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Inhaled Epoprostenol Augments Cold-Induced Vasodilation: A Double-Blind Crossover Trial
Theodore Tj Hartridge1, Scott McIntosh1, Emad Awad1
1Department of Emergency Medicine, University of Utah Health, Salt Lake City, UT.
Inhaled epoprostenol improved cold-induced vasodilation (CIVD) response, increasing finger temperatures during cold exposure. This prostacyclin analog may offer future frostbite prevention strategies.
Area of Science:
- Physiology
- Pharmacology
Background:
- Cold exposure causes peripheral vasoconstriction, followed by cold-induced vasodilation (CIVD).
- Enhanced CIVD response may reduce frostbite risk and improve dexterity.
- Intravenous prostacyclin (PGI2) analogs are used for severe frostbite; inhaled options are unexplored.
Purpose of the Study:
- To investigate the effect of inhaled epoprostenol, a PGI2 analog, on CIVD response.
- To assess continuous finger temperature changes during cold water immersion with inhaled epoprostenol versus placebo.
Main Methods:
- Double-blind, crossover study design.
- Fourteen healthy volunteers underwent cold water immersion.
- Continuous finger temperature measurement was used to assess CIVD response.
Main Results:
- Inhaled epoprostenol significantly increased mean finger temperature (9.16°C vs 8.34°C, p=0.027).
- Higher mean maxima (10.86°C vs 9.88°C, p=0.045) and mean minima (7.45°C vs 6.80°C, p=0.024) finger temperatures were observed with epoprostenol.
- No significant differences in CIVD cycle count; no adverse events like hypotension or hypothermia were reported.
Conclusions:
- Inhaled epoprostenol augmented the CIVD response, significantly increasing finger temperatures.
- Nebulized PGI2 analog delivery suggests potential for early frostbite intervention in remote settings.
- Further research is required to confirm epoprostenol's efficacy in frostbite management.
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