Early Rehabilitation in Critically ill Children: A Two Center Implementation Study*

Author:

Choong Karen12,Fraser Douglas D.3,Al-Farsi Ahmed1,Awlad Thani Saif1,Cameron Saoirse4,Clark Heather5,Cuello Carlos2,Debigaré Sylvie6,Ewusie Joycelyne7,Kennedy Kevin8,Kho Michelle E.9,Krasevich Kimberley1,Martin Claudio M.10,Thabane Lehana127,Nanji Jasmine1,Watts Catharine5,Simpson Andrea5,Todt Ashley6,Wong Jonathan5,Xie Feng2,Vu Michael11,Cupido Cynthia1,

Affiliation:

1. Department of Pediatrics, McMaster University, Hamilton, ON, Canada.

2. Department of Health Research Methods, Evidence and Impact, McMaster University, Hamilton, ON, Canada.

3. Department of Medicine, Division of Critical Care, Schulich School of Medicine and Dentistry, Western University, London, ON, Canada.

4. Lawson Health Research Institute, Children’s Hospital at London Health Sciences Center, London, ON, Canada.

5. McMaster Children’s Hospital, Hamilton, ON, Canada.

6. Family partner.

7. The Research Institute, Biostatistics Unit, St. Joseph’s Healthcare, Hamilton, ON, Canada.

8. School of Population and Public Health, University of British Columbia, Vancouver, BC, Canada.

9. School of Rehabilitation Science, McMaster University, Hamilton, ON, Canada.

10. Department of Pediatrics, Division of Critical Care, Schulich School of Medicine and Dentistry, Western University, London, ON, Canada.

11. Department of Family Medicine, McMaster University, Hamilton, ON, Canada.

Abstract

OBJECTIVES: To implement an early rehabilitation bundle in two Canadian PICUs. DESIGN AND SETTING: Implementation study in the PICUs at McMaster Children’s Hospital (site 1) and London Health Sciences (site 2). PATIENTS: All children under 18 years old admitted to the PICU were eligible for the intervention. INTERVENTIONS: A bundle consisting of: 1) analgesia-first sedation; 2) delirium monitoring and prevention; and 3) early mobilization. MEASUREMENTS AND MAIN RESULTS: Primary outcomes were the duration of implementation, bundle compliance, process of care, safety, and the factors influencing implementation. Secondary endpoints were the impact of the bundle on clinical outcomes such as pain, delirium, iatrogenic withdrawal, ventilator-free days, length of stay, and mortality. Implementation occurred over 26 months (August 2018 to October 2020). Data were collected on 1,036 patients representing 4,065 patient days. Bundle compliance was optimized within 6 months of roll-out. Goal setting for mobilization and level of arousal improved significantly (p < 0.01). Benzodiazepine, opioid, and dexmedetomidine use decreased in site 1 by 23.2% (95% CI, 30.8–15.5%), 26.1% (95% CI, 34.8–17.4%), and 9.2% (95% CI, 18.2–0.2%) patient exposure days, respectively, while at site 2, only dexmedetomidine exposure decreased significantly by 10.5% patient days (95% CI, 19.8–1.1%). Patient comfort, safety, and nursing workload were not adversely affected. There was no significant impact of the bundle on the rate of delirium, ventilator-free days, length of PICU stay, or mortality. Key facilitators to implementation included institutional support, unit-wide practice guidelines, dedicated PICU educators, easily accessible resources, and family engagement. CONCLUSIONS: A rehabilitation bundle can improve processes of care and reduce patient sedative exposure without increasing patient discomfort, nursing workload, or harm. We did not observe an impact on short-term clinical outcomes. The efficacy of a PICU-rehabilitation bundle requires ongoing study. Lessons learned in this study provide evidence to inform rehabilitation implementation in the PICU setting.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Critical Care and Intensive Care Medicine,Pediatrics, Perinatology and Child Health

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