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!!!!
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!
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
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
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)
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)
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
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
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
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
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
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