Any person, 16 years and over, 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. See antibiotic management section.
- Elderly patients may present with systemic compromise, with or without fever.
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
- Trigger (patient-identified source)
- Pain assessment – PQRST
- Pre-hospital treatment
- Past admissions
- Medical and surgical history including oncology or haematology diagnosis, recent surgery, invasive procedure or indwelling medical device
- Current medications
- Immunotherapy or chemotherapy drug regime, and last dosing
- Non-prescription drug or alcohol use
- Known allergies
- Contact with sick people
Signs and symptoms
- Confusion, agitation or irritability
- Respiratory distress or cough
- Tachycardia
- Fever, chills or rigors
- Abdominal pain
- Dysuria, frequency of urination or reduced urine output
- 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
- Recent surgery or wound
- Indwelling medical device
- Daily corticosteroids therapy
- Returned traveller
- Concurrent chemotherapy and radiotherapy
- Pregnancy
- Re-presentation within 48 hours
- Multi-resistant organisms alert in medical record
- Splenectomy or non-functioning spleen
Clinical
- Altered level of consciousness
- Shortness of breath
- Haemodynamic compromise in the elderly, with or without fever
- Poor perfusion, i.e. prolonged capillary refill, mottled skin or cool peripheries
- Tachycardia
- Hypotension
- Abdominal pain, distension or peritonism
- Non-blanching rash
Remember adult at risk: patient or carer concern, frailty, 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
Assessment | Intervention |
---|---|
General appearance/first impressions | Position of comfort Allocate to protective isolation space, if available Review the patient's febrile neutropenia management plan, if available |
Airway
Assessment | Intervention |
---|---|
Patency of airway | Maintain airway patency Consider airway opening manoeuvres and positioning |
Breathing
Assessment | Intervention |
---|---|
Respiratory rate and effort Auscultate chest (breath sounds) Oxygen saturation (SpO2) | Assist ventilation as clinically indicated Consider oxygen if dyspnoeic, titrate oxygen to maintain SpO2 over 93% Patients at risk of hypercapnia, maintain SpO2 at 88–92% |
Circulation
Assessment | Intervention |
---|---|
Perfusion (capillary refill, skin warmth and colour) Pulse Blood pressure Cardiac rhythm | Assess circulation Attach cardiac monitor and complete 12 lead ECG 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 |
IVC and/or pathology | Proceed to access central venous access device (CVAD), if trained and/or insert IV cannula, if trained If unable to obtain IV access, consider intraosseous, if trained |
Signs of shock: tachycardia and CRT 3 seconds and over and/or abnormal skin perfusion and/or hypotension | If signs of shock present and/or SBP less than 90 mmHg:
If no response in SBP, escalate as per local CERS protocol for further fluid order. |
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. See antibiotic management section.
- Patient without systemic compromise or shock: continue A to G assessment.
Disability
Assessment | Intervention |
---|---|
ACVPU | If ACVPU shows reduced level of consciousness, continue to 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
Assessment | Intervention |
---|---|
Temperature | Measure temperature |
Skin inspection, including posterior surfaces | Check and document any abnormalities |
Fluids
Assessment | Intervention |
---|---|
Hydration status: last ate, drank, bowels opened, passed urine or vomited | Commence strict fluid input and fluid output monitoring |
NBM | Consider clear fluids or NBM based on red flags and clinical severity |
Nausea and/or vomiting | If present, see nausea and/or vomiting section |
Glucose
Assessment | Intervention |
---|---|
BGL |
Measure BGL If BGL less than 4 mmol/L with NO decrease in level of consciousness (Yellow Zone criteria):
If BGL less than 4 mmol/L WITH a decrease in level of consciousness (Red Zone criteria) OR the patient is unable to tolerate oral intake:
If the patient is unconscious or peri-arrest:
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
- Patients with presumed sepsis are at high risk of clinical deterioration despite initial resuscitation with fluids and antibiotics.
- All patients presenting with fever following anticancer therapy should be managed as neutropenic and receive empiric antibiotics, until proven otherwise.
- Do not wait for white cell count (WCC) or neutrophil count before commencing antibiotics.
- The absence of fever in elderly patients is frequent, and infection should be suspected in those who have acute functional decline, including new or increasing confusion, falls, reduced oral intake and change in urinary habits.
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 (4 g + 0.5 g) IV once only
If known MRSA or risk of colonisation and/or CVAD in situ:
also give vancomycin 25 mg/kg (actual body weight) IV once only, maximum dose 3 g
Non-severe penicillin allergy
Give meropenem 1 g IV, once only
If known MRSA or risk of colonisation and/or CVAD in situ:
also give vancomycin 25 mg/kg (actual body weight) IV, once only, maximum dose 3 g
Life-threatening or uncertain penicillin allergy
If known MRSA or risk of colonisation and/or CVAD in situ:
give vancomycin 25 mg/kg (actual body weight) IV once only, maximum dose 3 g
Gentamicin dosing is based on BMI and whether there is known kidney impairment.
If gentamicin dose calculator available: use the gentamicin dose calculator. It will work out whether to use actual or adjusted body weight.
If no gentamicin dose calculator: use the BMI and adjusted body weight calculator on the webpage.
- BMI under 30: use actual body weight for gentamicin dose.
- BMI 30 and over: use adjusted body weight for gentamicin dose.
Gentamicin
Gentamicin dosing is based on BMI and whether there is known kidney impairment.
If using Gentamicin Dose Advisor in eMR: use the gentamicin dose calculator. It will work out whether to use actual or adjusted body weight.
If no Gentamicin Dose Advisor: use the BMI and adjusted body weight calculator on the webpage.
- BMI under 30: use actual body weight for gentamicin dose.
- BMI 30 and over: use adjusted body weight for gentamicin dose.
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.
Use the BMI calculator below to determine whether to use actual or adjusted body weight for gentamicin dosing.
Analgesia
Select pain score:
Pain score 1–3 (mild)
Give paracetamol 1000 mg orally once only
and/or ibuprofen 400 mg orally once only
Pain score 4–6 (moderate)
Give:
oxycodone (immediate release):
- 16–65 years: 5 mg orally and, if required, repeat once after 30 minutes, maximum dose 10 mg
- 65 years and over: 2.5 mg orally and, if required, repeat once after 30 minutes, maximum dose 5 mg
and/or paracetamol 1000 mg orally once only
and/or ibuprofen 400 mg orally once only
Pain score 7–10 (severe)
Give one of:
Fentanyl intranasal
- 16–65 years: 50 microg intranasally and, if required, repeat once after 5 minutes, maximum dose 100 microg. Dose to be divided between nostrils
- 65 years and over: 25 microg intranasally and, if required, repeat once after 5 minutes, maximum dose 50 microg. 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
Fentanyl IV
- 16–65 years: 50 microg IV and, if required, repeat once after 5 minutes, maximum dose 100 microg
- 65 years and over: 25 microg IV and, if required, repeat once after 5 minutes, maximum dose 50 microg
Morphine IV
- 16–65 years: 5 mg IV and, if required, repeat once after 5 minutes, maximum dose 10 mg
- 65 years and over: 2.5 mg IV and, if required, repeat once after 5 minutes, maximum dose 5 mg
Morphine IM
- 16–65 years: 5 mg IM and, if required, repeat once after 60 minutes, maximum dose 10 mg
- 65 years and over: 2.5 mg IM and, if required, repeat once after 60 minutes, maximum dose 5 mg
and/or paracetamol 1000 mg orally once only
and/or ibuprofen 400 mg orally once only
If pain does not improve with medication, escalate as per local CERS protocol.
Nausea and/or vomiting
If nausea and/or vomiting is present, give:
- metoclopramide 10 mg orally or IV/IM once only (over 20 years only)
- or ondansetron 4 mg orally or IV/IM. If symptoms persist after 60 minutes, repeat once, maximum dose 8 mg
- or prochlorperazine 5 mg orally once only or 12.5 mg IV/IM once only
Choice of antiemetic should be determined by cause of symptoms.
Radiology
- If chest thought to be source of infection 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 with lactate, Ca/Mg/PO4, group and hold
- Urinalysis: mid-stream (preferred), clean catch or catheter urine. Send for MC&S. Keep sample refrigerated if transport delayed
- Blood cultures: take two sets of blood cultures from two separate sites. If a patient has a central venous access device in situ, take 1 set of blood cultures from each lumen, and 1 set from a peripheral site
- Consider specific fever sources: wound swab, sputum culture, stool culture and respiratory viral screen
- Female of childbearing age: urine βHCG. If positive and within the first trimester, send serum βHCG for quantitative analysis
Medications
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 |
---|---|---|---|
Fentanyl H, R | 16–65 years: 65 years and over: | IV/intranasal | Pain score 7–10 Repeat once if required after 5 minutes to maximum dose |
Use actual or adjusted body weight as per BMI guide provided 16–18 years: 18–80 years: 80 years and over: Known kidney impairment and 18 years and over: | IV | Once only | |
1 mg | IM | Once only | |
200 mL | IV infusion over 15 minutes | Once only | |
Glucose 40% gel | 15 g | Buccal | Repeat after 15 minutes if required |
50 mL | Slow IV injection | Once only | |
Ibuprofen H, R | 400 mg | Oral | Pain score 1–10
Once only |
1 g | IV | Once only | |
Over 20 years: | Oral/IV/IM | Once only | |
Morphine H, R | 16–65 years:
65 years and over: | Pain score 7–10 | |
IV | Repeat once if required after 5 minutes | ||
IM | Repeat once if required after 60 minutes | ||
4 mg Maximum dose 8 mg | Oral/IV/IM | Repeat once if required after 60 minutes | |
16–65 years:
65 years and over: | Oral | Pain score 4–6 Repeat once if required after 30 minutes to maximum dose | |
Oxygen | 2–15 L/min, device dependent | Inhalation | Continuous |
1000 mg | Oral | Pain score 1–10 Once only | |
4 g + 0.5 g | IV | Once only | |
5 mg | Oral | Once only | |
OR | |||
12.5 mg | IV/IM | Once only | |
20 mL/kg Maximum dose 1000 mL | IV/intraosseous | Bolus Once only | |
25 mg/kg (actual body weight) Maximum dose 3 g | 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
- Government of South Australia. Febrile Neutropenia Management Guideline. Australia: SA Health; 2017 [cited 10 Feb 2023]. Available from: https://www.sahealth.sa.gov.au/wps/wcm/connect/
- Klastersky J, de Naurois J, Rolston K, et al. Management of febrile neutropaenia: ESMO Clinical Practice Guidelines. Ann Oncol. 2016 Sep;27(suppl 5):v111-v8. DOI: 10.1093/annonc/mdw325
- Long B, Targonsky E, Brém E. Just the facts: febrile neutropenia in the emergency department setting. Cjem. 2021 Jul;23(4):445-9. DOI: 10.1007/s43678-020-00055-x
- MIMS Australia. Clinical Resources. Australia: MIMS Australia Pty Ltd; 2022 [cited 2 Feb 2023]. Available from: https://www.mimsonline.com.au.acs.hcn.com.au/Search/Search.aspx
- NSW Health. Australian Medicines Handbook. Australia: Australian Government, NSW; 2022 [cited 13 Apr 2022]. Available from: https://amhonline.amh.net.au.acs.hcn.com.au/
- Rivera-Salgado D, Valverde-Muñoz K, Ávila-Agüero ML. [Febrile neutropenia in cancer patients: management in the emergency room]. Rev Chilena Infectol. 2018;35(1):62-71. DOI: 10.4067/s0716-10182018000100062
- Strasfeld L. Febrile neutropenia. London, UK: BMJ Best Practice; 2022 [cited 10 Feb 2023]. Available from: https://bestpractice.bmj.com/topics/en-gb/950
- Beasley R, Chien J, Douglas J, et al. Thoracic Society of Australia and New Zealand oxygen guidelines for acute oxygen use in adults: 'Swimming between the flags'. Respirology. 2015 Nov;20(8):1182-91. DOI: 10.1111/resp.12620
- Clinical Excellence Commission. Sepsis Management Plan- Adult Sepsis Pathway. NSW Australia: NSW Health,; 2014 [cited 10 Feb 2023]. Available from: https://www.cec.health.nsw.gov.au/__data/assets/pdf_file/0005/291803/Adult-Sepsis-Pathway.PDF
- Clinical Excellence Commission. Sepsis Kills Program. NSW Australia: NSW Health; 2022 [cited 10 Feb 2023]. Available from: https://www.cec.health.nsw.gov.au/keep-patients-safe/sepsis/program
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/adult/unwell-immunocompromised-person