Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
  • Physician-Scientist Development
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Immunology
    • Metabolism
    • Nephrology
    • Oncology
    • Pulmonology
    • All ...
  • Videos
  • Collections
    • In-Press Preview
    • Resource and Technical Advances
    • Clinical Research and Public Health
    • Research Letters
    • Editorials
    • Perspectives
    • Physician-Scientist Development
    • Reviews
    • Top read articles

  • Current issue
  • Past issues
  • Specialties
  • In-Press Preview
  • Resource and Technical Advances
  • Clinical Research and Public Health
  • Research Letters
  • Editorials
  • Perspectives
  • Physician-Scientist Development
  • Reviews
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
A phase I trial of low-dose inhaled carbon monoxide in sepsis-induced ARDS
Laura E. Fredenburgh, … , B. Taylor Thompson, Augustine M.K. Choi
Laura E. Fredenburgh, … , B. Taylor Thompson, Augustine M.K. Choi
Published December 6, 2018
Citation Information: JCI Insight. 2018;3(23):e124039. https://doi.org/10.1172/jci.insight.124039.
View: Text | PDF
Clinical Research and Public Health Clinical trials Pulmonology

A phase I trial of low-dose inhaled carbon monoxide in sepsis-induced ARDS

  • Text
  • PDF
Abstract

BACKGROUND. Acute respiratory distress syndrome (ARDS) is a prevalent disease with significant mortality for which no effective pharmacologic therapy exists. Low-dose inhaled carbon monoxide (iCO) confers cytoprotection in preclinical models of sepsis and ARDS. METHODS. We conducted a phase I dose escalation trial to assess feasibility and safety of low-dose iCO administration in patients with sepsis-induced ARDS. Twelve participants were randomized to iCO or placebo air 2:1 in two cohorts. Four subjects each were administered iCO (100 ppm in cohort 1 or 200 ppm in cohort 2) or placebo for 90 minutes for up to 5 consecutive days. Primary outcomes included the incidence of carboxyhemoglobin (COHb) level ≥10%, prespecified administration-associated adverse events (AEs), and severe adverse events (SAEs). Secondary endpoints included the accuracy of the Coburn-Forster-Kane (CFK) equation to predict COHb levels, biomarker levels, and clinical outcomes. RESULTS. No participants exceeded a COHb level of 10%, and there were no administration-associated AEs or study-related SAEs. CO-treated participants had a significant increase in COHb (3.48% ± 0.7% [cohort 1]; 4.9% ± 0.28% [cohort 2]) compared with placebo-treated subjects (1.97% ± 0.39%). The CFK equation was highly accurate at predicting COHb levels, particularly in cohort 2 (R2 = 0.9205; P < 0.0001). Circulating mitochondrial DNA levels were reduced in iCO-treated participants compared with placebo-treated subjects. CONCLUSION. Precise administration of low-dose iCO is feasible, well-tolerated, and appears to be safe in patients with sepsis-induced ARDS. Excellent agreement between predicted and observed COHb should ensure that COHb levels remain in the target range during future efficacy trials. TRIAL REGISTRATION. ClinicalTrials.gov NCT02425579. FUNDING. NIH grants P01HL108801, KL2TR002385, K08HL130557, and K08GM102695.

Authors

Laura E. Fredenburgh, Mark A. Perrella, Diana Barragan-Bradford, Dean R. Hess, Elizabeth Peters, Karen E. Welty-Wolf, Bryan D. Kraft, R. Scott Harris, Rie Maurer, Kiichi Nakahira, Clara Oromendia, John D. Davies, Angelica Higuera, Kristen T. Schiffer, Joshua A. Englert, Paul B. Dieffenbach, David A. Berlin, Susan Lagambina, Mark Bouthot, Andrew I. Sullivan, Paul F. Nuccio, Mamary T. Kone, Mona J. Malik, Maria Angelica Pabon Porras, Eli Finkelsztein, Tilo Winkler, Shelley Hurwitz, Charles N. Serhan, Claude A. Piantadosi, Rebecca M. Baron, B. Taylor Thompson, Augustine M.K. Choi

×

Figure 4

Coburn-Forster-Kane equation accurately predicts COHb levels in ARDS patients.

Options: View larger image (or click on image) Download as PowerPoint
Coburn-Forster-Kane equation accurately predicts COHb levels in ARDS pat...
The Coburn-Forster-Kane (CFK) equation was used to predict COHb levels at 60, 75, and 90 minutes using the measured COHb level at baseline and 20 minutes in subjects treated with 100 ppm (day 1, n = 4; day 2, n = 4; day 3, n = 2; day 5, n = 2) (A and C) or 200 ppm (day 1, n = 2; day 2, n = 4; day 3, n = 2; day 4, n = 4; day 5, n = 1) (B and D) iCO. Accuracy of the CFK equation in predicting COHb levels was analyzed by Spearman’s correlation and Bland-Altman plots using measured vs. predicted COHb levels and modeled using linear regression. (A) Correlation between predicted and measured COHb levels using the 20-minute COHb level and CFK equation in 100 ppm iCO–treated subjects in cohort 1 (Spearman’s r = 0.8614, P < 0.0001; goodness-of-fit R2 = 0.7186, P < 0.0001). (B) Correlation between predicted and measured COHb levels using the 20-minute COHb level and CFK equation in 200 ppm iCO–treated subjects in cohort 2 (Spearman’s r = 0.916, P < 0.0001; goodness-of-fit R2 = 0.9204, P < 0.0001). (C and D) Bland-Altman plots demonstrate excellent agreement between measured and predicted COHb levels in 100 ppm iCO–treated subjects in cohort 1 (C) and 200 ppm iCO–treated subjects in cohort 2 (D).

Copyright © 2025 American Society for Clinical Investigation
ISSN 2379-3708

Sign up for email alerts