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National Confidential Enquiry into Patient Outcome and Death
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Home/Studies/Stabilisation of the critically ill child
Stabilisation of the critically ill child

This study has been commissioned by Healthcare Quality Improvement Partnership HQIP
as part of the Child Health Clinical Outcome Review Programme as part of the current contract awarded in 2019.
For information on how we use data click here

Data collection for study To commence July 2025
Patient identification spreadsheet data collection Open
Clinical data collection Not open 
Organisational data collection Not open
Publication date December 2026

Aim
    • To identify good practice and areas for improvement in the quality of care provided to patients 0-18th birthday who are critically ill and require stabilisation
    • To review the impact of delivering that care on staff, patients and parent carers
Participation
All acute hospital providers where patients might be admitted will be asked to participate in the study.

Data collection
The timeframe from which data will be sampled will be between the 1st October 2024 – 31st March 2025

Patient identification spreadsheets
Patients will be identified for inclusion from hospital patient administration systems and via paediatric critical care transport team records.
Via hospital patient administration systems
Local reporters will be asked to populate the patient identification spreadsheet with the details of patients who were:
    • Admitted to critical care (level 2 (PHDU/HDU) or level 3 (PICU/ICU) care)
    • Seen in the Emergency Department and have one of the included SNOMED CT or OPCS codes (listed below):
    • Transferred to another hospital
If any one of the three criteria above are met, the patient should be included on the patient identification spreadsheet
SNOMED CT/OPCS codes for inclusion
SNOMED CT code OPCS code
General anaesthesia 50697003 Y80
Non-invasive ventilation 428311008 E85.2
Insertion of endotracheal tube 112798008 X56.
2X56.9
Insertion of catheter into artery 392247006 L70.4
Central venous cannula insertion 233527006 L91.2
Y53.9
Central venous cannula insertion Intraosseous cannulation 430824005 Y33.0

Via paediatric critical care transport team records
Local reporters in the Trusts/Health Boards where the paediatric critical care transport teams are based will be asked to populate the patient identification spreadsheet with the details of patients who were:
    • Discussed with a critical care/paediatric transport/retrieval team during stabilisation
    • Transferred by a critical care/paediatric transport/retrieval team
Exclusions
    • Patients admitted to the Neonatal Intensive Care Unit (NICU) or Special Care Baby Unit (SCBU)
    • Patients who are admitted as a result of trauma (ICD10 codes T00 – T88) to a major trauma centre (patients admitted as a result of trauma to a non-major trauma centre will still be included)
    • Patients admitted to independent hospitals
Clinician questionnaires
Two questionnaires will be used to collect clinical data for this study:
    • Stabilisation questionnaire
    • Critical care questionnaire (where applicable)
Up to 8 patients per hospital will be sampled for inclusion.

Case note extracts for review
Case notes will be requested for all patients included in the peer review aspect of the study.
Organisational questionnaires
An organisational questionnaire will be sent to all hospitals where patients (0-18th birthday) might be admitted
Please see the study protocol for more detailed information on the study methods.

Any other queries relating to this study should also be addressed to stabilisation@ncepod.org.uk
This page will be updated regularly so please check for further information.


 

Download links
  • Study protocol
  • Healthcare quality improvement plan
  • Patient identification spreadsheet for Local Reporters
  • Patient identification spreadsheet for Paediatric Critical Care Transport Teams
  • Study information poster for clinicians
  • Study information poster for young people and parent carers
  • Study information poster for young people and parent carers (easy read version)
  • Information leaflet for young people
  • Information leaflet for parent carers  

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