key: cord-0737202-ppk9y79d
authors: Reizine, Florian; Liard, Clémence; Pronier, Charlotte; Thibault, Vincent; Maamar, Adel; Gacouin, Arnaud; Tadié, Jean-Marc
title: Herpesviridae systemic reactivations in COVID-19 associated ARDS patients
date: 2021-11-17
journal: J Hosp Infect
DOI: 10.1016/j.jhin.2021.11.007
sha: aa98bbaeee111c657cf7a7baba1e3c5fb36e27ea
doc_id: 737202
cord_uid: ppk9y79d

nan

The clinical spectrum of Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) infection can lead to acute respiratory distress syndrome (ARDS), associated with immune dysfunctions and prolonged duration of mechanical ventilation (1), both responsible for secondary infection acquisition (MV) (2) . Along these lines, ARDS and prolonged MV are recognized risk-factors for herpesviridae systemic reactivations (HSR) that may affect the outcome of critically ill patients (3, 4) . However, the burden of these infectious events in severe COVID-19 patients remains poorly explored. Hence, in the present study, we describe the clinical features of HSR in COVID-19 associated ARDS patients.

All consecutive ARDS patients with polymerase chain reaction (PCR) confirmed COVID-19 admitted to the medical Intensive Care Unit (ICU) of Rennes University Hospital between March 12, 2020 and April 16, 2021 were reviewed. We retrospectively analyzed patients that were at least weekly monitored for Herpes Simplex Virus (HSV) and Cytomegalovirus (CMV) systemic replication by quantitative real time (RT) PCR. HSR were considered when viral DNA was detected by PCR (The lower limits of detection were 119 IU/ml for CMV with Altona RealStar CMV assay and 165 copies/ml for HSV-1 with Altona RealStar HSV assay). Respiratory samples for bacterial, fungal and viral (CMV, HSV and SARS-CoV-2 RT-PCR) examinations were also collected at least weekly. Ventilator associated pneumonia (VAP) were defined in accordance with international guidelines (5). The Mann-Whitney U test was used for quantitative data and qualitative data were compared using the Chi-square or Fisher-test, as appropriate. All statistical analyses were two-sided, and P values less than 0.05 were considered statistically significant. Analyses were performed using R software version 4.0.4. Our institutional ethical review board approved the study (N 20-56).

Over the study period, 122 patients with COVID-19 associated ARDS were included. Demographic and clinical features are listed in table 1. Patients were mainly male with a median age of 66 years. HSR was observed in 33 patients (27%), 27 patients experienced HSV viremia (21.9%) while 13 patients experienced CMV viremia (10.7%) and seven patients had co-reactivation. Viremia occurred at a median of 12 days following ICU admission (IQR 9-22). As shown in Table 1 , among patients experiencing HSR a wide proportion of them also presented herpesviridae respiratory reactivations while such viral respiratory reactivations were observed less often in patients without HSR (87.9% versus 23.6%; p<0.001) ( Table 1) . Patients with HSR were lymphopenic and experienced positive respiratory RT-PCRs for SARS-CoV-2 for longer durations. As shown in table 1, when analyzing clinical courses, patients with HSR had longer duration of MV and ICU length of stay (LOS). Finally, we also observed higher rates of VAP among these patients.

In this single-center study, 27% of patients admitted to the ICU for COVID-19-associated ARDS developed HSR. Such viral reactivations appeared to be associated with prolonged duration of MV and ICU length of stay, which is consistent with previous studies (3, 4) . We previously showed that respiratory CMV and HSV reactivations are often observed in critically ill COVID-19 patients (6) . Moreover, septic patients, even immunocompetent, are recognized at-risk for developing viral reactivations (7) that may be promoted by sepsis-induced immunosuppression (8) . Although associated with immune defects (i.e prolonged lymphopenia and positive respiratory SARS-CoV-2 RT-PCR), there is no clear evidence that viral reactivations have a direct impact on patients' outcomes in ICU. These infectious events could also be considered as a marker for disease severity (7) . Furthermore, pathophysiology of systemic reactivations is debated. Lungs are known to be major sites of herpesviridae latency. Since here we observed that a wide proportion of patients developing systemic reactivations also experienced previous (or concomitant) respiratory reactivations, we may suppose that respiratory reactivation is the first step before systemic dissemination which may be favored by immunosuppressive mechanisms in patients with sustained SARS-CoV2 infections.

Finally, our results suggest that HSR are common in ARDS COVID-19 patients and may influence the clinical courses of these critical patients. Direct clinical consequences of systemic herpesviridae reactivations and treatment of such infections remain to be investigated. 

Clinical characteristics and day-90 outcomes of 4244 critically ill adults with COVID-19: a prospective cohort study

Fungal and bacterial coinfections increase mortality of severely ill COVID-19 patients

Cytomegalovirus and herpes simplex virus effect on the prognosis of mechanically ventilated patients suspected to have ventilatorassociated pneumonia

Epidemiology of Multiple Herpes Viremia in Previously Immunocompetent Patients With Septic Shock

Management of Adults With Hospital-acquired and Ventilator-associated Pneumonia: 2016 Clinical Practice Guidelines by the Infectious Diseases Society of America and the

Herpes simplex virus and cytomegalovirus reactivations among severe COVID-19 patients

Herpes simplex virus lung infection in patients undergoing prolonged mechanical ventilation

Abbreviations: CRP: C-Reactive Protein; PaO2: arterial oxygen tension; FiO2: Fraction of inspired Oxygen; SAPS II: Simplified Acute Physiology Score II SOFA: Sequential Organ Failure Assessment ECMO: Extracorporeal Membrane Oxygenation; VAP: Ventilator Associated Pneumonia; ICU: Intensive Care Unit Obesity was defined as BMI>30, lymphopenia as lymphocyte count <1.10 9 /L and previous immunosuppression as immunosuppressive treatments including corticosteroids >0.5 mg/kg/day prednisone-equivalent within 30 days prior to inclusion, severe neutropenia <0.5 G/L of neutrophils, HIV seropositivity, bone marrow or solid organ transplantation. Declarations section Ethics approval and consent to participate Our

We thank Leo-Pol Rio for his help in data collection J o u r n a l P r e -p r o o f

The datasets from this study are available from the corresponding author on request.

The authors report no conflict of interest related to this work