Nitrous oxide for the treatment of complex regional pain syndrome: a randomized blinded trial

Complex Regional Pain Syndrome (CRPS) is a debilitating neuropathic condition often refractory to conventional treatments. N-methyl-D-aspartate (NMDA) receptor antagonists have a well-established role in the development and modulation of chronic neuropathic pain. Nitrous oxide is widely used and gen...

Full description

Saved in:
Bibliographic Details
Published inRegional anesthesia and pain medicine Vol. 49; no. 8; p. 573
Main Authors Hale, Jason, Xu, Jijun, Wang, Dong, Rodriguez-Patarroyo, Fabio, Bakal, Omer, Kopac, Orkun, Yamak Altinpulluk, Ece, Onal, Ozkan, Brooker, Jack E, Cruz, Miguel, Maurtua, Marco, Agudelo-Jimenez, Ruben, Sessler, Daniel I, Turan, Alparslan
Format Journal Article
LanguageEnglish
Published England BMJ Publishing Group LTD 01.08.2024
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Complex Regional Pain Syndrome (CRPS) is a debilitating neuropathic condition often refractory to conventional treatments. N-methyl-D-aspartate (NMDA) receptor antagonists have a well-established role in the development and modulation of chronic neuropathic pain. Nitrous oxide is widely used and generally safe anesthetic gas with NMDA receptor antagonist activity. We therefore tested the hypothesis that brief periods of nitrous oxide exposure reduce pain in patients with CRPS. Patients with a diagnosis of CRPS were randomized to either 2 hours of nitrous oxide exposure on three alternating days (Nitrous Oxide) versus a placebo air/oxygen mixture (Air-Oxygen). Our primary outcome was patient-reported pain scores at 1 week and 1 month. Secondary and exploratory outcomes were physical and mental health (PRMOIS-29 v2 survey), specific neuropathic pain symptoms (McGill short-form questionnaire), and opioid consumption. 44 patients participated in the study; 20 were randomized to Nitrous Oxide and 24 were assigned to Air-Oxygen. Pain scores did not differ significantly, with the estimated difference in means (Nitrous Oxide-Air-Oxygen) of -0.57 (95% CI: -1.42 to 0.28) points, p=0.19. There were also no differences detected in secondary outcomes, with the estimated difference in mean Z-scores for physical health (Nitrous Oxide-Air-Oxygen) of 0.13 (95% CI: -0.16 to 0.43), mental health 0.087 (95% CI: -0.31 to 0.48), and Patient Global Impression of Change score -0.7 (95% CI: -1.85 to 0.46). Compared with air/oxygen, 2 hours of nitrous oxide/oxygen exposure for three sessions did not provide meaningful therapeutic potential for patients with chronic CRPS. Our results do not support using nitrous oxide for the treatment of CRPS.
ISSN:1098-7339
1532-8651
DOI:10.1136/rapm-2023-104537