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.

Abstract

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.