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Study protocol for a two-center test of a nurse-implemented chronotherapeutic restoring bundle in critically ill children: RESTORE Resilience (R 2 ).

Authors :
Perry MA
Dawkins-Henry OS
Awojoodu RE
Blumenthal J
Asaro LA
Wypij D
Kudchadkar SR
Zuppa AF
Curley MAQ
Source :
Contemporary clinical trials communications [Contemp Clin Trials Commun] 2021 Aug 19; Vol. 23, pp. 100840. Date of Electronic Publication: 2021 Aug 19 (Print Publication: 2021).
Publication Year :
2021

Abstract

Often, pediatric intensive care environments are not conducive to healing the sick. Critically ill children experience disruptions in their circadian rhythms, which can contribute to delayed recovery and poor outcomes. We aim to test the hypothesis that children managed via RESTORE Resilience ( R <superscript>2</superscript> ), a nurse-implemented chronotherapeutic bundle, will experience restorative circadian rhythms compared to children receiving usual care. In this two-phased, prospective cohort study, two separate pediatric intensive care units in the United Sates will enroll a total of 20 baseline subjects followed by 40 intervention subjects, 6 months to less than 18 years of age, requiring invasive mechanical ventilation. During the intervention phase, we will implement the R <superscript>2</superscript> bundle, which includes: (1) a focused effort to replicate the child's pre-hospitalization daily routine, (2) cycled day-night lighting and sound modulation, (3) minimal yet effective sedation ( RESTORE ), (4) nighttime fasting with bolus enteral daytime feedings, (5) early progressive mobility ( PICU Up !), (6) continuity in nursing care, and (7) parent diaries. Our primary outcome is circadian activity ratio post-extubation. We hypothesize that children receiving R <superscript>2</superscript> will experience restored circadian rhythms as evidenced by decreased nighttime activity while in the PICU. Our exploratory outcomes include salivary melatonin levels; electroencephalogram (EEG) slow-wave activity; R <superscript>2</superscript> feasibility, adherence, and system barriers; levels of patient comfort; exposure to sedative medications; time to physiological stability; and parent perception of being well cared for. This paper describes the design, rationale, and implementation of R <superscript>2</superscript> .<br />Clinicaltrialsgov Identifier: NCT04695392.<br /> (© 2021 Published by Elsevier Inc.)

Details

Language :
English
ISSN :
2451-8654
Volume :
23
Database :
MEDLINE
Journal :
Contemporary clinical trials communications
Publication Type :
Academic Journal
Accession number :
34466711
Full Text :
https://doi.org/10.1016/j.conctc.2021.100840