Abstract

Improvements in clinical management of the preterm infant have reduced the rates of the two most common forms of brain injury, such as severe intraventricular hemorrhage and white matter injury, both of which are contributory factors in the development of cerebral palsy. Nonetheless, they remain a persistent challenge and are associated with a significant increase in the risk of adverse neurodevelopment outcomes. Repeated episodes of ischemia–reperfusion represent a common pathway for both forms of injury, arising from discordance between systemic blood flow and the innate regulation of cerebral blood flow in the germinal matrix and periventricular white matter. Nevertheless, establishing firm hemodynamic boundaries, as a part of neuroprotective strategy, has challenged researchers. Existing measures either demonstrate inconsistent relationships with injury, as in the case of mean arterial blood pressure, or are not feasible for long-term monitoring, such as cardiac output estimated by echocardiography. These challenges have led some researchers to focus on the mechanisms that control blood flow to the brain, known as cerebrovascular autoregulation. Historically, the function of the cerebrovascular autoregulatory system has been difficult to quantify; however, the evolution of bedside monitoring devices, particularly near-infrared spectroscopy, has enabled new insights into these mechanisms and how impairment of blood flow regulation may contribute to catastrophic injury. In this review, we first seek to examine how technological advancement has changed the assessment of cerebrovascular autoregulation in premature infants. Next, we explore how clinical factors, including hypotension, vasoactive medications, acute and chronic hypoxia, and ventilation, alter the hemodynamic state of the preterm infant. Additionally, we examine how developmentally linked or acquired dysfunction in cerebral autoregulation contributes to preterm brain injury. In conclusion, we address exciting new approaches to the measurement of autoregulation and discuss the feasibility of translation to the bedside.

Highlights

  • Premature infants weighing less than 1,500 g at birth are frequently affected by two specific forms of brain injury, such as intraventricular hemorrhage (IVH) and white matter injury (WMI)

  • This shift has been enabled by new technology, driving deeper investigation into the regulation of cerebral blood flow (CBF) in preterm infants, finding significant impairment of autoregulation as a major contributing factor to the development of IVH

  • Cerebrovascular autoregulatory system failure results in unstable CBF, generating the cycle of ischemia–reperfusion, which drives the mechanisms of preterm brain injury

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Summary

INTRODUCTION

Premature infants weighing less than 1,500 g at birth are frequently affected by two specific forms of brain injury, such as intraventricular hemorrhage (IVH) and white matter injury (WMI). Over the last 10 years, investigation has shifted from examination of systemic blood flow to detailed investigation of patterns of CBF This shift has been enabled by new technology, driving deeper investigation into the regulation of CBF in preterm infants, finding significant impairment of autoregulation as a major contributing factor to the development of IVH. Obstruction of the venous system, whether by pneumothorax impeding venous return, ventilator asynchrony or a change in head position caused an increase in hydrostatic pressure, again leads to the rupture of vessels in the capillary bed [5] Both mechanisms likely provide contributory components, with cycles of ischemia and reperfusion further weakening the vascular structures until the blood vessels can no longer tolerate the fluctuations and burst. Repeated ischemic episodes associated with any of these mechanisms will generate an inflammatory response, increasing the metabolic demand, utilizing a greater fraction of delivered oxygen, and potentiating further injury during the ischemic episode

REVIEW OF CEREBROVASCULAR AUTOREGULATORY SYSTEM
OVERVIEW OF METHODS FOR QUANTIFYING THE AUTOREGULATORY SYSTEM
LINK BETWEEN DYSFUNCTION IN AUTOREGULATION AND BRAIN INJURY
Findings
CONCLUSION

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