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Effects of early-life exposures to anesthesia on the brain

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Debate exists over the real-world consequences of these impacts. The effect size of early-life anesthesia exposure appears small, and may or may not be practically relevant. In 2016, the United States Food and Drug Administration issued a communication cautioning about "repeated or lengthy" exposure to general anesthetic prior to age three and suggested clinicians and caregivers weigh the risks and benefits of surgical procedures longer than three hours in this population.

Preclinical evidence

Studies in preclinical models have demonstrated that rodents and nonhuman primates that were exposed to general anesthesia in infancy developed neurodevelopmental problems later in life. Particularly in nonhuman primates, studies of exposures to anesthesia in infancy indicate that early-life anesthesia is associated with long-term changes in social behaviors, elevated anxiety and/or inhibition. At the cellular level, the exposure of rodents and nonhuman primates to anesthesia during infancy causes developmental neurotoxicity, including widespread neuronal and glial apoptosis, and deficits in synapse and mitochondria structures and functions. Exposures to anesthetics in early life can also cause genomic and epigenomic changes, including reduced levels of proteins that regulate the development and function of neurons, such as BDNF and immediate early genes. Multiple exposures to anesthesia have been found to confer greater deficits in neurotoxicity, cognition and social behavior than single exposures.

Nearly all anesthetics that are antagonists of NMDA receptors and/or agonists of GABAA receptors have been shown to cause developmental neurotoxicity and alter cognition and/or behavior. Neurotoxicity in rodents has been shown for inhalant anesthetics—such as sevoflurane, isoflurane, and desflurane—as well as intravenous anesthetics like ketamine and propofol. Studies in nonhuman primates have shown that neurotoxic and cognitive or behavioral effects caused by general anesthetics may be reduced by co-administration of agents such as dexmedetomidine, lithium, and pramipexole.

Limitations of preclinical studies

Many preclinical neurological findings are limited in their translatability to humans due to differences in brain complexity and development between humans and rodents, as well as the difficulty in controlling and monitoring rodent physiology for safety during exposures.

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