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Neutrophil count predicts clinical outcome in hospitalized COVID‐19 patients: Results from the NOR‐Solidarity trial

2021; Wiley; Volume: 291; Issue: 2 Linguagem: Inglês

10.1111/joim.13377

1365-2796

Trine Kåsine, Anne Ma Dyrhol‐Riise, Andreas Barratt‐Due, Anders Benjamin Kildal, Inge Christoffer Olsen, Kateřina Nezvalová‐Henriksen, Fridtjof Lund‐Johansen, Hedda Hoel, Aleksander Rygh Holten, Anders Tveita, Alexander Mathiessen, Mette Haugli, Ragnhild Eiken, Åse Berg, Asgeir Johannessen, Lars Heggelund, Tuva B. Dahl, Bente Halvorsen, Paweł Mielnik, Lan Ai Kieu Le, Lars Thoresen, Gernot Ernst, Dag Arne Lihaug Hoff, Hilde Skudal, Bård Reiakvam Kittang, Roy Bjørkholt Olsen, Birgitte Tholin, Carl Magnus Ystrøm, Nina Vibeche Skei, Raisa Hannula, Olav Dalgård, Ane‐Kristine Finbråten, Kristian Tonby, Saad Aballi, Fredrik Müller, Kristin Greve‐Isdahl Mohn, Marius Trøseid, Pål Aukrust, Thor Ueland,

Sepsis Diagnosis and Treatment

To the Editor: Despite numerous studies on SARS-CoV-2-induced inflammation, we still lack markers for rapid disease progression with admission to intensive care unit (ICU) or respiratory failure (RF). Few studies have evaluated the prognostic value of routine diagnostic repertoire available at most hospitals. The NOR-Solidarity trial is an independent add-on study to the WHO Solidarity trial, evaluating hydroxychloroquine (HCQ) and remdesivir compared to standard of care in hospitalized COVID-19 patients [1]. We explored whether standard biomarkers in peripheral blood could give information on ICU admission and RF in hospitalized COVID-19 patients. Adult patients admitted to 23 Norwegian hospitals with PCR-confirmed SARS-2-CoV-2 infection were eligible for participation. In this substudy, the routine biochemistry was related to (i) the need for ICU admission or (ii) RF defined as pO2/FiO2 (P/F ratio) < 26.6 kPa during the first 10 days of hospitalization. Routine peripheral blood samples were collected at inclusion and daily until discharge from the hospital, and outpatients were followed up 3 months after discharge. Markers included were C-reactive protein (CRP), ferritin, lactate dehydrogenase (LDH), haemoglobin, fibrinogen, procalcitonin (PCT), D-dimer, platelet count, total white blood cell count, monocyte, neutrophil and lymphocyte count. Exclusion criteria, intervention, ethical statement, details on viral load and SARS-CoV-2 antibodies and statistical analysis are given in the Supporting Information file. The NOR-Solidarity trial design and main results have recently been published. As reported, neither HCQ nor remdesivir had any significant impact on routine biochemistry, and laboratory data from all study arms were pooled prior to analysis [2].Of 184 randomized patients, 35 patients (19%) were admitted to ICU and 60 (33%) patients experienced RF. We first assessed the discriminatory properties of admission levels of markers focusing on markers with AUC ≥ 0.70 (Table S2) and determined cutoffs with Youden's index followed by stepwise Cox regression to identify independent candidates. Thus, ferritin and neutrophil counts were risk factors for ICU admission, whilst PCT, LDH and neutrophil counts were independently associated with RF. Similar results were observed excluding patients with bacterial co-infection (n = 4, Table S3). We calculated a lymphocyte–monocyte–neutrophil score [3], which gave good discrimination, but was not selected over neutrophil counts in multivariable analysis. Precision–recall curves revealed no benefit in combining markers and poor discriminatory properties for ICU admission, whilst combinations of markers gave better discrimination than either marker alone for RF (Fig. 1a). Thus, having above threshold levels of two markers, around 80% of these patients could be identified with close to 70% true positives. Kaplan–Meier and Cox regression analyses confirmed a high risk of RF and ICU admission with increasing number of markers above threshold levels (Fig. 1b). However, as shown in Fig. 1c, no beneficial effects of treatment were observed when comparing patients with less than two versus two or more elevated markers. All markers except neutrophils remained markedly elevated in patients with outcome, with a decline towards the end of the 10-day period (Fig. 1d). A total 121 patients completed 3-month follow-up. As shown in Table S4, a substantial number of patients had inflammatory markers above reference limits, in particular LDH (24%) and CRP (30%). We found no significant impact of treatment on clinical biomarkers at 3 months. Admission levels of several routine biochemical parameters (i.e., neutrophil counts, LDH, PCT and ferritin) gave independent prognostic information on disease severity in hospitalized COVID-19 patients. Flow cytometry of whole blood samples has shown that severe COVID-19 infection is characterized by a dramatic increase in immature neutrophils, associated with augmented systemic inflammation [4]. Moreover, neutrophils have been linked with development of COVID-19-associated acute respiratory distress syndrome and induction of thrombus formation through neutrophil extracellular traps, representing a potential therapeutic target in COVID-19 disease [5, 6]. Both ferritin, reflecting macrophage activation, and LDH, as a general marker of cell damage, correlate with severe disease manifestations and/or unfavourable outcome in COVID-19 patients [7, 8]. PCT is suggested to be a specific marker of bacterial-driven inflammation. However, we detected bacterial co-infections only in a few patients (2.2%) with negligible influence on our findings. Although our study population was small, bacterial infections seem to be rare in hospitalized COVID-19 patients, also reported in a large cohort study [9]. Approximately 25%–30% of the patients had persistent biochemical signs of systemic inflammation even 3 months after discharge, indicative of a long-lasting, low-grade systemic inflammation. Several reports suggest long-term complications in hospitalized COVID-19 patients several months after hospitalization [10]. Our findings suggest that routine biochemistry could give valuable prognostic information in these patients, both during the course of hospitalization and possibly during long-term follow-up. The authors declare no conflict of interest. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. 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