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Whole-body hypothermia in mild neonatal encephalopathy: protocol for a multicentre phase III randomised controlled trial.
Garegrat, Reema; Montaldo, Paolo; Burgod, Constance; Pant, Stuti; Mazlan, Munirah; Palanisami, Balamurugan; Chakkarapani, Ela; Woolfall, Kerry; Johnson, Samantha; Grant, Patricia Ellen; Land, Sarah; Mahmoud, Mariam; Brady, Tony; Cornelius, Victoria; Adams, Eleri; Dorling, Jon; Aladangadi, Narendra; Fleming, Paul; Pressler, Ronit; Shennan, Andrew; Petrou, Stavros; Soe, Aung; Basset, Paul; Shankaran, Seetha; Thayyil, Sudhin.
Afiliação
  • Garegrat R; Centre for Perinatal Neuroscience, Department of Brain Sciences, Imperial College London, Du Cane Road, London, W12 0HS, England. r.garegrat@imperial.ac.uk.
  • Montaldo P; Centre for Perinatal Neuroscience, Department of Brain Sciences, Imperial College London, Du Cane Road, London, W12 0HS, England.
  • Burgod C; Department of Woman, Child, and General and Specialized Surgery, University of Campania "Luigi Vanvitelli", Naples, Italy.
  • Pant S; Centre for Perinatal Neuroscience, Department of Brain Sciences, Imperial College London, Du Cane Road, London, W12 0HS, England.
  • Mazlan M; Centre for Perinatal Neuroscience, Department of Brain Sciences, Imperial College London, Du Cane Road, London, W12 0HS, England.
  • Palanisami B; Centre for Perinatal Neuroscience, Department of Brain Sciences, Imperial College London, Du Cane Road, London, W12 0HS, England.
  • Chakkarapani E; Neonatal Medicine, Liverpool Women's NHS Foundation Trust, Liverpool, UK.
  • Woolfall K; University of Bristol and St Michaels Hospital NHS Trust, Bristol, UK.
  • Johnson S; Public Health, Policy and Systems, University of Liverpool, Liverpool, UK.
  • Grant PE; Department of Population Health Sciences, University of Leicester, Leicester, UK.
  • Land S; Departments of Radiology and Pediatrics, Boston Children,s Hospital, Harvard Medical School, Boston, USA.
  • Mahmoud M; PEEPS HIE Charity, London, UK.
  • Brady T; Parent representative, London, UK.
  • Cornelius V; Sealed Envelope, London, USA.
  • Adams E; Imperial Clinical Trials Unit, Imperial College London, London, UK.
  • Dorling J; Neonatal Medicine, John Radcliffe Hospital NHS Trust, London, UK.
  • Aladangadi N; Neonatal Medicine, University Hospital Southampton NHS Trust, London, UK.
  • Fleming P; Neonatal Medicine, Homerton Healthcare NHS Foundation Trust, London, UK.
  • Pressler R; Neonatal Medicine, Homerton Healthcare NHS Foundation Trust, London, UK.
  • Shennan A; Department of Neurophysiology, Great Ormond Street Hospital, London, UK.
  • Petrou S; Department of Obstetrics, Kings College London, London, UK.
  • Soe A; Professor of Health Economics, University of Oxford, Oxford, UK.
  • Basset P; Oliver Fisher Neonatal Intensive Care Unit, Medway Maritime Hospital, Medway NHS Foundation Trust, Kent, UK.
  • Shankaran S; Stats Consultancy, London, UK.
  • Thayyil S; Department of Neonatal-Perinatal Medicine, Wayne State University, Detroit, MI, USA.
BMC Pediatr ; 24(1): 460, 2024 Jul 18.
Article em En | MEDLINE | ID: mdl-39026197
ABSTRACT

BACKGROUND:

Mild hypoxic ischemic encephalopathy is associated with sub optimal cognition and learning difficulties at school age. Although whole-body hypothermia reduces death and disability after moderate or severe encephalopathy in high-income countries, the safety and efficacy of hypothermia in mild encephalopathy is not known. The cooling in mild encephalopathy (COMET) trial will examine if whole-body hypothermia improves cognitive development of neonates with mild encephalopathy.

METHODS:

The COMET trial is a phase III multicentre open label two-arm randomised controlled trial with masked outcome assessments. A total of 426 neonates with mild encephalopathy will be recruited from 50 to 60 NHS hospitals over 2 ½ years following parental consent. The neonates will be randomised to 72 h of whole-body hypothermia (33.5 ± 0.5 C) or normothermia (37.0 ± 0.5 C) within six hours or age. Prior to the recruitment front line clinical staff will be trained and certified on expanded modified Sarnat staging for encephalopathy. The neurological assessment of all screened and recruited cases will be video recorded and centrally assessed for quality assurance. If recruitment occurs at a non-cooling centre, neonates in both arms will be transferred to a cooling centre for continued care, after randomisation. All neonates will have continuous amplitude integrated electroencephalography (aEEG) at least for the first 48 h to monitor for seizures. Predefined safety outcomes will be documented, and data collected to assess resource utilization of health care. A central team masked to trial group allocation will assess neurodevelopmental outcomes at 2 years of age. The primary outcome is mean difference in composite cognitive scores on Bayley scales of Infant and Toddler development 4th Edition.

DISCUSSION:

The COMET trial will establish the safety and efficacy of whole-body hypothermia for mild hypoxic ischaemic encephalopathy and inform national and international guidelines in high income countries. It will also provide an economic assessment of whole-body hypothermia therapy for mild encephalopathy in the NHS on cost-effectiveness grounds. TRIAL REGISTRATION NUMBER NCT05889507 June 5, 2023.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hipóxia-Isquemia Encefálica / Hipotermia Induzida Limite: Humans / Newborn Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hipóxia-Isquemia Encefálica / Hipotermia Induzida Limite: Humans / Newborn Idioma: En Ano de publicação: 2024 Tipo de documento: Article