Effects of pulsed inhaled nitric oxide delivery on the distribution of pulmonary perfusion in spontaneously breathing and mechanically ventilated anesthetized ponies

Author(s):  
Adam Auckburally ◽  
Maja K. Wiklund ◽  
Peter F. Lord ◽  
Göran Hedenstierna ◽  
Görel Nyman

Abstract OBJECTIVE To measure changes in pulmonary perfusion during pulsed inhaled nitric oxide (PiNO) delivery in anesthetized, spontaneously breathing and mechanically ventilated ponies positioned in dorsal recumbency. ANIMALS 6 adult ponies. PROCEDURES Ponies were anesthetized, positioned in dorsal recumbency in a CT gantry, and allowed to breathe spontaneously. Pulmonary artery, right atrial, and facial artery catheters were placed. Analysis time points were baseline, after 30 minutes of PiNO, and 30 minutes after discontinuation of PiNO. At each time point, iodinated contrast medium was injected, and CT angiography was used to measure pulmonary perfusion. Thermodilution was used to measure cardiac output, and arterial and mixed venous blood samples were collected simultaneously and analyzed. Analyses were repeated while ponies were mechanically ventilated. RESULTS During PiNO delivery, perfusion to aerated lung regions increased, perfusion to atelectatic lung regions decreased, arterial partial pressure of oxygen increased, and venous admixture and the alveolar-arterial difference in partial pressure of oxygen decreased. Changes in regional perfusion during PiNO delivery were more pronounced when ponies were spontaneously breathing than when they were mechanically ventilated. CLINICAL RELEVANCE In anesthetized, dorsally recumbent ponies, PiNO delivery resulted in redistribution of pulmonary perfusion from dependent, atelectatic lung regions to nondependent aerated lung regions, leading to improvements in oxygenation. PiNO may offer a treatment option for impaired oxygenation induced by recumbency.

2020 ◽  
Vol 60 ◽  
pp. 159-160 ◽  
Author(s):  
Michele Ferrari ◽  
Alessandro Santini ◽  
Alessandro Protti ◽  
Davide T. Andreis ◽  
Giacomo Iapichino ◽  
...  

2020 ◽  
Vol 14 ◽  
pp. 175346662093351 ◽  
Author(s):  
Raj Parikh ◽  
Carolyn Wilson ◽  
Janice Weinberg ◽  
Daniel Gavin ◽  
James Murphy ◽  
...  

1999 ◽  
Vol 27 (Supplement) ◽  
pp. 162A
Author(s):  
Richard Mink ◽  
Robert Ream ◽  
John Hauver ◽  
Barbara Kountzman ◽  
Laura Loftis ◽  
...  

1997 ◽  
Vol 113 (3) ◽  
pp. 435-442 ◽  
Author(s):  
Andreas Gamillscheg ◽  
Gerfried Zobel ◽  
Bernd Urlesberger ◽  
Jutta Berger ◽  
Drago Dacar ◽  
...  

1999 ◽  
Vol 83 (2) ◽  
pp. 321-324 ◽  
Author(s):  
L E Young ◽  
D J Marlin ◽  
R M McMurphy ◽  
K Walsh ◽  
P M Dixon

2009 ◽  
Vol 55 (2) ◽  
pp. 149-155 ◽  
Author(s):  
Tomas Javier ACOSTA ◽  
Mamadou Bousa BAH ◽  
Anna KORZEKWA ◽  
Izabela WOCLAWEK-POTOCKA ◽  
Wlodzimierz MARKIEWICZ ◽  
...  

Thorax ◽  
2021 ◽  
pp. thoraxjnl-2020-216128
Author(s):  
Samir Gupta ◽  
Rosalind Tang ◽  
Abdul Al-Hesayen

The hepatopulmonary syndrome (HPS) is defined by liver dysfunction, intrapulmonary vasodilatation and abnormal oxygenation. Hypoxaemia is progressive and liver transplant is the only effective treatment. Severe hypoxaemia is a life-threatening HPS complication, particularly after transplant. We evaluated gas-exchange and haemodynamic effects of invasive therapies in a consecutive sample of 26 pre-transplant patients. Inhaled nitric oxide significantly improved partial pressure of oxygen (12.4 mm Hg; p=0.001) without deleterious effects on cardiac output. Trendelenburg positioning resulted in a small improvement, and methylene blue did not, though individual responses were variable. Future studies should prospectively evaluate these strategies in severe post-transplant hypoxaemia.


2021 ◽  
Vol 66 (6) ◽  
pp. 1021-1028
Author(s):  
Stefano Gianni ◽  
Ryan W Carroll ◽  
Robert M Kacmarek, ◽  
Lorenzo Berra

1998 ◽  
Vol 43 ◽  
pp. 203-203 ◽  
Author(s):  
Mary E Wearden ◽  
Suzanne E Hegemier ◽  
Nusret Dzdic ◽  
Lynette K Rogers ◽  
Patricia L Ramsay ◽  
...  

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