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EM SAQsImmunocompromised host and febrile neutropenia

EM SAQs · Immunocompromised host and febrile neutropenia

Febrile neutropenia — definition, MASCC and empirical antibiotics

ACEM-style SAQ on FN definition, high-risk recognition, door-to-antibiotic targets, and IDSA-style regimens with doses.

10 marks10 min1 min readSource-verified ·

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Prompt
A 55-year-old man day 10 after induction chemotherapy for AML presents with a single oral temperature of 38.5°C. BP 100/60, HR 110, ANC 0.1×10⁹/L, tunnelled Hickman line in situ with mild exit-site erythema. Define febrile neutropenia, compute qualitative MASCC risk, outline the first 60 minutes including culture strategy, and give exact empirical antibiotic choices and doses including when to add vancomycin. (10 marks)

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Definition. Febrile neutropenia = ANC at or below 500 cells per microlitre plus fever 38.3 C or higher once or above 38.0 C maintained over one hour in a patient on chemotherapy / haematological malignancy / transplant immunosuppression.[6]

Risk. This patient is high risk: profound neutropenia (ANC 100), AML induction, inpatient-level illness, line infection concern. MASCC will be below 21 (symptom burden, inpatient at onset, age may score) — admit for IV therapy, since low MASCC scores carry worse outcomes; not an outpatient oral candidate.[5][6]

First 60 minutes. Resus assessment; blood cultures before antibiotics — all lumens of the Hickman plus a concurrent peripheral set; lactate, FBC, U&E, LFT, coag, CXR, urine. Do not wait for ANC confirmation if clinical FN. Initial doses of empirical antibacterials within 1 hour of triage with 4+ hours of monitoring. Fluids if hypotensive/lactataemic; early ICU if shock.[2][8]

Antibiotics. First-line anti-pseudomonal beta-lactam monotherapy — piperacillin-tazobactam IV (supported where resistance profiles do not mandate carbapenems), cefepime IV, ceftazidime IV, or a carbapenem (meropenem or imipenem) IV. Add vancomycin or teicoplanin for suspected catheter-related infection or MRSA cover; stop combination cover at 24 to 72 hours in the responder without a specific microbiologic indication. Source control for line infection with oncology/ID.[6][8][14]

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References6ShowHide
  1. [1]Freifeld AG, Bow EJ, Sepkowitz KA, et al. Clinical practice guideline for the use of antimicrobial agents in neutropenic patients with cancer: 2010 update by the Infectious Diseases Society of America. Clinical Infectious Diseases, 2011.PMID 21258094
  2. [2]Taplitz RA, Kennedy EB, Bow EJ, et al. Outpatient Management of Fever and Neutropenia in Adults Treated for Malignancy: American Society of Clinical Oncology and Infectious Diseases Society of America Clinical Practice Guideline Update. Journal of Clinical Oncology, 2018.PMID 29461916
  3. [5]Klastersky J, Paesmans M, Rubenstein EB, et al. The Multinational Association for Supportive Care in Cancer risk index: A multinational scoring system for identifying low-risk febrile neutropenic cancer patients. Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2000.PMID 10944139
  4. [6]Feghali F, Aoun C, Kabbara WK Evaluation of the Management of Febrile Neutropenia in a Tertiary Care Center. The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale, 2025.PMID 40236690
  5. [8]Lehrnbecher T, Robinson PD, Ammann RA, et al. Guideline for the Management of Fever and Neutropenia in Pediatric Patients With Cancer and Hematopoietic Cell Transplantation Recipients: 2023 Update. Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2023.PMID 36689694
  6. [14]Paul M, Yahav D, Bivas A, et al. Anti-pseudomonal beta-lactams for the initial, empirical, treatment of febrile neutropenia: comparison of beta-lactams. Cochrane database of systematic reviews, 2010.PMID 21069685
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