Feasibility and Acceptability of Methods to Collect Follow-Up Information From Parents 12 Months After Their Child's Emergency Admission to Pediatric Intensive Care.


Journal

Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies
ISSN: 1529-7535
Titre abrégé: Pediatr Crit Care Med
Pays: United States
ID NLM: 100954653

Informations de publication

Date de publication:
04 2019
Historique:
pubmed: 6 2 2019
medline: 12 5 2020
entrez: 6 2 2019
Statut: ppublish

Résumé

To evaluate the feasibility and acceptability of different methods of collecting follow-up data from parents 12 months after their child's emergency admission to a PICU. Mixed-methods explanatory sequential design. One regional PICU transport service and three PICUs in England. Children undergoing emergency transport to PICU recruited to an ongoing biomarker study whose parents consented to be contacted for follow-up 12 months after PICU admission. None. Parents or guardians who consented were asked to complete three questionnaires about their child's functional status, quality of life, and behavior 12 months after PICU admission. Parents were given a choice about method of questionnaire completion: postal, online, or telephone interview and also asked for telephone feedback about the process and the reasons for their choice. Of 486 parents who consented to be contacted at 12 months, 232 were successfully contacted. Consent to receive questionnaires was obtained in 218 of 232 (94%). Of the 218 parents, 102 (47%) chose to complete questionnaires online (with 77% completion rate), 91 (42%) chose to complete postal questionnaires (48% completion rate), and 25 (11%) chose to complete questionnaires by telephone interview (44% completion rate). Parents expressed different preferences for follow-up questionnaire completion. Response rates varied by completion method. Understanding and catering for parental preferences is an important factor in maximizing response rates for follow-up studies in intensive care.

Identifiants

pubmed: 30720671
doi: 10.1097/PCC.0000000000001892
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e199-e207

Commentaires et corrections

Type : CommentIn

Auteurs

Rachel Anne Pulham (RA)

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

Jo Wray (J)

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

Yael Feinstein (Y)

Cardiac Intensive Care Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.

Katherine Brown (K)

Cardiac Intensive Care Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.

Christine Pierce (C)

Paediatric Intensive Care Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.

Simon Nadel (S)

Paediatric Intensive Care Unit, St Mary's Hospital, Imperial College Healthcare NHS Trust, London, United Kingdom.

Nazima Pathan (N)

Department of Paediatrics, University of Cambridge, Cambridge, United Kingdom.

Elena Garralda (E)

Centre for Psychiatry, Imperial College London, London, United Kingdom.

Padmanabhan Ramnarayan (P)

Paediatric Intensive Care Unit, St Mary's Hospital, Imperial College Healthcare NHS Trust, London, United Kingdom.
Children's Acute Transport Service (CATS), Critical Care Division, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.

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