Bloodstream Infection Risk, Incidence, and Deaths for Hospitalized Patients during Coronavirus Disease Pandemic

Hospital-acquired infections are emerging major concurrent conditions during the coronavirus disease (COVID-19) pandemic. We conducted a retrospective review of hospitalizations during March‒October 2020 of adults tested by reverse transcription PCR for severe acute respiratory syndrome coronavirus 2. We evaluated associations of COVID-19 diagnosis with risk for laboratory-confirmed bloodstream infections (LCBIs, primary outcome), time to LCBI, and risk for death by using logistic and competing risks regression with adjustment for relevant covariates. A total of 10,848 patients were included in the analysis: 918 (8.5%) were given a diagnosis of COVID-19, and 232 (2.1%) had LCBIs during their hospitalization. Of these patients, 58 (25%) were classified as having central line‒associated bloodstream infections. After adjusting for covariates, COVID-19‒positive status was associated with higher risk for LCBI and death. Reinforcement of infection control practices should be implemented in COVID-19 wards, and review of superiority and inferiority ranking methods by National Healthcare Safety Network criteria might be needed.

Hospital-acquired infections are emerging major concurrent conditions during the coronavirus disease (COVID- 19) pandemic. We conducted a retrospective review of hospitalizations during March-October 2020 of adults tested by reverse transcription PCR for severe acute respiratory syndrome coronavirus 2. We evaluated associations of COVID-19 diagnosis with risk for laboratory-confi rmed bloodstream infections (LCBIs, primary outcome), time to LCBI, and risk for death by using logistic and competing risks regression with adjustment for relevant covariates. A total of 10,848 patients were included in the analysis: 918 (8.5%) were given a diagnosis of COVID-19, and 232 (2.1%) had LCBIs during their hospitalization. Of these patients, 58 (25%) were classifi ed as having central line-associated bloodstream infections. After adjusting for covariates, COVID-19-positive status was associated with higher risk for LCBI and death. Reinforcement of infection control practices should be implemented in COVID-19 wards, and review of superiority and inferiority ranking methods by National Healthcare Safety Network criteria might be needed.

laboratory-confirmed bloodstream infection (LCBI).
We also aimed to identify other potential risk factors for LCBI in hospitalized COVID-19 patients. We hypothesized that COVID-19 patients would have greater odds of acquiring an LCBI than hospitalized patients without COVID-19 after adjusting for relevant confounders, and that other risk factors might also be identified, which might serve as targets for interventions to reduce co-infection rates in this vulnerable group.

Study Design and Cohort
We conducted a retrospective cohort study of adult hospitalizations during March 25-October 27, 2020, at an academic, tertiary, acute-care facility in Miami, Florida, USA, which lacks capacity to give care with extracorporeal membrane oxygenation. Patients were included in the cohort if they had >1 reverse transcription PCR completed; patients could be included more than once if they were admitted to the hospital more than once over the study period. During the study period, all patients were screened by reverse transcription PCR before hospital admission. Although there were no specific exclusion criteria, the facility does not offer pediatric or obstetric services, so pregnant woman and patients <18 years of age were not included. A restricted cohort of patients that had central venous catheters at any point during their hospital stay was also considered.

Exposure and Outcomes
Our exposure of interest was COVID-19 positivity (determined by SARS-CoV-2 PCR testing) during the hospital stay. Patients who had >1 positive test result (from 7 days before admission up until discharge with or without preceding negative test results) were considered positive for COVID-19. Our primary outcome was LCBI. Secondary outcomes were death, time to LCBI (time from hospital admission to first positive blood culture per patient admission), and development of central line-associated bloodstream infection (CLABSI) evaluated by using the restricted cohort of patients who had a central venous catheter. We defined LCBIs and CLABSIs according to National Healthcare Safety Network (NHSN) 2020 criteria (9). In brief, LCBI is defined in these criteria as a single positive blood culture or molecular test result for a pathogen or 2 positive blood cultures for a commensal organism. CLABSI is defined as an LCBI associated with a central venous catheter in place for >2 calendar days (9).

Data Sources and Variables
We obtained information for each patient from the hospital system's electronic medical record by using EPIC software (https://www.epic.com). In addition to COVID-19 infection status and outcomes (including organism identification), we abstracted information on demographics (age, sex, race, primary insurance provider), organisms isolated from blood cultures, chronic health conditions, Elixhauser comorbidity conditions (10), body mass index, severity of acute illness (sequential organ failure assessment score [SOFA] during hospital day 1) (11), renal replacement therapy (either intermittent or continuous), invasive mechanical ventilation, care in the ICU, prone positioning (including persons using mechanical ventilation), central venous catheters, urinary catheters, systemic corticosteroids, tocilizumab, and remdesivir. For each of the resources other than prone positioning, we identified whether they were used and the total duration of use. For prone positioning, we were able to identify only use (not duration or timing of use). We also obtained data on hospital length of stay.

Statistical Analysis and Ethics
We described the cohort by using standard summary statistics. We made compared characteristics by outcome by using χ 2 and Kruskal-Wallis tests as appropriate. Our primary analysis was a risk for LCBI assessment by using multivariable logistic regression modeling with an exposure of COVID-19 status. We included all data elements except prone positioning, remdesivir, and tocilizumab as covariables, and resource elements were modeled as receipt/nonreceipt before development of LCBI (or hospital discharge if no LCBI). To ensure our results would not be confounded by deaths in hospitals, we recreated the same models for hospital survivors and decedents separately.
To consider secondary outcomes, we first used multivariable Cox proportional hazards modeling with censoring at hospital discharge and a competing risk for death to assess the association of COVID-19 positivity and time to LCBI. We then constructed a multivariable logistic regression model to assess the association of COVID-19 positivity with risk for death by hospital discharge. For this model, we included days of resource use as covariates.
We also constructed 3 models to evaluate for LCBI that developed >2 calendar days from admission, indicated as LCBI HAI. Next, we reconstructed the models (for our primary and 2 secondary outcomes) by using the restricted cohort of patients who had used central venous catheters to assess risk for and time to CLABSI and death. Finally, to identify risk factors for infection among COVID-19 patients, we constructed 3 multivariable logistic regression models: for LCBI among all COVID-19 patients, for LCBI HAI among all COVID-19 patients, and for CLABSI among COVID-19 patients who had central venous catheters.
Because of a large number of patients who had missing data regarding calculation of SOFA, we imputed this score for each model (using multivariable regression modeling, including all covariates and outcome). We conducted 2 sensitivity analyses to assess the robustness of our primary analysis: only patients with an available SOFA score, and all patients but not including SOFA as a model covariate.
Study approval was obtained from the University of Miami Institutional Review Board (#20200739). We performed all analyses by using the programming language R (R Foundation for Statistical Computing, https://www.r-project.org). Results were considered significant if p<0.05. Because we did not adjust for multiple comparisons, we considered all nonprimary analyses to be hypothesis generating.

Non-COVID-19 Risk Factors for LCBI, LCBI HAI, and CLABSI
In a subgroup analysis of only COVID-19 patients, we found that previous central line use was associated with an increased risk for LCBI (OR 8.11, 95% CI 2.40-37.3; p = 0.002) and LCBI HAI (OR 11.7, 95% CI 2.94-78.2; p = 0.002) ( Table 3). We found no major associations with use of remdesivir, steroids, or tocilizumab. Another finding in the subgroup analysis was that prone positioning did not have any major associations with risk for outcomes in patients who had COVID-19.

Discussion
Before the COVID-19 pandemic, HAIs were well-recognized as a cause of death (12   pandemic on HAIs and their outcomes, particularly LCBIs (3,13). Using data for >10,000 patients hospitalized after SARS-CoV-2 testing, we found that COVID-19 positivity was associated with a 3.88-fold increased odds of developing an LCBI. This finding might be related to COVID-19 itself or other variables not accounted for in our cohort, such as changes in supplementary nursing care or changes in infection control practices associated with the care of these patients. In addition, isolates responsible for LCBI and CLABSI in COVID-19 patients versus non-COVID-19 patients show major differences with regards to type and number of organisms. Prone positioning has proven benefits for patients who have non-COVID-19-associated acute respiratory distress syndrome requiring invasive mechanical ventilation (14). Studies have noted increases in use of prone positioning as treatment for critical care patients who have influenza (15) and, in recent months, data have emerged suggesting benefits of prone positioning for ventilated patients (16)(17)(18)(19)(20) and nonventilated patients who have COVID-19 (21). Although potential adverse effects, such as pressure ulcers (22) and deep venous thromboses (23), have been observed with prone positioning, we did not find any statistical association with our primary outcomes.
The strengths of our study stem from detailed clinical data (including organism identification) and severity of illness information (both acute and chronic) available to us. Our study is limited by a high rate of missing SOFA score data. However, the robustness of our results to sensitivity analyses, in which we excluded patients who had missing SOFA data and excluded SOFA as a model covariate, suggests that this limitation had minimal effect on our findings. Although our sample included >10,000 patients (of whom 918 patients had COVID-19), we included only patients from a single hospital, which might limit the generalizability of our results. In addition, several of the factors included in our models occurred after COVID-19 testing (our exposure), making it plausible that these factors are mediators rather than confounders of the association of COVID-19 with outcomes.
Another limitation of the study was our inability to include admission symptoms or central venous catheter insertion sites in the analysis. This limitation was largely caused by inconsistent documentation of these data points in a nondiscrete format in our electronic medical record. We also were not able to address markers of hospital operational stressors that might have varied over the time period of our study and might effect patient outcomes. Collinearity of clinical variables included in the models was also a concern. However, our evaluation identified only 2 variables that had higher correlation coefficients (previous mechanical ventilation and ICU stay) (Appendix Figure 4). A final limitation was the difficulty in analyzing dose and type of steroids and antimicrobial drugs given before and after bloodstream infections, as well as timing and duration of prone positioning.
As more data emerge regarding increases in HAIs during the COVID-19 pandemic (24), we propose that these challenges warrant reevaluation of the NHSN SIR methods for LCBI and CLABSI in COVID-19designated care areas. Further studies are needed to clarify the relationship between COVID-19 and non-LCBI infections to ascertain whether prone positioning, COVID-19-specific treatments, changes in adherence to infection control practices, or a combination of these variables might be associated with higher rates of other HAIs.
In conclusion, inpatient management of patients who have COVID-19 has brought many changes in treatment protocols and associated challenges, including adherence to infection control best practices. Established infection control best practices should be reemphasized among COVID-19 patients who might be at higher risk for LCBI, adding a concurrent condition to an already vulnerable population.