RECOGNITION
OF THE CRITICALLY
ILL CHILD
I. INTRODUCTION
Children are often
unable, or unwilling to
verbalize complaints. In
addition, symptoms and signs of sepsis or cardio-respiratory compromise are often vague and subtle in children.
The ability to
assess and recognize an ill
child early allows
for
simple interventions
and therapy such as ventilatory support,
fluid
resuscitation or early antibiotics to reverse potentially life- threatening cardiopulmonary instability.
II. ANATOMIC AND PHYSIOLOGICAL CONSIDERATIONS
The paediatric
respiratory
system is
ill-designed to cope
with an increased
work of breathing.
The reasons are multi-factorial
and include a relatively large tongue and
floppy epiglottis,
small
airways with increased airway resistance, and increased
chest wall compliance due to a cartilaginous
chest
wall.
Cardiac output is a function
of stroke volume and
heart rate. An infant has a limited ability to increase stroke volume in
response to shock, and therefore mounts a tachycardia response to compensate for
a drop in cardiac output. In
addition, children have a higher oxygen consumption
per kilogramme body weight
than
adults. As a result, they tolerate hypoxia poorly,
and may manifest with tachycardia as
a first sign of compensated
shock.
III. HISTORY
Functionality of the child is
a simple but effective measure of
how ill the child
is. Questions to ask include:
• Level
of activity/play
• Conscious level/irritability
• Feeding/fluid
intake
• Urine
output
Danger signs in the history include:
• High-pitched cry/inconsolable crying
• Grunting
• Cyanosis
• Apnoeic
episodes
• Pallor,
cool and clammy peripheries
• Shortness of breath
or dyspnoea
• Acute
change in mentation
• Focal seizures
• Bloody stool in a neonate
Is there a significant medical history such as:
• Maternal history of
GBS or other neonatal
infection risk factor (in a neonate)
• Congenital cardiac defects
• Primary immunodeficiency syndromes
• Chronic
steroid usage
• Haem-oncological
disorders on active chemotherapy
• History of adreno-cortical
deficiency e.g.
hypopituitarism, congenital adrenal
hyperplasia, hypothalamic or pituitary lesions
IV.
VITAL PARAMETERS
Hypotension is defined as
systolic BP:
< 60mmHg in a neonate
< 70mmHg in infants (one to12
months)
< 70mmHg + [2 x (Age in
Years)] in children one to
ten years
< 90mmHg in children >
ten years age
Mean arterial pressure can
be calculated as {50 + [2
x (Age in
Years)}mmHg.
Pulse pressure (systolic minus
diastolic BP) is usually greater
than 20mmHg. A widened pulse pressure is present in
distributive shock, a narrow pulse
pressure may suggest hypovolemic or cardiogenic shock. Unexplained
tachycardia may be one of
the first signs of
compensated shock.
V. PHYSICAL EXAMINATION
Clinical states
which can rapidly progress and are life-threatening include:
• Impending respiratory arrest
• Cardiovascular instability/cardiogenic
shock
• Sepsis/septic
shock
• Severe dehydration
• Seizures/altered mental
state
• Trauma
Danger signs in the physical
examination which
may
indicate an unwell child
include:
• General appearance:
- Mottling of
the skin
- Pallor
- Cool peripheries
- Lethargy/irritability
- Bulging tense fontanelles
- Purpuric rash
- Bruising/petechial rash
- Hyper-pyrexia (> 40°C)
• Respiratory system:
- Cyanosis
- Tachypnoea/bradypnoea by age
- Kussmaul’s
respirations
- Grunting
- Nasal flaring
- Retractions
- Audible stridor with drooling
• Cardiovascular:
- Delayed capillary refill time (> two seconds)
- Weak/thready pulses
- Tachycardia/bradycardia by age
- Cardiac arrhythmias
- New
onset murmur
- Gallop rhythm
- Absent
femoral pulses
(neonate)
• Neurological:
- Focal neurological signs
- Rapidly decreasing conscious level
or Glasgow Coma Score (GCS)
< 13
- Change in
mentation
- Asymmetrical pupillary reflex
• Trauma:
- Penetrating injury of
chest
or abdomen
- Suspected
spinal cord injury
- Flail chest
- Skull fracture
- Facial burns or
burns involving > 10% Body Surface Area (BSA)
If a danger sign is present in
the history and/or physical examination,
consider the following:
• Admit
for observation
• Call for senior
help if there is evidence of severe
respiratory distress, poor
perfusion and/or hypotension, obtundation/change in mentation, prolonged seizure or cardiac
arrhythmias
VI. INVESTIGATIONS
• Blood sugar: Exclude hypoglycaemia or
DKA
as a cause for obtundation
• Blood gas analysis with
electrolytes:
Evaluate for severe acidosis, sodium/potassium/calcium derangements
• Full Blood
Count, U/E/Cr and group and
match
• Imaging:
CXR to exclude pulmonary pathology,
cardiomegaly. CT head
if
there are concerns regarding intracranial pathology
• Septic screen including blood
and urine cultures if sepsis
is suspected. Consider
CSF
cultures
if an intra-cranial
infection is suspected
• LFT/coagulation
profile if
suspected liver dysfunction/bleeding diathesis
• Serum
lactate if available.
This reflects tissue hypoperfusion and can
be used as a marker of
response to therapy
• Metabolic screen if there is
unexplained
severe metabolic acidosis/
hypoglycaemia
• Drug toxicology
screen if suspected
VII. ACUTE TREATMENT
• Ensure adequate
oxygenation:
Administer 100% oxygen
nonrebreather facemask if hypoxia
is present
• Assess
and maintain a patent airway:
Consider intubation
and assisted ventilation if there
are
concerns about
hypoventilation or inability to maintain airway reflexes
• Evaluate for haemodynamic compromise: Secure IV access
early,
consider intra-osseous access
if venous
access
is difficult. Administer fluid resuscitation if there are signs of shock e.g. tachycardia,
prolonged capillary refill time,
cool peripheries. Give IV
crystalloids in aliquots of 20ml/kg boluses
and watch for
response. If there is suspicion of cardiogenic
shock, give
fluids
cautiously and consider early inotropic support (see
management of
shock).
• Correct
rapidly reversible, potentially life-threatening derangements.
This includes:
- Hypoglycaemia: IV
dextrose 10% 4–5ml/kg or
dextrose 25% 1–2ml/kg
- Hyponatraemia: IV
3% NaCl
2ml/kg over
30 minutes
- Hyperkalaemia: IV
insulin 0.1units/kg + IV
dextrose 50% 2ml/kg and/or sodium
polystyrene sulphonate
(kayexalate)
PR/oral 0.5–1g/kg
- Hypocalcaemia: IV
10%
Calcium chloride 0.2ml/kg over ten
minutes)
• Early antibiotic therapy if
sepsis is suspected
• Transfer patient
to an
appropriate
care
facility after
initial stabilisation
VIII. MONITORING
• Continuous
pulse oximetry, heart rate and respiratory rate monitoring
• Close BP monitoring: Consider invasive
BP
monitoring if there are
concerns
about haemodynamic instability
• Conscious level monitoring
• Urine
output as a marker of perfusion and end-organ
function
REFERENCES (BIBLIOGRAPHY)
1- 2005
American Heart
Association (AHA) Guidelines
for cardiopulmonary resuscitation
(CPR) and emergency cardiovascular care
(ECC) of pediatric
and neonatal patients: Pediatric advanced life support. Pediatrics. 2006;117(5):1005–1028.
2-
Advanced Life Support Group.
Advanced paediatric life
support: The practical approach.
4th ed. London: Blackwell Publishing;
2005.
3-
Mejia R, Serrao
K. Assessment of critically ill children. In:
Mejia R, editor. Pediatric
fundamental critical care
support. Mount Prospect, Ilinois: Society of Critical
Care Medicine;
2008. p.
1.1–121.
4- Shann F. Drug Doses.
13th ed. Melbourne: Collective Pty Ltd; 2005.
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