Evidence map›Paper›PMID 26997257›Full record

ArticleScientific reports2016

Treatment temperature and insult severity influence the neuroprotective effects of therapeutic hypothermia.

Thomas Wood, Damjan Osredkar, Maja Puchades, Elke Maes, Mari Falck, Torun Flatebø, Lars Walløe, Hemmen Sabir, Marianne Thoresen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 3 pooled it
24.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

63 citing papers in PubMed, 3 syntheses or guidelines pooled it, 109 citations in OpenAlex.

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  15. [Gastrodin improves microglia-mediated inflammatory response after hypoxic-ischemic brain damage in neonatal ratsNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2024
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3 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 4 countries.

Thomas WoodDepartment of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Damjan OsredkarDepartment of Paediatric Neurology, University Children's Hospital, Ljubljana, Slovenia.
Maja PuchadesDepartment of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Elke MaesDepartment of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Mari FalckDepartment of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Torun FlatebøDepartment of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Lars WalløeDepartment of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Hemmen SabirDepartment of General Pediatrics, Neonatology and Pediatric Cardiology, University Children's Hospital, Heinrich-Heine University, Düsseldorf, Germany.
Marianne ThoresenDepartment of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
University of Oslo · NODüsseldorf University Hospital · DELjubljana University Medical Centre · SIUniversity of Bristol · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapeutic hypothermia (HT) is standard care for moderate and severe neonatal hypoxic-ischaemic encephalopathy (HIE), the leading cause of permanent brain injury in term newborns. However, the optimal temperature for HT is still unknown, and few preclinical studies have compared multiple HT treatment temperatures. Additionally, HT may not benefit infants with severe encephalopathy. In a neonatal rat model of unilateral hypoxia-ischaemia (HI), the effect of five different HT temperatures was investigated after either moderate or severe injury. At postnatal-day seven, rat pups underwent moderate or severe HI followed by 5 h at normothermia (37 °C), or one of five HT temperatures: 33.5 °C, 32 °C, 30 °C, 26 °C, and 18 °C. One week after treatment, neuropathological analysis of hemispheric and hippocampal area loss, and CA1 hippocampal pyramidal neuron count, was performed. After moderate injury, a significant reduction in hemispheric and hippocampal loss on the injured side, and preservation of CA1 pyramidal neurons, was seen in the 33.5 °C, 32 °C, and 30 °C groups. Cooling below 33.5 °C did not provide additional neuroprotection. Regardless of treatment temperature, HT was not neuroprotective in the severe HI model. Based on these findings, and previous experience translating preclinical studies into clinical application, we propose that milder cooling should be considered for future clinical trials.

Indexed as

AnimalsAnimals, NewbornBrainCell CountDisease Models, AnimalFemaleHippocampusHyperthermia, InducedHypoxia-Ischemia, BrainMalePyramidal CellsRatsRats, WistarTemperatureTranslational Research, Biomedical

Identifiers

PMID26997257
PMCPMC4800445
OpenAlexW2322169884

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.