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National Collaborating Centre for Cancer (UK). Neutropenic Sepsis: Prevention and Management of Neutropenic Sepsis in Cancer Patients. London: National Institute for Health and Clinical Excellence (NICE); 2012 Sep. (NICE Clinical Guidelines, No. 151.)

Cover of Neutropenic Sepsis: Prevention and Management of Neutropenic Sepsis in Cancer Patients

Neutropenic Sepsis: Prevention and Management of Neutropenic Sepsis in Cancer Patients.

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Key priorities for implementation

Definition of neutropenia and fever

Information and support for patients and carers

Investigations appropriate for clinical management and risk stratification

Assessing the patient's risk of septic complications

  • A healthcare professional with competence in managing complications of anticancer treatment should assess the patient's risk of septic complications within 24 hours of presentation to secondary or tertiary care, basing the risk assessment on presentation features and using a validated risk scoring system1.

Reducing the risk of septic complications of anticancer treatment

  • For adult patients (aged 18 years and older) with acute leukaemias, stem cell transplants or solid tumours in whom significant neutropenia (neutrophil count 0.5 × 109 per litre or lower) is an anticipated consequence of chemotherapy, offer prophylaxis with a fluoroquinolone during the expected period of neutropenia only.

Timing of initial antibiotic treatment

Empiric intravenous antibiotic monotherapy or intravenous antibiotic dual therapy

Inpatient versus outpatient management strategies

  • Consider outpatient antibiotic therapy for patients with confirmed neutropenic sepsis and a low risk of developing septic complications, taking into account the patient's social and clinical circumstances and discussing with them the need to return to hospital promptly if a problem develops.

Duration of inpatient care

  • Offer discharge to patients having empiric antibiotic therapy for neutropenic sepsis only after:
    -

    the patient's risk of developing septic complications has been reassessed as low by a healthcare professional with competence in managing complications of anticancer treatment using a validated risk scoring system3 and

    -

    taking into account the patient's social and clinical circumstances and discussing with them the need to return to hospital promptly if a problem develops.

Footnotes

1

Examples of risk scoring systems include 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. 2000;18:3038–51. [PubMed: 10944139] and the modified Alexander rule for children (aged under 18). European Journal of Cancer. 2009;45:2843–9. [PubMed: 19616427].

2

At the time of publication (September 2012) piperacillin with tazobactam did not have a UK marketing authorisation for use in children aged under 2 years. The prescriber should follow relevant professional guidance, taking full responsibility for the decision. The child's parent or carer should provide informed consent, which should be documented. See the GMC's Good practice in prescribing medicines – guidance for doctors and the prescribing advice provided by the Joint Standing Committee on Medicines (a joint committee of the Royal College of Paediatrics and Child Health and the Neonatal and Paediatric Pharmacists Group) for further information.

3

Examples of risk scoring systems include 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. 2000;18:3038–51. [PubMed: 10944139] and the modified Alexander rule for children (aged under 18). European Journal of Cancer. 2009;45:2843–9. [PubMed: 19616427].

Copyright © National Collaborating Centre for Cancer, 2012.
Bookshelf ID: NBK373690

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