVERLOAD Neonates are born with excess Na+ • No Na REQUIRED IN FIRST 72HRS • Maintenance fluid should be only of hypotonic glucose solution (prevent hypoglycemia) • Replacement of insensible third space loss and small blood vol. loss - give isotonic fluid • If more blood loss - PRBC • MAXIMUM ALLLOWABLE BLOOD LOSS (MABL) = EBV(STARTING HCT – TARGET HCT)/STARTING HCT
  • 11. TEMPERATURE  Brown fat metabolism  MAINTAIN BODY HEAT  NON SHIVERING THERMOGENESIS •- INCREASED BODY SURFACE AREA •- LOWER HEAT RESERVES, LESS INSULATING FAT •- INABILITY TO SHIVER •- DECREASED KERATINISATION OF SKIN • RADIANT WARMERS, FLUID WARMERS • WARMED SURGICAL SOLUTIONS • PLASTIC WRAP TO PREVENT SKIN FROM GETTING WET • COVERING HEAD & OTHER AREAS BY PADDING VULNERABLE TO HYPOTHERMIA PREVENTION & MANAGEMENT  Brown fat  Differentiate at 26 – 30wks POG  Not present sufficiently in preterm  So more risk of hypothermia
  • 12. NERVOUS SYSTEM • Increased chances of intra-ventricular hemorrhage • Pain– neurological, physiological, hormonal and metabolic stress response is present NOCICEPTIVE SYSTEM AND STRESS RESPONSE • Transduction of pain functionally matures by 24 wks POG • Spinal cord transmission & supraspinal processing and integration mature at 30wks • But NT which modulate pain do not appear in descending pathway till 1st month of life • So results in • Increased intensity of pain • Increased duration • Hyperalgesia of injured tissue decrease pain threshold by 30-35% • Amounts to • Permanent structural and behavioral changes in neonates’ nervous system and somatic complaints later on
  • 13. REGIONAL ANAESTHESIA:  Distal end of spinal cord ends between L2 – L3.  They have more spinal fluid per body weight, hence require larger dose , duration of block is short.  Most common approach for epidural anaesthesia is caudally.
  • 14. Neonatal Pharmacology • Hepatic function immature. • Renal tubular function immature. • Less protein (albumin) ↓PPB & ↑Vd • Increased volume of distribution (Vd) – larger initial dosage of water soluble drugs (eg- Sch, antibiotics) • ↓Fat - slower redistribution in fat - ↑ duration of action eg: Thiopentone • Fentanyl ; redistributes to muscle ; ↑ duration of action
  • 15. Induction agents Propofol Moderate-to-severe hypotension, no effect on PVR Thiopentone Due to high Vd high doses required Inhalational agents Sevoflourane Has less effect on hemodynamics Desflurane Emergence is faster and beneficial in neonates in whom extubation is planned. Muscle relaxants Succinylcholine Newborns require higher dose of (2 mg/kg) Mivacurium, Rocuronium Predictable duration of action, provided the infant is normothermic and no significant cardiovascular side effects Opioids Fentanyl Minimal cardiovascular depression, used in critically ill neonates Local anaesthetics Bupivacaine Caudal/epidural-associated with higher blood level in neonates Chlorprocaine Can be used with greater safety in the newborns.
  • 16.  History - significant events at birth (asphyxia, meconium aspiration, Apgar score), review NICU care and ventilatory support  Examination  Investigations – CBC, RFT, electrolytes, ECHO, Chest X ray, blood gases  Counseling parents and consent Preoperative considerations
  • 17. Monitoring  ECG  Pulse oximeter – pre ductal and post ductal  Capnograph  Noninvasive blood pressure  Precordial stethoscope  Temperature probe  Urine output , invasive arterial pressure, central venous pressure in major surgeries  CVP catheters in right IJV – monitor CVP & secure iv line in anticipated blood loss or fluid shift  PICC line can give fluid but no CVP monitoring
  • 18. • Immediate postoperative extubation • Post anaesthetic apnoea is high in neonates <40 weeks • Fluid, electrolytes, glucose monitoring • Total parenteral nutrition • Continued NICU care and ventilation Postoperative considerations
  • 19. SURGICAL EMERGENCIES • Almost all surgical emergencies in neonates are urgencies & not emergencies • Can afford to wait for 24-48 hrs while baby is stabilised & allows for better foetal to neonatal transition • Maternal & Perinatal history which could provide important clues to diagnosis. • Rule out any associated anomalies especially congenital heart disease.
  • 20. FIRST WEEK OF LIFE : INTESTINAL OBSTRUCTION CONGENITAL DIAPHRAGMATIC HERNIA(CDH) TRACHEO-OESOPHAGEAL FISTULA(TOF) OMPHALOCELE & GASTROCHISIS MENINGOMYELOCELE SECOND WEEK OF LIFE: Hernia Necrotising enterocolitis(NEC) THIRD TO SIXTH WEEK OF LIFE : Pyloric stenosis
  • 21. TRACHEO-OESOPHAGEAL FISTULA(TOF) Incidence: 1: 3000 live births. • 50% associated with congenital anomalies. Associated anomalies: VATER –  Vertebral anomalies or ventricular septal defect  Anal atresia  TOF  Oesophageal atresia  Radial aplasia & renal anomalies VACTERL • Also includes Cardiac and limb anomalies.
  • 22. Type: 5 major varieties present MOST COMMON TYPE - TYPE C ( upper end blind with lower end communicating)  Fistula commonly occurs in posterior muscular part of trachea, just above carina.
  • 23. Embryology: Division of foregut occurs at 4th & 5th week of development. Incomplete division leads to FISTULA. Diagnosis: • Antenatally: maternal polyhydramnios & absence of stomach bubble on USG. • Postnatally: presents with 3 C’s of oesophageal atresia • choking • Coughing • cyanosis • Passage of NG tube meets with obstruction
  • 24. Clinical presentation: DEHYDRATION: proximal oesophagus doesn’t communicate with stomach. Aspiration pneumonia: reflux of stomach contents through distal oesophagus into trachea. Investigations:  Chest Xray – coiled catheter in blind proximal pouch
  • 25. PRE OPERATIVE STABILISATION: • NPO • IV access • Head up position • Treat dehydration : hydrate adequately, correct electrolyte imbalance • ASPIRATION PNEUMONIA : If reflux is high , gastrostomy is planned to protect pulmonary system • Fistula repair is taken up if neonate is in good health ANAESTHETIC MANAGEMENT INTRAOPERATIVE: AVOID EXCESSIVE POSITIVE PRESSURE VENTILATION INDUCTION & TRACHEAL INTUBATION:  UNSTABLE PT • Awake intubation with local anaesthesia and mild sedation  STABLE PT • Rapid sequence IV induction with muscle paralysis or • Inhalational induction with spontaneous ventilation without muscle relaxant
  • 26. ASSESSMENT OF ETT POSITION : • Goal: ETT just above the carina & just below the fistula (so that less gastric insufflation through the fistula) • Right main stem intubation & withdraw ETT until bilateral breath sounds. • Avoid positive pressure ventilation to decrease stomach distension via fistula • If fistula is too close to carina- selective endobronchial intubation till fistula ligation • ETT above fistula with spontaneous or gentle assisted ventilation • If fistula large and PPV needed - do gastrostomy to avoid gastric rupture • Stethoscope over axilla detects accidental rt. mainstem bronchial ETT advancement
  • 27. Patient position: • Lateral decubitus position • Posterolateral thoracotomy
  • 28. MAINTAINENCE: • O2 : N2O , Inhalational agent & spontaneous ventilation are used. • Maintain PaO2 50 – 70 mmHg or SaO2 87 – 92% to avoid retinopathy of prematurity. •Spontaneous ventilation with inhalational agents before doing the repair •controlled ventilation & muscle relaxant after doing the repair
  • 29. POST OPERATIVE: • Pharynx suctioned with a soft catheter & it must not reach anastomotic site. • Prolonged intensive respiratory Care. • Postop analgesia: epidural catheter, IV narcotics. •EXTUBATED Child with a clear chest who is awake & moving vigorously •continue controlled ventilation If pulmonary complication present
  • 30. Congenital diaphragmatic hernia • Incidence 1:4000-5000, M:F- 2:1 • M/C - POSTEROLAT - BOCHDALEK TYPE (90%) • THROUGH FORAMEN OF MORGAGNI – 10%
  • 31. PATHOGENESIS Herniation of viscera During branching of bronchi and PAs Interference with lung development Decreased bronchiolar branching Loss of lung mass: HYPOPLASIA Dysfunctional surfactant system ATELECTASIS AND RESPIRATORY DISTRESS
  • 32. Associated anomalies CVS Ductus arteriosus, septal defects, A-V valve defects, aortic arch hypoplasia, 50% CNS Neural tube defects, microcephaly 20% GIT Malrotation & atresia 10% Genito- urinary Hypospadias, renal dysplasia 10% Musculoskel etal Polydactyly, talipes 10% DELAYED CLOSURE OF PLEURO-PERITONEAL CANALS OR EARLY MIDGUT MIGRATION OR RESULTS IN CDH
  • 33. Pathophysiology Visceral herniation Abnormal lung development Abnormal pulmonary vasculature Atelectasis of the lung Systemic hypotension H Y P O X A E M I A Pulmonary hypoplasia Persistent pulmonary hypertension (PPHN)
  • 34. DIAGNOSIS USG • Polyhydramnios on prenatal USG • Intrathoracic gastric bubble • Mediastinal shift away from hernia CLINICAL FEATURES • ↑HR, ↑RR , CYANOSIS • Scaphoid (concave) abdomen clause of herniation Auscultation - no breath sounds bowel sounds in chest X ray - bowel loops in chest (m/c Lt. side) • NGT in stomach in chest
  • 35. • Initial stabilization with delayed surgery • Tracheal intubation and mechanical ventilation • Avoid hypothermia which causes ↑rt→lt shunt ↑ pvr ↑ o2 consumption • Decompress stomach by ngt • Avoid bag and mask ventilation (contraindicated) • Lung protective ventilatory strategy Low TV, RR high PIP≤ 25cm H2O PaCO245-60mm Hg - permissive hypercapina pH >7.3 (avoid acidosis - pulmonary vasoconstriction and decreases SPO2) Preductal SpO2 85%-95% AVOID rt→lt shunt PRE OP MANAGEMENT
  • 36. • Laboratory studies: CBC, RBS, serum electrolytes, cross matching, ABG • CXR: Air filled viscera in the chest, mediastinal shift • ECHO : Assessment of myocardial function, pulmonary hypertension, concurrent heart defects, R-L shunting INVESTIGATIONS
  • 37. Adequate venous access Gastric decompression Monitoring  Pre induction –Standard monitors, preductal & postductal pulse oximeter, precordial stethoscope  Post induction - Temperature, capnography, urine output, ± right radial arterial line, ± central venous access INTRAOPERATIVE MANAGEMENT
  • 38. • Choice of anaesthesia – Rapid sequence induction with succinylcholine/rocuronium or awake intubation • Maintenance- Isoflurane + O2+ air. Avoid N2O • Volume/ Pressure control ventilation – PIP<30cm H2O, RR 30-60/min • Analgesia- IV opioids, epidural • Active warming measures INTRAOPERATIVE MANAGEMENT
  • 39. Intraoperative complications • Acute desaturation- suspect pneumothorax on unaffected side • Sudden hypotension - RV failure, kinking of major blood vessels, abdominal compartment syndrome • Hypothermia • Hypoglycemia
  • 40. • Post operative ventilation in large hernia • Do not hyperventilate • Aim to maintain PaO2 >150 mmHg with least FiO2 • Slow weaning from oxygen over 48-72 hours • Abdominal compartment syndrome • Beware of Honeymoon phenomenon POSTOPERATIVE MANAGEMENT
  • 41. UPPER GIT LOWER GIT COMPRISES STOMACH , DUODENUM , PROXIMAL ILEUM TERMINAL ILEUM , COLON , RECTUM , ANUS CAUSES 1.Duodenal or ileal atresia. 2.Malrotation of midgut volvulus. 3.Peritoneal bands. 4.Intra abdominal hernia. 1.Meconium ileus. 2.Intussusception. 3.Imperporate anus INTESTINAL OBSTRUCTION Incidence: 1 : 1500 live births
  • 42. UPPER GIT LOWER GIT CLINICAL FEATURES  24 hrs of birth. Vomiting with initiation of feeding. Tender abdomen. Persistent vomiting leads to sodium loss, hypochloraemia, metabolic alkalosis.  bowel ischaemia – acidosis , bloody stools  2 – 7 days of birth. Increased abdominal distention. No passage of faeces. Vomiting is delayed.
  • 43. Anaesthetic management: • Aggressive correction with fluid & electrolytes, blood products • Sodium bicarbonate only in severe acidosis (Ph < 7.20) • Nasogastric tube suctioning and left open • Rapid sequence intubation is preferred to prevent aspiration • Procedure: combined general + caudal . • Advantages : light level of anaesthesia , muscle relaxation & early extubation. • Post operative ventilation in sick patients till condition stabilises.
  • 44. Abdominal wall defects • Most common are gastroschisis & omphalocoele • Although these conditions are embryologically unique anaesthetic management is essentially same
  • 45. Gastroschisis Omphalocoele Incidence 1:10000 1:4000-7000 Patho-physiology Interruption of ompalomescentric artery Non return of bowel from extra embryonic coelom Defect Open with inflamed, eodematous bowel Amnion cover outside, peritoneum inside Astd anomalies Rare High Defect size 2-5 cm, lateral 2-15 cm, midline Umbilical cord Adjacent to defect Apex of sac
  • 46. Surgical management • Primary closure- for small defects with not much viscero- abdominal disproportion • Staged repair- if complete reduction is not possible • Delayed closure- over weeks to months in very large omphalocoele
  • 47. Intraoperative management • Choice of anaesthesia – Modified rapid sequence induction with succinylcholine /rocuronium, maintenance- isoflurane+O2 + air. Avoid N2O • Adequate neuromuscular blockade to facilitate abdominal closure • Fluid - 10-20ml/kg boluses • Analgesia- IV opioids, regional techniques • Active warming
  • 48.  Intragastric <20mm Hg Intravesical pressures <20mm Hg PIP prior to abdominal closure < 35 cm H2O End tidal CO2<50mm Hg Urine output >0.5ml /kg/hr Criteria for safe abdominal closure
  • 49. Complications • Abdominal compartment syndrome • Dehydration & electrolyte imbalance • Hypothermia • Hypoglycaemia • B/L lower lobe atelectasis
  • 50. Post operative care • Continuation of mechanical ventilation for 24-48 hours • Judicious fluid therapy • Good analgesia • Initiating TPN