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Ventilator Liberation Practices in Pediatric Cardiac Critical Care
Amy J Romer1, Samer Abu-Sultaneh2, Michael G Gaies3
1Dr. Romer is affiliated with Division of Cardiac Critical Care Medicine, Department of Anesthesiology and Critical Care, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, Pennsylvania.
Insights
Ventilator liberation practices for critically ill children with cardiac disease lack standardized protocols. This study reveals significant variation in extubation readiness testing and post-extubation support, highlighting a need for improved guidelines and quality improvement initiatives.
Area of Science:
- Pediatric Critical Care
- Cardiology
- Respiratory Medicine
Background:
- Mechanical ventilation is prevalent in critically ill children with cardiac disease.
- Limited literature exists on ventilator liberation practices for this specific pediatric population.
- Understanding current practices is crucial for improving patient outcomes.
Purpose of the Study:
- To describe current ventilator liberation practices in critically ill children with cardiac disease.
- To identify variations in extubation readiness testing and post-extubation support.
- To highlight areas for protocol development and quality improvement.
Main Methods:
- An electronic survey was distributed to pediatric ICU attending physicians within the Pediatric Cardiac Critical Care Consortium.
- The survey evaluated institutional protocols and individual practices regarding ventilator liberation, extubation readiness testing (ERT), spontaneous breathing trials (SBT), and post-extubation support.
- 133 responses from 47 hospitals were analyzed.
Main Results:
- Only 47% of institutions reported ERT eligibility screening and 55% reported SBT protocols.
- Most respondents utilized SBTs (95%) and pressure support augmentation to CPAP (92%) for extubation assessment.
- Significant variation was observed in extubation readiness parameters (e.g., pulse oximetry, lactate, pH, mixed venous saturation) and post-extubation non-invasive respiratory support (NRS) use.
Conclusions:
- Standardized ERT eligibility screening and SBT protocols are lacking in approximately half of surveyed institutions.
- Wide variations in extubation readiness assessment and post-extubation respiratory support strategies exist.
- There is a clear need for protocol development aligned with clinical guidelines and multi-center quality improvement to establish best practices for ventilator liberation in pediatric cardiac patients.
Abstract:
Background: Mechanical ventilation is common in critically ill children with cardiac disease, but literature focused on ventilator liberation practices for this unique pediatric subpopulation is limited. We aimed to describe current ventilator liberation practices in critically ill children with cardiac disease. Methods: Through the Pediatric Cardiac Critical Care Consortium, an electronic survey was distributed to pediatric ICU attending physicians caring for patients with cardiac disease evaluating institutional protocols and individual practices around ventilator liberation including criteria for extubation readiness testing (ERT), ERT components, spontaneous breathing trial (SBT) method and duration, timing of extubation, and postextubation respiratory support. Results: We received 133 responses representing 47 hospitals. ERT eligibility screening and SBT protocols were reported at 22 (47%) and 26 (55%) of the 47 institutions, respectively. Most respondents used SBTs in their assessment of extubation readiness (95%) and pressure support augmentation to CPAP for SBT (92%). Most respondents reported a maximum dose threshold for epinephrine (81%), above which they would not extubate. Some indices used for determination of extubation readiness were used by nearly all respondents: pulse oximetry (92%), serum lactate (86%), and arterial pH (85%); but some respondents also report using mixed venous saturation (68%), ventricular function (62%), near-infrared spectroscopy (62%), and systemic atrioventricular valve regurgitation (53%). Reported use of noninvasive respiratory support (NRS) after extubation was common, up to 90% in selected subgroups. There was wide variation in the type of NRS used in all populations. Conclusions: ERT eligibility screening and SBT protocols were reported in only half of the institutions surveyed, and notable variation exists between parameters surrounding extubation readiness assessment and postextubation respiratory support. These data suggest opportunities to increase protocol development to align with established clinical practice guidelines around ERT and conduct multi-center quality improvement to identify best practices for ventilator liberation in this patient population.
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