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Cerebral Oximetry in Preterm Infants-To Use or Not to Use, That Is the Question
Gorm Greisen1, Mathias Lühr Hansen1, Marie Isabel Skov Rasmussen1
1Department of Neonatology, Rigshospitalet and Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
Insights
The SafeBoosC project evaluated cerebral oximetry in extremely preterm infants, finding potential harms outweigh benefits. This study advises caution with this monitoring tool in neonatal intensive care.
Area of Science:
- Neonatal intensive care
- Pediatric neurology
- Medical device evaluation
Background:
- Extremely preterm infants face high risks of death and brain injury.
- Cerebral oximetry is approved but may harm vulnerable infants.
- The SafeBoosC project prioritizes "do not disturb-unless necessary".
Purpose of the Study:
- To test patient-relevant benefits and harms of cerebral oximetry in extremely preterm infants.
- To evaluate the use of cerebral oximetry versus other monitoring modalities.
- To provide a perspective on cerebral oximetry's clinical use in neonates.
Main Methods:
- Randomized clinical trial design.
- Discussion of cerebral oximetry, pulse oximetry, electric cardiometry, and blood pressure monitoring.
- Analysis of measurement reliability, pathophysiological rationale, evidence, and costs.
Main Results:
- Potential tangible risks include skin breakdown and tube displacement.
- Mismanagement of cerebral oxygenation is a concern.
- Evidence for benefit and harms of cerebral oximetry requires careful consideration.
Conclusions:
- The risks associated with cerebral oximetry in extremely preterm infants warrant cautious use.
- Non-invasive monitoring modalities may offer alternatives for reducing hypoxic-ischemic brain injury.
- Further evidence is needed to guide the routine use of cerebral oximetry in neonatal care.
Abstract:
The Safeguarding the Brains of our smallest Children (SafeBoosC) project was initially established to test the patient-relevant benefits and harms of cerebral oximetry in extremely preterm infants in the setting of a randomized clinical trial. Extremely preterm infants constitute a small group of patients with a high risk of death or survival with brain injury and subsequent neurodevelopmental disability. Several cerebral oximeters are approved for clinical use, but the use of additional equipment may disturb and thereby possibly harm these vulnerable, immature patients. Thus, the mission statement of the consortium is "do not disturb-unless necessary." There may also be more tangible risks such as skin breakdown, displacement of tubes and catheters due to more complicated nursing care, and mismanagement of cerebral oxygenation as a physiological variable. Other monitoring modalities have relevance for reducing the risk of hypoxic-ischemic brain injury occurring during acute illness and have found their place in routine clinical care without evidence from randomized clinical trials. In this manuscript, we discuss cerebral oximetry, pulse oximetry, non-invasive electric cardiometry, and invasive monitoring of blood pressure. We discuss the reliability of the measurements, the pathophysiological rationale behind the clinical use, the evidence of benefit and harms, and the costs. By examining similarities and differences, we aim to provide our perspective on the use or non-use of cerebral oximetry in newborn infants during intensive care.
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