Due to maintenance currently being carried out, Subscription and PC renewal payments will be unavailable until Wednesday, 25th April 2018. Apologies for any inconvenience this may cause.
The Paediatric Early Warning System (PEWS) is a workstream of the National Clinical Programme for Paediatrics and Neonatology.
It provides a framework for care and empowers clinicians to act on behalf of a child with signs of deterioration or about whom they have clinical concerns.
It is designed to make hospital admissions safer for children and help staff care for deteriorating paediatric patients.
A National Clinical Guideline on the Irish Paediatric Early Warning System (PEWS) was published by the National Clinical Effectiveness Committee and Department of Health in November 2015 and updated in November 2016.
PEWS is designed for use in tertiary, regional and peripheral hospital settings.
It takes a multifaceted approach to improving clinical outcomes, using safety interventions such as:
The following resources are available to support PEWS implementation and training.
These resources replace all earlier editions and are correct from June 2017.
This toolkit contains the resources required by PEWS Governance Committees and senior management teams considering the implementation of PEWS.
The PEWS National Clinical Guideline provides the framework for implementation and should be referred to for guidance.
This toolkit contains the resources required by PEWS Leads, Trainers and Champions to facilitate training for implementation and ongoing retraining/updates.
You must refer to the PEWS National Clinical Guideline and the specific guidance for implementation / training when accessing and using these resources.
*Please contact email@example.com for these resources
The resources in this toolkit are to aid PEWS Governance bodies, leads, trainers and champions to undertake audit of process and outcome measures, as required by the PEWS National Clinical Guideline
These resources are also required for complying with HSE BIU KPI suite requirements.
We recognise that parents and carers know their children best and can be acutely aware that their child is unwell or 'just not right', sometimes before the physiological parameters become abnormal.
The concerns of parents, families and caregivers are a core scoring parameter in PEWS. An assessment of parent/carer concern is undertaken at every observation opportunity. Concern on the part of a parent/carer should merit appropriate consideration and may require escalation.
The resources in this toolkit will assist the bedside clinician in supporting parents to participate in the concern assessment and to aid parents in expressing their concern about their child.
These resources were adapted with kind permission from Birmingham Children’s Hospital Listening to You communication bundle. We are grateful for their support of this project.
The National PEWS Steering Group is chaired by Dr. John Fitzsimons, Clinical Director for Quality Improvement, HSE Quality Improvement Division.
Membership (as of June 2016):