Stellate Ganglion Block for the Treatment of COVID-19-Induced Olfactory Dysfunction: A Prospective Pilot Study
Andrew M Peterson1, Brevin J Miller1, Dorina Kallogjeri1
1Clinical Outcomes Research Office, Department of Otolaryngology-Head and Neck Surgery, Washington University School of Medicine in St Louis, St Louis, Missouri, USA.
Objective:
The objective of this study was to explore the safety and feasibility of stellate ganglion blocks (SGBs) to treat persistent COVID-19-induced olfactory dysfunction (OD). Secondarily, the goal was to determine effect sizes to plan a future randomized clinical trial.
Study Design:
Prospective case series.
Setting:
Quaternary Care Academic Medical Center.
Methods:
In this single-arm pilot trial, adult participants with a COVID-19 diagnosis ≥ 12 months prior to enrollment with OD underwent bilateral SGBs. Subjects were followed for 1 month after completion of SGB. The primary outcome measure was the change in the Clinical Global Impression-Improvement Scale for smell loss. Secondary outcome measures included changes in the University of Pennsylvania Smell Identification Test (UPSIT) and Olfactory Dysfunction Outcomes Rating (ODOR).
Results:
Twenty participants were enrolled with a mean (SD) age of 46 (11) years and a mean (SD) duration of OD of 21 (5) months. At 1 month, 10 (50%) participants experienced at least slight subjective improvement in their OD, 11 (55%) attained a clinically meaningful improvement in smell identification using the UPSIT, and 7 (35%) achieved a clinically meaningful improvement in olfactory-specific quality of life (QoL) measured by the ODOR. The median difference between UPSIT scores at baseline and 1 month was 6 (95% confidence interval: 3-11), exceeding the minimal clinically important difference of 4. There were no serious adverse events.
Conclusion:
Sequential SGBs for COVID-19-associated OD were safe and associated with modest improvements in subjective olfaction, odor identification, and olfactory-specific QoL. A placebo-controlled trial is warranted to determine the efficacy of SGBs for COVID-19-associated OD.
Insights
Stellate ganglion blocks (SGBs) show promise for treating persistent COVID-19-induced olfactory dysfunction (OD). This pilot study found SGBs to be safe, with 55% of participants showing improved smell identification and 35% reporting better quality of life.
Area of Science:
- Neurology
- Otolaryngology
- Infectious Disease
Background:
- Persistent olfactory dysfunction (OD) is a common sequela of COVID-19.
- Current treatments for post-COVID-19 OD have limited efficacy.
- Stellate ganglion blocks (SGBs) are an interventional treatment modality with potential applications in neurological and inflammatory conditions.
Purpose of the Study:
- To evaluate the safety and feasibility of SGBs for treating persistent COVID-19-induced OD.
- To determine effect sizes for future randomized clinical trials.
Main Methods:
- Prospective case series of adult participants with a history of COVID-19 and OD for at least 12 months.
- Bilateral SGBs were administered, followed by a 1-month observation period.
- Primary outcome: Clinical Global Impression-Improvement Scale. Secondary outcomes: University of Pennsylvania Smell Identification Test (UPSIT) and Olfactory Dysfunction Outcomes Rating (ODOR).
Main Results:
- Twenty participants (mean age 46 years, mean OD duration 21 months) were enrolled.
- At 1 month post-SGB, 50% reported subjective improvement in OD, 55% showed clinically meaningful improvement in UPSIT scores, and 35% improved in olfactory-specific quality of life (ODOR).
- The median improvement in UPSIT scores (6 points) exceeded the minimal clinically important difference.
Conclusions:
- Sequential SGBs appear to be a safe treatment for COVID-19-associated OD.
- Modest improvements were observed in subjective olfaction, odor identification, and quality of life.
- A placebo-controlled trial is recommended to confirm the efficacy of SGBs for this condition.
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