Development of a parent experience measure for paediatric critical care transport teams.


Journal

Nursing in critical care
ISSN: 1478-5153
Titre abrégé: Nurs Crit Care
Pays: England
ID NLM: 9808649

Informations de publication

Date de publication:
05 2022
Historique:
revised: 16 03 2021
received: 30 11 2020
accepted: 20 04 2021
pubmed: 25 5 2021
medline: 11 5 2022
entrez: 24 5 2021
Statut: ppublish

Résumé

A third of children admitted to paediatric intensive care units (PICUs) in the United Kingdom (UK) are transported by paediatric critical care transport services (PCCTs). Parents have described the transfer journey as particularly stressful. Critical care nurses have a key role in mitigating the impact of the journey on parents. Evaluating parents' experiences is important to inform service improvements. Our aim was to describe the development of a new measure of parents' experiences of PCCTs, derived from data collected in the Differences in access to Emergency Paediatric Intensive Care and care during Transport (DEPICT) study. A descriptive cross-sectional survey was used. As part of the DEPICT study, a 17-item transport experience questionnaire was developed and given to parents of children transported by PCCTs to 24 UK PICUs during a 12-month period. Analyses included exploratory factor analysis and a validation review by a PCCT stakeholder group. Families of 1722 children (1798 journeys) completed questionnaires. Five items were excluded from further analysis as correlation coefficients were <0.3. Two factors explained 53% of the variance and all 12 items loaded on one of these factors. Factor 1 (8 items) explained 47% of the variance, had excellent internal reliability and the clustered items were conceptually coherent with a specific relevance to PCCTs; these were offered for consideration, with other items possibly discarded. Twenty-eight PCCT clinicians reviewed the questions. Using a 70% agreement threshold, one additional, previously discarded, item was identified for inclusion, resulting in a nine-item experience measure. Our brief measure of parents' experience of critical care transport provides a standardized measure that can be used across all PCCTs, enabling national benchmarking of services and potentially increasing the collection and use of parent experience data to improve services. Being able to measure experience provides an opportunity to understand how to make services better to improve experience.

Sections du résumé

BACKGROUND
A third of children admitted to paediatric intensive care units (PICUs) in the United Kingdom (UK) are transported by paediatric critical care transport services (PCCTs). Parents have described the transfer journey as particularly stressful. Critical care nurses have a key role in mitigating the impact of the journey on parents. Evaluating parents' experiences is important to inform service improvements.
AIM AND OBJECTIVES
Our aim was to describe the development of a new measure of parents' experiences of PCCTs, derived from data collected in the Differences in access to Emergency Paediatric Intensive Care and care during Transport (DEPICT) study.
DESIGN
A descriptive cross-sectional survey was used.
METHODS
As part of the DEPICT study, a 17-item transport experience questionnaire was developed and given to parents of children transported by PCCTs to 24 UK PICUs during a 12-month period. Analyses included exploratory factor analysis and a validation review by a PCCT stakeholder group.
RESULTS
Families of 1722 children (1798 journeys) completed questionnaires. Five items were excluded from further analysis as correlation coefficients were <0.3. Two factors explained 53% of the variance and all 12 items loaded on one of these factors. Factor 1 (8 items) explained 47% of the variance, had excellent internal reliability and the clustered items were conceptually coherent with a specific relevance to PCCTs; these were offered for consideration, with other items possibly discarded. Twenty-eight PCCT clinicians reviewed the questions. Using a 70% agreement threshold, one additional, previously discarded, item was identified for inclusion, resulting in a nine-item experience measure.
CONCLUSION
Our brief measure of parents' experience of critical care transport provides a standardized measure that can be used across all PCCTs, enabling national benchmarking of services and potentially increasing the collection and use of parent experience data to improve services.
RELEVANCE TO CLINICAL PRACTICE
Being able to measure experience provides an opportunity to understand how to make services better to improve experience.

Identifiants

pubmed: 34028143
doi: 10.1111/nicc.12648
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Pagination

367-374

Subventions

Organisme : Health Services and Delivery Research Programme
ID : 15/136/45

Informations de copyright

© 2021 British Association of Critical Care Nurses.

Références

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Auteurs

Ruth E C Evans (REC)

Centre for Outcomes and Experience Research in Children's Health, Illness and Disability (ORCHID), Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.

Victoria Barber (V)

Centre for Outcomes and Experience Research in Children's Health, Illness and Disability (ORCHID), Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.

Sarah Seaton (S)

Department of Health Sciences, University of Leicester, Leicester, UK.

Elizabeth S Draper (ES)

Department of Health Sciences, University of Leicester, Leicester, UK.

Fatemah Rajah (F)

Yorkshire and Humber Infant and Children's Transport Service (Embrace), Barnsley, UK.

Christina Pagel (C)

Clinical Operational Research Unit, University College, London, UK.

Eithne Polke (E)

Children's Acute Transport Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.

Padmanabhan Ramnarayan (P)

Children's Acute Transport Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Respiratory, Critical Care and Anaesthesia Section, Infection, Immunity and Inflammation Research and Teaching Department, UCL GOS Institute of Child Health, London, UK.

Jo Wray (J)

Centre for Outcomes and Experience Research in Children's Health, Illness and Disability (ORCHID), Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Heart and Lung Directorate, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Institute of Cardiovascular Science, University College, London, UK.

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