Surviving the Pediatric Intensive Care Unit (PICU)
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: This is a non-interventional study..
- Who it may be relevant to
- Registry conditions: Post Intensive Care Syndrome (PICS). Basic parameters: 28 Days — 16 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Singapore
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Surviving the Pediatric Intensive Care Unit (PICU): Long-term Study to Understand and Improve Outcomes of PICU Survivors and Their Families
Overview
Improvement in pediatric intensive care unit (PICU) supportive care has led to improvement in clinical outcomes and decreased mortality in pediatric critical illness. However, PICU survivors are at risk of long-term health sequalae. Given the increased recognition of physical, cognitive, and psychological sequelae in PICU survivors, the concept of post-intensive care syndrome-pediatrics (PICS-p) has been proposed. Besides the PICU patient/survivor, the PICS-p framework also highlights the impacts of a child's critical illness has on the family. The impact of a PICU admission extends beyond the patient and parents, potentially affecting healthy siblings who are navigating their own developmental challenges. Healthy siblings may face emotional distress, increased responsibilities, and disruptions in their daily routines, all of which can contribute to long-term negative outcomes if unaddressed. Thus, this study consists of two cohorts to understand the long-term physical, cognitive, and psychological outcomes in PICU survivors and their families, and the short-term impacts on siblings of critically ill children.
Detailed description
The objectives of Helping to Optimize Patients' Experiences (HOPE) after Pediatric Critical Illness Cohort Study are:
1. \[Primary\] To characterize physical and cognitive health outcomes of PICU survivors. 2. \[Primary\] To investigate subgroups of critically ill children who have poor medium-term physical and cognitive health outcomes. 3. \[Primary\] To elucidate risk factors for poor physical and cognitive health outcomes in PICU survivors. 4. \[Exploratory\] To investigate the impact of physical and cognitive health of PICU survivors on overall family health.
The objectives of Singapore Health outcomes After Critical illness in Kids - Siblings (SHACK-S): Health Outcomes and Experiences of Healthy Siblings in the first 6 months after PICU discharge are:
1. \[Primary\] To describe and compare quality-of-life in healthy siblings at 1, 3 and 6 months after PICU discharge. 2. \[Primary\] To explore the experiences and support needs of healthy siblings 6 months after PICU discharge of a critically ill child. 3. \[Secondary\] To examine the experiences of recovery trajectory of healthy siblings.
Thus, HOPE cohort will provide information and insight regarding which groups of PICU patients and associated PICU therapies are associated with the highest risk for poor survivorship. The conduct of this study will also allow us to identify the challenges and find appropriate solutions in performing a cohort study with an emphasis on patient-reported outcomes (e.g., functional status, cognition and quality of life). Concurrently, the SHACK-S cohort will provide insights to understand the impacts of PICU admission on siblings and their recovery.
Interventions
- Other This is a non-interventional study.
This is a non-interventional study.
Primary outcome measures
- [HOPE] Pediatric Evaluation of Disability Inventory (PEDI-CAT) [Physical health outcomes of PICU survivors] [Time frame: Baseline, Hospital Discharge (up to 18 months post-PICU discharge), 6-, 12- and 18-month post-PICU discharge]
- [HOPE] Functional Status Scale (FSS) [Physical health outcomes of PICU survivors] [Time frame: Baseline, Hospital Discharge (up to 18 months post-PICU discharge), 6-, 12- and 18-month post-PICU discharge]
- [HOPE] Hand-grip strength test [Physical health outcomes of PICU survivors] [Time frame: Hospital Discharge (up to 18 months post-PICU discharge), 6-, 12- and 18-month post-PICU discharge]
- [HOPE] 6-minute walk test [Physical health outcomes of PICU survivors] [Time frame: Hospital Discharge (up to 18 months post-PICU discharge), 6-, 12- and 18-month post-PICU discharge]
- [HOPE] Developmental Profile-4 (DP-4) [Cognitive outcomes of PICU survivors] [Time frame: Baseline, 6-, 12- and 18-month post-PICU discharge]
- [HOPE] Bayley Scales of Infant and Toddler Development - 4th edition (Bayley-4) [Cognitive outcomes of PICU survivors] [Time frame: 6- and 18-month post-PICU discharge]
- [HOPE] National Institute of Health Toolbox - Cognition Battery (NIHTB-CB) [Cognitive outcomes of PICU survivors] [Time frame: Hospital Discharge (up to 18 months post-PICU discharge), 6-, 12- and 18-month post-PICU discharge]
- [HOPE] Strengths and Difficulty Questionnaire (SDQ) [Cognitive outcomes of PICU survivors] [Time frame: Baseline, 6-, 12- and 18-month post-PICU discharge]
- [SHACK-S] PedsQL 4.0 Short Form 15 (SF5) [Quality of Life in Siblings of Critically Ill Children] [Time frame: PICU discharge, 1-, 3-, and 6-month post-PICU discharge]
- [SHACK-S] Strengths and Difficulties Questionnaire (SDQ) [Experiences and Support Needs of Siblings of Critically Ill Children] [Time frame: 1-, 3-, and 6-month post-PICU discharge]
Secondary outcome measures (7)
- [HOPE] PedsQL 1.0 Infant Scales [Overall Family Health] [Time frame: Baseline, Hospital Discharge (up to 18 months post-PICU discharge), 6-, 12- and 18-month post-PICU discharge]
- [HOPE] PedsQL 4.0 Short Form 15 (SF15) [Overall Family Health] [Time frame: Baseline, Hospital Discharge (up to 18 months post-PICU discharge), 6-, 12- and 18-month post-PICU discharge]
- [HOPE] PedsQL 3.0 Cognitive Functioning Scales [Overall Family Health] [Time frame: Baseline, Hospital Discharge (up to 18 months post-PICU discharge), 6-, 12- and 18-month post-PICU discharge]
- [HOPE] Young Child PTSD Screen / Child and Adolescent PTSD Screen [Overall Family Health] [Time frame: 6-, 12- and 18-month post-PICU discharge]
- [HOPE] PedsQL 2.0 Family Impact Module [Overall Family Health] [Time frame: Baseline, Hospital Discharge (up to 18 months post-PICU discharge), 6-, 12- and 18-month post-PICU discharge]
- [HOPE] Patient Health Questionnaire-4 (PHQ-4) [Overall Family Health] [Time frame: PICU discharge, Hospital Discharge (up to 18 months post-PICU discharge), 6-, 12- and 18-month post-PICU discharge]
- [HOPE] PTSD Checklist for DSM-5 [Overall Family Health] [Time frame: 6-, 12- and 18-month post-PICU discharge]
Eligibility criteria
Inclusion criteria
\[HOPE Cohort\]
- Between 28 days - 16 years of age at PICU admission
- Have an expected PICU stay > 48 hours\*
\[SHACK-S Cohort\]
- Healthy children (aged 4 -16 years old) with critically ill sibling between 28 days - 16 years of age at PICU admission
- Has a critically ill sibling who has an expected PICU stay > 48 hours
- Lives in the same household as the critically ill sibling and parents prior to admission
Exclusion criteria
\[HOPE Cohort\]
- Do-Not-Resuscitate status
- Lack of informed consent
- Prior enrolment in this study
\[SHACK-S Cohort\]
- Children of critically ill sibling with Do-Not-Resuscitate status
- Children with condition listed on paediatric Complex Chronic Conditions (CCC) system Version 3.0 or with neurocognitive/neurodevelopmental delays or disorders
- Previous admission to PICU
- Lack of informed consent
- Prior enrolment in this study
- Note: For participating study sites without a dedicated PICU (e.g., sites where patients are managed in a combined ward under High Dependency (HD) or ICU status), PICU stay will be defined as the duration during which the patient is assigned an ICU status. The determination of ICU status will be made at the discretion of the respective site's study team and Site-PI.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Singapore · 2 centers
- National University Singapore — Singapore
- KK Women's and Children's Hospital — Singapore
Identifiers
NCT: NCT06812130 · ECOS Ref: 2024-3978