Background: ARDS is characterized by decreased functional residual capacity (FRC), heterogeneous lung injury, and severe hypoxemia. Tidal ventilation is preferentially distributed to ventilated alveoli. Aerosolized prostaglandin I exploits this pathophysiology by inducing local vasodilation, thereby increasing ventilation-perfusion matching and reducing hypoxemia. Therefore, aerosolized prostaglandin I efficacy may depend upon FRC. Both P /F and compliance of the respiratory system (C) are indirect signifiers of FRC and thus may partly determine the response to aerosolized prostaglandin I.
Methods: We reviewed the records of 208 ARDS subjects who received aerosolized prostaglandin I and had arterial blood gases done before and after the initiation of therapy, without other ventilator manipulations. Subjects were grouped according to baseline P /F (lowest: < 60, intermediate: 60-90, highest: > 90 mm Hg) and C (< 20, 20-29, 30-39, and ≥ 40 mL/cm HO) and by other factors, such as sepsis. Comparisons were analyzed by paired tests, or Kruskal-Wallis and Dunn post-tests. Multivariate logistic regression modeling was done to determine which of 18 clinically relevant factors were most predictive for responding to aerosolized prostaglandin I. α was set at .05.
Results: Mean P /F increased by 33 mm Hg (42%) upon initiation of prostaglandin I, with a responder rate of 62%. P /F increased significantly in all oxygenation groups. The highest baseline P /F group had the greatest improvement and responder rate (51 ± 63 mm Hg, and 82%). In addition, those with sepsis had a smaller improvement in P /F compared with those without sepsis (18 ± 35 vs 40 ± 55 mm Hg, = .002). Both P /F and responder rate increased as C improved, but between-group improvements were not as consistent. In the final model, the only factors that predicted a positive response to aerosolized prostaglandin I were baseline P /F (odds ratio 1.10 [1.004-1.205], = .042) and C (odds ratio 1.04 [1.01-1.08], = .02).
Conclusions: Aerosolized prostaglandin I improves oxygenation in approximately 60% of ARDS cases. A favorable response was most strongly associated with baseline P /F and C.
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http://dx.doi.org/10.4187/respcare.05268 | DOI Listing |
PLoS One
November 2024
HPIG, Ruminant Medicine Unit, Department of Clinical Sciences, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Non-steroidal anti-inflammatory drugs (NSAID) are not recommended for use against pneumonia in humans, but are commonly utilised against bovine respiratory disease. This study aimed to determine if the use of NSAIDs in the early phase of bovine respiratory syncytial virus (BRSV)-infection limits pulmonary inflammation. Four to nine-week old calves were infected with BRSV by aerosol and were treated with either meloxicam intravenously on day (D)4 (n = 5, MEL), acetylsalicylat-DL-lysin intravenously on D4 and D5 (n = 5, ASA), or were left untreated as controls (n = 5, CTR).
View Article and Find Full Text PDFSci Total Environ
February 2024
Univ. Grenoble Alpes, CNRS, INRAE, IRD, Grenoble INP, IGE, 38000 Grenoble, France. Electronic address:
Oxidative stress is a prominent pathway for the health effects associated with fine particulate matter (PM) exposure. Oxidative potential (OP) of PM has been associated to several health endpoints, but studies on its impact on biomarkers of oxidative stress remains insufficient. 300 pregnant women from the SEPAGES cohort (France) carried personal PM samplers for a week and OP was measured using ascorbic acid (AA) and dithiothreitol (DTT) assays, and normalized by 1) PM mass (OP) and 2) sampled air volume (OP).
View Article and Find Full Text PDFRespir Physiol Neurobiol
December 2022
Pathophysiology Program, Lovelace Biomedical Research Institute, Albuquerque, NM 87108, USA. Electronic address:
Exposure to aerosolized citric acid (CA, 150 mM) and prostaglandin E (PGE, 0.43 mM) for 10 min in guinea pigs reportedly produces the distinct cough patterns (Type I vs. II) and ventilatory responses (long-lasting hyperventilation vs.
View Article and Find Full Text PDFToxicol Sci
July 2022
Department of Physiology and Pharmacology, West Virginia University School of Medicine, Morgantown, West Virginia 26505-9229, USA.
Pregnancy requires rapid adaptations in the uterine microcirculation to support fetal development. Nanomaterial inhalation is associated with cardiovascular dysfunction, which may impair gestation. We have shown that maternal nano-titanium dioxide (nano-TiO2) inhalation impairs microvascular endothelial function in response to arachidonic acid and thromboxane (TXA2) mimetics.
View Article and Find Full Text PDFExpert Opin Drug Deliv
May 2022
Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, Stony Brook University Medical Center, Stony Brook, NY, USA.
Introduction: Critically ill mechanically ventilated patients routinely receive aerosol delivery of epoprostenol by continuous infusion of the nebulizer by syringe pump. This procedure is 'off-label' as no FDA approved drug presently exists. Without standardized protocols, therapy is based on prior experience with bronchodilators, limited studies of delivery systems and anecdotal clinical trials.
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