Document Detail

New Pharmacological Approaches in Infants with Hypoxic-Ischemic Encephalopathy.
MedLine Citation:
PMID:  22385055     Owner:  NLM     Status:  Publisher    
New knowledge of the pathophysiology and evolution of hypoxic-ischemic brain injuries has made feasible interventions to improve clinical outcomes for newborns surviving birth asphyxia. Brain injury following hypoxic-ischemic insult is a complex process evolving over hours to days, which provides a unique window of opportunity for neuroprotective treatment interventions. The specific pathologic processes preceding the onset of irreversible cerebral injury appear to be a combination of several mechanisms that are variable according to the severity and duration of the insult and to biochemical modifications in the brain. Advances in neuroimaging, brain monitoring techniques, and tissue biomarkers have improved the ability to diagnose, monitor, and care for newborn infants with neonatal encephalopathy, as well as to predict their outcome. The role of oxidative stress in newborn morbidity with respect to the higher risk of free radical damage in these babies is growing. However, challenges remain in early identification of infants at risk for neonatal encephalopathy, determination of timing and extent of hypoxic-ischemic brain injury, as well as optimal management and treatment duration. Potential neuroprotective strategies targeting different pathways leading to neuronal cell death in response to hypoxic-ischemic insult have been investigated: hypothermia, erythropoietin, iminobiotin, deferioxamine, magnesium, allopurinol, xenon, melatonin and statins. Hypothermia is currently the only recognized beneficial therapy. However, many infants still develop significant adverse outcomes. It is becoming evident that the association of moderate hypothermia with neuroprotective drugs may enhance the outcome. By virtue of their pleiotropic effects without toxic effects, melatonin and statins may act at different levels of the multiple mechanisms responsible for the progression of the neurodegenerative process and represent promising neuroprotectants, alone or as additional adjunctive therapy, for reducing brain injury and its long-term sequelae in infants. More clinical studies are needed to clarify the role of these potential neuroprotective drugs.
G Buonocore; G Turrisi; B W Kramer; W Balduini; S Perrone
Related Documents :
20378105 - A cohort study of developmental polychlorinated biphenyl (pcb) exposure in relation to ...
1932105 - Plasma lecithin-cholesterol acyltransferase activity and cholesterol and phospholipid l...
2271715 - Hypersomatotropism in the dysmature infant at term and preterm birth.
17094045 - The relationship among intrauterine growth, insulinlike growth factor i (igf-i), igf-bi...
15795535 - The effect of pre-eclampsia on the levels of coagulation and fibrinolysis factors in um...
22038875 - Responses of chimpanzees to a recently dead community member at gombe national park, ta...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-2-27
Journal Detail:
Title:  Current pharmaceutical design     Volume:  -     ISSN:  1873-4286     ISO Abbreviation:  -     Publication Date:  2012 Feb 
Date Detail:
Created Date:  2012-3-5     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9602487     Medline TA:  Curr Pharm Des     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Director of UOC Pediatria Neonatale, Policlinico S. Maria alle Scotte, AOUS, viale Bracci, 36, 53100 Siena, Italy. giuseppe.buonocore@unisi.It.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  The Use of Sildenafil in the Treatment of Persistent Pulmonary Hypertension of the Newborn: A Review...
Next Document:  Transient Tachypnea of the Newborn: The Treatment Strategies.