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Adib Mursyidi
A&E Department
 5-day-old boy brought to ED for very poor
feeding, lethargy. Full term SVD with
unremarkable prenatal and post natal history
 What is your next step?
 FREAK OUT!!!!
 Ill neonate  frightening entity for most
clinicians
 Neonatal = first 28 days of life, but may be
expanded to account for gestational age
 Generally  sign and symptoms are vague
and non-specific, can be fatal!
 Fever / hypothermia
 Abnormal tone (limping/stiff)
 Altered mental status (lethargy/irritability)
 Weak suck
 Poor feeding
 Jaundice
 Abnormal respiration
 Cyanosis or mottling
 Vomiting
FEEDINGTREND
 In breast feeding : 1 to 3 hourly, bottle : 6 to 9 in
24hr
 Lose up to 12% of birth weight during first 3-
7days
 After this time, gain 20-30g during first 3months
STOOLS
 Normal BF infants may go 5-7days without
stools OR 6-7 stools per day
 Color : no significant unless blood is present OR
acholic (white)
RESPIRATORY
 Range 40-60x per min
 Periodic breathing (alternating episodes of
rapid breathing with brief <5-10sec pause) 
usually normal
 Healthy infant sleeps median 16.2hr per day
 In non accidental head trauma  subtle
history with no obvious physical finding, non
specific
 Evaluation includingCT Scan, USG, MRI. Skull
X-ray might not helpful because infant can
have significant injury without skull fracture
 X-ray only likely to have positive findings if
the were visible sign of injury
 Child <2 years old might have occult
traumatic head injury and retinal hemorrhage
 Evaluation and stabilization of ABC’s
 Bedside glucose
 Temperature regulation
 If bruises or known of ICB
 Lab should include FBC, PT, APTT
 Neuroimaging should be done after stabilization
 Patient should be admitted to respective
team
 Skeletal survey and ophthalmologic exam should
be part of evaluation
 Always consider theTerribleT’s
▪ Tetralogy of Fallot (TOF)
▪ Tricuspid atresia (TA)
▪ Transposition of great vessels (TOGV)
▪ Total anomalous pulmonary venous return (TAPVR)
▪ Truncus arteriosus (TA)
 CHD might not detected in newborn nursery 
still adequate oxygenated blood through
systemic circulation via patent ductus arteriosus
(PDA)
 PDA closes by 2 weeks of age (delay in
detecting)
 Boot shaped heart
 Elevated cardiac apex
“Egg on a string”
“Snowman sign”
 Providing 100% O2 can help differentiating
between cardiac vs non-cardiac
 Non-cardiac at least have 10% increase in
pulse oximetry value, where in cardiac have
minimal changing in O2 saturation
 Hyperoxia test (ABG in room air, then repeat
ABG after 10min of 100% O2)
 In cardiac  minimal change in PaO2
 Examination should include BP in 4 extremities
 Murmur maybe audible, absence does not exclude
cardiac defect
 CXR, ECG and ECHO is diagnostic
 Prostaglandin E1 (PGE1) as bolus of IV 0.05mcg/kg
followed by IV infusion 0.05-0.01mcg/kg/min 
watchout for hypotension, seizure, apnea
 Definitive airway management for transportation
 Typically present with symptoms of
congestive heart failure. Causes:
 Acyanotic heart disease (ventricular septal defect,
atrial septal defect, patent ductus arteriosus,
coarctation of the aorta)
 Severe anemia
 Trauma
 Sepsis
 Metabolic abnormalities
 Thyrotoxicosis
 Classic symptoms: tachypnea, tachycardia,
hepatomegaly
 History include poor/slow feeding, sweating,
color change with feeding, poor weight gain
 Stabilization of ABC’s
 CXR, ECG, FBC, serum electrolyte
 ECHO  diagnostic of heart defect
 IV Furosemide 1mg/kg
 IV Dopamine 5-15mcg/kg/min, IV
Dobutamine 2.5-15mcg/kg/min for CVS
support
 Carefully not to overload this patient
 Cardiology consultation
 Mostly cause by RSV, adenovirus, influenza
 Classic symptoms : rhinorrhea, cough,
congestion, apnea, significant respiratory
distress and wheezing
 Depending on symptoms
 In severe, prolonged apnea accompanied by
bradycardia, unresponsive to O2 therapy,
may required intubation
 Nebulization with corticosteroid therapy
 Sepsis evaluation should be consider
 Admission in premature and other comorbid
(reactive airway disease)
 Present in the 1st week with vomiting,
hypoglycemia or shock
 Common cause in CAH : deficiency in 21
hydroxylase enzyme
 CAH diagnosed at birth by routine newborn
screening, but missed due inadequate blood,
lab error, inability to contact family
 Hypotension that unresponsive to fluids and
inotropes leads to suspicion of CAH
 Stabilization of ABC’s
 Bedside glucose, serum electrolytes (usually
had hyponatremia and hyperkalemia)
 IV Hydrocortisone 25-50mg/m2, imperative
to treat hypoglycemia
 HyperK in this patient response to fluids,
however in symptomatic with ECG changes,
calcium chloride, sodium bicarbonate, insulin
and glucose may be needed
 Develop in infant born to mother with Grave’s
disease
 Cause by transmission of maternalTS
immunoglobin
 Present with poor feeding, failure to thrive,
tachycardia, irritability, hyperthermia,
vomiting, diarrhea, jaundice,
thrombocytopenia, respiratory distress, heart
failure and shock
 Diagnosis is difficult without clear history of
Grave’s disease from mother
 Evaluation should includeThyroid function
test
 Stabilization withABC’s
 IV Propranolol 0.25 mg/kg for the tachycardia
 IV Propylthiouracil (PTU) 1.25 mg/kg followed
 Lugol's solution 1-5 drops by mouth
 Given 1 hour after the PTU
 This will help to control the hypermetabolic state
 Admit with endocrine consultation
 Delay/unrecognized/uncommon and not part
of routine screening and symptoms
 Non specific symptoms such as poor
feeding, vomiting, failure to thrive,
tachycardia, tachypnea, or irritability
 Occasionally symptoms of seizures, lethargy,
hypoglycemia, apnea, temperature instability,
and acidosis.
 Physical exam findings are usually normal
 Stabilization withABC’s
 Bedside glucose
 FBC, serum electrolytes, pH, lactate,
ammonia, LFT, urinalysis for reducing
substances and ketones
 Main goal : stop exposure to protein that
maybe converted to toxic metabolic and clear
the body of toxic byproduct
 In any rectal temperature >38 C
 Sign and symptoms : poor feeding, irritability,
apnea, hypothermia, jaundice, rashes,
increased sleeping, seizures, or vomiting
 Maternal and fully physical exam might help
 Stabilization withABC’s
 Full septic evaluation : CBC, blood culture,
urinalysis, urine culture, cerebral spinal fluid
[CSF] culture and analysis, and CXR
 To administer broad spectrum antibiotic in
sepsis / life threatening symptoms
 In neonatal herpes  early recognition and
treat with acyclovir may decrease mortality
 IVAmpicillin 50-100mg/kg and IV Gentamicin
2mg/kg
OR
 IV Cefotaxime 50-100mg/kg
 IV Acyclovir 20mg/kg
 Inappropriate mixing of water and powdered
formula
 Overdilution of concentrated liquid of
premixed formula
 This may result life threatening electrolyte
disturbances or failure to thrive
 Hyponatremia may present as seizures and
immediate correction to stop seizure
 Malrotation caused by abnormal rotation of
bowel in utero  result in an unfixed portion
of bowel that may later twist on itself 
resulting volvulus and bowel ischemia/death
 Diagnoses as early in 1st month of life
 Symptoms include bilious emesis and poor
feeding, lethargy and shock in advanced state
 Stabilization of ABC’s
 Fluids resuscitation,
NGT placement,
surgical consultation
 AXR might normal,
sign of bowel
obstruction or classic
double bubble sign
 Life threatening, might unrecognized
 History of constipation, with additionally
history of unable to pass meconium in 1st
24hours of life
 Poor feeding, vomiting, irritability, abdominal
distention, hematochezia and shock
 Stabilization of ABC’s
 Fluid resuscitation
 Administration of broad spectrum antibiotic
 AXR : enlarged or dilated section of colon
 Need surgical consultation
 Classical disease of premature neonates
 Similar presentation with Hirschsprung
enterocolitis
 Management includes stabilization of ABC,
fluid resuscitation, NGT placement
 AXR demonstrate pneumatosis intestinalis /
portal air
 Administration of broad spectrum antibiotic
and surgical consultation
 Most common, neonate may represent
normal healthy baby
 Evaluation depend on presentation
 ED management include stabilization, lab
evaluation
 Based on hospital protocal
 Uncommon in this group, can be result from
maternal ingestion in BF mother,
homeopathic remedies, drug overuse
 Most common “teething gel”
 ED management primarily supportive and
based on clinical presentation
 Hospitalization might required for
observation and monitoring
 Neonate suspect with seizure difficult to
diagnose
 History can include their newborn not acting
right or more somnolent
 Neonate had immature cortical development,
seizure activity might not tonic-clonic
 Symptoms include lip-smacking, abnormal
eye or tongue movement, pedaling, apnea
 Describing event “frightening to the observer
and is characterized by some combination of
apnea, color change, marked change in muscle
tone, choking, or gagging”
 ED management : depending on historical
information provided by observer and
examination
 Hospitalization maybe appropriate for
observing and monitoring
 Common differential diagnosis of ALTE
 Sepsis/Meningitis/Encephalitis
 Pneumonia/RSV
 Hypothermia/hypoglycemia
 Anemia
 ICB
 Acid base disturbance/Electrolyte abnormalities/IEM
 Seizures
 GERD
 Child abuse
 Further history
 Feeding well previously, 2oz every 2hours
 Starting to sucking poorly and taking less than
half oz every feeding
 On examination  difficult to arouse, slightly
jaundiced and mottled, other examination
unremarkable
 Temp 35.5, HR 190, RR 50, BP 66/38, CRT
>2sec
 IV access obtained via scalp
 FBC :WCC raise, electrolyte normal. UFEME
clear.
 Infant was given IV NS 20ml/kg bolus and
started on maintenance fluids
 IV Ampicillin and IV Gentamicin was initiated
 LP was performed : no evidence of meningitis
 Blood C&S showed Group B Strep
 Antibiotic was changed to penicillin in view of
sensitivity and continue for 10days
 Infant was discharge well after 12 days of
hospitalization
 Neonatal emergencies may provoke anxiety
in ED clinician
 Mnemonics “THE MISFITS” is a helpful tools
 Infant  rare entity
 Sign and symptoms are non specific
 To treat unstable neonate  narrow down
diagnosis  begin life-sustaining treatment
 ensure safe disposition
 References
 Evidence Based Review of Neonatal Emergencies
in Pediatrics, Aug 2010
 Medscape Emergency Medicine : Neonatal
Emergencies
 Pediatric Protocol 3rd edition, 2013
Neonatal Emergency and Common Problems in Emergency Department

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Neonatal Emergency and Common Problems in Emergency Department

  • 2.  5-day-old boy brought to ED for very poor feeding, lethargy. Full term SVD with unremarkable prenatal and post natal history  What is your next step?  FREAK OUT!!!!
  • 3.
  • 4.  Ill neonate  frightening entity for most clinicians  Neonatal = first 28 days of life, but may be expanded to account for gestational age  Generally  sign and symptoms are vague and non-specific, can be fatal!
  • 5.  Fever / hypothermia  Abnormal tone (limping/stiff)  Altered mental status (lethargy/irritability)  Weak suck  Poor feeding  Jaundice  Abnormal respiration  Cyanosis or mottling  Vomiting
  • 6. FEEDINGTREND  In breast feeding : 1 to 3 hourly, bottle : 6 to 9 in 24hr  Lose up to 12% of birth weight during first 3- 7days  After this time, gain 20-30g during first 3months STOOLS  Normal BF infants may go 5-7days without stools OR 6-7 stools per day  Color : no significant unless blood is present OR acholic (white)
  • 7. RESPIRATORY  Range 40-60x per min  Periodic breathing (alternating episodes of rapid breathing with brief <5-10sec pause)  usually normal  Healthy infant sleeps median 16.2hr per day
  • 8.
  • 9.  In non accidental head trauma  subtle history with no obvious physical finding, non specific  Evaluation includingCT Scan, USG, MRI. Skull X-ray might not helpful because infant can have significant injury without skull fracture  X-ray only likely to have positive findings if the were visible sign of injury  Child <2 years old might have occult traumatic head injury and retinal hemorrhage
  • 10.  Evaluation and stabilization of ABC’s  Bedside glucose  Temperature regulation  If bruises or known of ICB  Lab should include FBC, PT, APTT  Neuroimaging should be done after stabilization  Patient should be admitted to respective team  Skeletal survey and ophthalmologic exam should be part of evaluation
  • 11.
  • 12.  Always consider theTerribleT’s ▪ Tetralogy of Fallot (TOF) ▪ Tricuspid atresia (TA) ▪ Transposition of great vessels (TOGV) ▪ Total anomalous pulmonary venous return (TAPVR) ▪ Truncus arteriosus (TA)  CHD might not detected in newborn nursery  still adequate oxygenated blood through systemic circulation via patent ductus arteriosus (PDA)  PDA closes by 2 weeks of age (delay in detecting)
  • 13.  Boot shaped heart  Elevated cardiac apex
  • 14. “Egg on a string”
  • 16.  Providing 100% O2 can help differentiating between cardiac vs non-cardiac  Non-cardiac at least have 10% increase in pulse oximetry value, where in cardiac have minimal changing in O2 saturation  Hyperoxia test (ABG in room air, then repeat ABG after 10min of 100% O2)  In cardiac  minimal change in PaO2
  • 17.  Examination should include BP in 4 extremities  Murmur maybe audible, absence does not exclude cardiac defect  CXR, ECG and ECHO is diagnostic  Prostaglandin E1 (PGE1) as bolus of IV 0.05mcg/kg followed by IV infusion 0.05-0.01mcg/kg/min  watchout for hypotension, seizure, apnea  Definitive airway management for transportation
  • 18.  Typically present with symptoms of congestive heart failure. Causes:  Acyanotic heart disease (ventricular septal defect, atrial septal defect, patent ductus arteriosus, coarctation of the aorta)  Severe anemia  Trauma  Sepsis  Metabolic abnormalities  Thyrotoxicosis
  • 19.  Classic symptoms: tachypnea, tachycardia, hepatomegaly  History include poor/slow feeding, sweating, color change with feeding, poor weight gain
  • 20.  Stabilization of ABC’s  CXR, ECG, FBC, serum electrolyte  ECHO  diagnostic of heart defect  IV Furosemide 1mg/kg  IV Dopamine 5-15mcg/kg/min, IV Dobutamine 2.5-15mcg/kg/min for CVS support  Carefully not to overload this patient  Cardiology consultation
  • 21.  Mostly cause by RSV, adenovirus, influenza  Classic symptoms : rhinorrhea, cough, congestion, apnea, significant respiratory distress and wheezing
  • 22.  Depending on symptoms  In severe, prolonged apnea accompanied by bradycardia, unresponsive to O2 therapy, may required intubation  Nebulization with corticosteroid therapy  Sepsis evaluation should be consider  Admission in premature and other comorbid (reactive airway disease)
  • 23.
  • 24.  Present in the 1st week with vomiting, hypoglycemia or shock  Common cause in CAH : deficiency in 21 hydroxylase enzyme  CAH diagnosed at birth by routine newborn screening, but missed due inadequate blood, lab error, inability to contact family  Hypotension that unresponsive to fluids and inotropes leads to suspicion of CAH
  • 25.  Stabilization of ABC’s  Bedside glucose, serum electrolytes (usually had hyponatremia and hyperkalemia)  IV Hydrocortisone 25-50mg/m2, imperative to treat hypoglycemia  HyperK in this patient response to fluids, however in symptomatic with ECG changes, calcium chloride, sodium bicarbonate, insulin and glucose may be needed
  • 26.  Develop in infant born to mother with Grave’s disease  Cause by transmission of maternalTS immunoglobin  Present with poor feeding, failure to thrive, tachycardia, irritability, hyperthermia, vomiting, diarrhea, jaundice, thrombocytopenia, respiratory distress, heart failure and shock
  • 27.  Diagnosis is difficult without clear history of Grave’s disease from mother  Evaluation should includeThyroid function test
  • 28.  Stabilization withABC’s  IV Propranolol 0.25 mg/kg for the tachycardia  IV Propylthiouracil (PTU) 1.25 mg/kg followed  Lugol's solution 1-5 drops by mouth  Given 1 hour after the PTU  This will help to control the hypermetabolic state  Admit with endocrine consultation
  • 29.
  • 30.  Delay/unrecognized/uncommon and not part of routine screening and symptoms  Non specific symptoms such as poor feeding, vomiting, failure to thrive, tachycardia, tachypnea, or irritability  Occasionally symptoms of seizures, lethargy, hypoglycemia, apnea, temperature instability, and acidosis.  Physical exam findings are usually normal
  • 31.  Stabilization withABC’s  Bedside glucose  FBC, serum electrolytes, pH, lactate, ammonia, LFT, urinalysis for reducing substances and ketones  Main goal : stop exposure to protein that maybe converted to toxic metabolic and clear the body of toxic byproduct
  • 32.
  • 33.  In any rectal temperature >38 C  Sign and symptoms : poor feeding, irritability, apnea, hypothermia, jaundice, rashes, increased sleeping, seizures, or vomiting  Maternal and fully physical exam might help
  • 34.  Stabilization withABC’s  Full septic evaluation : CBC, blood culture, urinalysis, urine culture, cerebral spinal fluid [CSF] culture and analysis, and CXR  To administer broad spectrum antibiotic in sepsis / life threatening symptoms  In neonatal herpes  early recognition and treat with acyclovir may decrease mortality
  • 35.  IVAmpicillin 50-100mg/kg and IV Gentamicin 2mg/kg OR  IV Cefotaxime 50-100mg/kg  IV Acyclovir 20mg/kg
  • 36.
  • 37.  Inappropriate mixing of water and powdered formula  Overdilution of concentrated liquid of premixed formula  This may result life threatening electrolyte disturbances or failure to thrive  Hyponatremia may present as seizures and immediate correction to stop seizure
  • 38.  Malrotation caused by abnormal rotation of bowel in utero  result in an unfixed portion of bowel that may later twist on itself  resulting volvulus and bowel ischemia/death  Diagnoses as early in 1st month of life  Symptoms include bilious emesis and poor feeding, lethargy and shock in advanced state
  • 39.  Stabilization of ABC’s  Fluids resuscitation, NGT placement, surgical consultation  AXR might normal, sign of bowel obstruction or classic double bubble sign
  • 40.  Life threatening, might unrecognized  History of constipation, with additionally history of unable to pass meconium in 1st 24hours of life  Poor feeding, vomiting, irritability, abdominal distention, hematochezia and shock
  • 41.  Stabilization of ABC’s  Fluid resuscitation  Administration of broad spectrum antibiotic  AXR : enlarged or dilated section of colon  Need surgical consultation
  • 42.  Classical disease of premature neonates  Similar presentation with Hirschsprung enterocolitis  Management includes stabilization of ABC, fluid resuscitation, NGT placement  AXR demonstrate pneumatosis intestinalis / portal air  Administration of broad spectrum antibiotic and surgical consultation
  • 43.  Most common, neonate may represent normal healthy baby  Evaluation depend on presentation  ED management include stabilization, lab evaluation  Based on hospital protocal
  • 44.
  • 45.  Uncommon in this group, can be result from maternal ingestion in BF mother, homeopathic remedies, drug overuse  Most common “teething gel”  ED management primarily supportive and based on clinical presentation  Hospitalization might required for observation and monitoring
  • 46.  Neonate suspect with seizure difficult to diagnose  History can include their newborn not acting right or more somnolent  Neonate had immature cortical development, seizure activity might not tonic-clonic  Symptoms include lip-smacking, abnormal eye or tongue movement, pedaling, apnea
  • 47.
  • 48.
  • 49.  Describing event “frightening to the observer and is characterized by some combination of apnea, color change, marked change in muscle tone, choking, or gagging”  ED management : depending on historical information provided by observer and examination  Hospitalization maybe appropriate for observing and monitoring
  • 50.  Common differential diagnosis of ALTE  Sepsis/Meningitis/Encephalitis  Pneumonia/RSV  Hypothermia/hypoglycemia  Anemia  ICB  Acid base disturbance/Electrolyte abnormalities/IEM  Seizures  GERD  Child abuse
  • 51.  Further history  Feeding well previously, 2oz every 2hours  Starting to sucking poorly and taking less than half oz every feeding  On examination  difficult to arouse, slightly jaundiced and mottled, other examination unremarkable  Temp 35.5, HR 190, RR 50, BP 66/38, CRT >2sec
  • 52.  IV access obtained via scalp  FBC :WCC raise, electrolyte normal. UFEME clear.  Infant was given IV NS 20ml/kg bolus and started on maintenance fluids  IV Ampicillin and IV Gentamicin was initiated  LP was performed : no evidence of meningitis  Blood C&S showed Group B Strep
  • 53.  Antibiotic was changed to penicillin in view of sensitivity and continue for 10days  Infant was discharge well after 12 days of hospitalization
  • 54.  Neonatal emergencies may provoke anxiety in ED clinician  Mnemonics “THE MISFITS” is a helpful tools  Infant  rare entity  Sign and symptoms are non specific  To treat unstable neonate  narrow down diagnosis  begin life-sustaining treatment  ensure safe disposition
  • 55.  References  Evidence Based Review of Neonatal Emergencies in Pediatrics, Aug 2010  Medscape Emergency Medicine : Neonatal Emergencies  Pediatric Protocol 3rd edition, 2013