Inhaled Nitric Oxide for Modulation of Ischemia–Reperfusion Injury in Lung Transplantation

Botha, Phil, Jeyakanthan, Mylvaganam, Rao, Jagan, Fisher, Andrew, Prabhu, Mahesh, Dark, John and Clark, Stephen (2007) Inhaled Nitric Oxide for Modulation of Ischemia–Reperfusion Injury in Lung Transplantation. The Journal of Heart and Lung Transplantation, 26 (11). pp. 1199-1205. ISSN 1053-2498

Full text not available from this repository. (Request a copy)
Official URL: http://www.sciencedirect.com/science/article/pii/S...

Abstract

Background
The prophylactic administration of inhaled nitric oxide (NO) during reperfusion after lung transplantation has been shown to reduce neutrophil-induced injury in animal models. There remain questions regarding efficacy in the clinical setting and concerns regarding increased free radical injury. We sought to assess the efficacy of NO in reducing neutrophil infiltration and associated injury if administered from the very onset of reperfusion in clinical lung transplantation.

Methods
Twenty bilateral sequential lung transplant recipients were randomized to receive 20-ppm inhaled NO (NO group) or a standard anesthetic gas mixture (control group) from the onset of ventilation. Bronchoalveolar lavage was performed immediately prior to implantation and after 30 minutes of reperfusion and analyzed for inflammatory cytokine levels and free radical surrogates. Primary graft dysfunction (PGD) scoring was performed prospectively for 72 hours post-transplant.

Results
The prophylactic administration of NO during the first 30 minutes of reperfusion had no statistically significant effect on the development of Grade II to III PGD (5 of 10 in NO group and 7 of 10 in control group, p = 0.36) or gas exchange (area under the curve: 429 ± 296 vs 336 ± 306; p = 0.64) in the NO and control groups, respectively. Pulmonary neutrophil sequestration, as measured by the transpulmonary arteriovenous neutrophil difference, was not influenced by the administration of NO. Prophylactic NO did not significantly alter the concentration of interleukin-8, myeloperoxidase or nitrotyrosine during transplantation.

Conclusions
This study could not demonstrate a significant effect of inhaled NO during the first 30 minutes of reperfusion in the prevention of neutrophil injury and primary graft dysfunction after lung transplantation.

Item Type: Article
Subjects: B100 Anatomy, Physiology and Pathology
Department: Faculties > Health and Life Sciences > School of Life Sciences > Applied Sciences
Depositing User: Becky Skoyles
Date Deposited: 28 Apr 2015 14:42
Last Modified: 10 Aug 2015 11:47
URI: http://nrl.northumbria.ac.uk/id/eprint/22260

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year

View more statistics


Policies: NRL Policies | NRL University Deposit Policy | NRL Deposit Licence