Figure 1: Potential negative impact of cytokine release syndrome.
Patrick Nemechek1* Guido Antonelli2 Ariel Braida21Nemechek Autonomic Medicine, Buckeye Arizona, USA
2Hospital Zonal Virgen del Carmen de Zárate, Zárate, Buenos Aires, Argentina
*Corresponding author: Patrick Nemechek, Nemechek Autonomic Medicine, Buckeye Arizona, USA, E-mail: email@example.com
Objective: Evaluate the safety and efficacy of transcutaneous vagus nerve stimulation in preventing respiratory failure and improving survival in hospitalized COVID-19 patients.
Design, Setting, and Participants: Final analysis of an ongoing single-arm, uncontrolled open-label, and observational trial to assess the transcutaneous vagus nerve stimulation (tVNS) in hospitalized SARS-CoV-2 infected subjects. Eligible subjects are 18 years old or older, requiring hospitalization for COVID-19 pneumonia.
Results: The 51 subjects enrolled with a mean age of 53.6 (22-85) years. Mechanical ventilation was required in only 3 (5.9%) cases. Of those receiving mechanical ventilation, 1 survived, and 2 died. Of all 51 hospitalized patients, 9 (17.6%) subjects died, with 7 cases (13.7%) directly attributable to respiratory failure. Relative to other reported COVID-19 hospitalization outcomes data, our mortality rate of 17.6% (9 of 51) is lower than many other reported cohorts 10.2%-50%. Only 5.9% (3 of 51) of subject’s required mechanical ventilation compared to 7.4%-79% of subjects requiring mechanical ventilation in other cohorts. Adverse events associated with tVNS occurred in only 2 subjects (3.4%) and consisted of reversible oral paresthesia and orthostatic hypotension.
Conclusion and Relevance: Our study evaluated the impact of tVNS in hospitalized patients diagnosed with COVID-19 pneumonia. The use of tVNS resulted in a low rate of adverse events, infrequent mechanical ventilation, and a high rate of survival. Several other studies using various therapies have ranges of mortality (14-50%) and the requirement of mechanical ventilation (7-79%). Considering the study was done in a resource-limited public hospital, it is important to note that the mortality rate and the frequency of mechanical ventilation were less than other reported COVID-19 cohorts. Only mild and self-limiting adverse events tVNS occurred in 2 subjects highlighting the safety of vagus stimulation.
Vagus nerve stimulation; VNS; SARS-CoV-2; COVID-19; Mechanical ventilation; Mortality; Cytokine storm; Cytokine release syndrome
VNS: Vagus Nerve Stimulation; CRS: Cytokine Release Syndrome; IL: Interleukin; TNF: Tumor Necrosis Factor; CAP: Cholinergic Anti-inflammatory Pathway; ARDS: Acute Respiratory Distress Syndrome
As the severe acute respiratory syndrome coronavirus 2 (SARSCoV-2) pandemic continues and thousands of individuals die daily from COVID-19 worldwide, a more effective therapeutic option is essential. Infection with SARS-CoV-2 is characterized by a dramatic cytokine storm in some patients with COVID-19 . Often referred to as Cytokine Release Syndrome (CRS), this storm is due to the release of high levels of pro-inflammatory cytokines such as interleukin (IL)-1 β, IL-6, tumor necrosis factor (TNF), chemokines by respiratory epithelial, dendritic cells, and macrophages. The surge of pro-inflammatory cytokines has the potential to contribute to the multitude of pathological changes seen in severe COVID-19 patients (Figure 1).
We hypothesize that CRS can be dampened with a subsequent improvement in the patient’s clinical outcome by activating the vagaldriven cholinergic anti-inflammatory pathway (CAP). Boezaart AP, et al., published a case report of two individuals with COVID-19 who both experienced significant reductions in IL-6 and CRP levels using 60 minutes of taVNS per day. Both individuals had COVID-19 pneumonia and were essentially free of respiratory symptoms by the end of the treatment course (16 and 18 days) with taVNS . Additionally, Staats P, et al. reported on the clinical improvement in two individuals with SARS-CoV-2 respiratory symptoms .
First described by Borovikova and Tracey, the CAP controls cytokine release via afferent vagal signaling into the dorsal vagal complex (DVC) [4,5]. The DVC is responsible for receiving and processing that vagal afferent signaling [4-6]. After the impulse is analyzed by the DVC, efferent impulses via sympathetic (spinal cord) and parasympatheitic (vagus nerve) pathways result in the release of acetylcholine (ACh) secretion at the site of injury that terminates the release of pro-inflammatory cytokines.
Individuals may have suppressed vagus nerve functionality partially reflected in low heart rate variability (HRV). Depressed vagal tone leads to functional impairment of CAP resulting in excessive cytokine distribution (cytokine storm) followed by tissue injury, pulmonary dysfunction, ARDS, and immune suppression, whereas in the case of ANS balance, controlled cytokine distribution is generating tissue repair and virus elimination.
The CAP is a neural reflex capable of decreasing the release of proinflammatory cytokines and is modulated by the vagus nerve. Electric neuromodulation of the vagus nerve inhibits TNF synthesis during endotoxemia, ischemia/reperfusion injury, hemorrhagic shock, septic peritonitis, and other excessive cytokine disorder modulation during endotoxemia ischemia/reperfusion injury, hemorrhagic shock, septic peritonitis, and other excessive cytokine disorders .
Vagus nerve stimulation (VNS) can play an essential role in managing patients with SARS-CoV-2 infection . The vagus nerve widely innervates multiple organs, especially the lungs and gastrointestinal tract. When the electrical stimulation is applied transcutaneously at the ear (taVNS), afferent fibers are stimulated, thereby activating the central autonomic network and resulting in activation of the efferent fibers of both the right and left vagus nerves as well as sympathetic fibers within the spinal cord and potential activation of the HPA axis . The cumulative effect of ta VNS is the improvement of the inflammatory modulation . taVNS therapy is uncomplicated, safe, inexpensive, and treatment might suppress the CRS enough to improve the clinical course in COVID-19 patients requiring hospitalization (Figure 2).
Figure 2: Potential beneficial effect of vagus nerve stimulation in COVID-19 patients.
An observational trial was designed to explore the safety and potential benefit of transcutaneous auricular vagus nerve stimulation in hospitalized patients infected with COVID-19 [9-12].
Study design and participants
This is an open-label, observational trial designed to see if taVNS stimulation was safe and might improve clinical outcomes for patients hospitalized with COVID-19 pneumonia. The protocol was approved by the ethical committee of Hospital Zonal Virgen del Carmen de Zárate, Zárate, Buenos Aires, Argentina. Written informed consent was obtained from all individuals before enrollment.
Eligible subjects are 18 years old or older, have a positive or presumed positive test for SARS-CoV-2, and require hospitalization for symptoms consistent with COVID-19 pneumonia. Study enrollment began in July 2020 with a planned minimal enrollment of 50 subjects. A total of 51 subjects were enrolled.
- Patients older than 18 years of age.
- Tested positive or suspected/presumed positive for SARS-CoV-2 infection.
- Patients requiring hospital admission with evidence of pneumonia and/or pneumopathy.
- Patients showing fever or respiratory symptoms with radiological findings of pneumonia or pneumopathy
- Respiratory distress ( ≧ 30 breaths/ min) or Oxygen saturation ≤ 93% at rest in ambient air; or oxygen saturation ≤ 97 % with O2 >5L/min.
- The patient provides signed and witnessed Informed Consent.
- Already enrolled in an experimental trial for SARS-CoV-2 or COVID-19 therapy.
- Potentially life-threatening heart rhythm.
- Pregnancy or potential pregnancy.
- Current implantation of an electrical and/or neurostimulator device, including but not limited to a cardiac pacemaker or defibrillator, vagal neurostimulator, deep brain stimulator, spinal stimulator, bone growth stimulator, or cochlear implant.
- History of an aneurysm, intracranial hemorrhage, brain tumors, or significant head trauma.
- Belongs to a vulnerable population or has any condition such that his or her ability to provide informed consent, comply with the follow-up requirements, or provide self-assessments is compromised (e.g., homeless, developmentally disabled, and prisoner).
Intervention with vagus nerve stimulation
After obtaining written consent, patients were assigned to receive 5 minutes of transcutaneous vagus nerve stimulation (tVNS) with an electronic neuromodulation device (Vitality Smart cable, Nemechek Technologies, figure 3). Stimulation parameters are 10 Hz, 800uS, biphasic pulse wave with the voltage set at 10v below the perception threshold) and was applied every 6 hours for up to 14 days.
Figure 3: taVNS is powered and controlled by iPod (Apple, Inc.)
The electrical stimulation was delivered through a small clip that makes contact within the concha and the back of the ear (Figure 4). The ear and the clip contact points are cleaned with an alcohol swab before each treatment. After the placement of the clip, the voltage was slowly increased until the subject could perceive the current. The voltage was set just below the level of perception by slowly reducing the current until it was no longer detectable by the subject.
Figure 4: Concha Clip Placement.
All other therapies (antivirals, steroids, immunoglobulin) as determined by the managing physician were allowed.
Primary outcome measures are as follows:
1. Survival without the need for mechanical ventilation on day 14. [time frame: 14 days from symptom onset] is to be considered a positive outcome.
a. Patients needing mechanical ventilator utilization (including non-invasive Ventilation, NVI) or death will be considered a negative outcome.
b. New do not resuscitate (DNR) orders will be considered a negative event at the date of the DNR.
2. Survival [time frame: 14 days].
a. Overall survival.
3. Cumulative incidence of successful tracheal extubation (defined as duration extubation >48 h) at day 14 [time frame: 14 days].
a. Death or DNR order will be considered a competing negative event.
Between July 7th and September 1st, 2020, 51 subjects (29 men and 22 women) with a mean age of 53.6 years (22-85) were enrolled in the study. The majority of subjects had comorbidities that included hypertension (66.7%), diabetes (18%), cardiovascular disease (11.8%), obesity (25.5%), and chronic kidney disease (5.9%). The mean oxygen saturation level on admission was 93.2% [range 79-98%], and oxygen saturation levels reached a low mean of 90.2% [range 79-97] during the hospitalization (Table 1).
|Survivor (%)||Non-Survivor (%)|
|Of Total Patients||42(82.4)||9(17.6)|
|Admission O2 sat%, Mean||79-98% [mean 93.2]||87-97% [mean 92.0]|
|No Mech. Vent.||41(97.6)||7(77.8)|
|Rec’d Mech. Vent.||1(3.4)||2(22.2)|
Table 1: Comparison of survivors and non-survivors.
Thirty-four subjects (66.6%) were treated with tVNS 4 times per day for 5 minutes. Because of a staffing emergency during an outbreak of COVID-19 amongst hospital staff, an additional 17 subjects (33.3%) only received tVNS only twice daily during their hospital stay. Survival between 2 versus 4 tVNS treatments per day was nearly identical (Table 2).
|VNS BID (%)||VNS QID (%)|
|Of Total Patients||17 (36.2)||30(63.8)|
|Admission O2 sat%, Mean||85-97% [mean 93.8]||79-98% [mean 92.3]|
|Survive||14 (82.4)||24 (80.0)|
|Mortality||3 (17.6)||6 (20.0)|
|No mech. Vent.||41 (97.6)||7 (77.8)|
|Rec’d Mech. Vent.||1 (3.4)||2 (22.2)|
Table 2: Comparison of 2 versus 4 tVNS treatments per day.
In addition to tVNS, all subjects received oxygen and dexamethasone, and 9 subjects (17.6%) received hyperimmune globulin as the only other forms of an investigational therapy for COVID-19 and were equally split between those receiving tVNS BID versus QID.
Of the initial 51 subjects treated with tVNS, 82.4% (n=42) survived, with only 3.4% (n=1) of the survivors requiring mechanical ventilation. Of the 9 non-survivors, 7 died from respiratory failure attributed to COVID-19 pneumonia, and only 2 received mechanical ventilation. Two non-survivors died from diabetic ketoacidosis, and bacterial septicemia felt to be related to advance AIDS.
Of the 51 survivors, 97.6% (n=41) did so without the need for mechanical ventilation. There was no significant difference in the oxygen saturation levels at the time of admission between survivors on non-survivors. Survivors had more comorbid diagnoses than non-survivors, but the numbers are too small to draw any statistical conclusions.
Both survivors and non-survivors had comorbid diagnoses, but a higher number of comorbid conditions were seen in those not requiring mechanical ventilation.
Patients treated with tVNS had a low need for mechanical ventilation. Of all 51 subjects, only 3 (5.9%) received mechanical ventilation. Of subjects not receiving mechanical ventilation, overall survival was 85.4% (Table 3).
|Mechanical Ventilation (%)||Non-Mechanical Ventilation (%)||Total (%)|
|Mortality||2(66.7)||7 (14.6)||9 (17.6)|
|Admission O2 sat%||93-98%, [mean
|79-99% [mean 93.0]|
|Obesity||1 (33.3)||12 (25)||13 (25.5)|
|Diabetes Mellitus||1 (33.3)||17 (35.4)||18 (35.3)|
|Hypertension||3 (100)||31 (64.6)||34 (66.7)|
|CAD/CVA||1(33.3)||5 (10.4)||6 (11.8)|
|Renal||-||3 (6.3)||3 (5.9)|
Table 3: Comparison of patients requiring or not requiring mechanical ventilation.
Adverse events associated with tVNS occurred in only 2 subjects (3.9%) and consisted of oral paresthesia and orthostatic hypotension. Both of which were described as mild by the managing physician and resolved spontaneously. These did not occur with the use of a lower voltage during subsequent treatments with vagal stimulation. Both patients with AE from tVNS survived. It is unknown if these adverse effects were directly attributable to taVNS.
Comparison to other cohorts
A control group is ideally used to provide a relative standard against which therapy is compared. Because of the outbreak of SARS-CoV-2 among hospital staff and the rapidly escalating number of SARS-CoV-2 cases arriving within the hospital, the study was modified to limited staff contact with infected patients unless clinically necessary, and the control group was eliminated from the study. As such, a comparison to other reported cohort data on overall mortality and the frequency of mechanical ventilation is outlined. The data is stratified according to the number of hospitalized subjects reported for each cohort.
Although our analysis details only treated patients, one can see that overall mortality is either lower or similar to other reported cohorts when vagus nerve stimulation is incorporated in the treatment regimen (Table 4) [13-20].
|Cohort||Number of Hospitalized patients||Overall Mortality (%)||Require Mechanical ventilation|
|Seattle, U.S ||24||12 (50%)||18 (75%)|
|Argentena - VNS||51||9 (17.6%)||3 (5.9%)|
|China ||191||54 (28.2%)||32 (16.6%)|
|New York, U.S ||257||101 (39%)||203 (79%)|
|New York, U.S ||393||40 (10.2%)||130 (33%)|
|Louisiana, U.S ||1382||325 (23.5%)||364 (26.3%)|
|New York, U.S ||1999||292 (14.6%)||445 (22.2%)|
|United Kingdom ||6678||2212 (33.1%)||497 (7.4%)|
|United States ||11721||2514 (21.5%)||1967 (16.8%)|
Table 4: Comparison of mortality and mechanical ventilation rates among other published cohorts.
We are aware that comparison with each different cohort should be made with caution as we are unable to delineate the relative available treatments between each of these reported cohorts. That being said, the patients in each of these cohorts received a wide variety of treatments reflecting the resources available and the prevailing treatment approaches taken by each cohort group.
While vaccination against SARS-CoV-2 improves hospitalization and mortality rates in wealthier countries, shortages of SARS-CoV-2 vaccines and basic medical supplies such as oxygen are still leading to widespread death from COVID-19 . The use of a vagus nerve stimulator offers a treatment option that holds the potential to alter the course of the infection in hospitalized individuals infected with SARS-CoV-2.
Implementation of tVNS as a treatment option can be instituted quickly within any hospital. Technicians can be trained very quickly, tVNS is safe, the devices are inexpensive, and can be run off an inexpensive smart phone. Similar to a fingertip pulse oximeter, a single device can be easily decontaminated and used among multiple patients.
Electrical stimulation of the vagus nerve can modulate the working point of the inflammatory response in a wide variety of potentially lethal medical conditions (endotoxemia, ischemia/reperfusion injury, hemorrhagic shock, septic peritonitis) . A growing number of publications agree with our position that tVNS can blunt the surge of inflammatory cytokines found in COVID-19 pneumonia and could favorably alter the course of the illness.
Scientific purists will emphatically state that no treatment should be put into practice without fully controlled clinical trials. In general, I wholeheartedly agree with this principle, but the dire reality faced by many communities not yet vaccinated against SARS-CoV-2needs actionable therapeutic options immediately. Treatment of patients with tVNS offers them a potentially beneficial, safe, and inexpensive therapy when faced with little to no other options.
Our results suggest that transcutaneous vagus nerve stimulation (tVNS) in hospitalized patients requiring oxygen support or having respiratory distress is a safe, rapid, and technically simple process that could easily be deployed in developing countries. Because of the lack of a control group, it is difficult to comment on the efficacy accurately. We believe a well-designed controlled clinical trial of taVNS is warranted.
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Aritcle Type: RESEARCH ARTICLE
Citation: Nemechek P, Antonelli G, Braida A (2021) Transcutaneous Vagus Nerve Stimulation is Associated with Lower Mechanical Ventilation and Mortality in COVID-19 Patients. J Emerg Dis Virol 6(2): dx.doi.org/10.16966/2473-1846.165
Copyright: © 2021 Nemechek P, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.