• Rachel Anne Pulham, Jo Wray, Yael Feinstein, Katherine Brown, Christine Pierce, Simon Nadel, Nazima Pathan, Elena Garralda, and Padmanabhan Ramnarayan.
• Centre for Outcomes & Experience Research in Children's Health, Illness & Disability (ORCHID), Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.
• Pediatr Crit Care Me. 2019 Apr 1; 20 (4): e199-e207.

ObjectivesTo 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.DesignMixed-methods explanatory sequential design.SettingOne regional PICU transport service and three PICUs in England.PatientsChildren 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.InterventionsNone.Measurements And Main ResultsParents 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).ConclusionsParents 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.

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