Abstract
293
Word Count: 2,797
Tables: 2
Figures: 3
The Kids Are Not Alright: A Preliminary Report of Post-COVID Syndrome in
University Students
Julie Walsh-Messinger, PhD1,2* Hannah Manis, BS1 Alison Vrabec, BA1 Jenna Sizemore,1
Karyn Bishof, BS3 Marcella Debidda, PhD4 Dolores Malaspina, MD MSPH5
Noah Greenspan DPT4
1Department of Psychology, University of Dayton, 300 College Park, Dayton, OH 45469
2Department of Psychiatry, Wright State University Boonshoft School of Medicine, 2555
University Blvd, Dayton, OH 45324
3Long-Hauler Advocacy Project, Boca Raton, FL
4Pulmonary Wellness Foundation, 218 East 36th Street, Apartment BB, New York, NY 10016
5Departments of Psychiatry, Neuroscience, and Genetics and Genomics, Icahn School of
Medicine at Mount Sinai, 1 Gustave L. Levy Place, New York, NY 10029
*Corresponding Author:
Julie Walsh-Messinger, PhD
Department of Psychology
University of Dayton
300 College Park
Dayton, OH 45469-1430
Phone: (937) 229-1380
Fax: (937) 229-3900
E-mail:
[email protected]
Keywords
SARS-CoV-2; COVID-19; coronavirus; post-COVID syndrome; long COVID; long-
haulers; young adults; university students
Funding: This work was supported by NIMH R01MH110418 (DM)
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NOTE: This preprint reports new research that has not been certified by peer review and should not be used to guide clinical practice.
Abstract
Background: Post-COVID syndrome is increasingly recognized by the medical community but
has not been studied exclusively in young adults. This preliminary report investigates the
prevalence and features of protracted symptoms in non-hospitalized university students who
experienced mild-to-moderate acute illness.
Methods
148 students completed an online study to earn research credit for class. Data from
COVID-19 positive participants with symptoms ≥ 28 days (N=22) were compared to those who
fully recovered (N=21) and those not diagnosed with COVID-19 (N=58).
Results
51% of participants who contracted COVID-19 (N=43) experienced symptoms ≥ 28
days and were classified as having post-COVID syndrome; all but one (96%) were female.
During acute illness the post-COVID group, compared to those who fully recovered,
experienced significantly more chest pain (64% vs 14%; P=.002), fatigue (86% vs 48%;
P=.009), fever (82% vs 48%; P=.02), olfactory impairment (82% vs 52%; P=.04), headaches
(32% vs 5%; P<.05), and diarrhea (32% vs 5%; P<.05). Compared to those not diagnosed with
COVID-19, the post-COVID syndrome group more frequently experienced exercise intolerance
(43% vs. 0%; P<.001), dyspnea (43% vs. 0%; P<.001), chest pain (31% vs 7%; P=.002),
olfactory impairment (19% vs 0%; P=.004), lymphadenopathy (19% vs 0%; P=.004), gustatory
impairment (14% vs 0%; P=.02), and appetite loss (36% vs 14%; P=.02).
Interpretation: Our results contradict the perception that this “yet to be defined” post-COVID
syndrome predominantly affects middle-aged adults and suggest that exercise intolerance,
dyspnea, chest pain, chemosensory impairment, lymphadenopathy, rhinitis, and appetite loss
may differentiate post-COVID syndrome from general symptoms of pandemic, age, and
academic related stress. These findings are also consistent with previous reports that females
are more vulnerable to this post viral syndrome. Large-scale population-based studies are
essential to discerning the magnitude and characterization of post-COVID syndrome in young
adults as well as more diverse populations.
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Introduction
The novel SARS-CoV-2 virus, first reported in Wuhan in late 2019, is an international
pandemic that has infected over 58 million and resulted in over 1.3 million deaths as of
November 23, 2020. The initial expectation that mild and moderate COVID-19, the disease
caused by SARS-CoV-2, would resolve within 2-3 weeks has been challenged by anecdotal
reports of prolonged and debilitating symptoms in COVID-19 survivors.1-3 Studies, such as Carfì
et al’s Italian case series which found that 87.4% of 143 cases who were hospitalized for
COVID-19 continued to experience symptoms two months after their positive test result,
4 have
resulted in increasing recognition of prolonged symptoms and disability for adults who were
hospitalized with severe COVID-19.
Young adults are widely considered to have a low risk of significant COVID-19
symptoms, but newer studies estimate that many infected adolescents and young adults may
require hospitalization.
5,6 The notion that COVID-19 has a minimal impact on the health of
young adults is contrary to a CDC report which found one in five individuals without pre-existing
medical conditions who were between 18-34 years old contracted the disease reported via
telephone contact that they were still symptomatic three weeks after their positive test.
7 This
assertion is further contradicted by reports in September and October, 2020 of three healthy
male university student fatalities directly related to COVID-19, two of whom were athletes.
8 As
there are currently no reports of protracted symptoms in non-hospitalized young adults who
contracted COVID-19, this preliminary report investigates the prevalence and features of post-
COVID syndrome in a sample of university students with mild to moderate acute illness severity.
Methods
Participants
Undergraduate students (N=195) at a private, Catholic, Midwestern university completed
an online study about COVID-19 testing, symptoms, course of illness, treatment, and current
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functioning between October 7 and November 11, 2020. Participants were recruited through
SONA, an online research study management system, and the self-report measures were
administered through Qualtrics (QualtricsXM, Provo, UT). The study was approved by the
University of Dayton Research Review and Ethics Committee, a subcommittee of the
Institutional Review Board, and participants provided voluntary informed consent obtained in
accordance with the Declaration of Helsinki. Participants were compensated for their time with
research experience credit for class.
Measures
A health survey, developed for this study by JWM and KB, asked about demographics,
medical history, COVID-19 testing and results, course of illness, treatment, and past and current
COVID-19 symptoms, including fever, pharyngitis, lymphadenopathy, cough, dyspnea, rhinitis,
myalgias, fatigue, diarrhea, constipation, appetite loss, nausea, emesis (excluding alcohol
related incidents), headache, and chemosensory impairment. The survey also asked about
post-COVID onset of exercise intolerance, hypertension, hypotension, tachycardia, bradycardia,
brain fog, and impaired concentration, memory, and sleep. Overall severity of illness and
treatment were assessed with questions 2a, 2b, and 2c from the COVID Experiences (COVEX)
Symptoms and Diagnoses module.
9
Perceived stress over the past month was assessed with the Perceived Stress Scale
(PSS).10 The 10-items on this self-report measure are rated on a 5-point Likert scale from
“never” to “very often” and are summed to yield a total score that can range from 0 to 40.
Depression severity over the past two weeks was measured with the Center for
Epidemiological Studies Depression Scale – Revised (CESD-R).11 The 20-item self-report
questionnaire produces an overall severity score that ranges from 0 to 60, as well as subscale
scores for Dysphoria and Sleep (subscales range from 0-9), Anhedonia, Appetite,
Thinking/Concentration, Guilt, Fatigue, Agitation, and Suicidal Ideation (subscales range from 0-
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6).
The Generalized Anxiety Disorder-7 (GAD-7)12 was used to assess generalized anxiety
severity over the past two weeks. The seven self-report items are rated on a 4-point scale from
“not at all” to “nearly every day” and total scores can range from 0 to 28.
Main Outcome Variables
The primary outcomes measures were COVID-19 positivity and duration of symptoms.
Secondary outcomes included treatment utilization, depression, anxiety, and perceived stress.
Statistical analysis
SPSS (version 27.0) was used for data analysis, which was conducted by JWM.
Descriptive statistics of all measures were examined to identify key features of the data (e.g.,
non-normal distribution, outliers, skewness) that might influence inferential methods. All
variables were determined to be normally distributed, with the exception of age days since
illness onset, and depression severity, which were positively skewed.
Differences between the participants who reported full recovery within 28 days (N=21)
and those with post-COVID syndrome (defined as protracted symptoms
≥ 28 days; N=22) were
assessed with independent samples t-tests for normally distributed continuous variables or
Mann Whitney U-tests for non-normally distributed continuous variables that were not. Cohen’s
d, Common Language Effect Size (CLES) and 95% confidence intervals [CI] were computed
using the Psychometrica online calculator.
12 Chi-Square and Fisher’s Exact tests were used to
examine group differences in categorical variables, the latter employed when cell counts were
<5, with Cramer’s V computed for effect sizes. Reported P-values are all two-tailed.
Role of the Funding Source
The funder had no role in the study design, data collection, analysis, interpretation, writing of
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this manuscript or decision to submit to The Lancet for publication. JWM, HM, AV, and JS had
access to all of the data. The corresponding author, JWM, had final responsibility for the
decision to submit the manuscript for publication, to which all authors agreed.
Results
Of the 215 students who enrolled in the study, 93% completed the self-report measures
(N=195). Excluded from analyses were 27 students who had no COVID-19 testing or diagnosis,
seven who did not know their test results, four with missing data, and nine who were <28 days
post onset of COVID-19 at the time they completed the measures, yielding a final sample size of
148 (see Figure 1). The university requirement that students produce a negative COVID-19 test
before returning to campus for the Fall 2020 semester was the most frequent reason for COVID-
19 testing (38%), followed by COVID-19 symptoms (26%), close contact with a known positive
case (23%), random testing (7%), and other reasons (6%), which included peace of mind and
requirement prior to a medical procedure.
One third of the sample (N=52) reported a positive COVID-19 test result or diagnosis.
Participants primarily had their diagnosis confirmed by PCR testing (76%); however, seven
(16%) were unable to obtain testing but were diagnosed by a clinician, and four (9%) had a
negative test but were nonetheless diagnosed as having COVID-19 by a clinician in light of
smell loss and other symptoms. Means, standard deviations, and frequency counts for all
demographic measures are presented in Table 1.
Post-COVID syndrome participants compared to recovered participants
Demographics
While 91% of COVID-19 positive participants reported “full recovery” from acute illness,
51% (N=22) continued to experience protracted symptoms, of whom 59% (N=13) had persistent
symptoms for
≥ 50 days. The number of days since the onset of COVID-19 ranged from 28 to
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291 and the groups did not differ (U=171.00; Z=-1.46; P=.15; CLES=0.56; CI, -0.40 to 0.80).
The recovered group reported an average of seven days from onset to symptom remission.
There were significantly more females in the post-COVID syndrome group compared to the
recovered group (
Χ 2=5.88, P=.02, Cramer’s V=0.37). The groups did not differ with regard to
age, race, ethnicity, cigarette smoking, or vaping (all P’s≥ .11).
The rates of pre-existing chronic illnesses were low across both groups. The most
frequently reported chronic illness was allergic rhinitis, which was endorsed by 29% of
recovered participants and 36% of the post-COVID syndrome group. One participant in the
post-COVID group reported a history of hypertension and irritable bowel syndrome, one had
endometriosis and fibromyalgia, and three others reported asthma. One recovered participant
reported obesity, two endorsed asthma, and one had a rare connective tissue disorder.
Symptomatology and severity
One participant in each group reported a severe course of illness (e.g. severe dyspnea
or complications leading to pneumonia). Even with these cases excluded, the post-COVID
syndrome group more frequently reported moderate illness severity compared to the majority of
the recovered group who were asymptomatic (N=1) or reported a mild course (P=.01; Cramer’s
V=0.43).
During acute illness, the post-COVID syndrome group, compared to the recovered
group, experienced significantly more chest pain chest pain (P=.002; Cramer’s V=0.51), fatigue
(
Χ 2=6.86; P=.009; Cramer’s V=0.40), fever (Χ 2=5.32; P=.02; Cramer’s V=0.40), olfactory
impairment (Χ 2=4.24; P=.04; Cramer’s V=0.31), headaches (P<.05; Cramer’s V=0.35), and
diarrhea (P.14). The number of symptoms experienced during acute
illness was significantly higher in the post-COVID syndrome group (t=-2.77; P=.008; d=0.82; CI,
0.24 to 1.42) who were also more likely to have sought medical treatment (Χ 2=9.79; P=.002;
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Cramer’s V=0.47).
Depression severity was higher in the post-COVID syndrome group (U=148.00; Z=-2.02;
P=.04; CLES=0.58; CI, -0.31 to 0.90); however, the only depression subscales that differed
were Sleep (U=145.5; Z=-2.11; P=.04; CLES=0.61; CI, -0.21 to 0.99), and Thinking (U=146.00;
Z=-2.41; P=.02; CLES=0.64; CI, -0.12 to 1.09), with a marginal difference for Appetite
(U=157.00; Z=-1.93; P=.05; CLES=0.66; CI, -0.02 to 1.21). Perceived stress and anxiety also
did not differ between the groups (P’s ≥ .47).
Characterization of participants with post-COVID syndrome
The number of symptoms and/or complications experienced by the post-COVID
syndrome group in the past week ranged from 2 to 33 (M=7.00±7.60), with mean symptom
severity (rated on a 5-point scale from “mild” to “severe”) ranging from 1.0 - 3.21 (M=1.74±
0.78). Impaired concentration was the most frequently reported symptom, followed by
headache, rhinitis, exercise intolerance, dyspnea, sleep impairment, brain fog, appetite loss,
fatigue, and chest pain. None of the study participants were hospitalized; however, six (27%)
reported in-person contact with at least one healthcare provider (e.g., primary care physician,
university health center, urgent care, or emergency room) and eight others (36%) reported
telehealth contact. Despite experiencing serious symptoms including chest pain, dyspnea, and
exercise intolerance, eight participants (36%) reported no contact with any healthcare
professional.
Comparison of Post-COVID syndrome to COVID negative participants
As some of the current symptoms endorsed by the post-COVID syndrome group could
be attributed to allergic rhinitis or other viral infections, we compared the frequency of their
symptoms to those endorsed by COVID negative participants for whom current symptom data
was available (N=58) and who served as an ecologically valid normative sample. The post-
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COVID syndrome group more frequently reported exercise intolerance (P<.001; Cramer’s
V=0.60), dyspnea (P<.001; Cramer’s V=0.60), chest pain (P=.002; Cramer’s V=0.38), olfactory
impairment (P=.005; Cramer’s V=0.38), lymphadenopathy (P=.004; Cramer’s V=0.37), rhinitis
(
Χ 2=8.57; P=.003; Cramer’s V=0.33) and gustatory impairment (P=.017; Cramer’s V=0.33) and
appetite loss (Χ 2=5.08; P=.02; Cramer’s V=0.25; Figure 3). Notably, one or more of the eight
aforementioned symptoms were endorsed by all but one post-COVID syndrome participant
(M=1.91±0.41).
While the results did not reach statistical significance, fever (P=.06; Cramer’s V=0.24),
fatigue (
Χ 2=3.40; P=.07; Cramer’s V=0.21), and hypertension (P=0.07; Cramer’s V=0.26)
tended to also be more frequent in the post-COVID syndrome group with moderate effect sizes.
There were no differences in frequency of pharyngitis, myalgias, diarrhea, constipation,
hypotension, tachycardia, bradycardia, brain fog, and sleep, memory, and concentration
impairment (all P’s>.10). Post-COVID syndrome participants also endorsed a greater number of
current symptoms (U=315.00; Z=-3.54; P<.001; CLES=0.71; CI, 0.16 to 1.36) and greater mean
severity of current symptoms (U=375.00; Z=-2.88; P=.004; CLES=0.53; CI, -0.48 to 0.72)
compared to COVID negative participants. Severity of depression, anxiety, and perceived stress
did not significantly differ between the groups (all P’s
≥ .200).
Discussion
The importance of understanding the COVID-19 disease in young adults cannot be
overstated, as the weekly number of such cases reported to the CDC is increasing over time
and especially as students have returned to campus settings.
13 This preliminary study
contradicts the perception that this “yet to be defined” post-COVID syndrome predominantly
affects middle-aged adults, as just over half of our young adult sample reported at least two
COVID-19 symptoms and/or related complications 30 days post illness onset, at minimum; a
majority were still symptomatic more than 50 days later. Our comparison of post-COVID
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syndrome participants to those never diagnosed with COVID-19 suggests that the protracted
symptoms experienced by the post-COVID syndrome group are not merely due to stress
associated with the current pandemic or college attendance.
Of paramount concern is that a third of the post-COVID syndrome group had not had
contact with a healthcare provider, despite serious symptoms, including dyspnea, exercise
intolerance, chest pain, and chemosensory impairment. The current message in the United
States that COVID-19 is benign and/or a short lived illness in young adults is inconsistent with
reports that adolescents and young adults may require hospitalization,5,6 and several recent
fatalities in healthy university students.8
Understandably, scientific efforts since the outbreak of SARS-CoV-2 have predominantly
focused on prevention (e.g., vaccine development, studying the efficacy of social distancing and
masks, developing early detection tests) and development of treatment approaches to reduce
the morbidity and mortality associated with COVID-19, with little attention within the scientific
and medical community to the lingering effects of the disease. As a result, individuals with
protracted COVID symptoms, frequently referred to as “long-haulers” or “long COVID” in the
media, formed social-media based support groups which have spearheaded advocacy efforts.
Surveys conducted by such advocacy groups suggest that a heterogeneous, multisystemic
constellation of symptoms and complications are experienced by these individuals,14,15 which
has prompted more recent attention to post-COVID syndrome in the medical literature16-19 and is
consistent with our present findings.
The only longitudinal study of putatively recovered COVID-19 cases found that 98% of
201 participants were still experiencing symptoms four months post illness onset, including
fatigue, myalgias, headaches, cardiorespiratory and gastrointestinal symptoms.20 Consistent
with these symptoms, multi-organ magnetic resonance imaging (MRI) detected impairment in
one or more organs, including heart, lungs, kidneys, liver, pancreas, and spleen in 70% of the
sample. Few of these participants had any pre-existing health conditions and only 18% were
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hospitalized during acute illness. While it remains unknown whether some or all of those with
post-COVID syndrome will eventually return to their pre-COVID level of health and functioning,
post-COVID morbidity is likely to place a substantial burden on healthcare systems that are
already depleted by their response to acute COVID-19.
Notably, all but one of the post-COVID syndrome participants in this study were female.
While mortality from COVID-19 is sexually dimorphic, with males accounting for approximately
70% of deaths,
21 the present findings suggest that females are more prone to a prolonged
course of illness and/or post-COVID-19 complications, similar to the preprint findings from the
Mayo Clinic.
20 Innate and immune responses are stronger in females than in males.22 It is
plausible that the more active female immune system may be an advantage in clearing the
virus, but this could be a double-edged sword if the female immune activation produces a
lingering syndrome. This sexually dimorphic immune response is further supported by a recent
study which found that 12.5% of males but only 2.6% of females with severe COVID-19 had
neutralizing immunoglobulin G (IgG) autoantibodies against interferons which could explain
some of the increased male mortality.
23
Limitations
To our knowledge, this is the first report of post-COVID syndrome in young adults and
the first to focus exclusively on non-hospitalized cases. However, this study is not without
limitations. The sample of positive students is small, although consistent with the positivity rates
on campus.
24 Additionally, the lack of age and racial and ethnic diversity in the sample may limit
the generalizability of our findings to more diverse university populations.
Given the low specificity rates of PCR testing, we cannot say with confidence that all
students who tested negative for COVID-19 and were never clinician diagnosed did not have
the illness. As asymptomatic infections are well documented,25,26 it’s possible that a few of our
unaffected students could have also been infected, lowering the proportion with persistent
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symptoms. However, all students who returned to campus were required to get tested prior to
their arrival and the university has been randomly testing up to 1,000 students a week. In our
sample, 14% of those who were asymptomatic and randomly tested reported a positive result,
which reduces the likelihood that a significant number of asymptomatic students are
represented in this sample. Still, even if all participants had been infected, a persistent disabling
syndrome minimally affected 15% of the sample. Finally, this study relies on retrospective self-
report data and longitudinal studies are needed to provide a more nuanced understanding of the
long-term sequelae of post-COVID syndrome.
Conclusion
Our results suggest that young adults are experiencing protracted symptoms and
complications post-COVID. There is overwhelming anecdotal evidence that some who contract
COVID-19 do not recover within 2-3 weeks; however, the proportion of those who experience
post-COVID syndrome at a population level remains unknown. Large-scale population-based
studies in larger, more diverse samples are essential to discerning the magnitude and
characterization of post-COVID syndrome. Until such studies are executed, we urge the medical
and scientific community to consider young adults vulnerable to post-COVID syndrome and to
closely monitor those who contract COVID-19 for lingering viral effects.
Conflict of Interest
NG is the Founder of the Pulmonary Wellness Foundation, under which he opened the
Pulmonary Wellness Foundation’s COVID Rehabilitation & Recovery Clinic. He also serves as a
consultant for PulmonX. All other authors declare no conflicts of interest.
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Acknowledgements
Thank you to the following students for their assistance with data
collection and Qualtrics programming: Jenna Kilian, Julie Mitchell, Piper Sereno, Madeline
Scherer, Maya Quale, Macy Newburg, and Patricia Sabal.
References
1. Bernstein L. Nobody has very clear answers for them’: Doctors search for treatments for
covid-19 long-haulers. The Washington Post 2020, October 16.
2. Ducharme J. Have We Been Thinking About Long-Haul Coronavirus All Wrong? Time
2020, October 16.
. CC-BY-NC-ND 4.0 International licenseIt is made available under a
is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity.(which was not certified by peer review)preprint
The copyright holder for thisthis version posted November 29, 2020. ; https://doi.org/10.1101/2020.11.24.20238261doi: medRxiv preprint
3. Yong E. Longhaulers are redefining COVID-19. The Atlantic 2020, August 19.
4. Carfì A, Bernabei R, Landi F, for the Geme lli Against C-P-ACSG. Persistent Symptoms in
Patients After Acute COVID-19. JAMA 2020;324:603-5.
5. DeBiasi RL, Song X, Delaney M, et al. Severe COVID-19 in Children and Young Adults in
the Washington, DC Metropolitan Region. J Pediatr 2020.
6. Liao J, Fan S, Chen J, et al. Epidemiological and Clinical Characteristics of COVID-19 in
Adolescents and Young Adults. The Innovation 2020;1:100001.
7. Tenforde MW, Kim SS, Lindsell CJ, et al. Symptom Duration and Risk Factors for Delayed
Return to Usual Health Among Outpatients with COVID-19 in a Multistate Health Care
Systems Network Morb Mortal Wkly Rep 2020;69:993-8.
8. Seltzer R, Redden E. COVID Roundup: U of Dayton Freshman Dies. Inside Higher Ed
October 26, 2020.
9. Fisher PW, Desai P, Klotz J, et al. COVID-19 Experiences (COVEX). 2020.
10. Cohen S, Kamarck T, & Mermelstein R. A global measure of perceived stress. Journal of
Health and Social Behavior 2020; 24:386-396
11. Eaton WW, Smith C, Ybarra M, Muntaner C, Tien A. Center for Epidemiologic Studies
Depression Scale: Review and Revision (CESD and CESD-R). The use of psychological
testing for treatment planning and outcomes assessment: Instruments for adults, Volume
3, 3rd ed. Mahwah, NJ, US: Lawrence Erlbaum Associates Publishers; 2004:363-77.
12. Spitzer RL, Kroenke K, Williams JB, Löwe B. A brief measure for assessing generalized
anxiety disorder: the GAD-7. Arch Intern Med 2006;166:1092-7.
13. Lenhard W, Lenhard A. Computation of Effect Sizes. 2017. Retrieved from:
https://www.psychometrica.de/effect_size.html
14. Bixler D, Miller A.D., Mattison CP, et al. SARS-CoV-2–Associated Deaths Among Persons
Aged <21 Years — United States, February 12–July 31, 2020. Morb Mortal Wkly Rep
2020;69:1324–9.
. CC-BY-NC-ND 4.0 International licenseIt is made available under a
is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity.(which was not certified by peer review)preprint
The copyright holder for thisthis version posted November 29, 2020. ; https://doi.org/10.1101/2020.11.24.20238261doi: medRxiv preprint
15. Bishoff K, Project LA. COVID-19 Confirmed Case Longhauler Only Survey: 1,700
Respondants. 2020.
16. Lambert NJ, Corps S. COVID-19 “Long Hauler” Symptoms Survey Report. 2020.
17. Baig AM. Chronic COVID Syndrome: Need for an appropriate medical terminology for
Long-COVID and COVID Long-Haulers. Journal of Medical Virology 2020.
18. Greenhalgh T, Knight M, A’Court C, Buxton M, Husain L. Management of post-acute
covid-19 in primary care. BMJ 2020;370:m3026.
19. Halpin S, O'Connor R, Sivan M. Long COVID and chronic COVID syndromes. Journal of
Medical Virology 2020.
20. Mahase E. Covid-19: What do we know about “long covid”? BMJ 2020;370:m2815.
21. Dennis A, Wamil M, Kapur S, et al. Multi-organ impairment in low-risk individuals with long
COVID. medRxiv 2020:2020.10.14.20212555.
22. Griffith DM, Sharma G, Holliday CS, et al. Men and COVID-19: A Biopsychosocial
Approach to Understanding Sex Differences in Mortality and Recommendations for
Practice and Policy Interventions. Prev Chronic Dis 2020; 17 2020;17.
23. Ghosh S, Klein RS. Sex Drives Dimorphic Immune Responses to Viral Infections. The
Journal of Immunology 2017;198:1782.
24. Bastard P, Rosen LB, Zhang Q, et al. Autoantibodies against type I IFNs in patients with
life-threatening COVID-19. Science 2020;370:eabd4585.
25. Spicker K. New coronavirus cases back in double digits at University of Dayton. Dayton
Daily News 2020 September 9.
26. Gudbjartsson DF, Helgason A, Jonsson H, et al. Spread of SARS-CoV-2 in the Icelandic
Population. New England Journal of Medicine 2020;382:2302-15.
27. Wang Y, Liu Y, Liu L, Wang X, Luo N, Li L. Clinical Outcomes in 55 Patients With Severe
Acute Respiratory Syndrome Coronavirus 2 Who Were Asymptomatic at Hospital
Admission in Shenzhen, China. The Journal of Infectious Diseases 2020;221:1770-4.
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Table 1. Demographic characteristics of the COVID negative, COVID positive recovered, and post-COVID syndrome
groups.
COVID
Negative†
N=58
COVID
Recovered
N=21
Post-COVID
Syndrome
N=22
Age, years — M ± SD 18.91 ± 1.04 18.95 ± 0.74 19.86 ± 3.03
Sex — n (%)
Male 21 (36.2) 7 (33.3) 1 (4.5)
Female 37 (63.8) 14 (66.7) 21 (95.5)
Race — n (%)
Non-White 6 (10.3) 0 (0.00) 1 (4.5)
White 52 (89.7) 21 (100) 21 (95.5)
Ethnicity — n (%)
Hispanic 5 (8.6) 1 (4.8) 1 (4.5)
Not Hispanic 53 (91.4) 20 (95.2) 21 (95.5)
Cigarette Use — n (%)
None 52 (89.7) 21 (100.0) 18 (81.08)
Yes, but not daily 6 (10.3) 0 (0.0) 4 (18.2)
Use of Vaping Devices — n (%)
None 39 (67.2) 14 (66.7) 16 (72.7)
Yes, but not daily 14 (22.1) 6 (28.8) 5 (22.7)
Yes, daily 5 (8.6) 1 (4.8) 1 (4.5)
†Demographic data are only reported for participants for which current symptom data was available.
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is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity.(which was not certified by peer review)preprint
The copyright holder for thisthis version posted November 29, 2020. ; https://doi.org/10.1101/2020.11.24.20238261doi: medRxiv preprint
Table 2. Characteristics of acute COVID-19 experienced by the COVID positive recovered and post-COVID syndrome
groups.
COVID
Recovered
N=21
Post-COVID
Syndrome
N=22
Days post COVID-19 onset, M ± SD 93.50 ± 72.75 79.32± 70.23
Number of COVID-19 symptoms during acute illness, M ± SD 5.24 ± 2.91 9.09 ± 3.91
Overall COVID-19 severity — n (%)
Mild 16 (76.2) 8 (36.4)
Moderate 4 (19) 13 (59.1)
Severe 1 (4.8) 1 (4.5)
Treatment — n (%)
Saw healthcare provider in person (e.g. clinic, doctor’s office, university
health center, urgent care, or emergency room) 2 (9.5) 6 (27.4)
Spoke to a healthcare provider over the phone, by email, or online 4 (19.0) 8 (36.4)
No contact with a healthcare provider 14 (71.4) 8 (36.4)
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The copyright holder for thisthis version posted November 29, 2020. ; https://doi.org/10.1101/2020.11.24.20238261doi: medRxiv preprint
Figure 1. Breakdown of included and excluded study participants
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Figure 2. Symptoms reported by COVID recovered and post-COVID syndrome participants
during acute illness. Bars represent the percentage of each group who endorsed each
symptom.
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The copyright holder for thisthis version posted November 29, 2020. ; https://doi.org/10.1101/2020.11.24.20238261doi: medRxiv preprint
Figure 3. Symptoms endorsed over the past week by post-COVID syndrome participants and
those who tested negative for COVID-
19. Bars represent the percentage of those who endorsed
the symptom in each group.
d
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The copyright holder for thisthis version posted November 29, 2020. ; https://doi.org/10.1101/2020.11.24.20238261doi: medRxiv preprint
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