Therapies for neonatal encephalopathy: Targeting the latent, secondary and tertiary phases of evolving brain injury.

Journal Article (Journal Article)

In term and near-term neonates with neonatal encephalopathy, therapeutic hypothermia protocols are well established. The current focus is on how to improve outcomes further and the challenge is to find safe and complementary therapies that confer additional protection, regeneration or repair in addition to cooling. Following hypoxia-ischemia, brain injury evolves over three main phases (latent, secondary and tertiary), each with a different brain energy, perfusion, neurochemical and inflammatory milieu. While therapeutic hypothermia has targeted the latent and secondary phase, we now need therapies that cover the continuum of brain injury that spans hours, days, weeks and months after the initial event. Most agents have several therapeutic actions but can be broadly classified under a predominant action (e.g., free radical scavenging, anti-apoptotic, anti-inflammatory, neuroregeneration, and vascular effects). Promising early/secondary phase therapies include Allopurinol, Azithromycin, Exendin-4, Magnesium, Melatonin, Noble gases and Sildenafil. Tertiary phase agents include Erythropoietin, Stem cells and others. We review a selection of promising therapeutic agents on the translational pipeline and suggest a framework for neuroprotection and neurorestoration that targets the evolving injury.

Full Text

Duke Authors

Cited Authors

  • Chakkarapani, AA; Aly, H; Benders, M; Cotten, CM; El-Dib, M; Gressens, P; Hagberg, H; Sabir, H; Wintermark, P; Robertson, NJ; Newborn Brain Society Guidelines and Publications Committee,

Published Date

  • June 12, 2021

Published In

Start / End Page

  • 101256 -

PubMed ID

  • 34154945

Electronic International Standard Serial Number (EISSN)

  • 1878-0946

Digital Object Identifier (DOI)

  • 10.1016/j.siny.2021.101256

Language

  • eng

Conference Location

  • Netherlands