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Neonatal magnesium sulphate for neuroprotection: A systematic review and meta-analysis.
Shepherd, Emily; Karim, Tasneem; McIntyre, Sarah; Goldsmith, Shona; Keir, Amy; Badawi, Nadia; Hunt, Rod W; Galinsky, Robert.
Afiliación
  • Shepherd E; Women and Kids Theme, South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.
  • Karim T; Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia.
  • McIntyre S; Cerebral Palsy Alliance Research Institute, Sydney Medical School, The University of Sydney, Sydney, New South Wales, Australia.
  • Goldsmith S; Cerebral Palsy Alliance Research Institute, Sydney Medical School, The University of Sydney, Sydney, New South Wales, Australia.
  • Keir A; Cerebral Palsy Alliance Research Institute, Sydney Medical School, The University of Sydney, Sydney, New South Wales, Australia.
  • Badawi N; Cerebral Palsy Alliance Research Institute, Sydney Medical School, The University of Sydney, Sydney, New South Wales, Australia.
  • Hunt RW; Women and Kids Theme, South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.
  • Galinsky R; Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia.
Dev Med Child Neurol ; 66(9): 1157-1172, 2024 Sep.
Article en En | MEDLINE | ID: mdl-38468452
ABSTRACT

AIM:

To review the evidence of the effects of neonatal magnesium sulphate for neuroprotection in perinatal asphyxia and hypoxic-ischaemic encephalopathy (HIE).

METHOD:

This was a systematic review of randomized controlled trials (RCTs) (with meta-analysis) and non-RCTs assessing magnesium sulphate for treating perinatal asphyxia and HIE at 35 weeks or more gestation (primary

outcomes:

neonatal death and death or long-term major neurodevelopmental disability).

RESULTS:

Twenty-five RCTs (2099 infants) and four non-RCTs (871 infants) were included, 23 in low- and middle-income countries (LMICs). In RCTs, reductions in neonatal death with magnesium sulphate versus placebo or no treatment (risk ratio [RR] = 0.68; 95% confidence interval [CI] = 0.53-0.86; 13 RCTs), and magnesium sulphate with melatonin versus melatonin alone (RR = 0.74; 95% CI = 0.58-0.95; one RCT) were observed. No difference in neonatal death was seen for magnesium sulphate with therapeutic hypothermia versus therapeutic hypothermia alone (RR = 0.66, 95% CI = 0.34-1.26; three RCTs), or magnesium sulphate versus phenobarbital (RR = 3.00; 95% CI = 0.86-10.46; one RCT). No reduction in death or long-term neurodevelopmental disability (RR = 0.52; 95% CI = 0.14-1.89; one RCT) but reductions in several short-term adverse outcomes were observed with magnesium sulphate. Evidence was low- to very-low certainty because of risk of bias and imprecision.

INTERPRETATION:

Given the uncertainty of the current evidence, further robust neonatal magnesium sulphate research is justified. This may include high-quality studies to determine stand-alone effects in LMICs and effects with and after therapeutic hypothermia in high-income countries.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Asfixia Neonatal / Fármacos Neuroprotectores / Hipoxia-Isquemia Encefálica / Sulfato de Magnesio Límite: Humans / Newborn Idioma: En Revista: Dev Med Child Neurol Año: 2024 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Asfixia Neonatal / Fármacos Neuroprotectores / Hipoxia-Isquemia Encefálica / Sulfato de Magnesio Límite: Humans / Newborn Idioma: En Revista: Dev Med Child Neurol Año: 2024 Tipo del documento: Article País de afiliación: Australia