TY - JOUR
T1 - Evolution of neurologic symptoms in non-hospitalized COVID-19 “long haulers”
AU - Ali, Sareen T.
AU - Kang, Anthony K.
AU - Patel, Tulsi R.
AU - Clark, Jeffrey R.
AU - Perez-Giraldo, Gina S.
AU - Orban, Zachary S.
AU - Lim, Patrick H.
AU - Jimenez, Millenia
AU - Graham, Edith L.
AU - Batra, Ayush
AU - Liotta, Eric M.
AU - Koralnik, Igor J.
N1 - Publisher Copyright:
© 2022 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.
PY - 2022/7
Y1 - 2022/7
N2 - Objective: We characterized the evolution of neurologic symptoms and self-perceived recovery of non-hospitalized COVID-19 “long haulers” 6–9 months after their initial Neuro-COVID-19 clinic evaluation. Methods: In this follow-up study on the first 100 patients, 50 SARS-CoV-2 laboratory-positive (SARS-CoV-2+), and 50 laboratory-negative (SARS-CoV-2−), evaluated at our Neuro-COVID-19 clinic between May and November 2020, patients completed phone questionnaires on their neurologic symptoms, subjective impression of recovery and quality of life. Results: Of 52 patients who completed the study (27 SARS-CoV-2+, 25 SARS-CoV-2−) a median 14.8 (range 11–18) months after symptom onset, mean age was 42.8 years, 73% were female, and 77% were vaccinated for SARS-CoV-2. Overall, there was no significant change in the frequency of most neurologic symptoms between first and follow-up evaluations, including “brain fog” (81 vs. 71%), numbness/tingling (69 vs. 65%), headache (67 vs. 54%), dizziness (50 vs. 54%), blurred vision (34 vs. 44%), tinnitus (33 vs. 42%), and fatigue (87 vs. 81%). However, dysgeusia and anosmia decreased overall (63 vs. 27%, 58 vs. 21%, both p < 0.001). Conversely, heart rate and blood pressure variation (35 vs. 56%, p = 0.01) and gastrointestinal symptoms (27 vs. 48%, p = 0.04) increased at follow-up. Patients reported improvements in their recovery, cognitive function, and fatigue, but quality of life measures remained lower than the US normative population (p < 0.001). SARS-CoV-2 vaccination did not have a positive or detrimental impact on cognitive function or fatigue. Interpretation: Non-hospitalized COVID-19 “long haulers” continue to experience neurologic symptoms, fatigue, and compromised quality of life 14.8 months after initial infection.
AB - Objective: We characterized the evolution of neurologic symptoms and self-perceived recovery of non-hospitalized COVID-19 “long haulers” 6–9 months after their initial Neuro-COVID-19 clinic evaluation. Methods: In this follow-up study on the first 100 patients, 50 SARS-CoV-2 laboratory-positive (SARS-CoV-2+), and 50 laboratory-negative (SARS-CoV-2−), evaluated at our Neuro-COVID-19 clinic between May and November 2020, patients completed phone questionnaires on their neurologic symptoms, subjective impression of recovery and quality of life. Results: Of 52 patients who completed the study (27 SARS-CoV-2+, 25 SARS-CoV-2−) a median 14.8 (range 11–18) months after symptom onset, mean age was 42.8 years, 73% were female, and 77% were vaccinated for SARS-CoV-2. Overall, there was no significant change in the frequency of most neurologic symptoms between first and follow-up evaluations, including “brain fog” (81 vs. 71%), numbness/tingling (69 vs. 65%), headache (67 vs. 54%), dizziness (50 vs. 54%), blurred vision (34 vs. 44%), tinnitus (33 vs. 42%), and fatigue (87 vs. 81%). However, dysgeusia and anosmia decreased overall (63 vs. 27%, 58 vs. 21%, both p < 0.001). Conversely, heart rate and blood pressure variation (35 vs. 56%, p = 0.01) and gastrointestinal symptoms (27 vs. 48%, p = 0.04) increased at follow-up. Patients reported improvements in their recovery, cognitive function, and fatigue, but quality of life measures remained lower than the US normative population (p < 0.001). SARS-CoV-2 vaccination did not have a positive or detrimental impact on cognitive function or fatigue. Interpretation: Non-hospitalized COVID-19 “long haulers” continue to experience neurologic symptoms, fatigue, and compromised quality of life 14.8 months after initial infection.
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U2 - 10.1002/acn3.51570
DO - 10.1002/acn3.51570
M3 - Article
C2 - 35607826
AN - SCOPUS:85130446449
SN - 2328-9503
VL - 9
SP - 950
EP - 961
JO - Annals of clinical and translational neurology
JF - Annals of clinical and translational neurology
IS - 7
ER -