Evidence map›Paper›PMID 37215599›Full record

ReviewFrontiers in pediatrics2023

Development of a neonatal Göttingen Minipig model for dose precision in perinatal asphyxia: technical opportunities, challenges, and potential further steps.

Marina-Stefania Stroe, Lieselotte Van Bockstal, Allan Valenzuela, Miriam Ayuso, Karen Leys, Pieter Annaert, Sebastien Carpentier, Anne Smits, Karel Allegaert, Adrian Zeltner and 3 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
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

13 authors at 4 institutions in 2 countries.

Marina-Stefania StroeComparative Perinatal Development, University of Antwerp, Antwerp, Belgium.
Lieselotte Van BockstalComparative Perinatal Development, University of Antwerp, Antwerp, Belgium.
Allan ValenzuelaComparative Perinatal Development, University of Antwerp, Antwerp, Belgium.
Miriam AyusoComparative Perinatal Development, University of Antwerp, Antwerp, Belgium.
Karen LeysDrug Delivery and Disposition, KU Leuven, Leuven, Belgium.
Pieter AnnaertDrug Delivery and Disposition, KU Leuven, Leuven, Belgium.
Sebastien CarpentierFacility for Systems Biology Mass Spectrometry, KU Leuven, Leuven, Belgium.
Anne SmitsNeonatal Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.
Karel AllegaertDepartment of Development and Regeneration, KU Leuven, Leuven, Belgium.
Adrian ZeltnerGöttingen Minipigs A/S, Dalmose, Denmark.
Antonius MulderNeonatal Intensive Care Unit, Antwerp University Hospital, Antwerp, Belgium.
Chris Van GinnekenComparative Perinatal Development, University of Antwerp, Antwerp, Belgium.
Steven Van CruchtenComparative Perinatal Development, University of Antwerp, Antwerp, Belgium.
University of Antwerp · BEKU Leuven · BEAntwerp University Hospital · BEErasmus MC · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Animal models provide useful information on mechanisms in human disease conditions, but also on exploring (patho)physiological factors affecting pharmacokinetics, safety, and efficacy of drugs in development. Also, in pediatric patients, nonclinical data can be critical for better understanding the disease conditions and developing new drug therapies in this age category. For perinatal asphyxia (PA), a condition defined by oxygen deprivation in the perinatal period and possibly resulting in hypoxic ischemic encephalopathy (HIE) or even death, therapeutic hypothermia (TH) together with symptomatic drug therapy, is the standard approach to reduce death and permanent brain damage in these patients. The impact of the systemic hypoxia during PA and/or TH on drug disposition is largely unknown and an animal model can provide useful information on these covariates that cannot be assessed separately in patients. The conventional pig is proven to be a good translational model for PA, but pharmaceutical companies do not use it to develop new drug therapies. As the Göttingen Minipig is the commonly used pig strain in nonclinical drug development, the aim of this project was to develop this animal model for dose precision in PA. This experiment consisted of the instrumentation of 24 healthy male Göttingen Minipigs, within 24 h of partus, weighing approximately 600 g, to allow the mechanical ventilation and the multiple vascular catheters inserted for maintenance infusion, drug administration and blood sampling. After premedication and induction of anesthesia, an experimental protocol of hypoxia was performed, by decreasing the inspiratory oxygen fraction (FiO

Indexed as

anesthesiaanimal modelpediatric drug developmentperinatal asphyxiaprecision dosingtherapeutic hypothermia

Identifiers

PMID37215599
PMCPMC10195037
OpenAlexW4377565307

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.