Evidence map›Paper›PMID 26320156›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2015

Effects of inhaled CO administration on acute lung injury in baboons with pneumococcal pneumonia.

Laura E Fredenburgh, Bryan D Kraft, Dean R Hess, R Scott Harris, Monroe A Wolf, Hagir B Suliman, Victor L Roggli, John D Davies, Tilo Winkler, Alex Stenzler and 5 more

2 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.4field-weighted citation impact, top 19% 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.

NCT03799874 phase2completednot on this mapstarted 2019, after this paper: background citation

A Phase II Trial of Inhaled Carbon Monoxide for the Treatment of Acute Respiratory Distress Syndrome (ARDS)

TypeinterventionalSponsorBrigham and Women's HospitalRan2019 to 2021Enrolled4ConditionsAcute Respiratory Distress SyndromeArmsInhaled Carbon Monoxide at 200 ppm, Inhaled Medical air
NCT04870125 phase1terminatednot on this mapstarted 2023, after this paper: background citation

A Phase Ib Trial of Inhaled Carbon Monoxide for the Treatment of Pneumonia and Sepsis-Induced Acute Respiratory Distress Syndrome (ARDS)

TypeinterventionalSponsorBrigham and Women's HospitalRan2023 to 2024Enrolled5ConditionsAcute Respiratory Distress Syndrome, SepsisArmsInhaled Carbon Monoxide at CFK equation-determined personalized dose (200-500 ppm to achieve a COHb level of 6-8%), Inhaled Medical air
3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 36 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Humidified Warmed COFrontiers in medicine · 2020
    Article
  13. Animal Models ofInternational journal of molecular sciences · 2019
    Review
  14. Article
  15. Review
  16. Inhalation therapies in acute respiratory distress syndrome.Annals of translational medicine · 2017
    Review
  17. Article
  18. Review
  19. Review
  20. Carbon monoxide in the treatment of sepsis.American journal of physiology. Lung cellular and molecular physiology · 2015
    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

15 authors at 5 institutions in 1 country.

Laura E FredenburghDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts; lfredenburgh@rics.bwh.harvard.edu.
Bryan D KraftDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Duke University Medical Center, Durham, North Carolina;
Dean R HessDepartment of Respiratory Care, Massachusetts General Hospital, Boston, Massachusetts; Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts;
R Scott HarrisDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts;
Monroe A WolfDepartment of Anesthesiology, Duke University Medical Center, Durham, North Carolina;
Hagir B SulimanDepartment of Anesthesiology, Duke University Medical Center, Durham, North Carolina;
Victor L RoggliDepartment of Pathology, Duke University Medical Center, Durham, North Carolina;
John D DaviesDepartment of Respiratory Care, Duke University Medical Center, Durham, North Carolina;
Tilo WinklerDepartment of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts;
Alex Stenzler12th Man Technologies, Garden Grove, California; and.
Rebecca M BaronDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts;
B Taylor ThompsonDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts;
Augustine M ChoiDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Weill Cornell Medical College, New York, New York.
Karen E Welty-WolfDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Duke University Medical Center, Durham, North Carolina;
Claude A PiantadosiDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Duke University Medical Center, Durham, North Carolina; Department of Anesthesiology, Duke University Medical Center, Durham, North Carolina; Department of Pathology, Duke University Medical Center, Durham, North Carolina;
Duke Medical Center · USMassachusetts General Hospital · USBrigham and Women's Hospital · USDuke University Hospital · USCornell University · US

Funding

Mesenchymal Stromal Cell Conditioning by Carbon MonoxideP01HL108801 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI CHOI, AUGUSTINE M · 2011 to 2015
$13.8M
The Role of HEME Oxygenase in Hyperoxic Lung InjuryR01HL055330 · NHLBI · YALE UNIVERSITY · PI CHOI, AUGUSTINE M, CHOI, MARY E · 1998 to 2021
$6.6M
HEME OXYGENASE 1--LUNG VASCULAR CELL HYPOXIC RESPONSER01HL060234 · NHLBI · YALE UNIVERSITY · PI CHOI, AUGUSTINE M, CHOI, MARY E · 1999 to 2017
$5.8M
NHLBI NIH HHS P01 HL108801NHLBI NIH HHS R01 HL055330NHLBI NIH HHS R01 HL060234
6 · The paper itself

Abstract

Inhaled carbon monoxide (CO) gas has therapeutic potential for patients with acute respiratory distress syndrome if a safe, evidence-based dosing strategy and a ventilator-compatible CO delivery system can be developed. In this study, we used a clinically relevant baboon model of Streptococcus pneumoniae pneumonia to 1) test a novel, ventilator-compatible CO delivery system; 2) establish a safe and effective CO dosing regimen; and 3) investigate the local and systemic effects of CO therapy on inflammation and acute lung injury (ALI). Animals were inoculated with S. pneumoniae (10(8)-10(9) CFU) (n = 14) or saline vehicle (n = 5); in a subset with pneumonia (n = 5), we administered low-dose, inhaled CO gas (100-300 ppm × 60-90 min) at 0, 6, 24, and/or 48 h postinoculation and serially measured blood carboxyhemoglobin (COHb) levels. We found that CO inhalation at 200 ppm for 60 min is well tolerated and achieves a COHb of 6-8% with ambient CO levels ≤ 1 ppm. The COHb level measured at 20 min predicted the 60-min COHb level by the Coburn-Forster-Kane equation with high accuracy. Animals given inhaled CO + antibiotics displayed significantly less ALI at 8 days postinoculation compared with antibiotics alone. Inhaled CO was associated with activation of mitochondrial biogenesis in the lung and with augmentation of renal antioxidative programs. These data support the feasibility of safely delivering inhaled CO gas during mechanical ventilation and provide preliminary evidence that CO may accelerate the resolution of ALI in a clinically relevant nonhuman primate pneumonia model.

Indexed as

Acute Lung InjuryAdministration, InhalationAnimalsAnti-Bacterial AgentsAntioxidantsCarbon MonoxideCarboxyhemoglobinDisease Models, AnimalEquipment DesignHumansKidneyLungMalePapioPneumonia, PneumococcalRespiration, ArtificialAnti-Bacterial AgentsAntioxidantsCarbon MonoxideCarboxyhemoglobincarbon monoxideCoburn-Forster-Kane equationdrug delivery systemspneumoniaStreptococcus pneumoniae

Identifiers

PMID26320156
PMCPMC4609940
OpenAlexW2280270379

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.