Nutritional management in newborn babies receiving therapeutic hypothermia: two retrospective observational studies using propensity score matching
Nutritional management in newborn babies receiving therapeutic hypothermia: two retrospective observational studies using propensity score matching
Background: therapeutic hypothermia is standard of care for babies with moderate to severe hypoxic- ischaemic encephalopathy. There is limited evidence to inform provision of nutrition during hypothermia.
Objectives: to assess the association during therapeutic hypothermia between (1) enteral feeding and outcomes, such as necrotising enterocolitis and (2) parenteral nutrition and outcomes, such as late-onset bloodstream infection.
Design: a retrospective cohort study using data held in the National Neonatal Research Database and applying propensity score methodology to form matched groups for analysis.
Setting: NHS neonatal units in England,Wales and Scotland.
Participants: babies born at ≥ 36 gestational weeks between 1 January 2010 and 31 December 2017 who received therapeutic hypothermia for 72 hours or who died during treatment.
Interventions: enteral feeding analysis - babies who were enterally fed during therapeutic hypothermia (intervention) compared with babies who received no enteral feeds during therapeutic hypothermia (control). Parenteral nutrition analysis - babies who received parenteral nutrition during therapeutic hypothermia (intervention) compared with babies who received no parenteral nutrition during therapeutic hypothermia (control).
Outcome measures: primary outcomes were severe and pragmatically defined necrotising enterocolitis (enteral feeding analysis) and late-onset bloodstream infection (parenteral nutrition analysis). Secondary outcomes were survival at neonatal discharge, length of neonatal stay, breastfeeding at discharge, onset of breastfeeding, time to first maternal breast milk, hypoglycaemia, number of days with a central line in situ, duration of parenteral nutrition, time to full enteral feeds and growth.
Results: a total of 6030 babies received therapeutic hypothermia. Thirty-one per cent of babies received enteral feeds and 25% received parenteral nutrition. Seven babies (0.1%) were diagnosed with severe necrotising enterocolitis, and further comparative analyses were not conducted on this outcome. A total of 3236 babies were included in the matched enteral feeding analysis. Pragmatically defined necrotising enterocolitis was rare in both groups (0.5% vs. 1.1%) and was lower in babies who were fed during hypothermia (rate difference -0.5%, 95% confidence interval -1.0% to -0.1%; p = 0.03). Higher survival to discharge (96.0% vs. 90.8%, rate difference 5.2%, 95% confidence interval 3.9% to 6.6%; p < 0.001) and higher breastfeeding at discharge (54.6% vs. 46.7%, rate difference 8.0%, 95% confidence interval 5.1% to 10.8%; p < 0.001) rates were observed in enterally fed babies who also had a shorter neonatal stay (mean difference -2.2 days, 95% confidence interval -3.0 to -1.2 days). A total of 2480 babies were included in the matched parenteral nutrition analysis. Higher levels of late-onset bloodstream infection were seen in babies who received parenteral nutrition (0.3% vs. 0.9%, rate difference 0.6%, 95% confidence interval 0.1% to 1.2%; p = 0.03). Survival was lower in babies who did not receive parenteral nutrition (90.0% vs. 93.1%, rate difference 3.1%, 95% confidence interval 1.5% to 4.7%; p < 0.001).
Limitations: propensity score methodology can address imbalances in observed confounders only. Residual confounding by unmeasured or poorly recorded variables cannot be ruled out. We did not analyse by type or volume of enteral or parenteral nutrition.
Conclusions: necrotising enterocolitis is rare in babies receiving therapeutic hypothermia, and the introduction of enteral feeding is associated with a lower risk of pragmatically defined necrotising enterocolitis and other beneficial outcomes, including rates of higher survival and breastfeeding at discharge. Receipt of parenteral nutrition during therapeutic hypothermia is associated with a higher rate of late-onset infection but lower mortality. These results support introduction of enteral feeding during therapeutic hypothermia.
Future work: randomised trials to assess parenteral nutrition during therapeutic hypothermia.
Trial registration: Current Controlled Trials ISRCTN474042962.
Gale, Chris
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Jeyakumaran, Dusha
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Battersby, Cheryl
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Ougham, Kayleigh
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Ojha, Shalini
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Culshaw, Lucy
473ba88d-5898-475a-941b-9a412518f773
Selby, Ella
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Dorling, Jon
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Longford, Nicholas
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June 2021
Gale, Chris
210b7c81-9a39-460a-9ab3-54fe92a69f8e
Jeyakumaran, Dusha
4af51f70-a8d5-42db-a5c9-5dfbf703a274
Battersby, Cheryl
24ba455f-7f54-427c-8732-3007926ee5ce
Ougham, Kayleigh
123d563f-55f0-4069-89c4-4418aa8044af
Ojha, Shalini
adc62cc2-df92-446f-8ad2-4c0cf006d689
Culshaw, Lucy
473ba88d-5898-475a-941b-9a412518f773
Selby, Ella
4b3cbd8b-c0aa-4941-b5df-383349c18d41
Dorling, Jon
e55dcb9a-a798-41a1-8753-9e9ff8aab630
Longford, Nicholas
2f3303da-6aa2-49e7-bb14-df151389aee2
Gale, Chris, Jeyakumaran, Dusha, Battersby, Cheryl, Ougham, Kayleigh, Ojha, Shalini, Culshaw, Lucy, Selby, Ella, Dorling, Jon and Longford, Nicholas
(2021)
Nutritional management in newborn babies receiving therapeutic hypothermia: two retrospective observational studies using propensity score matching.
Health Technology Assessment, 25 (36).
(doi:10.3310/HTA25360).
Abstract
Background: therapeutic hypothermia is standard of care for babies with moderate to severe hypoxic- ischaemic encephalopathy. There is limited evidence to inform provision of nutrition during hypothermia.
Objectives: to assess the association during therapeutic hypothermia between (1) enteral feeding and outcomes, such as necrotising enterocolitis and (2) parenteral nutrition and outcomes, such as late-onset bloodstream infection.
Design: a retrospective cohort study using data held in the National Neonatal Research Database and applying propensity score methodology to form matched groups for analysis.
Setting: NHS neonatal units in England,Wales and Scotland.
Participants: babies born at ≥ 36 gestational weeks between 1 January 2010 and 31 December 2017 who received therapeutic hypothermia for 72 hours or who died during treatment.
Interventions: enteral feeding analysis - babies who were enterally fed during therapeutic hypothermia (intervention) compared with babies who received no enteral feeds during therapeutic hypothermia (control). Parenteral nutrition analysis - babies who received parenteral nutrition during therapeutic hypothermia (intervention) compared with babies who received no parenteral nutrition during therapeutic hypothermia (control).
Outcome measures: primary outcomes were severe and pragmatically defined necrotising enterocolitis (enteral feeding analysis) and late-onset bloodstream infection (parenteral nutrition analysis). Secondary outcomes were survival at neonatal discharge, length of neonatal stay, breastfeeding at discharge, onset of breastfeeding, time to first maternal breast milk, hypoglycaemia, number of days with a central line in situ, duration of parenteral nutrition, time to full enteral feeds and growth.
Results: a total of 6030 babies received therapeutic hypothermia. Thirty-one per cent of babies received enteral feeds and 25% received parenteral nutrition. Seven babies (0.1%) were diagnosed with severe necrotising enterocolitis, and further comparative analyses were not conducted on this outcome. A total of 3236 babies were included in the matched enteral feeding analysis. Pragmatically defined necrotising enterocolitis was rare in both groups (0.5% vs. 1.1%) and was lower in babies who were fed during hypothermia (rate difference -0.5%, 95% confidence interval -1.0% to -0.1%; p = 0.03). Higher survival to discharge (96.0% vs. 90.8%, rate difference 5.2%, 95% confidence interval 3.9% to 6.6%; p < 0.001) and higher breastfeeding at discharge (54.6% vs. 46.7%, rate difference 8.0%, 95% confidence interval 5.1% to 10.8%; p < 0.001) rates were observed in enterally fed babies who also had a shorter neonatal stay (mean difference -2.2 days, 95% confidence interval -3.0 to -1.2 days). A total of 2480 babies were included in the matched parenteral nutrition analysis. Higher levels of late-onset bloodstream infection were seen in babies who received parenteral nutrition (0.3% vs. 0.9%, rate difference 0.6%, 95% confidence interval 0.1% to 1.2%; p = 0.03). Survival was lower in babies who did not receive parenteral nutrition (90.0% vs. 93.1%, rate difference 3.1%, 95% confidence interval 1.5% to 4.7%; p < 0.001).
Limitations: propensity score methodology can address imbalances in observed confounders only. Residual confounding by unmeasured or poorly recorded variables cannot be ruled out. We did not analyse by type or volume of enteral or parenteral nutrition.
Conclusions: necrotising enterocolitis is rare in babies receiving therapeutic hypothermia, and the introduction of enteral feeding is associated with a lower risk of pragmatically defined necrotising enterocolitis and other beneficial outcomes, including rates of higher survival and breastfeeding at discharge. Receipt of parenteral nutrition during therapeutic hypothermia is associated with a higher rate of late-onset infection but lower mortality. These results support introduction of enteral feeding during therapeutic hypothermia.
Future work: randomised trials to assess parenteral nutrition during therapeutic hypothermia.
Trial registration: Current Controlled Trials ISRCTN474042962.
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Published date: June 2021
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This report presents independent research funded by the National Institute for Health Research (NIHR). The views and opinions expressed by authors in this publication are those of the authors and do not necessarily reflect those of the NHS, the NIHR, NETSCC, the HTA programme or the Department of Health and Social Care. If there are verbatim quotations included in this publication the views and opinions expressed by the interviewees are those of the interviewees and do not necessarily reflect those of the authors, those of the NHS, the NIHR, NETSCC, the HTA programme or the Department of Health and Social Care.
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This project was funded by the National Institute for Health Research (NIHR) Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 25, No. 36. See the NIHR Journals Library website for further project information.
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Declared competing interests of authors: Chris Gale reports grants from the Medical Research Council (MRC) (London, UK) and the National Institute for Health Research (NIHR) during the conduct of the study, and grants from NIHR, Mason Medical Research Foundation (London, UK), Rosetrees Trust (Edgeware, UK) and from the Canadian Institute for Health Research (Ottawa, ON, Canada), outside the submitted work. He reports a grants from Chiesi Pharmaceuticals (Parma, Italy) outside the submitted work for a research study and a personal fee from Chiesi Pharmaceuticals to support attendance at an educational meeting. Chris Gale is vice chairperson of the NIHR Research for Patient Benefit London Regional Assessment Panel (2016–present). Chris Gale was an unremunerated member of the Neonatal Data Analysis Unit Steering Board that oversees the National Neonatal Research Database (2014–20). Cheryl Battersby reports personal fees from AbbVie Pharmaceuticals (Maidenhead, UK) and Chiesi Pharmaceuticals, outside the submitted work. Cheryl Battersby sits on the NIHR Health Technology Assessment (HTA) Prioritisation Panel for Maternal, Child and Mental Health Care (2019–present) Cheryl Battersby is an unremunerated member of the National Neonatal Research Database Steering Board (April 2020 to present). Shalini Ojha reports grants from the MRC and the Arts and Humanities Research Council (Swindon, UK), outside the work. Jon Dorling reports grants from Nutrinia Ltd (Ramat Gan, Israel), outside the submitted work. The grant from Nutrinia Ltd in 2018 was for part of his salary to work as an expert advisor on a trial. He was a member of the NIHR HTA General Board (2017–18) and the NIHR HTA, Newborn and Child Health Panel (2013–18). Nicholas Longford’s post is in part funded by the Healthcare Quality Improvement Programme (London, UK) as part of the National Neonatal Audit Programme (London, UK). Nicholas Longford reports grants from Chiesi Pharmaceuticals, outside the submitted work.
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The research reported in this issue of the journal was funded by the HTA programme as project number 16/79/03. The contractual start date was in September 2017. The draft report began editorial review in December 2019 and was accepted for publication in June 2020. The authors have been wholly responsible for all data collection, analysis and interpretation, and for writing up their work. The HTA editors and publisher have tried to ensure the accuracy of the authors’ report and would like to thank the reviewers for their constructive comments on the draft document. However, they do not accept liability for damages or losses arising from material published in this report.
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Local EPrints ID: 485023
URI: http://eprints.soton.ac.uk/id/eprint/485023
ISSN: 1366-5278
PURE UUID: 5abe35d5-bcc1-46b5-96ea-e43b22dad700
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Date deposited: 28 Nov 2023 17:38
Last modified: 18 Mar 2024 04:16
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Author:
Chris Gale
Author:
Dusha Jeyakumaran
Author:
Cheryl Battersby
Author:
Kayleigh Ougham
Author:
Shalini Ojha
Author:
Lucy Culshaw
Author:
Ella Selby
Author:
Jon Dorling
Author:
Nicholas Longford
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