Longitudinal Progression of Patients with Long COVID Treated in a Post-COVID Clinic: A Cross-Sectional Survey

Author:

Hurt Ryan T.123,Yadav Siddhant1,Schroeder Darrell R.4,Croghan Ivana T.14ORCID,Mueller Michael R.1,Grach Stephanie L.1ORCID,Aakre Christopher A.1,Gilman Elizabeth A.1,Stephenson Christopher R.1,Overgaard Joshua1,Collins Nerissa M.1,Lawson Donna K.15,Thompson Ann M.1,Natividad Lasonya T.1,Mohamed Elfadil Osman3,Ganesh Ravindra1ORCID

Affiliation:

1. Department of Internal Medicine, Division of General Internal Medicine, Mayo Clinic, Rochester, MN, USA

2. Department of Internal Medicine, Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA

3. Department of Internal Medicine, Division of Endocrinology, Diabetes, Metabolism and Nutrition, Mayo Clinic, Rochester, MN, USA

4. Division of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA

5. Department of Internal Medicine, Division of Hospital Internal Medicine, Mayo Clinic, Rochester, MN, USA

Abstract

Background: In addition to the morbidity and mortality associated with acute infection, COVID-19 has been associated with persistent symptoms (>30 days), often referred to as Long COVID (LC). LC symptoms often cluster into phenotypes, resembling conditions such as fibromyalgia, postural orthostatic tachycardiac syndrome (POTS), and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). LC clinics have been established to best address the needs of LC patients and continuity of care. We developed a cross-sectional survey to assess treatment response through our LC Clinic (LCC). Methods: A 25-question survey (1-10 Likert scale) was expert- and content-validated by LCC clinicians, patients, and patient advocates. The survey assessed LC symptoms and the helpfulness of different interventions, including medications and supplements. A total of 852 LCC patients were asked to complete the survey, with 536 (62.9%) responding. Results: The mean time from associated COVID-19 infection to survey completion was 23.2 ± 6.4 months. The mean age of responders was 52.3 ± 14.1 (63% females). Self-reported symptoms were all significantly improved ( P < .001) from the initial visit to the LCC (baseline) to the time of the follow-up survey. However, only 4.5% (24/536) of patients rated all symptoms low (1-2) at the time of the survey, indicating low levels of full recovery in our cohort. The patients rated numerous interventions as being helpful, including low-dose naltrexone (45/77; 58%), vagal nerve stimulation (18/34; 53%), and fisetin (28/44; 64%). Conclusions: Patients report general improvements in symptoms following the initial LCC visit, but complete recovery rates remain low at 23.2 ± 6.4 months.

Funder

GHR Foundation

National Center for Advancing Translational Sciences

Publisher

SAGE Publications

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