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Characteristics and prognosis of bloodstream infection in patients with COVID-19 admitted in the ICU: an ancillary study of the COVID-ICU study

A Correction to this article was published on 11 January 2022

This article has been updated



Patients infected with the severe acute respiratory syndrome coronavirus 2 (SARS-COV 2) and requiring intensive care unit (ICU) have a high incidence of hospital-acquired infections; however, data regarding hospital acquired bloodstream infections (BSI) are scarce. We aimed to investigate risk factors and outcome of BSI in critically ill coronavirus infectious disease-19 (COVID-19) patients.

Patients and methods

We performed an ancillary analysis of a multicenter prospective international cohort study (COVID-ICU study) that included 4010 COVID-19 ICU patients. For the present analysis, only those with data regarding primary outcome (death within 90 days from admission) or BSI status were included. Risk factors for BSI were analyzed using Fine and Gray competing risk model. Then, for outcome comparison, 537 BSI-patients were matched with 537 controls using propensity score matching.


Among 4010 included patients, 780 (19.5%) acquired a total of 1066 BSI (10.3 BSI per 1000 patients days at risk) of whom 92% were acquired in the ICU. Higher SAPS II, male gender, longer time from hospital to ICU admission and antiviral drug before admission were independently associated with an increased risk of BSI, and interestingly, this risk decreased over time. BSI was independently associated with a shorter time to death in the overall population (adjusted hazard ratio (aHR) 1.28, 95% CI 1.05–1.56) and, in the propensity score matched data set, patients with BSI had a higher mortality rate (39% vs 33% p = 0.036). BSI accounted for 3.6% of the death of the overall population.


COVID-19 ICU patients have a high risk of BSI, especially early after ICU admission, risk that increases with severity but not with corticosteroids use. BSI is associated with an increased mortality rate.


As a consequence of severe acute respiratory syndrome coronavirus-2 (SARS-COV 2) epidemic, intensive care units (ICU) worldwide faced a surge of critically ill patients who are at risk of developing bacterial infections, in particular patients requiring mechanical ventilation (MV) [1,2,3]. Although pulmonary bacterial infections (co-infection and nosocomial infections) have been extensively studied in ICU patients [1, 2, 4], conflicting results are reported, due to differences in infection definitions. Conversely, bloodstream infection (BSI) have been less studied, and among the 10 studies published to date [3, 5,6,7,8,9,10,11,12], only 2 focused on ICU patients [3, 9]. The first one was a single-center study that included 78 patients, and found a high incidence of BSI (45 episodes in 31 patients, e.g., 39% of patients with at least one episode) [9]. The second one, a case–cohort study that matched 235 ICU patients with coronavirus disease 2019 (COVID-19) to 235 patients without, found that COVID-19 patients had a higher rate of BSI than non-COVID-19 patients [3]. A third study included 100 BSI out of a cohort of 2005 patients, but although most bacteremia occurred in ICU patients, the baseline population was not exclusively hospitalized in the ICU [11]. Therefore, data regarding BSI (incidence, risk factors and prognosis) specifically in ICU patients are lacking.

We conducted this study to evaluate the incidence, risk factors and prognosis of hospital acquired BSI in patients with SARS-CoV-2 pneumonia hospitalized in the ICU.


Study design, patients

We performed an ancillary analysis of the COVID-ICU study. COVID-ICU was a multi-center, observational, and prospective cohort study conducted in 149 ICUs from 138 centers, across three countries (France, Switzerland, and Belgium) and has been described elsewhere [13]. It received approval from the ethical committee of the French Intensive Care Society (CE-SRLF 20–23) and Swiss and Belgium ethical committees following local regulations. All patients or close relatives were informed that their medical data were anonymously included in the COVID-ICU cohort. Patients and relatives had the possibility not to participate in the study. In case of refusal, the data were not collected accordingly. This manuscript follows the STROBE statement for reporting cohort studies.

For this report, we restricted the analysis to patients in whom the BSI status (yes/no) and day 90 status were known: these data were available for 4010 out of the 4747 patients included in the COVID-ICU study [13]. Data regarding incidence and risk factors were analyzed from this population. In a second set of analysis, to assess the attributable mortality of BSI, we matched 537 patients with BSI to 537 controls (patients without BSI) using a propensity score matching [14].

Data collection

Day-1 was defined as the first day when the patient was in ICU at 10:00 AM. Each day, the study investigators completed a standardized electronic case report form. Baseline information collected at ICU admission were: age, gender, body mass index (BMI), active smoking, Simplified Acute Physiology Score (SAPS) II score [15], Sequential Organ Failure Assessment (SOFA) [16], comorbidities, immunodeficiency (if present), the date of the first symptom, dates and times of hospital and ICU admissions, and presence or not of co-infection at ICU admission [17]. Acute respiratory distress syndrome (ARDS) severity was assessed using Berlin definition [18]. Data collected daily from day 1 to day 15 and then at days 21, 45, 60 and 90 were the following: use of immunomodulatory drugs (interferon, tocilizumab or monoclonal antibodies), antiviral drug, antibiotics, anticoagulants and glucocorticoids; occurrence of BSI or ventilator-associated pneumonia (VAP); procedures during ICU stay (mechanical ventilation (MV), extracorporeal membrane oxygenation (ECMO), renal replacement therapy (RRT)). The number of days at risk for BSI was the number of days in hospital from the 48th hour of stay until ICU discharge for patients without BSI or until the first occurrence of BSI for patients with BSI.

For each positive blood culture, investigators could point out the micro-organisms responsible for infection among a restricted list: Enterobacteriaceae, Pseudomonas aeruginosa, Acinetobacter baumannii, Streptococcus pneumonia, Group A or B Streptococcus, Enteroccoccus spp., methicillin-susceptible Staphylococcus aureus, methicillin-resistant Staphylococcus aureus, Haemophilus influenza, anaerobes or other. Therefore, “other” denotes all micro-organisms not present in the preceding list and were not specified. Since some patients may have polymicrobial blood culture, investigators could declare as many micro-organisms that needed for a single blood sample.

The following outcomes were also recorded: occurrence of thrombosis [19], duration of MV, vital status at ICU and hospital discharge and 28, 60 and 90 days after ICU admission.

Objectives and definition

Primary objective was to describe the incidence of bloodstream infection in patients hospitalized in the ICU for severe COVID-19 pneumonia. Secondary objectives were to describe risk factors for BSI, and to evaluate the attributable mortality of BSI.

Our study focused on hospital acquired BSI which was defined as a positive blood culture occurring ≥ 48 h after hospital admission, whereas ICU-acquired BSI was defined as a positive blood culture if it occurred ≥ 48 h after ICU admission. Therefore, patients were at risk of BSI from 48 h after hospital admission until hospital discharge, either dead or alive. Ventilator-free days at day 90 was defined as the number of days alive and breathing spontaneously (i.e., without mechanical ventilation) at day 90 after ICU admission [20]. ICU-free days at day 90 was defined as the number of days alive and outside the ICU at day 90 after ICU admission.

Statistical analysis

Statistical analysis was performed with the statistical software R 3.4.3. Incidence rate and prevalence were expressed with the 95 percent confidence interval (95% CI). Categorical variables were expressed as number (percentage) and continuous variables as median and interquartile range [IQR]. When appropriate, the chi-square test and the Fisher’s exact test were used to compare categorical variables. The Mann–Whitney U test and the Wilcoxon test were used for continuous variables when applicable. All tests were two-sided, and a P value less than 0.05 was considered statistically significant.

Competitive risk analysis was used to estimate the probability of developing a BSI, with discharge and death being competing events. Using the “cmprsk” package we performed a Fine and Gray model to estimate sub-distribution hazard ratio (sdHR) of ICU death [14]. Therefore, sdHR > 1 indicates that those with exposure will be seen to have a quicker time to BSI. Conversely, a sdHR < 1 indicates a longer time before BSI onset for those exposed. A multivariable cox proportional hazard model was used for survival analysis. Variables associated with event (either BSI or death) with a p value < 0.2 in univariate analysis were included in multivariable model. Of note, for outcome comparison, only the first BSI was taken into account.

Because BSI acquisition was considered as a transition state from admission to discharge or death, patients with BSI were included in the group with BSI from first BSI onset only, to take into account immortal time bias associate with exposure.

To draw unbiased marginal estimates of exposure effect, a propensity-score matched analysis was performed. Propensity score was calculated for each patient and correspond to his probability to develop BSI and to die. As potential confounders, we included for propensity-score calculation all non-redundant variables associated with BSI (event) or death (outcome) with p value ≤ 0.05 in the Fine and Gray (BSI) or Cox model (death) multivariable analysis. Then, using the “MatchIt” package, a k-nearest neighbor algorithm was used for propensity-score matching with a 1:1 ratio: each patient with BSI was matched with 1 patient without BSI with the nearest propensity-score. The balance between matched groups was evaluated by the analysis of the standardized differences before and after weighting. A post-matching difference < 0.1 was considered as an optimal bias reduction. Multivariable Cox proportional hazard model and Kaplan–Meier survival curves were used for survival analysis in the propensity-matched analysis.


Among the 4747 patients included in the COVID-ICU database, 4010 had all data available and were included in the current analysis (Fig. 1). Their median [IQR] age was 62 [54–70] years, with admission SAPS II and SOFA scores of 37 [28–49] and 5 [3–8], respectively. ARDS criteria were objective in 3231 (81%), of whom 776 (19%), 1,635 (41%) and 820 had mild, moderate and severe ARDS, respectively. Finally 283 (7%) had a bacterial co-infection on admission.

Fig. 1
figure 1

Flow chart of the study. ICU, intensive care unit. BSI, bloodstream infection. *1243 (989 in the no BSI group and 245 in the BSI group) patients had missing data among variables used for matching process and were, therefore, excluded from matched analysis

Among these 4,010 patients, 780 (19.5%) experienced a total of 1066 episodes of BSI (1 [1, 2] episode per patient with BSI) through 103,293 patients-days at risk. Therefore, incidence rate was 10.3 BSI per 1000 patients-days. First episode of BSI occurred after a median [IQR] of 9 [5–13] days after hospital admission (Fig. 2). BSI was considered as ICU-acquired in 714 (92%) of patients with at least one BSI episode. Baseline characteristics of patients, according to their status (BSI or not) are displayed in Table 1. Briefly, patients experiencing BSI had higher disease severity on ICU admission, and were more likely to have severe lung disease, as assessed by the ARDS severity and the higher number of patients intubated upon admission. Micro-organisms responsible for infections are given in the Additional file 1: Table S1 (see Online Supplement). Of note, 104 (13%) of the 780 BSI patients relapsed (> 1 BSI episode with the same micro-organism), especially those infected with Methicillin-resistant Staphylococcus aureus (OR 4.2, 95% CI [1.4–12.8]; p = 0.012) or Pseudomonas aeruginosa (OR 2.9, 95% CI [1.2–6.8]; p = 0.017).

Fig. 2
figure 2

Cumulative incidence of bloodstream infection (BSI) as a function of time. ICU: intensive care unit. In 40 out of the 780 patients with BSI, BSI occurred after 21 days in the ICU. Precise day of BSI occurrence for these 40 patients is not known

Table 1 Baseline characteristics of patients according to their status, namely, bloodstream infection or not

Risk factors for BSI

Risk factors for BSI in univariate and multivariable analysis are given in Table 2. Higher SAPS II, male gender, longer time from hospital to ICU admission, antiviral drug before admission, intubation during period at risk for BSI, renal replacement therapy during period at risk for BSI, antibiotic use prior to BSI were independently associated with occurrence of BSI and interestingly, the risk to develop BSI decreased over time (Table 2 and Fig. 2).

Table 2 Risk factors for bloodstream infection, using a Fine and Gray competing risk analysis

Risk factors for day-90 death

Risk factors associated with death at day 90 are reported in Table 3. After adjusting for potential confounders using Cox model multivariable analysis, BSI occurring during hospital stay remained associated with day-90 mortality (HR 1.28, 95% CI 1.05–1.56). In a sensitive analysis in which BSI patients in whom the micro-organism responsible for infection was notified as “others” were excluded (n = 434), BSI remained independently associated with a shorter time to death (aHR1.41, 95% CI 1.08–1.84).

Table 3 Risk factors for death for the whole population

Univariate and multivariable Cox analysis of factors associated with day-90 death in the 780 patients with BSI is shown in Additional file 1: Table S3. Age, frailty scale [21], SOFA score the day of BSI, co-infection at admission, antibiotic and tocilizumab use during period at risk for BSI were associated with increased risk of day-90 death.

Propensity score matched analysis

None redundant baseline characteristics independently associated with day-90 death and/or BSI (i.e., SAPS II, frailty scale, ARDS severity, hypertension, diabetes mellitus, male gender, time from hospital admission to ICU admission, antiviral before admission, intubation before admission, nurse/patients ratio) were included for propensity score calculation. Only patients without missing data regarding these variables were included for matching procedure (Fig. 1). Thereafter 537 patients with BSI were matched with 537 without BSI. Density of propensity scores in each groups are reported in Additional file 1: Fig. S1, and baseline characteristics were well balanced (Additional file 1: Table S2).

Outcomes of matched patients with and without BSI are given in Table 4: patients with BSI had worse outcomes than patients without BSI with longer hospital and ICU length of stay, less day-90 ICU- and ventilator-free days, and higher mortality rate. Probability of death with time was higher among patients with BSI (HR 1.26; 95% CI [1.03–1.54]) (Fig. 3). Relative risk of death was 1.19 and number needed to harm was 16. Therefore, attributable mortality fraction of BSI in the overall population (n = 4010) was 3.6%.

Table 4 Outcomes among 537 patients with bloodstream infection and their 537 propensity-matched patients without bloodstream infection
Fig. 3
figure 3

Kaplan–Meier analysis of survival in the matched patients with (n = 537) and without (n = 537) bloodstream infection (BSI). ICU: intensive care unit


In this study, we show that among a large population of COVID-19 patients requiring ICU, BSI was frequent, occurring in 19.5% of patients. Various risk factors for BSI were identified, with higher SAPS II, male gender, longer time from hospital to ICU admission, antiviral drug before admission, intubation being associated with increased risk of BSI. Another result was that BSI was independently associated with increased day-90 mortality.

Several studies having evaluated BSI in COVID-19 patients have been published to date, most of them mixing ICU and non-ICU patients, with incidence of BSI ranging from 2.7 to 5.6% [5, 6, 8, 10, 11]. Only 2 studies focused on ICU patients: a single-center study found that 31 out of 78 patients (39%) experienced at least one episode of BSI [9]; and a larger multicenter study of 235 COVID-19 patients found a 14.9% incidence of BSI [3]. In this study, the authors matched their COVID-19 patients to 235 ICU patients without COVID-19, and they found a lower rate of BSI in patients without COVID (3.4%). However, they did not evaluate the mortality attributable to BSI. A more recent multicenter case–control study matched, among 2,005 patients with COVID-19, 100 patients with BSI to 100 patients without BSI (matched on age, gender, and severity) [11]. The authors found that immunomodulatory drugs were not associated with an increased risk of BSI, but that BSI was associated with a higher mortality risk. However, this study did not focus on ICU patients. Our results are line with these data and complete them: our incidence of bacteremia was close to that of the largest ICU study published to date [3], and we showed for the first time that ICU-acquired BSI was associate with an excess death rate. This attributable mortality was in line with previous reports in non COVID-19 patients, ranking from 2.1 to 5.2% [14, 22]. Further studies are needed to better understand association between BSI and death in critically ill patients.

Given the high number of patients included in the COVID-ICU study and the high number of BSI, we were able to explore risk factors for BSI in ICU patients. Beyond traditional risk factors, unexpected results were observed for two variables: renal replacement therapy and number of day at risk being associated with lower risk of developing BSI. For the first variable, we assume that patients needing renal replacement therapy have a high probability of early death, competing with BSI occurrence. Similarly, use of epinephrine was not associated with an increased risk of BSI. For the second one, it suggests that patients have a higher risk of BSI soon after admission, while facing a more severe condition, whereas this risk decreases over time, with clinical improvement. Caregivers should be careful about BSI early after admission. Interestingly, corticosteroids use was not associated with increased risk of BSI. In a recent multicenter observational study, use of dexamethasone was not associated with an increased risk of BSI [23]. Similar results were found in another case–control study [11]. Data regarding immunomodulatory drug use and risk of BSI are discordant in ICU patients: a recent randomized placebo-controlled trial found no increased risk of infection with tocilizumab use [24]. Abelenda-Alonso et al. found no association between tocilizumab use and BSI [11], whereas Buetti et al. found an association between its use and BSI; however, in that study, the small sample size limits any firm conclusion [3]. In our study, although few patients received tocilizumab, its use was not associated with an increased risk of BSI. However, those experiencing BSI after tocilizumab use had an increased mortality as compared with BSI patients who did not received this agent. Combined with the lack of effect of anti-IL6 drugs in the most severe patients, their use should be cautiously outweighed in ICU patients. Similarly, BSI patients with previous antibiotic exposure had an increased risk of death. We hypothesized that antibiotic pressure selected resistant microorganisms in which empiric therapy was more likely to fail. This result supports a strict antibiotic stewardship program in COVID-19 setting.

Several limitations of our study should be underlined. First, some data are missing, which is inherent to this kind of multicenter observational study [13]. In particular, the main objective of the COVID-ICU study was not to evaluate infectious complications of ICU patients suffering from COVID-19. Therefore, we lack of important data, such as pathogen responsible for BSI (the list of bacteria available was restricted and for more than 50% of BSI episodes, pathogen responsible for infection is not known). Other relevant missing values were date of BSI occurrence after day 21 (for 40 patients, BSI occurred after day 21 but without additional precision), susceptibility of pathogen responsible for infection (wild type, multi-drug resistant…) appropriateness and duration of antimicrobial treatment. Second, this study was performed during the first wave, between March and May 2020. Since care of COVID-19 ICU patients has changed with improvement over time, and differ from one country to another, results might be different in different countries and among different waves of the pandemic. In particular, with the widespread use of corticosteroids and the increased use of anti-IL-6 drugs, incidence of BSI and outcomes may be different. Third, we defined BSI as a single positive blood culture. For some pathogens such as Staphylococcus epidermidis, 2 blood cultures taken apart are required to define BSI. We, therefore, might have overestimated the rate of BSI. However, the rate of BSI in our study was similar to other reports [3, 11] and lower than other [9]. Moreover, other studies found a high rate of BSI due to Staphylococcus epidermidis [12]. In our study, BSI patients infected with unknown pathogen and those infected with an identified micro-organism had similar outcomes, and should be both similarly considered. Fourth, as BSI occurred during ICU stay, we should acknowledge immortal time bias [25]. However, this bias would lead to underestimation of mortality risk associated with BSI, since patients experiencing this event are those surviving longer enough, whereas those who died early have short time of exposition but were even included in control group.

In conclusion, BSI is a frequent complication of critically ill COVID-19 patients, especially early after ICU admission and is associated with increased severity at admission but not with corticosteroids use. BSI is associated with an increased mortality rate.

Availability of data and materials

The data sets generated during the current study are available from the corresponding author on reasonable request.

Change history


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We thank all investigators from the COVID-ICU Bacteremia Study Group, who were involved in the development of this study: S Nseir, K Razazi, M Fartoukh, G Voiriot, A Rouzé, CE Luyt, V Maxime, P Moine, F Santi, R Bounab, D Annane, N Massart, P Fillatre, F Legay, N Barbarot, F Bruneel, M Amara, S Marque-Juillet, A Ferre.

We gratefully acknowledge all the French, Belgian, and Swiss clinical research centers, COVID-ICU investigators, the medical students, Polytechnic University students, and patients involved in the study. Participating sites and COVID-ICU investigators: CHU Angers, Angers, France (Alain Mercat, Pierre Asfar, François Beloncle, Julien Demiselle), APHP—Hôpital Bicêtre, Le Kremlin-Bicêtre, France (Tài Pham, Arthur Pavot, Xavier Monnet, Christian Richard), APHP—Hôpital Pitié Salpêtrière, Paris, France (Alexandre Demoule, Martin Dres, Julien Mayaux, Alexandra Beurton), CHU Caen Normandie—Hôpital Côte de Nacre, Caen, France, (Cédric Daubin, Richard Descamps, Aurélie Joret, Damien Du Cheyron), APHP—Hôpital Cochin, Paris, France (Frédéric Pene, Jean-Daniel Chiche, Mathieu Jozwiak, Paul Jaubert), APHP—Hôpital Tenon, Paris (France, Guillaume Voiriot, Muriel Fartoukh, Marion Teulier, Clarisse Blayau), CHRU de Brest—La Cavale Blanche, Brest, France (Erwen L'Her, Cécile Aubron, Laetitia Bodenes, Nicolas Ferriere), Centre Hospitalier de Cholet, Cholet, France (Johann Auchabie, Anthony Le Meur, Sylvain Pignal, Thierry Mazzoni), CHU Dijon Bourgogne, Dijon, France (Jean-Pierre Quenot, Pascal Andreu, Jean-Baptiste Roudau, Marie Labruyère), CHU Lille—Hôpital Roger Salengero, Lille, France (Saad Nseir, Sébastien Preau, Julien Poissy, Daniel Mathieu), Groupe Hospitalier Nord Essonne, Longjumeau, France (Sarah Benhamida, Rémi Paulet, Nicolas Roucaud, Martial Thyrault), APHM—Hopital Nord, Marseille, France (Florence Daviet, Sami Hraiech, Gabriel Parzy, Aude Sylvestre), Hôpital de Melun-Sénart, Melun, France (Sébastien Jochmans, Anne-Laure Bouilland, Mehran Monchi), Élément Militaire de Réanimation du SSA, Mulhouse, France (Marc Danguy des Déserts, Quentin Mathais, Gwendoline Rager, Pierre Pasquier), CHU Nantes—Hôpital Hotel Dieu, Nantes, France (Jean Reignier, Amélie Seguin, Charlotte Garret, Emmanuel Canet), CHU Nice—Hôpital Archet, Nice, France (Jean Dellamonica, Clément Saccheri, Romain Lombardi, Yanis Kouchit), Centre Hospitalier d'Orléans, Orléans, France (Sophie Jacquier, Armelle Mathonnet, Mai-Ahn Nay, Isabelle Runge), Centre Hospitalier Universitaire de la Guadeloupe, Pointe-à-Pitre, France (Frédéric Martino, Laure Flurin, Amélie Rolle, Michel Carles), Hôpital de la Milétrie, Poitiers, France (Rémi Coudroy, Arnaud W Thille, Jean-Pierre Frat, Maeva Rodriguez), Centre Hospitalier Roanne, Roanne, France (Pascal Beuret, Audrey Tientcheu, Arthur Vincent, Florian Michelin), CHU Rouen—Hôpital Charles Nicolle, Rouen, France (Fabienne Tamion, Dorothée Carpentier, Déborah Boyer, Christophe Girault ), CHRU Tours—Hôpital Bretonneau, Tours, France (Valérie Gissot, Stéphan Ehrmann, Charlotte Salmon Gandonniere, Djlali Elaroussi), Centre Hospitalier Bretagne Atlantique, Vannes, France (Agathe Delbove, Yannick Fedun, Julien Huntzinger, Eddy Lebas), CHU Liège, Liège, Belgique (Grâce Kisoka, Céline Grégoire, Stella Marchetta, Bernard Lambermont), Hospices Civils de Lyon—Hôpital Edouard Herriot, Lyon, France (Laurent Argaud, Thomas Baudry, Pierre-Jean Bertrand, Auguste Dargent), Centre Hospitalier Du Mans, Le Mans, France (Christophe Guitton, Nicolas Chudeau, Mickaël Landais, Cédric Darreau), Centre Hospitalier de Versailles, Le Chesnay, France (Alexis Ferre, Antoine Gros, Guillaume Lacave, Fabrice Bruneel), Hôpital Foch, Suresnes, France (Mathilde Neuville, Jérôme Devaquet, Guillaume Tachon, Richard Gallot), Hôpital Claude Galien, Quincy sous Senart, France (Riad Chelha, Arnaud Galbois, Anne Jallot, Ludivine Chalumeau Lemoine), GHR Mulhouse Sud-Alsace, Mulhouse, France (Khaldoun Kuteifan, Valentin Pointurier, Louise-Marie Jandeaux, Joy Mootien), APHP—Hôpital Antoine Béclère, Clamart, France (Charles Damoisel, Benjamin Sztrymf), APHP—Hôpital Pitié-Salpêtrière, Paris, France (Matthieu Schmidt, Alain Combes, Juliette Chommeloux, Charles Edouard Luyt), Hôpital Intercommunal de Créteil, Créteil, France (Frédérique Schortgen, Leon Rusel, Camille Jung), Hospices Civils de Lyon—Hôpital Neurologique, Lyon, France (Florent Gobert), APHP—Hôpital Necker, Paris, France (Damien Vimpere, Lionel Lamhaut), Centre Hospitalier Public du Cotentin—Hôpital Pasteur, Cherbourg-en-cotentin, France (Bertrand Sauneuf, Liliane Charrrier, Julien Calus, Isabelle Desmeules), CHU Rennes—Hôpital du Pontchaillou, Rennes, France (Benoît Painvin, Jean-Marc Tadie), CHU Strasbourg—Hôpital Hautepierre, Strasbourg, France (Vincent Castelain, Baptiste Michard, Jean-Etienne Herbrecht, Mathieu Baldacini), APHP—Hôpital Pitié Salpêtrière, Paris, France (Nicolas Weiss, Sophie Demeret, Clémence Marois, Benjamin Rohaut), Centre Hospitalier Territorial Gaston-Bourret, Nouméa, France (Pierre-Henri Moury, Anne-Charlotte Savida, Emmanuel Couadau, Mathieu Série), Centre Hospitalier Compiègne-Noyon, Compiègne, France (Nica Alexandru), Groupe Hospitalier Saint-Joseph, Paris, France (Cédric Bruel, Candice Fontaine, Sonia Garrigou, Juliette Courtiade Mahler), Centre hospitalier mémorial de Saint-Lô, Saint-Lô, France (Maxime Leclerc, Michel Ramakers), Grand Hôpital de l'Est Francilien, Jossigny, France (Pierre Garçon, Nicole Massou, Ly Van Vong, Juliane Sen), Gustave Roussy, Villejuif, France (Nolwenn Lucas, Franck Chemouni, Annabelle Stoclin), Centre Hospitalier Intercommunal Robert Ballanger, Aulnay-sous-Bois, France (Alexandre Avenel, Henri Faure, Angélie Gentilhomme, Sylvie Ricome), Hospices Civiles de Lyon—Hôpital Edouard Herriot, Lyon, France (Paul Abraham, Céline Monard, Julien Textoris, Thomas Rimmele), Centre Hospitalier d'Avignon, Avignon, France (Florent Montini), Groupe Hospitalier Diaconesses—Croix Saint Simon, Paris, France (Gabriel Lejour, Thierry Lazard, Isabelle Etienney, Younes Kerroumi), CHU Clermont-Ferrand—Hôpital Gabriel Montpied, Clermont Ferrand, France (Claire Dupuis, Marine Bereiziat, Elisabeth Coupez, François Thouy), Hôpital d'Instruction des Armées Percy, Clamart, France (Clément Hoffmann, Nicolas Donat, Anne Chrisment, Rose-Marie Blot), CHU Nancy—Hôpital Brabois, Vandoeuvre-les-Nancy, France (Antoine Kimmoun, Audrey Jacquot, Matthieu Mattei, Bruno Levy), Centre Hospitalier de Vichy, Vichy, France (Ramin Ravan, Loïc Dopeux, Jean-Mathias Liteaudon, Delphine Roux), Hopital Pierre Bérégovoy, Nevers, France (Brice Rey, Radu Anghel, Deborah Schenesse, Vincent Gevrey), Centre Hospitalier de Tarbes, Tarbes, France (Jermy Castanera, Philippe Petua, Benjamin Madeux), Hôpitaux Civils de Colmar—Hôpital Louis pasteur, Colmar, France (Otto Hartman), CHU Charleroi—Hôpital Marie Curie, Bruxelles, Belgique (Michael Piagnerelli, Anne Joosten,Cinderella Noel, Patrick Biston), Centre hospitalier de Verdun Saint Mihiel, Saint Mihiel, France (Thibaut Noel), CH Eure-Seine—Hôpital d'Evreux-Vernon, Evreux, France (Gurvan LE Bouar, Messabi Boukhanza, Elsa Demarest, Marie-France Bajolet), Hôpital René Dubos, Pontoise, France (Nathanaël Charrier, Audrey Quenet, Cécile Zylberfajn, Nicolas Dufour), APHP—Hôpital Lariboisière, Paris, France (Buno Mégarbane, Sébastian Voicu, Nicolas Deye, Isabelle Malissin), Centre Hospitalier de Saint-Brieuc, Saint-Brieuc, France (François Legay, Matthieu Debarre, Nicolas Barbarot, Pierre Fillatre), Polyclinique Bordeaux Nord Aquitaine, Bordeaux, France (Bertrand Delord, Thomas Laterrade, Tahar Saghi, Wilfried Pujol), HIA Sainte Anne, Toulon, France (Pierre Julien Cungi, Pierre Esnault, Mickael Cardinale), Grand Hôpital de l'Est Francilien, Meaux, France (Vivien Hong Tuan Ha, Grégory Fleury, Marie-Ange Brou, Daniel Zafimahazo), HIA Robert Picqué, Villenave d'Ornon, France (David Tran-Van, Patrick Avargues, Lisa Carenco), Centre Hospitalier Fontainebleau, Fontainebleau, France (Nicolas Robin, Alexandre Ouali, Lucie Houdou), Hôpital Universitaire de Genève, Genève, Suisse (Christophe Le Terrier, Noémie Suh, Steve Primmaz, Jérome Pugin), APHP—Hôpital Beaujon, Clichy, France (Emmanuel Weiss, Tobias Gauss, Jean-Denis Moyer, Catherine Paugam Burtz), Groupe Hospitalier Bretage Sud, Lorient, France (Béatrice La Combe, Rolland Smonig, Jade Violleau, Pauline Cailliez), Centre Hospitalier Intercommunal Toulon, La Seyne sur Mer, France (Jonathan Chelly), Centre Hospitalier de Dieppe, Dieppe, France (Antoine Marchalot, Cécile Saladin, Christelle Bigot), CHU de Martinique, Fort-de-France, France (Pierre-Marie Fayolle, Jules Fatséas, Amr Ibrahim, Dabor Resiere), Hôpital Fondation Adolphe de Rothchild, Paris, France (Rabih Hage, Clémentine Cholet, Marie Cantier, Pierre Trouiler), APHP—Bichat Claude Bernard, Paris, France (Philippe Montravers, Brice Lortat-Jacob, Sebastien Tanaka, Alexy Tran Dinh), APHP—Hôpital Universitaire Paris Sud, Bicêtre, France (Jacques Duranteau, Anatole Harrois, Guillaume Dubreuil, Marie Werner), APHP—Hôpital Européen Georges Pompidou, Paris, France (Anne Godier, Sophie Hamada, Diane Zlotnik, Hélène Nougue), APHP, GHU Henri Mondor, Créteil, France (Armand Mekontso-Dessap, Guillaume Carteaux, Keyvan Razazi, Nicolas De Prost), APHP—Hôpitaux Universitaires Henri Mondor, Créteil, France (Nicolas Mongardon, Nicolas Mongardon, Meriam Lamraoui, Claire Alessandri, Quentin de Roux), APHP—Hôpital Lariboisière, Paris, France (Charles de Roquetaillade, Benjamin G. Chousterman, Alexandre Mebazaa, Etienne Gayat), APHP—Hôpital Saint-Antoine, Paris, France (Marc Garnier, Emmanuel Pardo, Lea Satre-Buisson, Christophe Gutton), APHP Hôpital Saint-Louis, Paris, France (Elise Yvin, Clémence Marcault, Elie Azoulay, Michael Darmon), APHP—Hôpital Saint-Antoine, Paris, France (Hafid Ait Oufella, Geoffroy Hariri, Tomas Urbina, Sandie Mazerand), APHP—Hôpital Raymond Pointcarré, Garches, France (Nicholas Heming, Francesca Santi, Pierre Moine, Djillali Annane), APHP—Hôpital Pitié Salpêtrière, Paris, France (Adrien Bouglé, Edris Omar, Aymeric Lancelot, Emmanuelle Begot), Centre Hospitalier Victor Dupouy, Argenteuil, France (Gaétan Plantefeve, Damien Contou, Hervé Mentec, Olivier Pajot), CHU Toulouse—Hôpital Rangueil, Toulouse, France (Stanislas Faguer, Olivier Cointault, Laurence Lavayssiere, Marie-Béatrice Nogier), Centre Hospitalier de Poissy, Poissy, France (Matthieu Jamme, Claire Pichereau, Jan Hayon, Hervé Outin), APHP—Hôpital Saint-Louis, Paris, France (François Dépret, Maxime Coutrot, Maité Chaussard, Lucie Guillemet), Clinique du MontLégia, CHC Groupe-Santé, Liège, Belgique (Pierre Goffin, Romain Thouny, Julien Guntz, Laurent Jadot), CHU Saint-Denis, La Réunion, France (Romain Persichini), Centre Hospitalier de Tourcoing, Tourcoing, France (Vanessa Jean-Michel, Hugues Georges, Thomas Caulier), Centre Hospitalier Henri Mondor d'Aurillac, Aurillac, France (Gaël Pradel, Marie-Hélène Hausermann, Thi My Hue Nguyen-Valat, Michel Boudinaud), Centre Hospitalier Saint Joseph Saint Luc, Lyon, France (Emmanuel Vivier, Sylvène Rosseli, Gaël Bourdin, Christian Pommier) Centre Hospitalier de Polynésie Française, Polynésie, France (Marc Vinclair, Simon Poignant, Sandrine Mons), Ramsay Générale de Santé, Hôpital Privé Jacques Cartier, Massy, France (Wulfran Bougouin), Centre Hospitalier Alpes Léman, Contamine sur Arve, France (Franklin Bruna, Quentin Maestraggi, Christian Roth), Hospices Civils de Lyon—Hôpital de la Croix Rousse, Lyon, France (Laurent Bitker, François Dhelft, Justine Bonnet-Chateau, Mathilde Filippelli), Centre Cardiologique du Nord, Saint-Denis, France (Tristan Morichau-Beauchant, Stéphane Thierry, Charlotte Le Roy, Mélanie Saint Jouan), GHU—Hôpital Saint-Anne, Paris, France (Bruno Goncalves, Aurélien Mazeraud, Matthieu Daniel, Tarek Sharshar) CHR Metz—Hôpital Mercy, Metz, France (Cyril Cadoz, Rostane Gaci, Sébastien Gette, Guillaune Louis), APHP—Hôpital Paul Brousse, Villejuif, France (Sophe-Caroline Sacleux, Marie-Amélie Ordan), CHRU Nancy—Hôpital Central, Nancy, France (Aurélie Cravoisy, Marie Conrad, Guilhem Courte, Sébastien Gibot), Centre Hospitalier d’Ajaccio, Ajaccio, France (Younès Benzidi, Claudia Casella, Laurent Serpin, Jean-Lou Setti), Centre Hospitalier de Bourges, Bourges, France (Marie-Catherine Besse, Anna Bourreau), Centre hospitalier de la Côte Basque, Bayonne, France (Jérôme Pillot, Caroline Rivera, Camille Vinclair, Marie-Aline Robaux), Hospices Civils de Lyon—Hôpital de la Croix Rousse, Lyon, France (Chloé Achino, Marie-Charlotte Delignette, Tessa Mazard, Frédéric Aubrun), CH Saint-Malo, Saint-Malo, France (Bruno Bouchet, Aurélien Frérou, Laura Muller, Charlotte Quentin), Centre Hospitalier de Mulhouse, Mulhouse, France (Samuel Degoul), Centre Hospitalier de Briançon, Briançon, France (Xavier Stihle, Claude Sumian, Nicoletta Bergero, Bernard Lanaspre), CHU Nice, Hôpital Pasteur 2, Nice, France (Hervé Quintard, Eve Marie Maiziere), Centre Hospitalier des Pays de Morlaix, Morlaix, France (Pierre-Yves Egreteau, Guillaume Leloup, Florin Berteau, Marjolaine Cottrel), Centre Hospitalier Valence, Valence, France (Marie Bouteloup, Matthieu Jeannot, Quentin Blanc, Julien Saison), Centre Hospitalier Niort, Niort, France (Isabelle Geneau, Romaric Grenot, Abdel Ouchike, Pascal Hazera), APHP—Hôpital Pitié Salpêtrière, Paris, France (Anne-Lyse Masse, Suela Demiri, Corinne Vezinet, Elodie Baron, Deborah Benchetrit, Antoine Monsel), Clinique du Val d'Or, Saint Cloud, France (Grégoire Trebbia, Emmanuelle Schaack, Raphaël Lepecq, Mathieu Bobet), Centre Hospitalier de Béthune, Béthune, France (Christophe Vinsonneau, Thibault Dekeyser, Quentin Delforge, Imen Rahmani), Groupe Hospitalier Intercommunal de la Haute-Saône, Vesoul, France (Bérengère Vivet, Jonathan Paillot, Lucie Hierle, Claire Chaignat, Sarah Valette), Clinique Saint-Martin, Caen, France (Benoït Her, Jennifier Brunet), Ramsay Générale de Santé, Clinique Convert, Bourg en Bresse, France (Mathieu Page, Fabienne Boiste, Anthony Collin), Hôpital Victor Jousselin, Dreux, France(Florent Bavozet, Aude Garin, Mohamed Dlala, Kais Mhamdi), Centre Hospitalier de Troye, Troye, France, (Bassem Beilouny, Alexandra Lavalard, Severine Perez), CHU de ROUEN-Hôpital Charles Nicolle, Rouen, France (Benoit Veber, Pierre-Gildas Guitard, Philippe Gouin, Anna Lamacz), Centre Hospitalier Agen-Nérac, Agen, France (Fabienne Plouvier, Bertrand P Delaborde, Aïssa Kherchache, Amina Chaalal), APHP—Hôpital Louis Mourier, Colombes, France (Jean-Damien Ricard, Marc Amouretti, Santiago Freita-Ramos, Damien Roux), APHP—Hôpital Pitié-Salpêtrière, Paris, France (Jean-Michel Constantin, Mona Assefi, Marine Lecore, Agathe Selves), Institut Mutualiste Montsouris, Paris, France (Florian Prevost, Christian Lamer, Ruiying Shi, Lyes Knani), CHU Besançon—Hôpital Jean Minjoz, Besançon, France, (Sébastien Pili Floury, Lucie Vettoretti), APHP—Hôpital Universitaire Robert-Debré, Paris, France (Michael Levy, Lucile Marsac, Stéphane Dauger, Sophie Guilmin-Crépon), CHU Besançon—Hôpital Jean Minjoz, Besançon, France, (Hadrien Winiszewski, Gael Piton, Thibaud Soumagne, Gilles Capellier); Médipôle Lyon-Villeurbanne, Vileurbanne, France, (Jean-Baptiste Putegnat, Frédérique Bayle, Maya Perrou, Ghyslaine Thao), APHP—Ambroise Paré, Boulogne-Billancourt, France (Guillaume Géri, Cyril Charron, Xavier Repessé, Antoine Vieillard-Baron), CHU Amiens Picardie, Amiens, France (Mathieu Guilbart, Pierre-Alexandre Roger, Sébastien Hinard, Pierre-Yves Macq), Hôpital Nord-Ouest, Villefranche-sur-Saône, France (Kevin Chaulier, Sylvie Goutte), CH de Châlons en Champagne, Châlons en Champagne, France (Patrick Chillet, Anaïs Pitta, Barbara Darjent, Amandine Bruneau), CHU Angers, Angers, France (Sigismond Lasocki, Maxime Leger, Soizic Gergaud, Pierre Lemarie), CHU Grenoble Alpes, Grenoble, France (Nicolas Terzi, Carole Schwebel, Anaïs Dartevel, Louis-Marie Galerneau), APHP—Hôpital Européen Georges Pompidou, Paris, France (Jean-Luc Diehl, Caroline Hauw-Berlemont, Nicolas Péron, Emmanuel Guérot), Hôpital Privé d'Antony, Antony, France (Abolfazl Mohebbi Amoli, Michel Benhamou, Jean-Pierre Deyme, Olivier Andremont), Institut Arnault Tzanck,Saint Laurent du Var, France (Diane Lena, Julien Cady, Arnaud Causeret, Arnaud De La Chapelle) ; Centre Hospitalier d’ Angoulême, Angoulême, France (Christophe Cracco, Stéphane Rouleau, David Schnell) ; Centre Hospitalier de Cahors, Cahors, France (Camille Foucault), Centre hospitalier de Carcassonne, Carcassonne, France (Cécile Lory) ; CHU Nice—Hôpital L’Archet 2, Nice, France (Thibault Chapelle, Vincent Bruckert, Julie Garcia, Abdlazize Sahraoui); Hôpital Privé du Vert Galant, Tremblay-en-France, France (Nathalie Abbosh, Caroline Bornstain, Pierre Pernet); Centre Hospitalier de Rambouillet, Rambouillet, France (Florent Poirson, Ahmed Pasem, Philippe Karoubi); Hopitaux du Léman, Thonon les Bains, France (Virginie Poupinel, Caroline Gauthier, François Bouniol, Philippe Feuchere), Centre Hospitalier Victor Jousselin, Dreux, France (Florent Bavozet, Anne Heron), Hôpital Sainte Camille, Brie sur Marne, France (Serge Carreira, Malo Emery, Anne Sophie Le Floch, Luana Giovannangeli), Hôpital d’instruction des armées Clermont-Tonnerre, Brest, France (Nicolas Herzog, Christophe Giacardi, Thibaut Baudic, Chloé Thill), APHP—Hôpital Pitié Salpêtrière, Paris, France (Said Lebbah, Jessica Palmyre, Florence Tubach, David Hajage); APHP—Hôpital Avicenne, Bobigny, France (Nicolas Bonnet, Nathan Ebstein, Stéphane Gaudry, Yves Cohen); Groupement Hospitalier la Rochelle Ré Amis, La Rochelle, France (Julie Noublanche, Olivier Lesieur); Centre Hospitalier Intercommunal de Mont de Marsan et du Pays des Sources, Mont de Marsan, France (Arnaud Sément, Isabel Roca-Cerezo, Michel Pascal, Nesrine Sma); Centre Hospitalier Départemental de Vendée, La-Roche-Sur-Yon, France (Gwenhaël Colin, Jean-Claude Lacherade, Gauthier Bionz, Natacha Maquigneau); Pôle Anesthésie-Réanimation, CHU Grenoble (Pierre Bouzat, Michel Durand, Marie-Christine Hérault, Jean-Francois Payen)


This study was funded by the Fondation APHP and its donators through the program “Alliance Tous Unis Contre le Virus”, the Direction de la Recherche Clinique et du Développement, and the French Ministry of Health and the foundation of the University hospitals of Geneva, Geneva, Switzerland. The funder had no role in the design and conduct of the study, collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication. This study was funded by Ministère des Affaires Sociales, de la Santé et des Droits des Femmes.

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NM, VL, PF, FB and CEL designed the study, interpreted the data and wrote the manuscript. NM and PF performed statistical analysis. All authors made significant intellectual concept. All authors read and approved the final manuscript.

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Correspondence to Charles-Edouard Luyt.

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Human research ethics committee approval for the study was the ethical committee of the French Intensive Care Society (CE-SRLF 20-23) following our local regulations.

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Not applicable.

Competing interests

CEL has served as consultant for Bayer Healthcare, Carmat and Thermo Fisher Brahms, and received lecture fees from MSD, Aerogen and BioMérieux, outside the submitted work. The other authors have no conflicts of interest to declare in relationship to this manuscript.

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The original online version of this article was revised: The heading of third column in table 4, was mistakenly mentioned as “n = 537” instead of “Patients without BSI n = 537”.

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Supplementary results.

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Massart, N., Maxime, V., Fillatre, P. et al. Characteristics and prognosis of bloodstream infection in patients with COVID-19 admitted in the ICU: an ancillary study of the COVID-ICU study. Ann. Intensive Care 11, 183 (2021).

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