Paediatric ECAT protocol

Unwell immunocompromised person

P3.4 Published: December 2023 Printed on 19 May 2024

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Any person, 4 weeks to 15 years, presenting unwell with or without fever, who has recently (within 14 days) received chemotherapy or other potential cause of immunocompromise.

Escalate immediately as per local CERS protocol.

This protocol is intended to be used by registered and enrolled nurses within their scope of practice and as outlined in The Use of Emergency Care Assessment and Treatment Protocols (PD2024_011). Sections marked triangle or diamond indicate the need for additional prerequisite education prior to use. Check the medication table for dose adjustments and links to relevant reference texts.

Unwell immunocompromised person with systemic compromise or shock

  • Give antibiotics within 30 minutes of starting this protocol if a medical or nurse practitioner is unavailable.

History prompts, signs and symptoms

These are not exhaustive lists. Maintain an open mind and be aware of cognitive bias.

History prompts

  • Presenting complaint
  • Onset of symptoms
  • Patient-identified source
  • Pain assessment
  • Pre-hospital treatment
  • Past admissions
  • Medical and surgical history, including oncology or haematology diagnosis, recent surgery or invasive procedure and indwelling medical device
  • Current medications
  • Immunotherapy or chemotherapy drug regime, and last dosing
  • Contact with sick people
  • History of other drug or alcohol use
  • Immunisation status
  • Known allergies
  • Current weight

Signs and symptoms

  • Respiratory distress or cough
  • Tachycardia
  • Pallor
  • Fever, chills or rigors
  • Abdominal pain
  • Dysuria and/or frequency
  • Irritability
  • Lethargy

Red flags

Recognise: identify indicators of actual or potential clinical severity and risk of deterioration.

Respond: carefully consider alternative ECAT protocol. Escalate as per clinical reasoning and local CERS protocol, and continue treatment.

Historical

  • Organ transplant recipient
  • Indwelling medical device
  • Daily corticosteroids therapy
  • Recent surgery or wound
  • Parental concern
  • Clinician concern
  • Multi-resistant organisms alert in medical record
  • Splenectomy or non-functioning spleen

Clinical

  • Altered level of consciousness or floppy
  • Respiratory distress or grunting
  • Tachypnoea
  • Hypoxia
  • Poor perfusion, i.e. prolonged capillary refill over 3 seconds, mottled skin and  cool peripheries
  • Tachycardia
  • Hypotension (late sign)
  • Bounding pulse
  • Abdominal pain or rigidity
  • Non-blanching rash

Remember child or adolescent at risk: patient or carer concern, suspected non-accidental injury or neglect, multiple comorbidities or unplanned return.

Clinical assessment and specified intervention (A to G)

If the patient has any Yellow or Red Zone observations or additional criteria (as per the relevant NSW Standard Emergency Observation Chart), refer and escalate as per local CERS protocol and continue treatment.

Position

AssessmentIntervention

General appearance/first impressions

Position of comfort

Allocate to protective isolation space

Review the patient's febrile neutropenia management plan if available

Airway

AssessmentIntervention

Patency of airway

Maintain airway patency

Consider airway opening manoeuvres and positioning

Breathing

AssessmentIntervention

Respiratory rate and work of breathing

Consider auscultation of chest (breath sounds)

Oxygen saturation (SpO2)

Assist ventilation as clinically indicated

Apply oxygen to maintain SpO2 over 93%

Circulation

AssessmentIntervention

Perfusion (capillary refill, skin warmth and colour)

Heart rate

Blood pressure

Cardiac rhythm

Assess circulation

Attach cardiac monitor if BP/HR are within the Yellow or Red Zones, or where clinically relevant, e.g. irregular pulse, palpitations, syncope, shock, respiratory compromise, cardiac history or clinical concern

Consider 12 lead ECG

IVC and/or pathology

Proceed to access the central venous access device (CVAD), if trained

and/or insert IV cannula, if trained

If unable to obtain IV access, consider intraosseous, if trained

See pathology section

Signs of shock:

tachycardia and CRT 3 seconds and over

and/or abnormal skin perfusion

and/or hypotension

If signs of shock present:

  • give sodium chloride 0.9% at 20 mL/kg IV/intraosseous bolus once only, maximum dose 1000 mL
  • give antibiotics. See antibiotic management section

Unwell immunocompromised person with systemic compromise or shock

  • Give antibiotics within 30 minutes of starting this protocol if a medical or nurse practitioner is unavailable.
  • Patient without systemic compromise or shock: continue A to G and refer to antibiotic management section.

Disability

AssessmentIntervention
AVPU

If AVPU shows reduced level of consciousness, continue to assess GCS, pupillary response and limb strength

GCS, pupillary response and limb strength

Obtain baseline and repeat assessment as clinically indicated

Pain

Assess pain. If indicated, give early analgesia as per analgesia section then resume A to G assessment

Exposure

AssessmentIntervention
Temperature

Measure temperature

Head-to-toe inspection, including posterior surfaces

Check and document any abnormalities

Fluids

AssessmentIntervention

Hydration status

Commence strict fluid input and fluid output monitoring

Glucose

Assessment Intervention

BGL

Measure BGL. See medication table for 40% glucose gel dosing

If BGL between 2 mmol/L and 3 mmol/L and NOT symptomatic (Yellow Zone criteria):

  • give quick-acting carbohydrate:
    • Up to 12 months: milk feed and/or 40% glucose gel buccal
    • 12 months and over: sugary soft drink or fruit juice or 40% glucose gel buccal
  • reassess BGL in 15–30 minutes and repeat treatment until BGL over 3 mmol/L

If BGL less than 2 mmol/L OR symptomatic (Red Zone criteria) OR unable to tolerate oral glucose:

  • give 40% glucose gel buccally in incremental doses, as tolerated, while establishing IV access
  • give 10% glucose, 2 mL/kg by slow IV injection once only
  • if IV access delayed, give:
    • Up to 25 kg: glucagon 0.5 mg IM, once only
    • 25 kg and over: glucagon 1 mg IM, once only
  • reassess BGL in 15 minutes

Once stabilised, give patient long-acting carbohydrate and continue to check BGL hourly, or as clinically indicated

Repeat and document assessment and observations to monitor responses to interventions, identify developing trends and clinical deterioration. Escalate care as required according to the local CERS protocol.

Focused assessment

Focused assessment should not delay antibiotic administration.

Consider relevant focused assessment according to findings.

Precautions and notes

  • All patients presenting with fever following anticancer therapy should be managed as neutropenic and receive empiric antibiotics, until proven otherwise.
  • Patients with presumed sepsis are at high risk of clinical deterioration despite initial resuscitation with fluids and antibiotics.
  • Do not wait for white cell count (WCC) or neutrophil count before commencing antibiotics.
  • Some patients with serious infection may present without fever or with hypothermia.
  • Bacteraemia is present in up to one-third of children with febrile neutropenia.

Interventions and diagnostics

Antibiotic management

Suspected febrile neutropenia with systemic compromise or shock: give antibiotics within 30 minutes if a medical or nurse practitioner is unavailable.

Suspected febrile neutropenia without systemic compromise or shock: give antibiotics within 60 minutes if a medical or nurse practitioner is unavailable.

Attempt blood cultures and sampling prior to giving antibiotics, but do not delay treatment.

Initial antibiotics

Select one:

No known allergies

Give piperacillin + tazobactam 100 mg/kg IV once only, maximum dose 4 g. Note: dose is expressed as the piperacillin component

and if known MRSA or risk of colonisation and/or CVAD in situ:

also give vancomycin 15 mg/kg IV once only, maximum dose 750 mg

Non-severe penicillin allergy

Give meropenem 20 mg/kg IV once only, maximum dose 1 g

and if known MRSA or risk of colonisation and/or CVAD in situ:

also give vancomycin 15 mg/kg IV once only, maximum dose 750 mg

Life-threatening or uncertain penicillin allergy

Give vancomycin 15 mg/kg IV once only, maximum dose 750 mg

Gentamicin

Only give gentamicin if there is systemic compromise or shock and/or life threatening penicillin allergy.

Do not give gentamicin if patient has:

  • pre-existing significant auditory impairment or vestibular condition
  • history of hypersensitivity reaction to aminoglycoside
  • myasthenia gravis
  • history of aminoglycoside-induced vestibular or auditory toxicity, or first degree relative has history of same.

If the patient has any of the above contraindications, continue to give the other antibiotics and seek advice about gentamicin.

Give gentamicin:

  • 1 month–10 years: 7.5 mg/kg IV once only, maximum dose 320 mg
  • 10–15 years: 7 mg/kg IV once only, maximum dose 560 mg


Analgesia

Select pain score:

Pain score 1–3 (mild)

Give paracetamol 15 mg/kg orally once only, maximum dose 1000 mg

and/or ibuprofen, if 3 months and over, 10 mg/kg orally once only, maximum dose 400 mg

Pain score 4–6 (moderate)

Give:

oxycodone (immediate release):

  • 1–12 months: 0.05 mg/kg orally once only, maximum dose 0.5 mg
  • 12 months and over: 0.1 mg/kg orally once only, maximum dose 5 mg

and/or paracetamol 15 mg/kg, orally once only, maximum dose 1000 mg

and/or ibuprofen, if 3 months and over, 10 mg/kg orally once only, maximum dose 400 mg

Pain score 7–10 (severe)

Give one of:

Fentanyl intranasal
  • 12 months and over: 1.5 microg/kg intranasally, maximum single dose 75 microg and, if required, repeat once after 5 minutes, maximum total dose 3 microg/kg or 150 microg, whichever is less. Dose to be divided between nostrils

Note: ensure an extra 0.1 mL is drawn up for the first dose to account for the dead space in the mucosal atomiser device

Morphine IV
  • 1–12 months: 0.05 mg/kg IV, maximum single dose 0.5 mg and, if required, repeat once after 5 minutes, maximum total dose 0.1 mg/kg or 1 mg, whichever is less
  • 12 months and over: 0.1 mg/kg IV, maximum single dose 5 mg and, if required, repeat once after 5 minutes, maximum total dose 0.2 mg/kg or 10 mg, whichever is less

and/or paracetamol 15 mg/kg orally once only, maximum dose 1000 mg

and/or ibuprofen, if 3 months and over, 10 mg/kg orally once only, maximum dose 400 mg

If pain does not improve with medication, escalate as per local CERS protocol.

Consider non-pharmacological pain relief (appendix).


Nausea and/or vomiting

If nausea and/or vomiting is present and over 6 months give:

ondansetron:

  • 8–15 kg: 2 mg, orally once only
  • 15–30 kg: 4 mg, orally once only
  • Over 30 kg: 8 mg, orally once only.

Procedural analgesia

For pain relief required during procedures only, not used to replace appropriate analgesia.

Sucrose 24%

  • 1–18 months: give 1–2 mL orally per procedure
  • Maximum dose:
    • 1–3 months: up to 5 mL in 24 hours
    • 3–18 months: up to 10 mL in 24 hours.

Repeat as needed up to the maximum dose.


Radiology

  • If chest thought to be source or source is difficult to determine: CXR

Pathology

Attempt blood cultures and sampling prior to giving antibiotics, but do not delay treatment.

  • FBC, UEC, LFT, VBG, Ca/Mg/PO4, group and hold, blood cultures
  • Blood cultures: if the patient has a central venous access device in situ, it is recommended to take 1 set of blood cultures from each lumen (minimum of two sets collected).
  • Urinalysis:
    • Patient who can void in the toilet: mid-stream urine
    • Patient who is not toilet trained: clean catch or catheter urine
    • Send for MC&S. Keep the sample refrigerated if transport is delayed.
  • Consider using for specific fever sources: wound swab, sputum culture, stool culture and respiratory viral screen

Medications

The patient’s weight is mandatory for calculating fluid and medication doses.

The Broselow Tape or APLS weight table (appendix) can be used only in circumstances where the patient cannot be weighed.

The shaded sections in this protocol are only to be used by registered nurses who have completed the required education.

Drag the table right to view more columns or turn your phone to landscape

Drug Dose Route Frequency

12 months and over:
1.5 microg/kg

Maximum single dose 75 microg
Maximum total dose of 3 microg/kg or 150 microg, whichever is less

Intranasal

Pain score 7–10

Repeat once if required after 5 minutes to maximum dose

1 month–10 years: 7.5 mg/kg
Maximum dose 320 mg

10–15 years: 7 mg/kg
Maximum dose 560 mg

IV

Once only

Up to 25 kg:
0.5 mg

25 kg and over:
1 mg

IM

Once only

2 mL/kg

Slow IV injection

Once only

Glucose 40% gel
(0.4 g/mL)

4 weeks1 year:
200 mg/kg (=0.5 mL/kg)

15 years: 5 g

611 years: 10 g

12 years and over : 15 g

Buccal

Repeat after 15 minutes if required

Ibuprofen H, R

3 months and over:
10 mg/kg

Maximum dose 400 mg

Oral

Pain score 1–10

Once only

20 mg/kg

Maximum dose 1 g

IV

Once only

1–12 months:
0.05 mg/kg
Maximum single dose 0.5 mg
Maximum total dose 0.1 mg/kg or 1 mg, whichever is less

12 months and over:
0.1 mg/kg
Maximum single dose 5 mg
Maximum total dose 0.2 mg/kg or 10 mg, whichever is less

IV

Pain score 7–10

Repeat once if required after 5 minutes to maximum dose

Over 6 months and 8–15 kg:
2 mg

15–30 kg:
4 mg

Over 30 kg:
8 mg

Oral

Once only

1–12 months:
0.05 mg/kg
Maximum dose 0.5 mg

12 months and over:
0.1 mg/kg
Maximum dose 5 mg

Oral

Pain score 4–6

Once only

Oxygen

0.25–15 L/min, device dependent

Inhalation

Continuous

Paracetamol H

15 mg/kg

Maximum dose 1000 mg

Oral

Pain score 1–10

Once only

100 mg/kg

Maximum dose 4 g

Note: dose is expressed as the piperacillin component

IV

Once only

20 mL/kg

Maximum dose 1000 mL

IV/intraosseous

Bolus

Once only

Sucrose 24%

1–18 months:
1–2 mL per procedure

Maximum dose
1–3 months:
Up to 5 mL in 24 hours

3–18 months:
Up to 10 mL in 24 hours

Oral

Used during procedures only

Repeat if required to maximum dose

15 mg/kg

Maximum dose 750 mg

IV

Once only

Medications with contraindications or requiring dose adjustment are marked:

  • H for patients with known hepatic impairment
  • R for patients with known renal impairment.

Escalate to medical or nurse practitioner.

References

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Evidence informed

Information was drawn from evidence-based guidelines and a review of latest available research. For more information, see the development process.

Collaboration

This protocol was developed by the ECAT Working Group, led by the Agency for Clinical Innovation. The group involved expert medical, nursing and allied health representatives from local health districts across NSW. Consensus was reached on all recommendations included within this protocol.

Currency Due for review: Jan 2026. Based on a regular review cycle.
Feedback Email ACI-ECIs@health.nsw.gov.au

Accessed from the Emergency Care Institute website at https://aci.health.nsw.gov.au/ecat/paediatric/unwell-immunocompromised-person

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