Evidence map›Paper›PMID 25281639›Full record

ReviewAmerican journal of physiology. Lung cellular and molecular physiology2014

Animal models of bronchopulmonary dysplasia. The preterm baboon models.

Bradley A Yoder, Jacqueline J Coalson

Open access · greenAbstract readReview
In one paragraph

Review in American journal of physiology. Lung cellular and molecular physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 3 pooled it
8.2field-weighted citation impact, top 2% 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

36 citing papers in PubMed, 3 syntheses or guidelines pooled it, 76 citations in OpenAlex.

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  16. Present and Future of Bronchopulmonary Dysplasia.Journal of clinical medicine · 2020
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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

2 authors at 2 institutions in 1 country.

Bradley A YoderDepartment of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah; and bradley.yoder@hsc.utah.edu.
Jacqueline J CoalsonDepartment of Pathology, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
The University of Texas Health Science Center at San Antonio · USUniversity of Utah · US

Funding

COLLABORATIVE PROGRAM IN BPDU01HL052636 · NHLBI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI COALSON, JACQUELINE JONES · 1999 to 2007
$18.1M
COLLABORATIVE PROGRAM IN BPDR10HL052636 · NHLBI · SOUTHWEST FOUNDATION FOR BIOMEDICAL RES · PI COALSON, JACQUELINE JONES · 1994 to 1994
–
GROWTH MODULATORS AND LONG TERM LUNG MATURATION IN BPDR10HL052646 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI COALSON, JACQUELINE JONES · 1994 to 1994
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COLLABORATIVE PROGRAM IN BPDU10HL052636 · NHLBI · SOUTHWEST FOUNDATION FOR BIOMEDICAL RES · PI COALSON, JACQUELINE JONES · 1994 to 1998
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GROWTH MODULATORS AND LONG TERM LUNG MATURATION IN BPDU10HL052646 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI COALSON, JACQUELINE JONES · 1994 to 1998
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NHLBI NIH HHS HL52636NHLBI NIH HHS HL52646
6 · The paper itself

Abstract

Much of the progress in improved neonatal care, particularly management of underdeveloped preterm lungs, has been aided by investigations of multiple animal models, including the neonatal baboon (Papio species). In this article we highlight how the preterm baboon model at both 140 and 125 days gestation (term equivalent 185 days) has advanced our understanding and management of the immature human infant with neonatal lung disease. Not only is the 125-day baboon model extremely relevant to the condition of bronchopulmonary dysplasia but there are also critical neurodevelopmental and other end-organ pathological features associated with this model not fully discussed in this limited forum. We also describe efforts to incorporate perinatal infection into these preterm models, both fetal and neonatal, and particularly associated with Ureaplasma/Mycoplasma organisms. Efforts to rekindle the preterm primate model for future evaluations of therapies such as stem cell replacement, early lung recruitment interventions coupled with noninvasive surfactant and high-frequency nasal ventilation, and surfactant therapy coupled with antioxidant or anti-inflammatory medications, to name a few, should be undertaken.

Indexed as

Bronchopulmonary DysplasiaDisease Models, AnimalRespiration, ArtificialAnimalsAnti-Inflammatory AgentsAntioxidantsHumansInflammationPapioPulmonary SurfactantsUreaplasmaUreaplasma InfectionsAnti-Inflammatory AgentsAntioxidantsPulmonary Surfactantsbaboonbronchopulmonary dysplasialungpreterm infantureaplasma

Identifiers

PMID25281639
PMCPMC4269686
OpenAlexW2079490745

What OpenQuestion holds

Textmetadata
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.