Cited by 2,862Neonatal and fetal brain pathologyThermal Regulation in MedicineInfant Development and Preterm Care

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Whole-body hypothermia for neonates with hypoxic-ischemic encephalopathy

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Shankaran, Seetha, Laptook, Abbot R., Ehrenkranz, Richard A., Tyson, Jon E., McDonald, Scott A., Donovan, Edward F., Fanaroff, Avroy A., Poole, W. Kenneth, Wright, Linda L., Higgins, Rosemary D., Finer, Neil N., Carlo, Waldemar A., Duara, Shahnaz, Oh, William, Cotten, C. Michael, Stevenson, David K., Stoll, Barbara J., Lemons, James A., Guillet, Ronnie, Jobe, Alan H.·2005·New England Journal of Medicine

DOI 10.1056/nejmcps050929

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Abstract

BACKGROUND: Hypothermia is protective against brain injury after asphyxiation in animal models. However, the safety and effectiveness of hypothermia in term infants with encephalopathy is uncertain. METHODS: We conducted a randomized trial of hypothermia in infants with a gestational age of at least 36 weeks who were admitted to the hospital at or before six hours of age with either severe acidosis or perinatal complications and resuscitation at birth and who had moderate or severe encephalopathy. Infants were randomly assigned to usual care (control group) or whole-body cooling to an esophageal temperature of 33.5 degrees C for 72 hours, followed by slow rewarming (hypothermia group). Neurodevelopmental outcome was assessed at 18 to 22 months of age. The primary outcome was a combined end point of death or moderate or severe disability. RESULTS: Of 239 eligible infants, 102 were assigned to the hypothermia group and 106 to the control group. Adverse events were similar in the two groups during the 72 hours of cooling. Primary outcome data were available for 205 infants. Death or moderate or severe disability occurred in 45 of 102 infants (44 percent) in the hypothermia group and 64 of 103 infants (62 percent) in the control group (risk ratio, 0.72; 95 percent confidence interval, 0.54 to 0.95; P=0.01). Twenty-four infants (24 percent) in the hypothermia group and 38 (37 percent) in the control group died (risk ratio, 0.68; 95 percent confidence interval, 0.44 to 1.05; P=0.08). There was no increase in major disability among survivors; the rate of cerebral palsy was 15 of 77 (19 percent) in the hypothermia group as compared with 19 of 64 (30 percent) in the control group (risk ratio, 0.68; 95 percent confidence interval, 0.38 to 1.22; P=0.20). CONCLUSIONS: Whole-body hypothermia reduces the risk of death or disability in infants with moderate or severe hypoxic-ischemic encephalopathy.

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Development and reliability of a system to classify gross motor function in children with cerebral palsy
Palisano, R. J., Rosenbaum, P., Walter, S. D., Russell, D., Wood, E. P., & Galuppi, B. E. (1997) · Developmental Medicine & Child Neurology · doi:10.1111/j.1469-8749.1997.tb07414.x · Cited by 6,728
Bayley Scales of Infant Development
(2007) · Sage eBooks · doi:10.4135/9781412952644.n48 · Cited by 4,242
Selective head cooling with mild systemic hypothermia after neonatal encephalopathy: multicentre randomised trial
Gluckman, P. D., Wyatt, J. S., Azzopardi, D., Ballard, R., Edwards, A. D., Ferriero, D. M., Polin, R. A., Robertson, C. M., Thoresen, M., Whitelaw, A., et al. (2005) · The Lancet · doi:10.1016/s0140-6736(05)17946-x · Cited by 2,270
Small Differences in Intraischemic Brain Temperature Critically Determine the Extent of Ischemic Neuronal Injury
Busto, R., Dietrich, W. D., Globus, M. Y. ‐., Valdés, I., Scheinberg, P., & Ginsberg, M. D. (1987) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1987.127 · Cited by 1,786
Dramatic neuronal rescue with prolonged selective head cooling after ischemia in fetal lambs.
Gunn, A. J., Gunn, T. R., de Haan, H. H., Williams, C. E., & Gluckman, P. D. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119153 · Cited by 622
Moderate hypothermia in neonatal encephalopathy: Efficacy outcomes
Eicher, D. J., Wagner, C. L., Katikaneni, L., Hulsey, T. C., Bass, W. T., Kaufman, D. A., Horgan, M. J., Languani, S., Bhatia, J. J. S., Givelichian, L. M., et al. (2004) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2004.06.014 · Cited by 581
Prediction of neuromotor outcome in perinatal asphyxia: evaluation of MR scoring systems.
Barkovich, A. J., Hajnal, B. L., Vigneron, D. B., Sola, A. M., Partridge, J. C., Allen, F., & Ferriero, D. M. (1998) · PubMed Central · Cited by 525
Assessment of Neonatal Encephalopathy by Amplitude-integrated Electroencephalography
Al-Naqeeb, N., Edwards, A. D., Cowan, F. M., & Azzopardi, D. (1999) · PEDIATRICS · doi:10.1542/peds.103.6.1263 · Cited by 458
Amplitude integrated EEG 3 and 6 hours after birth in full term neonates with hypoxic–ischaemic encephalopathy
Toet, M. C., Hellström-Westas, L. K., Groenendaal, F., Eken, P., & de Vries, L. S. (1999) · Archives of Disease in Childhood Fetal & Neonatal · doi:10.1136/fn.81.1.f19 · Cited by 439
Delayed and prolonged post-ischemic hypothermia is neuroprotective in the gerbil
Colbourne, F., & Corbett, D. (1994) · Brain Research · doi:10.1016/0006-8993(94)90488-x · Cited by 418

Show all 36 references

Research works printed but not linked: 2

Kuluz JW, 1993, Am J Physiol, 265, H824
Barkovich AJ, 1998, AJNR Am J Neuroradiol, 19, 143

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Perinatal asphyxia.
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Therapeutic hypothermia in experimental models of focal and global cerebral ischemia and intracerebral hemorrhage
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Authors: Shankaran, S., Laptook, A. R., Ehrenkranz, R. A., Tyson, J. E., McDonald, S. A., Donovan, E. F., Fanaroff, A. A., Poole, W. K., Wright, L. L., Higgins, R. D., Finer, N. N., Carlo, W. A., Duara, S., Oh, W., Cotten, C. M., Stevenson, D. K., Stoll, B. J., Lemons, J. A., Guillet, R., & Jobe, A. H.
Affiliations: Wayne State University (US)
Women & Infants Hospital of Rhode Island (US)
Yale University (US)
RTI International (US)
University of Cincinnati (US)
Rainbow Babies & Children's Hospital (US)
National Institutes of Health (US)
University of California San Diego (US)
University of Alabama at Birmingham (US)
University of Miami (US)
Duke Medical Center (US)
Stanford University (US)
Emory University (US)
Indiana University School of Medicine (US)
University of Rochester (US)
ORCID: Shankaran, Seetha
Laptook, Abbot R.
McDonald, Scott A.
Higgins, Rosemary D.
Carlo, Waldemar A.
Duara, Shahnaz
Cotten, C. Michael
Stevenson, David K.
Stoll, Barbara J.
Guillet, Ronnie
Jobe, Alan H.
Venue: New England Journal of Medicine
Publisher: Massachusetts Medical Society
Published: 2005-10-13
Volume: 353
Issue: 15
Pages: 1574-1584
ISSN: 0028-4793 (ISSN-L)
1533-4406
DOI: 10.1056/nejmcps050929
OpenAlex: W2164127547
Cited by: 2,862
References: 36
Citations by year: 2026: 95 · 2025: 152 · 2024: 157 · 2023: 121 · 2022: 118 · 2021: 155 · 2020: 123 · 2019: 129 · 2018: 152 · 2017: 152 · 2016: 143 · 2015: 170 · 2014: 131 · 2013: 141 · 2012: 166
FWCI: 89.20
Type: journal article
Language: en
Open access: bronze
doi.org
Locations: New England Journal of Medicine (publishedVersion)
PubMed (publishedVersion)
UWA Profiles and Research Repository (UWA) (submittedVersion)
Funders: National Center for Research Resources (5-M01-RR-00044, M01RR008084, M01-RR00039, M01RR000125, M01-RR 00750, M01 RR-00125, M01 RR 0039-43, M01RR000750, M-01 RR 00070, M01RR000044, M01RR000070, M01RR000039, M01-RR-08084)
Eunice Kennedy Shriver National Institute of Child Health and Human Development (U10HD040498, (U10 HD27871, U10 HD 27853, U10HD027880, U10 HD27880, U10 HD 40461, U10HD40521, U10HD21385, U10HD 21397, U10HD40498, U10HD27851, U10 HD34216, U10HD40492, U01HD36790, U10‐HD‐27904, U10HD021397, U10HD027904, U10HD027856, U10HD040689, U10HD027871, U10-HD21373, U10HD027853, U10HD040492, U10HD034216, U10HD021373, U10HD021385, U10HD40689, U10 HD27856, U10HD040521, U01HD036790, U10HD027851, U10HD040461)
Topics: Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Neonatal and fetal brain pathology
Health Sciences › Medicine › Critical Care and Intensive Care Medicine › Thermal Regulation in Medicine
Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Infant Development and Preterm Care
Keywords: whole-body hypothermia, hypoxic-ischemic encephalopathy, neonates, neuroprotection, cerebral palsy, neurodevelopmental outcomes, perinatal asphyxia, acidosis, term infants, mortality, disability
MeSH terms: Acidosis, Asphyxia Neonatorum, Blindness, Cerebral Palsy, Developmental Disabilities, Female, Follow-Up Studies, Humans, Hypothermia, Induced, Infant, Newborn, Obstetric Labor Complications, Male, Pregnancy, Pregnancy Complications, Hypoxia-Ischemia, Brain, Hearing Loss

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Whole-body hypothermia for neonates with hypoxic-ischemic encephalopathy

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