Trial Report Safety and Changes in Health-Related Quality of Life After Epidural Oxygen Injection for [LC]: A Multicenter Retrospective Study, 2026, Inaba et al

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Safety and Changes in Health-Related Quality of Life After Epidural Oxygen Injection for Long COVID/Post-COVID Syndrome: A Multicenter Retrospective Study

Inaba, Tasuku; Takagi, Kiyoshi; Atsuchi, Masamichi; Atsuchi, Shoko; Tamura, Noriko; Takahashi, Koichi; Yoshida, Kentaro; Abo, Masahiro

Background/Objectives
Long COVID/post-COVID-19 syndrome is associated with persistent symptoms, including fatigue, headache, and autonomic dysfunction, leading to impaired health-related quality of life (HRQoL).

Although epidural oxygen injections have been used in patients with chronic post-traumatic headache and mild traumatic brain injury, their safety and therapeutic effects have not been systematically evaluated.

Methods
In this multicenter retrospective study, patients with Long COVID/post-COVID-19 syndrome who underwent their first epidural oxygen injection between April 2022 and December 2025 were included. Safety was assessed by reviewing adverse events.

HRQoL was evaluated using the Japanese version of the 36-Item Short-Form Health Survey version 2 (SF-36v2®) before treatment and approximately one month afterward. Paired SF-36v2® scores were compared using the Wilcoxon signed-rank test with Bonferroni correction.

Results
Forty-two patients were included (mean age, 31.9 ± 16.2 years; 21 males). The mean interval between COVID-19 infection and treatment was 16.7 ± 12.8 months. Adverse events occurred in eight patients (subcutaneous emphysema, n = 5; dyspnea, n = 2; back pain, n = 1); they all resolved spontaneously within one week, with no deaths, hospitalizations, or long-term sequelae.

Paired SF-36v2® data were available for 35 patients. The median scores improved across all domains, with the greatest increase observed in vitality (+25.0 points). All improvements remained significant after Bonferroni correction.

Conclusions
Epidural oxygen injection demonstrated a favorable short-term safety profile and was associated with improved HRQoL in patients with Long COVID/post-COVID-19 syndrome. Prospective controlled studies using objective outcome measures are needed to confirm efficacy and clarify the underlying mechanisms.

Web | DOI | PMC | PDF | Journal of Clinical Medicine | Open Access
 
Does anyone have thoughts on whether this would translate to mecfs and pots, and for those who are severe?

It was only 1 month follow up too, hard to know if its only a temp reset, placebo, natural fluctuation of disease anyway.
 
Does anyone have thoughts on whether this would translate to mecfs and pots, and for those who are severe?

It was only 1 month follow up too, hard to know if its only a temp reset, placebo, natural fluctuation of disease anyway.
With no control group and only subjective outcomes I wouldn’t put much emphasis on the changes. The recent LDN trial was a prime example of how much bias you can generate, or the fecal transplant for IBS. ~40 % were «responders» in both groups.
 
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