ABSTRACT
The present study is part of DRAGON, a prospective multicentre European project aimed at improving the diagnosis of COVID-19. The primary aim of this study is to evaluate BAL role in detecting coexisting infections. Secondary aims are BAL impact on the management of COVID patients, characteristics of BAL cellularity in COVID patients, and safety of BAL in COVID patients and for healthcare providers. The study was carried out in 2021. It involved hospitalized patients in non-ICU wards at Careggi University Hospital in Florence, at CHU of Liege and at Morgagni Hospital Bologna University/Forli. All patients underwent BAL for microbiological and cytological analysis. Coinfections were detected in 35 out of 115 patients. In 34% of cases we demonstrated the presence of lymphocytic alveolitis;in 49% of cases a neutrophilic alveolitis and in 7% of cases we observed the presence of a mixed lymphocytic/neutrophilic alveolitis. All patients tested positive for Sars-Cov-2 PCR nasal swabs on admission. BAL was positive for Sars-Cov-2 in all cases, 7 PCR nasal swab performed at the time of the BAL were negative. No major adverse events were demonstrated in the 24 hours after BAL in enrolled patients. There were no cases of infection among health care workers involved in bronchoscopic procedures. Coinfections in COVID-19 patients are common. BAL is a safe tool to identify the presence of coinfections and help clinicians manage these patients correctly. BAL cellularity in covid patients shows a predominance of neutrophils, particularly in cases of co-infection. Our data suggests an earlier negativisation of nasopharyngeal swab compared to BAL.
ABSTRACT
BACKGROUND: The new coronavirus 19 disease (COVID-19) represents the current worldwide emergency. According to past evidence, a simple biomarker, such as low free triiodothyronine (fT3) levels, within the framework of euthyroid sick syndrome (ESS), might help to identify patients with unfavourable outcomes. OBJECTIVE: Evaluation of ESS significance in hospitalized mild COVID-19 patients. DESIGN: Prospective study, from 1 April 2020 to 31 May 2021. PARTICIPANTS: COVID-19 patients with mild disease at hospital admission. MAIN MEASURES: At hospital admission, eligible patients underwent a complete thyroid function evaluation. Subjects with previous thyroid disease or with thyroid-interfering medications were excluded. Levels of fT3 were correlated to biochemical markers and to patient outcome, the latter considered as favourable in the event of infection recovery and unfavourable in the event of death or transfer to an intensive care unit (ICU). KEY RESULTS: Of 600 screened patients, 506 were eligible for this study. Of those, 94 (19%) died during hospitalization and 80 (18%) required a transfer to ICU. The most frequent thyroid disorder was ESS (57%). Admission levels of fT3 were significantly lower within the unfavourable outcome subgroup (p < 0.001) and were negatively associated with several poor prognostic markers, including IL-6 (p < 0.001). In Kaplan-Meier and Cox regression analyses, fT3 was independently associated with poor outcome and death (p = 0.005 and p = 0.037, respectively). A critical fT3 threshold for levels < 2.7 pmol/l (sensitivity 69%, specificity 61%) was associated with a 3.5-fold increased risk of negative outcome (95%CI 2.34-5.34). CONCLUSION: Low fT3 levels, in the framework of ESS, resulted as being a valid predictor of unfavourable outcomes in a very early stage population of COVID-19.