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Prophylactic Oral Dextrose Gel and Neurosensory Impairment at 2-Year Follow-up of Participants in the hPOD Randomized Trial.
Edwards, Taygen; Alsweiler, Jane M; Crowther, Caroline A; Edlin, Richard; Gamble, Greg D; Hegarty, Joanne E; Lin, Luling; McKinlay, Christopher J D; Rogers, Jenny A; Thompson, Benjamin; Wouldes, Trecia A; Harding, Jane E.
Afiliação
  • Edwards T; Liggins Institute, University of Auckland, Auckland, New Zealand.
  • Alsweiler JM; Department of Paediatrics: Child and Youth Health, University of Auckland, Auckland, New Zealand.
  • Crowther CA; Newborn Services, Auckland City Hospital, Auckland, New Zealand.
  • Edlin R; Liggins Institute, University of Auckland, Auckland, New Zealand.
  • Gamble GD; Health Systems, School of Population Health, University of Auckland, Auckland, New Zealand.
  • Hegarty JE; Liggins Institute, University of Auckland, Auckland, New Zealand.
  • Lin L; Newborn Services, Auckland City Hospital, Auckland, New Zealand.
  • McKinlay CJD; Liggins Institute, University of Auckland, Auckland, New Zealand.
  • Rogers JA; Liggins Institute, University of Auckland, Auckland, New Zealand.
  • Thompson B; Kidz First Neonatal Care, Counties Manukau Health, Auckland, New Zealand.
  • Wouldes TA; Liggins Institute, University of Auckland, Auckland, New Zealand.
  • Harding JE; School of Optometry and Vision Science, Waterloo, Ontario, Canada.
JAMA ; 327(12): 1149-1157, 2022 03 22.
Article em En | MEDLINE | ID: mdl-35315885
ABSTRACT
Importance Prophylactic oral dextrose gel reduces neonatal hypoglycemia, but later benefits or harms remain unclear.

Objective:

To assess the effects on later development of prophylactic dextrose gel for infants born at risk of neonatal hypoglycemia. Design, Setting, and

Participants:

Prospective follow-up of a multicenter randomized clinical trial conducted in 18 Australian and New Zealand hospitals from January 2015 to May 2019. Participants were late preterm or term at-risk infants; those randomized in 9 New Zealand centers (n = 1359) were included and followed up between January 2017 and July 2021.

Interventions:

Infants were randomized to prophylactic 40% dextrose (n = 681) or placebo (n = 678) gel, 0.5 mL/kg, massaged into the buccal mucosa 1 hour after birth. Main Outcomes and

Measures:

The primary outcome of this follow-up study was neurosensory impairment at 2 years' corrected age. There were 44 secondary outcomes, including cognitive, language, and motor composite Bayley-III scores (mean [SD], 100 [15]; higher scores indicate better performance).

Results:

Of eligible infants, 1197 (91%) were assessed (581 females [49%]). Neurosensory impairment was not significantly different between the dextrose and placebo gel groups (20.8% vs 18.7%; unadjusted risk difference [RD], 2.09% [95% CI, -2.43% to 6.60%]; adjusted risk ratio [aRR], 1.13 [95% CI, 0.90 to 1.41]). The risk of cognitive and language delay was not significantly different between the dextrose and placebo groups (cognitive 7.6% vs 5.3%; RD, 2.32% [95% CI, -0.46% to 5.11%]; aRR, 1.40 [95% CI, 0.91 to 2.17]; language 17.0% vs 14.7%; RD, 2.35% [95% CI, -1.80% to 6.50%]; aRR, 1.19 [95% CI, 0.92 to 1.54]). However, the dextrose gel group had a significantly higher risk of motor delay (2.5% vs 0.7%; RD, 1.81% [95% CI, 0.40% to 3.23%]; aRR, 3.79 [95% CI, 1.27 to 11.32]) and significantly lower composite scores for cognitive (adjusted mean difference [aMD], -1.30 [95% CI, -2.55 to -0.05]), language (aMD, -2.16 [95% CI, -3.86 to -0.46]), and motor (aMD, -1.40 [95% CI, -2.60 to -0.20]) performance. There were no significant differences between groups in the other 27 secondary outcomes. Conclusions and Relevance Among late preterm and term infants born at risk of neonatal hypoglycemia, prophylactic oral 40% dextrose gel at 1 hour of age, compared with placebo, resulted in no significant difference in the risk of neurosensory impairment at 2 years' corrected age. However, the study may have been underpowered to detect a small but potentially clinically important increase in risk, and further research including longer-term follow-up is required. Trial Registration anzctr.org.au Identifier ACTRN12614001263684.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos de Sensação / Glucose / Hipoglicemia Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Female / Humans / Male / Newborn Idioma: En Revista: JAMA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Nova Zelândia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos de Sensação / Glucose / Hipoglicemia Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Female / Humans / Male / Newborn Idioma: En Revista: JAMA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Nova Zelândia