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Implementation of risk stratified antibiotic therapy for neutropenic fever: what are the risks?
Author(s) -
Wierema J.,
Konecny P.,
Links M.
Publication year - 2013
Publication title -
internal medicine journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.596
H-Index - 70
eISSN - 1445-5994
pISSN - 1444-0903
DOI - 10.1111/imj.12251
Subject(s) - medicine , antibiotic therapy , intensive care medicine , neutropenia , antibiotics , chemotherapy , microbiology and biotechnology , biology
Background A new national guideline for the management of febrile patients with severe neutropenia uses a risk stratification score to tailor treatment. Aims To evaluate the implementation of this guideline in a metropolitan teaching hospital. Methods A protocol was developed for implementation of the national guidelines for patients with neutropenic fever or at risk because of recent chemotherapy. Medical records of all patients presenting with fever to the haematology and oncology service for 3 months in 2011 were audited. Patients with a neutrophil count between 0.5 and 1.0 × 10 9 / L were classified as borderline neutropenia. Results Eighty‐one episodes of fever were treated on the protocol. Forty‐three per cent of patients were neutropenic. Uptake of the policy was low (35%) despite concerted efforts. The sensitivity and specificity of the M ultinational A ssociation for S upportive C are in C ancer score was 86% and 24% respectively. The readmission rate with fever was 19.2%. Median time to antibiotics was 60 min. Outcomes were similar for the neutropenic fever and borderline groups. Increasing treatment complexity was the major barrier to implementation. Conclusions The majority of presentations with cancer and fever following chemotherapy do not have neutropenia but have similar outcomes when treated on the same pathway. The utility of the M ultinational A ssociation for S upportive C are in C ancer score was limited by uptake and specificity. Reducing time to antibiotics administration and readmission rates were identified as priorities. Implementation was labour‐intensive and faced significant barriers. Prioritisation of evidence for translation requires attention to local priorities and implementation complexity. These results argue for a single sepsis guideline with treatment of cancer as a high‐risk group.