AI Article Synopsis

  • Symptomatic patients who recovered from acute COVID-19 face significant respiratory challenges and require extensive follow-up care, impacting both their health and healthcare systems.
  • A study of 275 patients showed that a high percentage had impaired lung function and chest abnormalities three months post-infection, indicating potential long-term effects of the virus.
  • Anti-S serological levels emerged as a key indicator, correlating with lung diffusion capacity and previous severity of COVID-19, while other serological markers did not show significant links to health outcomes.

Article Abstract

Medical follow-up of symptomatic patients after acute Coronavirus Disease 2019 (COVID-19) results in major burdens on patients and healthcare systems. The value of serological markers as part of this follow-up remains undetermined. We aimed to evaluate the clinical implications of serological markers for follow-up of acute COVID-19. For this purpose, we conducted an observational cohort study of patients 3 months after acute COVID-19. Participants visited a respiratory-clinic between October 2020 and March 2021, and completed pulmonary function tests (PFTs), serological tests, symptom-related questionnaires, and chest CT scans. Overall, 275 patients were included at a median of 82 days (IQR 64-111) post infection. 162 (59%) patients had diffusing capacity for carbon monoxide corrected for hemoglobin (DLCOc) below 80%, and 69 (25%) had bilateral chest abnormalities on CT scan. In multivariate analysis, anti-S levels were an independent predictor for DLCOc (β = - 0.14, p = 0.036). Anti-S levels were also associated with severe COVID-19 and older age, and correlated with anti-nucleocapsid (r = 0.30, p < 0.001) and antibodies to receptor binding domain (RBD, r = 0.37, p < 0.001). Other serological variables were not associated with clinical outcomes. In conclusion, symptomatic patients 3-months after COVID-19 had high respiratory symptomatic burden, in which anti-S levels were significantly associated with previous severe COVID-19 and DLCOc.

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Source
http://dx.doi.org/10.1007/s10238-023-01139-5DOI Listing

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