Evidence map›Paper›PMID 28685297›Full record

ArticlePharmaceutical research2017

Hemodynamic Effects of Lipid-Based Oxygen Microbubbles via Rapid Intravenous Injection in Rodents.

Katherine J Black, Andrew T Lock, Lindsay M Thomson, Alexis R Cole, Xiaoqi Tang, Brian D Polizzotti, John N Kheir

Abstract read
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In one paragraph

Article in Pharmaceutical research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. A microfluidic device for real-time on-demand intravenous oxygen delivery.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  6. 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

7 authors at 1 institution in 1 country.

Katherine J BlackDepartment of Cardiology at Boston Children's Hospital, 300 Longwood Avenue, Boston, Massachusetts, 02115, USA.
Andrew T LockDepartment of Cardiology at Boston Children's Hospital, 300 Longwood Avenue, Boston, Massachusetts, 02115, USA.
Lindsay M ThomsonDepartment of Cardiology at Boston Children's Hospital, 300 Longwood Avenue, Boston, Massachusetts, 02115, USA.
Alexis R ColeDepartment of Cardiology at Boston Children's Hospital, 300 Longwood Avenue, Boston, Massachusetts, 02115, USA.
Xiaoqi TangDepartment of Cardiology at Boston Children's Hospital, 300 Longwood Avenue, Boston, Massachusetts, 02115, USA.
Brian D PolizzottiDepartment of Cardiology at Boston Children's Hospital, 300 Longwood Avenue, Boston, Massachusetts, 02115, USA. brian.polizzotti@childrens.harvard.edu.
John N KheirDepartment of Cardiology at Boston Children's Hospital, 300 Longwood Avenue, Boston, Massachusetts, 02115, USA. john.kheir@childrens.harvard.edu.ORCID http://orcid.org/0000-0001-6080-8739
Boston Children's Hospital · US

Funding

Boston Biomedical Innovation CenterU54HL119145 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI GOLAN, DAVID E., LOSCALZO, JOSEPH · 2013 to 2021
$18.8M
Advanced Research Projects Agency W81XWH-11-2-0041Advanced Research Projects Agency W81XWH-15-1-0544National Heart, Lung, and Blood Institute U54HL119145
6 · The paper itself

Abstract

purposeLow oxygen levels, or hypoxemia, is a common cause of morbidity and mortality in critically ill patients. Hypoxemia is typically addressed by increasing the fraction of inspired oxygen, the use of mechanical ventilation, or more invasive measures. Recently, the injection of oxygen gas directly into the bloodstream by packaging it within lipid-based oxygen microbubbles (LOMs) has been explored. The purpose of this work is to examine the acute hemodynamic effects of intravenous injections of LOMs.

methodsLOMs composed of 1,2-distearoyl-sn-glycero-3-phosphocoline and cholesterol were manufactured using a process of shear homogenization under an oxygen headspace. A 5 mL aliquot of either PlasmaLyte A, or low (37%) or high (55%) concentration LOMs (n = 10 per group) was injected over a 1 min period into Sprague Dawley rats instrumented for measurement of cardiac index and pulmonary (PVR) and systemic (SVR) vascular resistance during a 60 min observation period. Hemodynamics were compared between groups by linear mixed modeling.

resultsApproximately 10

conclusionsLOMs may be injected in quantities sufficient to deliver clinically meaningful volumes of oxygen but cause significant decrements in blood pressure and elevations in PVR.

Indexed as

HemodynamicsAnimalsBlood PressureCholesterolHumansHypoxiaInjections, IntravenousMaleMicrobubblesOxygenParticle SizePhosphatidylcholinesPulmonary ArteryRatsRats, Sprague-DawleyRespiration, Artificial1,2-distearoyllecithinCholesterolOxygenPhosphatidylcholineshemodynamicshypoxiamicrobubbleoxygenphospholipid

Identifiers

PMID28685297
OpenAlexW2724989342

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.