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Updated: Jul 5, 2025

A Neonatal Imaging Model of Gram-Negative Bacterial Sepsis
Published on: August 12, 2020
Sepsis epidemiology in Australian and New Zealand children (SENTINEL): protocol for a multicountry prospective
Elliot Long, Meredith L Borland1,2, Shane George3,4,5
1Department of Emergency Medicine, Perth Children's Hospital, Perth, Western Australia, Australia.
Insights
This study analyzes childhood sepsis in Australia and New Zealand, identifying key factors for improving diagnosis and treatment. Understanding sepsis burden is crucial for developing new interventions to improve pediatric outcomes.
Area of Science:
- Pediatric critical care medicine
- Infectious disease epidemiology
- Health services research
Background:
- Childhood sepsis is a significant global health issue, causing millions of deaths annually and substantial healthcare costs.
- Current therapies and outcomes for sepsis have seen little improvement over decades due to challenges in diagnosis and disease variability.
- There is a critical need to better understand the epidemiology and management of childhood sepsis to inform effective interventions.
Purpose of the Study:
- To characterize the burden of community-acquired childhood sepsis in Australia and New Zealand, including incidence, severity, outcomes, and costs.
- To prospectively evaluate sepsis diagnostic criteria and risk stratification tools in pediatric patients.
- To describe sepsis therapies, quality of care, parental awareness, and parent-reported outcomes to guide future research.
Main Methods:
- A prospective observational study involving children up to 18 years presenting with suspected sepsis across 12 emergency departments in Australia and New Zealand.
- Collection of detailed clinical data, including vital signs, biomarkers, management strategies, and patient outcomes (mortality, length of stay, parent-reported outcomes).
- Evaluation of existing and novel diagnostic and risk stratification criteria, alongside characterization of antimicrobial use and guideline adherence.
Main Results:
- Data collection on presenting characteristics, management, and outcomes for pediatric sepsis cases is ongoing.
- Analysis will determine sepsis epidemiology, validate risk stratification tools, and assess antimicrobial stewardship and guideline adherence.
- Parental awareness and parent-reported outcomes will be documented to provide a comprehensive view of the sepsis experience.
Conclusions:
- This study will provide crucial insights into the epidemiology and clinical management of childhood sepsis in Australia and New Zealand.
- Findings will inform the design of interventional trials aimed at improving diagnostic accuracy and therapeutic effectiveness.
- Understanding the multifaceted aspects of sepsis care is fundamental for enhancing outcomes in affected children.
Introduction:
Sepsis affects 25.2 million children per year globally and causes 3.4 million deaths, with an annual cost of hospitalisation in the USA of US$7.3 billion. Despite being common, severe and expensive, therapies and outcomes from sepsis have not substantially changed in decades. Variable case definitions, lack of a reference standard for diagnosis and broad spectrum of disease hamper efforts to evaluate therapies that may improve sepsis outcomes. This landscape analysis of community-acquired childhood sepsis in Australia and New Zealand will characterise the burden of disease, including incidence, severity, outcomes and cost. Sepsis diagnostic criteria and risk stratification tools will be prospectively evaluated. Sepsis therapies, quality of care, parental awareness and understanding of sepsis and parent-reported outcome measures will be described. Understanding these aspects of sepsis care is fundamental for the design and conduct of interventional trials to improve childhood sepsis outcomes.
Methods And Analysis:
This prospective observational study will include children up to 18 years of age presenting to 12 emergency departments with suspected sepsis within the Paediatric Research in Emergency Departments International Collaborative network in Australia and New Zealand. Presenting characteristics, management and outcomes will be collected. These will include vital signs, serum biomarkers, clinician assessment of severity of disease, intravenous fluid administration for the first 24 hours of hospitalisation, organ support therapies delivered, antimicrobial use, microbiological diagnoses, hospital and intensive care unit length-of-stay, mortality censored at hospital discharge or 30 days from enrolment (whichever comes first) and parent-reported outcomes 90 days from enrolment. We will use these data to determine sepsis epidemiology based on existing and novel diagnostic criteria. We will also validate existing and novel sepsis risk stratification criteria, characterise antimicrobial stewardship, guideline adherence, cost and report parental awareness and understanding of sepsis and parent-reported outcome measures.
Ethics And Dissemination:
Ethics approval was received from the Royal Children's Hospital of Melbourne, Australia Human Research Ethics Committee (HREC/69948/RCHM-2021). This included incorporated informed consent for follow-up. The findings will be disseminated in a peer-reviewed journal and at academic conferences.
Trial Registration Number:
ACTRN12621000920897; Pre-results.
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